Obesity: A neuroimmunometabolic perspective
Abstract
Neuroimmunology and immunometabolism are burgeoning topics of study, but the intersection of these two fields is scarcely considered. This interplay is particularly prevalent within adipose tissue, where immune cells and the sympathetic nervous system (SNS) have an important role in metabolic homeostasis and pathology, namely in obesity. In the present Review, we first outline the established reciprocal adipose-SNS relationship comprising the neuroendocrine loop facilitated primarily by adipose tissue-derived leptin and SNS-derived noradrenaline. Next, we review the extensive crosstalk between adipocytes and resident innate immune cells as well as the changes that occur in these secretory and signalling pathways in obesity. Finally, we discuss the effect of SNS adrenergic signalling in immune cells and conclude with exciting new research demonstrating an immutable role for SNS-resident macrophages in modulating SNS-adipose crosstalk. We posit that the latter point constitutes the existence of a new field - neuroimmunometabolism.
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Induction of beige adipocytes by exercise or functional enhancement of existing brown adipose tissue improves total energy expenditure and insulin sensitivity, contributing to fat and weight loss.
“induction of beige adipocytes by exercise or functional enhancement of existing BAT has shown to improve total energy expenditure and insulin sensitivity, contributing to fat and weight loss [16,17,18,19]”
IL-6 directly increases GLP-1 in mice and stimulates the sympathetic nervous system, increasing white adipose tissue lipolysis and browning and brown adipose tissue thermogenesis.
“It has been shown to directly increase GLP-1 in mice [73] and to stimulate SNS, increasing WAT lipolysis and “browning” and BAT thermogenesis [19].”
IL-6 enhances SNS output.
“enhancing SNS output [19] (3b)”
Cites
Obesity is associated with macrophage accumulation in adipose tissue
Weisberg, S. P., McCann, D., Desai, M., Rosenbaum, M., Leibel, R. L., & Ferrante, A. W. (2003) · Journal of Clinical Investigation · doi:10.1172/jci200319246 · Cited by 10,041 · see citing works
The metabolic phenotype in obesity: Fat mass, body fat distribution, and adipose tissue function
Goossens, G. H. (2017) · Obesity Facts · doi:10.1159/000471488 · Cited by 8,481 · see citing works
Adipose Expression of Tumor Necrosis Factor-α: Direct Role in Obesity-Linked Insulin Resistance
Hotamisligil, G. S., Shargill, N. S., & Spiegelman, B. M. (1993) · Science · doi:10.1126/science.7678183 · Cited by 7,518 · see citing works
Xu, H., Barnes, G. T., Yang, Q., Tan, G., Yang, D., Chou, C. J., Sole, J., Nichols, A., Ross, J. S., Tartaglia, L. A., et al. (2003) · Journal of Clinical Investigation · doi:10.1172/jci200319451 · Cited by 6,760 · see citing works
Obesity induces a phenotypic switch in adipose tissue macrophage polarization
Lumeng, C. N., Bodzin, J. L., & Saltiel, A. R. (2007) · Journal of Clinical Investigation · doi:10.1172/jci29881 · Cited by 4,664 · see citing works
Identification and Importance of Brown Adipose Tissue in Adult Humans
Cypess, A. M., Lehman, S., Williams, G., Tal, I., Rodman, D., Goldfine, A. B., Kuo, F. C., Palmer, E. L., Tseng, Y.-H., Doria, A., et al. (2009) · New England Journal of Medicine · doi:10.1056/nejmoa0810780 · Cited by 4,399 · see citing works
Mutation of the mouse klotho gene leads to a syndrome resembling ageing
Kuro-o, M., Matsumura, Y., Aizawa, H., Kawaguchi, H., Suga, T., Utsugi, T., Ohyama, Y., Kurabayashi, M., Kaname, T., Kume, E., et al. (1997) · Nature · doi:10.1038/36285 · Cited by 3,837 · see citing works
TLR4 links innate immunity and fatty acid-induced insulin resistance
Shi, H., Kokoeva, M. V., Inouye, K., Tzameli, I., Yin, H., & Flier, J. S. (2006) · Journal of Clinical Investigation · doi:10.1172/jci28898 · Cited by 3,690 · see citing works
Kim, H. J., Park, S. Y., Choi, Y. J., Han, S. J., Lee, K. W., & Kim, D. J. (2013) · Hormone Research in Paediatrics · doi:10.1159/000348848 · Cited by 3,061 · see citing works
Targeted disruption of the melanocortin-4 receptor results in obesity in mice
Huszar, D., Lynch, C. A., Fairchild-Huntress, V., Dunmore, J. H., Fang, Q., Berkemeier, L. R., Gu, W., Kesterson, R. A., Boston, B. A., Cone, R. D., et al. (1997) · Cell · doi:10.1016/s0092-8674(00)81865-6 · Cited by 3,030 · see citing works
Macrophages, inflammation, and insulin resistance
Olefsky, J. M., & Glass, C. K. (2010) · Annual Review of Physiology · doi:10.1146/annurev-physiol-021909-135846 · Cited by 2,733 · see citing works
Kanda, H. (2006) · Journal of Clinical Investigation · doi:10.1172/jci26498 · Cited by 2,682 · see citing works
The adipocyte-secreted protein Acrp30 enhances hepatic insulin action
Berg, A. H., Combs, T. P., Du, X., Brownlee, M., & Scherer, P. E. (2001) · Nature Medicine · doi:10.1038/90992 · Cited by 2,526 · see citing works
Leptin activates anorexigenic POMC neurons through a neural network in the arcuate nucleus
Cowley, M. A., Smart, J. L., Rubinstein, M., Cerdán, M. G., Diano, S., Horvath, T. L., Cone, R. D., & Low, M. J. (2001) · Nature · doi:10.1038/35078085 · Cited by 2,356 · see citing works
Protection from obesity-induced insulin resistance in mice lacking TNF-α function
Uysal, K. T., Wiesbrock, S. M., Marino, M. W., & Hotamisligil, G. S. (1997) · Nature · doi:10.1038/39335 · Cited by 2,234 · see citing works
Inflammatory mechanisms linking obesity and metabolic disease
Saltiel, A. R., & Olefsky, J. M. (2017) · Journal of Clinical Investigation · doi:10.1172/jci92035 · Cited by 2,212 · see citing works
Fruebis, J., Tsao, T., Javorschi, S., Ebbets-Reed, D., Erickson, M., Yen, F. T., Bihain, B. E., & Lodish, H. F. (2001) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.98.4.2005 · Cited by 1,987 · see citing works
Stein, M., Keshav, S., Harris, N., & Gordon, S. (1992) · The Journal of experimental medicine · doi:10.1084/jem.176.1.287 · Cited by 1,960 · see citing works
Role of melanocortinergic neurons in feeding and the agouti obesity syndrome
Fan, W., Boston, B. A., Kesterson, R. A., Hruby, V. J., & Cone, R. D. (1997) · Nature · doi:10.1038/385165a0 · Cited by 1,902 · see citing works
The role of neuropeptide Y in the antiobesity action of the obese gene product
Stephens, T. W., Basinski, M., Bristow, P. K., Bue-Valleskey, J. M., Burgett, S. G., Craft, L., Hale, J., Hoffmann, J., Hsiung, H. M., Kriauciunas, A., et al. (1995) · Nature · doi:10.1038/377530a0 · Cited by 1,498 · see citing works
CCR2 modulates inflammatory and metabolic effects of high-fat feeding
Weisberg, S. P., Hunter, D., Huber, R., Lemieux, J., Slaymaker, S., Vaddi, K., Charo, I., Leibel, R. L., & Jr., A. W. F. (2006) · Journal of Clinical Investigation · doi:10.1172/jci24335 · Cited by 1,497 · see citing works
CCR2 modulates inflammatory and metabolic effects of high-fat feeding
Weisberg, S. P. (2006) · Journal of Clinical Investigation · doi:10.1172/jci24335c1 · Cited by 1,424 · see citing works
Eosinophils Sustain Adipose Alternatively Activated Macrophages Associated with Glucose Homeostasis
Wu, D., Molofsky, A. B., Liang, H.-E., Ricardo-González, R. R., Jouihan, H. A., Bando, J. K., Chawla, A., & Locksley, R. M. (2011) · Science · doi:10.1126/science.1201475 · Cited by 1,361 · see citing works
The role of estrogens in control of energy balance and glucose homeostasis
Mauvais-Jarvis, F., Clegg, D. J., & Hevener, A. L. (2013) · Endocrine Reviews · doi:10.1210/er.2012-1055 · Cited by 1,329 · see citing works
Yokota, T., Oritani, K., Takahashi, I., Ishikawa, J., Matsuyama, A., Ouchi, N., Kihara, S., Funahashi, T., Tenner, A. J., Tomiyama, Y., et al. (2000) · Blood · doi:10.1182/blood.v96.5.1723 · Cited by 1,294 · see citing works
Metabolic Instruction of Immunity
Buck, M. D., Sowell, R., Kaech, S. M., & Pearce, E. L. (2017) · Cell · doi:10.1016/j.cell.2017.04.004 · Cited by 1,233 · see citing works
Monocyte chemoattractant protein 1 in obesity and insulin resistance
Sartipy, P., & Loskutoff, D. J. (2003) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1133870100 · Cited by 1,199 · see citing works
Mountjoy, K. G., Mortrud, M. T., Low, M. J., Simerly, R. B., & Cone, R. D. (1994) · Molecular Endocrinology · doi:10.1210/mend.8.10.7854347 · Cited by 1,157 · see citing works
Structure-Function Studies of the Adipocyte-secreted Hormone Acrp30/Adiponectin
Pajvani, U. B., Du, X., Combs, T. P., Berg, A. H., Rajala, M. W., Schulthess, T., Engel, J., Brownlee, M., & Scherer, P. E. (2003) · Journal of Biological Chemistry · doi:10.1074/jbc.m207198200 · Cited by 1,090 · see citing works
Agouti protein is an antagonist of the melanocyte-stimulating-hormone receptor
Lu, D., Willard, D. H., Patel, I. R., Kadwell, S. H., Overton, L. K., Kost, T., Luther, M., Chen, W., Woychik, R. P., Wilkison, W. O., et al. (1994) · Nature · doi:10.1038/371799a0 · Cited by 1,075 · see citing works
Type 2 innate lymphoid cells control eosinophil homeostasis
Nussbaum, J. C., Dyken, S. J. V., von Moltke, J., Cheng, L. E., Mohapatra, A., Molofsky, A. B., Thornton, E. E., Krummel, M. F., Chawla, A., Liang, H.-E., et al. (2013) · Nature · doi:10.1038/nature12526 · Cited by 1,069 · see citing works
Alternatively activated macrophages produce catecholamines to sustain adaptive thermogenesis
Nguyen, K. D., Qiu, Y., Cui, X., Goh, Y. P. S., Mwangi, J., David, T., Mukundan, L., Brombacher, F., Locksley, R. M., & Chawla, A. (2011) · Nature · doi:10.1038/nature10653 · Cited by 1,038 · see citing works
Nguyen, M. T. A., Favelyukis, S., Nguyen, A.-K., Reichart, D., Scott, P. A., Jenn, A., Liu-Bryan, R., Glass, C. K., Neels, J. G., & Olefsky, J. M. (2007) · Journal of Biological Chemistry · doi:10.1074/jbc.m706762200 · Cited by 1,035 · see citing works
Activation of Human Brown Adipose Tissue by a β3-Adrenergic Receptor Agonist
Cypess, A. M., Weiner, L. S., Roberts‐Toler, C., Franquet, E., Kessler, S., Kahn, P. A., English, J., Chatman, K., Trauger, S. A., Doria, A., et al. (2015) · Cell Metabolism · doi:10.1016/j.cmet.2014.12.009 · Cited by 1,024 · see citing works
Receptor-mediated regional sympathetic nerve activation by leptin.
Haynes, W. G., Morgan, D. A., Walsh, S. A., Mark, A. L., & Sivitz, W. I. (1997) · Journal of Clinical Investigation · doi:10.1172/jci119532 · Cited by 979 · see citing works
Neutrophils mediate insulin resistance in mice fed a high-fat diet through secreted elastase
Talukdar, S., Oh, D. Y., Bandyopadhyay, G. K., Li, D., Xu, J., McNelis, J., Lu, M. M., Li, P., Yan, Q., Zhu, Y., et al. (2012) · Nature Medicine · doi:10.1038/nm.2885 · Cited by 966 · see citing works
Fibrosis and adipose tissue dysfunction.
Sun, K., Tordjman, J., Clément, K., & Scherer, P. E. (2013) · Cell Metabolism · doi:10.1016/j.cmet.2013.06.016 · Cited by 960 · see citing works
Fetuin-A acts as an endogenous ligand of TLR4 to promote lipid-induced insulin resistance
Pal, D., Dasgupta, S., Kundu, R., Maitra, S., Das, G., Mukhopadhyay, S., Ray, S., Majumdar, S. S., & Bhattacharya, S. (2012) · Nature Medicine · doi:10.1038/nm.2851 · Cited by 922 · see citing works
Lumeng, C. N.-K., DelProposto, J. B., Westcott, D. J., & Saltiel, A. R. (2008) · Diabetes · doi:10.2337/db08-0872 · Cited by 919 · see citing works
Leptin Increases Hypothalamic Pro-opiomelanocortin mRNA Expression in the Rostral Arcuate Nucleus
Schwartz, M. W., Seeley, R. J., Woods, S. C., Weigle, D. S., Campfield, L. A., Burn, P., & Baskin, D. G. (1997) · Diabetes · doi:10.2337/diab.46.12.2119 · Cited by 879 · see citing works
Molofsky, A. B., Nussbaum, J. C., Liang, H.-E., Dyken, S. J. V., Cheng, L. E., Mohapatra, A., Chawla, A., & Locksley, R. M. (2013) · The Journal of Experimental Medicine · doi:10.1084/jem.20121964 · Cited by 879 · see citing works
Qiu, Y., Nguyen, K. D., Odegaard, J. I., Cui, X., Tian, X., Locksley, R. M., Palmiter, R. D., & Chawla, A. (2014) · Cell · doi:10.1016/j.cell.2014.03.066 · Cited by 869 · see citing works
Kratz, M., Coats, B. R., Hisert, K. B., Hagman, D. K., Mutskov, V. J., Peris, E., Schoenfelt, K. Q., Kuzma, J. N., Larson, I. A., Billing, P. S., et al. (2014) · Cell Metabolism · doi:10.1016/j.cmet.2014.08.010 · Cited by 828 · see citing works
Adiponectin induces the anti-inflammatory cytokines IL-10 and IL-1RA in human leukocytes
Wolf, A. M., Wolf, D. G. F., Rumpold, H. F., Enrich, B., & Tilg, H. (2004) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2004.08.145 · Cited by 821 · see citing works
Leptin Activates Hypothalamic CART Neurons Projecting to the Spinal Cord
Elias, C. F., Lee, C., Kelly, J., Aschkenasi, C. J., Ahima, R. S., Couceyro, P. R., Kuhar, M. J., Saper, C. B., & Elmquist, J. K. (1998) · Neuron · doi:10.1016/s0896-6273(00)80656-x · Cited by 809 · see citing works
Cawthorn, W. P., & Sethi, J. K. (2007) · FEBS Letters · doi:10.1016/j.febslet.2007.11.051 · Cited by 792 · see citing works
Reduced Adipose Tissue Oxygenation in Human Obesity
Pasarica, M., Sereda, O. R., Redman, L. M., Albarado, D. C., Hymel, D. T., Roan, L. E., Rood, J. C., Burk, D. H., & Smith, S. R. (2009) · Diabetes · doi:10.2337/db08-1098 · Cited by 786 · see citing works
βAR Signaling Required for Diet-Induced Thermogenesis and Obesity Resistance
Bachman, E. S., Dhillon, H., Zhang, C.-Y., Cinti, S., Bianco, A. C., Kobilka, B. K., & Lowell, B. B. (2002) · Science · doi:10.1126/science.1073160 · Cited by 782 · see citing works
A Switch from White to Brown Fat Increases Energy Expenditure in Cancer-Associated Cachexia
Petruzzelli, M., Schweiger, M., Schreiber, R., Campos‐Olivas, R., Tsoli, M., Allen, J., Swarbrick, M. M., Rose‐John, S., Rincón, M., Robertson, G. R., et al. (2014) · Cell Metabolism · doi:10.1016/j.cmet.2014.06.011 · Cited by 752 · see citing works
Leptin Receptor Immunoreactivity in Chemically Defined Target Neurons of the Hypothalamus
Håkansson, M., Brown, H., Ghilardi, N., Skoda, R. C., & Meister, B. (1998) · Journal of Neuroscience · doi:10.1523/jneurosci.18-01-00559.1998 · Cited by 731 · see citing works
Weight loss and lipolysis promote a dynamic immune response in murine adipose tissue
Kosteli, A., Sugaru, E., Haemmerle, G., Martin, J. F., Lei, J., Zechner, R., & Ferrante, A. W. (2010) · Journal of Clinical Investigation · doi:10.1172/jci42845 · Cited by 726 · see citing works
Obesity, Inflammation, Toll-Like Receptor 4 and Fatty Acids
Rogero, M. M., & Calder, P. C. (2018) · Nutrients · doi:10.3390/nu10040432 · Cited by 720 · see citing works
Kang, K., Reilly, S. M., Karabacak, V., Gangl, M. R., Fitzgerald, K., Hatano, B., & Lee, C.-H. (2008) · Cell Metabolism · doi:10.1016/j.cmet.2008.04.002 · Cited by 699 · see citing works
Cousin, B., Cinti, S., Morroni, M., Raimbault, S., Ricquier, D., Pénicaud, L., & Casteilla, L. (1992) · Journal of Cell Science · doi:10.1242/jcs.103.4.931 · Cited by 665 · see citing works
Selective deletion of leptin receptor in neurons leads to obesity
Cohen, P., Zhao, C., Cai, X., Montez, J. M., Rohani, S., Feinstein, P. G., Mombaerts, P., & Friedman, J. M. (2001) · Journal of Clinical Investigation · doi:10.1172/jci13914 · Cited by 657 · see citing works
The role of peripheral immune cells in the CNS in steady state and disease
Prinz, M., & Priller, J. (2017) · Nature Neuroscience · doi:10.1038/nn.4475 · Cited by 657 · see citing works
Adiponectin Promotes Macrophage Polarization toward an Anti-inflammatory Phenotype
Ohashi, K., Parker, J. L., Ouchi, N., Higuchi, A., Vita, J. A., Gokce, N., Pedersen, A. A., Kalthoff, C., Tullin, S., Sams, A., et al. (2010) · Journal of Biological Chemistry · doi:10.1074/jbc.m109.088708 · Cited by 646 · see citing works
UCP1 in Brite/Beige Adipose Tissue Mitochondria Is Functionally Thermogenic
Shabalina, I. G., Petrovič, N., de Jong, J. M. A., Kalinovich, A., Cannon, B., & Nedergaard, J. (2013) · Cell Reports · doi:10.1016/j.celrep.2013.10.044 · Cited by 637 · see citing works
Greenstein, A. S., Khavandi, K., Withers, S., Sonoyama, K., Clancy, O., Jeziorska, M., Laing, I., Yates, A. P., Pemberton, P. W., Malik, R. A., et al. (2009) · Circulation · doi:10.1161/circulationaha.108.821181 · Cited by 616 · see citing works
Local Proliferation of Macrophages Contributes to Obesity-Associated Adipose Tissue Inflammation
Amano, S. U., Cohen, J. L., Vangala, P., Tencerová, M., Nicoloro, S. M. C., Yawe, J. C., Shen, Y., Czech, M., & Aouadi, M. (2014) · Cell Metabolism · doi:10.1016/j.cmet.2013.11.017 · Cited by 613 · see citing works
GLP-1 agonism stimulates brown adipose tissue thermogenesis and browning through hypothalamic AMPK
Beiroa, D., Imbernon, M., Gallego, R., Senra, A., Herranz, D., Villarroya, F., Serrano, M., Fernø, J., Salvador, J., Escalada, J., et al. (2014) · Diabetes · doi:10.2337/db14-0302 · Cited by 602 · see citing works
Human Leptin Stimulates Proliferation and Activation of Human Circulating Monocytes
Santos‐Álvarez, J., Goberna, R., & Sánchez‐Margalet, V. (1999) · Cellular Immunology · doi:10.1006/cimm.1999.1490 · Cited by 600 · see citing works
Lee, Y. S., Kim, J.-W., Osborne, O., Oh, D. Y., Sasik, R., Schenk, S., Chen, A., Chung, H., Murphy, A., Watkins, S. M., et al. (2014) · Cell · doi:10.1016/j.cell.2014.05.012 · Cited by 598 · see citing works
Distinct Hypothalamic Neurons Mediate Estrogenic Effects on Energy Homeostasis and Reproduction
Xu, Y., Nedungadi, T. P., Zhu, L., Sobhani, N., Irani, B. G., Davis, K. E., Zhang, X., Zou, F., Gent, L. M., Hahner, L. D., et al. (2011) · Cell Metabolism · doi:10.1016/j.cmet.2011.08.009 · Cited by 597 · see citing works
Saturated fatty acids activate TLR-mediated proinflammatory signaling pathways
Huang, S., Rutkowsky, J. M., Snodgrass, R. G., Ono‐Moore, K. D., Schneider, D. A., Newman, J. W. I., Adams, S. H., & Hwang, D. H. (2012) · Journal of Lipid Research · doi:10.1194/jlr.d029546 · Cited by 591 · see citing works
Selective deletion of leptin receptor in neurons leads to obesity
Cohen, P., Zhao, C., Cai, X., et al. (2001) · Journal of Clinical Investigation · doi:10.1172/jci200113914 · Cited by 554 · see citing works
Ruan, H., Hacohen, N., Golub, T. R., Parijs, L. V., & Lodish, H. F. (2002) · Diabetes · doi:10.2337/diabetes.51.5.1319 · Cited by 531 · see citing works
Proinflammatory Phenotype of Perivascular Adipocytes
Chatterjee, T. K., Stoll, L. L., Denning, G. M., Harrelson, A. L., Blomkalns, A. L., Idelman, G., Rothenberg, F. G., Neltner, B. S., Romig‐Martin, S. A., Dickson, E. W., et al. (2009) · Circulation Research · doi:10.1161/circresaha.108.182998 · Cited by 526 · see citing works
Melanocortin receptors in leptin effects
Seeley, R. J., Yagaloff, K. A., Fisher, S. L., Burn, P., Thiele, T. E., van Dijk, G., Baskin, D. G., & Schwartz, M. W. (1997) · Nature · doi:10.1038/37016 · Cited by 522 · see citing works
Pirzgalska, R. M., Seixas, E., Seidman, J. S., Link, V. M., Martínez‐Sánchez, N., Mahú, I., Mendes, R., Gres, V., Kubasova, N., Morris, I., et al. (2017) · Nature Medicine · doi:10.1038/nm.4422 · Cited by 497 · see citing works
Sympathetic Neuro-adipose Connections Mediate Leptin-Driven Lipolysis
Zeng, W., Pirzgalska, R. M., Pereira, M. M. A., Kubasova, N., Barateiro, A., Seixas, E., Lu, Y.-H., Kozlova, A., Voss, H., Martins, G. G., et al. (2015) · Cell · doi:10.1016/j.cell.2015.08.055 · Cited by 490 · see citing works
Sfrp5 Is an Anti-Inflammatory Adipokine That Modulates Metabolic Dysfunction in Obesity
Ouchi, N., Higuchi, A., Ohashi, K., Oshima, Y., Gokce, N., Shibata, R., Akasaki, Y., Shimono, A., & Walsh, K. (2010) · Science · doi:10.1126/science.1188280 · Cited by 490 · see citing works
Leptin targets in the mouse brain
Scott, M. M., Lachey, J. L., Sternson, S. M., Lee, C. E., Elias, C. F., Friedman, J. M., & Elmquist, J. K. (2009) · Journal of Comparative Neurology · doi:10.1002/cne.22025 · Cited by 484 · see citing works
Adipocyte lipolysis and insulin resistance
Morigny, P., Houssier, M., Mouisel, É., & Langin, D. (2015) · Biochimie · doi:10.1016/j.biochi.2015.10.024 · Cited by 471 · see citing works
Adiponectin differentially regulates cytokines in porcine macrophages
Wulster-Radcliffe, M. C., Ajuwon, K. M., Wang, J., Christian, J. A., & Spurlock, M. E. (2004) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2004.02.130 · Cited by 464 · see citing works
Sympathetic and sensory innervation of brown adipose tissue
Bartness, T. J., Vaughan, C. H., & Song, C. K. (2010) · International Journal of Obesity · doi:10.1038/ijo.2010.182 · Cited by 459 · see citing works
Saberi, M., Woods, N.-B., de Luca, C., Schenk, S., Lu, J. C., Bandyopadhyay, G., Verma, I. M., & Olefsky, J. M. (2009) · Cell Metabolism · doi:10.1016/j.cmet.2009.09.006 · Cited by 456 · see citing works
Inflammasome-driven catecholamine catabolism in macrophages blunts lipolysis during ageing
Camell, C. D., Sander, J., Spadaro, O., Lee, A., Nguyen, K. Y., Wing, A., Goldberg, E. L., Youm, Y.-H., Brown, C. W., Elsworth, J., et al. (2017) · Nature · doi:10.1038/nature24022 · Cited by 456 · see citing works
Estradiol Regulates Brown Adipose Tissue Thermogenesis via Hypothalamic AMPK
de Morentin, P. B. M., González‐García, I., Martins, L., Lage, R., Fernández-Mallo, D., Martínez‐Sánchez, N., Ruíz-Pino, F., Liu, J. T., Morgan, D. A., Pinilla, L., et al. (2014) · Cell Metabolism · doi:10.1016/j.cmet.2014.03.031 · Cited by 452 · see citing works
Role of innate and adaptive immunity in obesity-associated metabolic disease
McLaughlin, T., Ackerman, S. E., Shen, L., & Engleman, E. G. (2017) · Journal of Clinical Investigation · doi:10.1172/jci88876 · Cited by 444 · see citing works
CNS origins of the sympathetic nervous system outflow to brown adipose tissue
Bamshad, M., Song, C. K., & Bartness, T. J. (1999) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.1999.276.6.r1569 · Cited by 437 · see citing works
Orexigen-sensitive NPY/AgRP pacemaker neurons in the hypothalamic arcuate nucleus
van den Top, M., Lee, K., Whyment, A. D., Blanks, A. M., & Spanswick, D. (2004) · Nature Neuroscience · doi:10.1038/nn1226 · Cited by 435 · see citing works
Peraldi, P., Hotamisligil, G. S., Buurman, W. A., White, M. F., & Spiegelman, B. M. (1996) · Journal of Biological Chemistry · doi:10.1074/jbc.271.22.13018 · Cited by 412 · see citing works
Adrenergic activation of triiodothyronine production in brown adipose tissue
Silva, J. E., & Larsen, P. R. (1983) · Nature · doi:10.1038/305712a0 · Cited by 401 · see citing works
Browning of Subcutaneous White Adipose Tissue in Humans after Severe Adrenergic Stress
Sidossis, L. S., Porter, C. C., Saraf, M. K., Børsheim, E., Radhakrishnan, R. S., Chao, T., Ali, A., Chondronikola, M., Mlcak, R. P., Finnerty, C. C., et al. (2015) · Cell Metabolism · doi:10.1016/j.cmet.2015.06.022 · Cited by 394 · see citing works
Production of Chemokines by Perivascular Adipose Tissue
Henrichot, E., Juge-Aubry, C. E., Pernin, A., Pache, J., Velebit, V., Dayer, J., Meda, P., Chizzolini, C., & Meier, C. A. (2005) · Arteriosclerosis Thrombosis and Vascular Biology · doi:10.1161/01.atv.0000188508.40052.35 · Cited by 382 · see citing works
β 2 -adrenergic receptor–mediated negative regulation of group 2 innate lymphoid cell responses
Moriyama, S., Brestoff, J. R., Flamar, A.-L., Moeller, J. B., Klose, C. S. N., Rankin, L. C., Yudanin, N. A., Monticelli, L. A., Putzel, G., Rodewald, H.-R., et al. (2018) · Science · doi:10.1126/science.aan4829 · Cited by 379 · see citing works
Brown adipose tissue in the parametrial fat pad of the mouse
Young, P., Arch, J. R. S., & Ashwell, M. (1984) · FEBS Letters · doi:10.1016/0014-5793(84)80822-4 · Cited by 377 · see citing works
Kreier, F., Fliers, E., Voshol, P. J., van Eden, C. G., Havekes, L. M., Kalsbeek, A., Heijningen, C. L. V., Sluiter, A. A., Mettenleiter, T. C., Romijn, J. A., et al. (2002) · Journal of Clinical Investigation · doi:10.1172/jci15736 · Cited by 363 · see citing works
Adrenergic regulation of innate immunity: a review
Scanzano, A., & Cosentino, M. (2015) · Frontiers in Pharmacology · doi:10.3389/fphar.2015.00171 · Cited by 360 · see citing works
Effect of Diet and Cold Exposure on Norepinephrine Turnover in Brown Adipose Tissue of the Rat
Young, J. B., Saville, E., Rothwell, N. J., Stock, M. J., & Landsberg, L. (1982) · Journal of Clinical Investigation · doi:10.1172/jci110541 · Cited by 356 · see citing works
Hui, X. H., Gu, P., Zhang, J., Nie, T., Pan, Y., Wu, D., Feng, T., Zhong, C., Wang, Y., Lam, K. S. L., et al. (2015) · Cell Metabolism · doi:10.1016/j.cmet.2015.06.004 · Cited by 349 · see citing works
Central nervous system origins of the sympathetic nervous system outflow to white adipose tissue
Bamshad, M., Aoki, V. T., Adkison, M., Warren, W. S., & Bartness, T. J. (1998) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.1998.275.1.r291 · Cited by 344 · see citing works
Kreier, F., Fliers, E., Voshol, P. J., van Eden, C. G., Havekes, L. M., Kalsbeek, A., Heijningen, C. L. V., Sluiter, A. A., Mettenleiter, T. C., Romijn, J. A., et al. (2002) · Journal of Clinical Investigation · doi:10.1172/jci0215736 · Cited by 331 · see citing works
Fischer, K., Ruiz, H. H., Jhun, K., Finan, B., Oberlin, D. J., van der Heide, V., Kalinovich, A., Petrovič, N., Wolf, Y., Clemmensen, C., et al. (2017) · Nature Medicine · doi:10.1038/nm.4316 · Cited by 326 · see citing works
Role of hypoxia in obesity-induced disorders of glucose and lipid metabolism in adipose tissue.
Yin, J., Gao, Z., He, Q., Zhou, D., Guo, Z., & Ye, J. (2009) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.90760.2008 · Cited by 319 · see citing works
LTB4 promotes insulin resistance in obese mice by acting on macrophages, hepatocytes and myocytes
Li, P., Oh, D. Y., Bandyopadhyay, G. K., Lagakos, W., Talukdar, S., Osborn, O., Johnson, A., Chung, H., Mayoral, R., Maris, M., et al. (2015) · Nature Medicine · doi:10.1038/nm.3800 · Cited by 318 · see citing works
Hypothalamic AMPK: a canonical regulator of whole-body energy balance
López, M., Nogueiras, R., Tena‐Sempere, M., & Diéguez, C. (2016) · Nature Reviews Endocrinology · doi:10.1038/nrendo.2016.67 · Cited by 312 · see citing works
Lee, B.-C., Kim, M., Pae, M., Yamamoto, Y., Eberlé, D., Shimada, T., Kamei, N., Park, H.-S., Sasorith, S., Woo, J. R., et al. (2016) · Cell Metabolism · doi:10.1016/j.cmet.2016.03.002 · Cited by 303 · see citing works
Ruan, H., Miles, P. D. G., Ladd, C. M., Ross, K. N., Golub, T. R., Olefsky, J. M., & Lodish, H. F. (2002) · Diabetes · doi:10.2337/diabetes.51.11.3176 · Cited by 297 · see citing works
Leptin revisited: its mechanism of action and potential for treating diabetes
Coppari, R., & Bjørbæk, C. (2012) · Nature Reviews Drug Discovery · doi:10.1038/nrd3757 · Cited by 295 · see citing works
Short-term Cold Acclimation Recruits Brown Adipose Tissue in Obese Humans
Hanssen, M. J. W., van der Lans, A. A. J. J., Brans, B. T., Joris Hoeks, J., Jardon, K. M. C., Schaart, G., Mottaghy, F. M., Schrauwen, P., & Lichtenbelt, W. D. V. M. (2015) · Diabetes · doi:10.2337/db15-1372 · Cited by 293 · see citing works
Sensory and sympathetic nervous system control of white adipose tissue lipolysis
Bartness, T. J., Shrestha, Y. B., Vaughan, C. H., Schwartz, G. J., & Song, C. K. (2010) · Molecular and Cellular Endocrinology · doi:10.1016/j.mce.2009.08.031 · Cited by 289 · see citing works
Chi, J., Wu, Z., Choi, C. H. J., Nguyen, L., Tegegne, S., Ackerman, S. E., Crane, A., Marchildon, F., Tessier-Lavigne, M., & Cohen, P. (2018) · Cell Metabolism · doi:10.1016/j.cmet.2017.12.011 · Cited by 285 · see citing works
Leptin and brain–adipose crosstalks
Caron, A., Lee, S., Elmquist, J. K., & Gautron, L. (2018) · Nature Reviews Neuroscience · doi:10.1038/nrn.2018.7 · Cited by 284 · see citing works
O-GlcNAc Transferase Enables AgRP Neurons to Suppress Browning of White Fat
Ruan, H.-B., Dietrich, M. O., Liu, Z.-W., Zimmer, M. R., Li, M.-D., Singh, J. P., Zhang, K., Yin, R., Wu, J., Horvath, T. L., et al. (2014) · Cell · doi:10.1016/j.cell.2014.09.010 · Cited by 281 · see citing works
Macrophage recruitment in obese adipose tissue
Bai, Y., & Sun, Q. (2015) · Obesity Reviews · doi:10.1111/obr.12242 · Cited by 279 · see citing works
Pedersen, S. B., Kristensen, K., Hermann, P. A., Katzenellenbogen, J. A., & Richelsen, B. (2004) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/jc.2003-031327 · Cited by 276 · see citing works
Mattioli, B., Straface, E., Quaranta, M. G., Giordani, L., & Viora, M. (2005) · The Journal of Immunology · doi:10.4049/jimmunol.174.11.6820 · Cited by 267 · see citing works
Orexin Is Required for Brown Adipose Tissue Development, Differentiation, and Function
Sellayah, D., Bharaj, P., & Sikder, D. (2011) · Cell Metabolism · doi:10.1016/j.cmet.2011.08.010 · Cited by 259 · see citing works
Saturated Fatty Acids Do Not Directly Stimulate Toll-Like Receptor Signaling
Erridge, C., & Samani, N. J. (2009) · Arteriosclerosis Thrombosis and Vascular Biology · doi:10.1161/atvbaha.109.194050 · Cited by 258 · see citing works
Inouye, K. E., Shi, H., Howard, J. K., Daly, C. H., Lord, G. M., Rollins, B. J., & Flier, J. S. (2007) · Diabetes · doi:10.2337/db07-0425 · Cited by 252 · see citing works
Brown-adipose-tissue macrophages control tissue innervation and homeostatic energy expenditure
Wolf, Y., Boura‐Halfon, S., Cortese, N., Haimon, Z., Shalom, H. S., Kuperman, Y., Kalchenko, V., Brandis, A. S., David, E., Segal-Hayoun, Y., et al. (2017) · Nature Immunology · doi:10.1038/ni.3746 · Cited by 251 · see citing works
Leptin: a potential regulator of polymorphonuclear neutrophil bactericidal action?
Caldefie‐Chezet, F., Poulin, A.-M., Tridon, A., Sion, B., & Vasson, M. (2001) · Journal of Leukocyte Biology · doi:10.1189/jlb.69.3.414 · Cited by 249 · see citing works
Zhang, Y., Kerman, I. A., Laque, A., Nguyen, P., Faouzi, M., Louis, G. W., Jones, J. C., Rhodes, C. J., & Münzberg, H. (2011) · Journal of Neuroscience · doi:10.1523/jneurosci.3223-10.2011 · Cited by 240 · see citing works
Fujisaka, S., Usui, I., Ikutani, M., Aminuddin, A., Takikawa, A., Tsuneyama, K., Mahmood, A., Goda, N., Nagai, Y., Takatsu, K., et al. (2013) · Diabetologia · doi:10.1007/s00125-013-2885-1 · Cited by 239 · see citing works
Cereijo, R., Gavaldà-Navarro, A., Cairó, M., Quesada-López, T., Villarroya, J., Morón-Ros, S., Sánchez-Infantes, D., Peyrou, M., Iglesias, R., Mampel, T., et al. (2018) · Cell Metabolism · doi:10.1016/j.cmet.2018.07.015 · Cited by 236 · see citing works
Bäckberg, M., Hervieu, G. J., Wilson, S., & Meister, B. (2002) · European Journal of Neuroscience · doi:10.1046/j.0953-816x.2001.01859.x · Cited by 235 · see citing works
Hams, E., Locksley, R. M., McKenzie, A. N. J., & Fallon, P. G. (2013) · The Journal of Immunology · doi:10.4049/jimmunol.1301176 · Cited by 232 · see citing works
Martínez‐Sánchez, N., Seoane‐Collazo, P., Contreras, C., Varela, L., Villarroya, J., Rial‐Pensado, E., Buqué, X., Aurrekoetxea, I., Delgado, T. C., Vázquez‐Martínez, R., et al. (2017) · Cell Metabolism · doi:10.1016/j.cmet.2017.06.014 · Cited by 231 · see citing works
Expression of leptin receptors and response to leptin stimulation of human natural killer cell lines
Zhao, Y., Sun, R., You, L., Gao, C., & Tian, Z. (2003) · Biochemical and Biophysical Research Communications · doi:10.1016/s0006-291x(02)02838-3 · Cited by 229 · see citing works
Sympathetic innervation of white adipose tissue and its regulation of fat cell number
Bowers, R. R., Festuccia, W. T., Song, C. K., Shi, H., Migliorini, R. H., & Bartness, T. J. (2004) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.00558.2003 · Cited by 221 · see citing works
Emerging Complexities in Adipocyte Origins and Identity
Sánchez-Gurmaches, J., Hung, C., & Guertin, D. A. (2016) · Trends in Cell Biology · doi:10.1016/j.tcb.2016.01.004 · Cited by 215 · see citing works
Leptin Regulation of Agrp and Npy mRNA in the Rat Hypothalamus
Körner, J., Savontaus, E., Chua, S. C., Leibel, R. L., & Wardlaw, S. L. (2001) · Journal of Neuroendocrinology · doi:10.1046/j.1365-2826.2001.00716.x · Cited by 213 · see citing works
An update on physical health and economic consequences of overweight and obesity
Chu, D., Nguyệt, N. T. M., Dinh, T. C., Lien, N. V. T., Nguyen, K. H., Ngọc, V. T. N., Tao, Y., Sơn, L. H., Le, D., Nga, V. B., et al. (2018) · Diabetes & Metabolic Syndrome Clinical Research & Reviews · doi:10.1016/j.dsx.2018.05.004 · Cited by 212 · see citing works
Bartness, T. J., & Song, C. K. (2007) · Journal of Lipid Research · doi:10.1194/jlr.r700006-jlr200 · Cited by 209 · see citing works
Murano, I., Barbatelli, G., Giordano, A., & Cinti, S. (2009) · Journal of Anatomy · doi:10.1111/j.1469-7580.2008.01001.x · Cited by 208 · see citing works
Tan, K. S., Nackley, A. G., Satterfield, K., Maixner, W., Diatchenko, L., & Flood, P. M. (2007) · Cellular Signalling · doi:10.1016/j.cellsig.2006.06.007 · Cited by 204 · see citing works
Jiang, H., Ding, X., Cao, Y., Wang, H., & Zeng, W. (2017) · Cell Metabolism · doi:10.1016/j.cmet.2017.08.016 · Cited by 204 · see citing works
Tsatsanis, C., Zacharioudaki, V., Androulidaki, A., Dermitzaki, E., Charalampopoulos, I., MINAS, V., Gravanis, A., & Margioris, A. N. (2005) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2005.07.197 · Cited by 203 · see citing works
Leptin induction of UCP1 gene expression is dependent on sympathetic innervation
Scarpace, P. J., & Matheny, M. E. (1998) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.1998.275.2.e259 · Cited by 202 · see citing works
Neural connections between the hypothalamus and the liver
Uyama, N., Geerts, A., & Reynaert, H. (2004) · The Anatomical Record Part A: Discoveries in Molecular, Cellular, and Evolutionary Biology · doi:10.1002/ar.a.20086 · Cited by 201 · see citing works
Immunologic and endocrine functions of adipose tissue: implications for kidney disease
Zhu, Q., & Scherer, P. E. (2018) · Nature Reviews Nephrology · doi:10.1038/nrneph.2017.157 · Cited by 200 · see citing works
Energy balance regulation by thyroid hormones at central level
López, M., Álvarez, C. V., Nogueiras, R., & Diéguez, C. (2013) · Trends in Molecular Medicine · doi:10.1016/j.molmed.2013.04.004 · Cited by 199 · see citing works
Burn Induces Browning of the Subcutaneous White Adipose Tissue in Mice and Humans
Patsouris, D., Qi, P., Abdullahi, A., Stanojcic, M., Chen, P., Parousis, A., Amini‐Nik, S., & Jeschke, M. G. (2015) · Cell Reports · doi:10.1016/j.celrep.2015.10.028 · Cited by 186 · see citing works
Dahlman, I., Forsgren, M., Sjögren, A., Nordström, E. A., Kaaman, M., Näslund, E., Attersand, A., & Arner, P. (2006) · Diabetes · doi:10.2337/db05-1421 · Cited by 184 · see citing works
Nogueiras, R., Pérez-Tilve, D., Veyrat-Durebex, C., Morgan, D. A., Varela, L., Haynes, W. G., Patterson, J. T., Disse, E., Pfluger, P. T., López, M., et al. (2009) · The Journal of Neuroscience · doi:10.1523/jneurosci.5977-08.2009 · Cited by 182 · see citing works
TNF-α-Induced Insulin Resistance In Vivo and Its Prevention by Troglitazone
Miles, P. D. G., Romeo, O. M., Higo, K., Cohen, A., Rafaat, K., & Olefsky, J. M. (1997) · Diabetes · doi:10.2337/diab.46.11.1678 · Cited by 182 · see citing works
Catecholaminergic innervation of white adipose tissue in Siberian hamsters
Youngstrom, T. G., & Bartness, T. J. (1995) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.1995.268.3.r744 · Cited by 180 · see citing works
Giordano, A., Song, C. K., Bowers, R. R., Ehlen, J. C., Frontini, A., Cinti, S., & Bartness, T. J. (2006) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.00679.2005 · Cited by 177 · see citing works
Spite, M. R., Hellmann, J. L., Tang, Y., Mathis, S., Kosuri, M., Bhatnagar, A., Jala, V. R., & Haribabu, B. (2011) · The Journal of Immunology · doi:10.4049/jimmunol.1100196 · Cited by 177 · see citing works
Molecular pathways linking adipose innervation to insulin action in obesity and diabetes mellitus
Guilherme, A., Henriques, F. D. S., Bedard, A. H., & Czech, M. (2019) · Nature Reviews Endocrinology · doi:10.1038/s41574-019-0165-y · Cited by 173 · see citing works
Effects of Bariatric Surgery on Human Small Artery Function
Aghamohammadzadeh, R., Greenstein, A. S., Yadav, R., Jeziorska, M., Hama, S., Soltani, F., Pemberton, P., Ammori, B. J., Malik, R. A., Soran, H., et al. (2013) · Journal of the American College of Cardiology · doi:10.1016/j.jacc.2013.04.027 · Cited by 169 · see citing works
Fukui, Y., Masui, S., Osada, S., Umesono, K., & Motojima, K. (2000) · Diabetes · doi:10.2337/diabetes.49.5.759 · Cited by 168 · see citing works
Thyroid hormones induce browning of white fat
Martínez‐Sánchez, N., Moreno‐Navarrete, J. M., Contreras, C., Rial‐Pensado, E., Fernø, J., Nogueiras, R., Diéguez, C., Fernández‐Real, J. M., & López, M. (2016) · Journal of Endocrinology · doi:10.1530/joe-16-0425 · Cited by 166 · see citing works
Tang, X., Guilherme, A., Chakladar, A., Powelka, A. M., Konda, S., Virbasius, J. V., Nicoloro, S. M. C., Straubhaar, J., & Czech, M. (2006) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0507660103 · Cited by 164 · see citing works
Adipocyte-Derived Serum Amyloid A3 and Hyaluronan Play a Role in Monocyte Recruitment and Adhesion
Han, C. Y., Subramanian, S., Chan, C. K., Omer, M., Chiba, T., Wight, T. N., & Chait, A. (2007) · Diabetes · doi:10.2337/db07-0218 · Cited by 163 · see citing works
Salmeterol: a potent and long‐acting inhibitor of inflammatory mediator release from human lung
Butchers, P. R., Vardey, C. J., & Johnson, M. W. (1991) · British Journal of Pharmacology · doi:10.1111/j.1476-5381.1991.tb12487.x · Cited by 158 · see citing works
Grailer, J. J., Haggadone, M. D., Sarma, J. V., Zetoune, F. S., & Ward, P. A. (2014) · Journal of Innate Immunity · doi:10.1159/000358524 · Cited by 157 · see citing works
Regulation of Adipocyte Formation by GLP-1/GLP-1R Signaling
Challa, T. D., Beaton, N., Arnold, M., Rudofsky, G., Langhans, W., & Wolfrum, C. (2012) · Journal of Biological Chemistry · doi:10.1074/jbc.m111.310342 · Cited by 149 · see citing works
Kirk, E. A., Sagawa, Z. K., McDonald, T. O., O'Brien, K. D., & Heinecke, J. W. (2008) · Diabetes · doi:10.2337/db07-1061 · Cited by 149 · see citing works
Park, P., McMullen, M. R., Huang, H., Thakur, V., & Nagy, L. E. (2007) · Journal of Biological Chemistry · doi:10.1074/jbc.m701419200 · Cited by 148 · see citing works
Effect of acute cold exposure on norpinephrine turnover rates in rat white adipose tissue
Garófalo, M. A. R., Kettelhut, Í. D. C., Roselino, J. E. S., & Migliorini, R. H. (1996) · Journal of the Autonomic Nervous System · doi:10.1016/0165-1838(96)00037-9 · Cited by 146 · see citing works
Wong, C. K., Cheung, P. F., & Lam, C. W. K. (2007) · European Journal of Immunology · doi:10.1002/eji.200636866 · Cited by 143 · see citing works
Barquissau, V., Beuzelin, D., Pisani, D. F., Béranger, G. E., Mairal, A., Montagner, A., Roussel, B., Tavernier, G., Marques, M.-A., Moro, C., et al. (2016) · Molecular Metabolism · doi:10.1016/j.molmet.2016.03.002 · Cited by 141 · see citing works
Brito, N. A., Brito, M. N., & Bartness, T. J. (2008) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.00068.2008 · Cited by 137 · see citing works
Jiang, Y., Berry, D. C., & Graff, J. M. (2017) · eLife · doi:10.7554/elife.30329 · Cited by 135 · see citing works
Estrogens and the control of energy homeostasis: a brain perspective
López, M., & Tena‐Sempere, M. (2015) · Trends in Endocrinology and Metabolism · doi:10.1016/j.tem.2015.06.003 · Cited by 134 · see citing works
THE EFFECT OF AUTONOMIC GANGLIONIC BLOCKADE UPON SERUM FREE FATTY ACID LEVELS IN MAN *
Bogdonoff, M. D., Weissler, A. M., & Merritt, F. L. (1960) · Journal of Clinical Investigation · doi:10.1172/jci104117 · Cited by 134 · see citing works
Adiponectin Inhibits Pro-inflammatory Signaling in Human Macrophages Independent of Interleukin-10
Folco, E. J. E., Rocha, V. Z., Lopez-Ilasaca, M. A., & Libby, P. (2009) · Journal of Biological Chemistry · doi:10.1074/jbc.m109.019786 · Cited by 133 · see citing works
Youngstrom, T. G., & Bartness, T. J. (1998) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.1998.275.5.r1488 · Cited by 133 · see citing works
Engin, A. (2017) · Advances in experimental medicine and biology · doi:10.1007/978-3-319-48382-5_13 · Cited by 124 · see citing works
Sympathetic but not sensory denervation stimulates white adipocyte proliferation
Foster, M. T., & Bartness, T. J. (2006) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.00197.2006 · Cited by 123 · see citing works
Adiponectin Induces Pro-inflammatory Programs in Human Macrophages and CD4+ T Cells
Cheng, X., Folco, E. J. E., Shimizu, K., & Libby, P. (2012) · Journal of Biological Chemistry · doi:10.1074/jbc.m112.409516 · Cited by 122 · see citing works
Monjo, M., Rodríguez, A. M., Palou, A., & Roca, P. (2003) · Endocrinology · doi:10.1210/en.2003-0537 · Cited by 122 · see citing works
Niijima, A. (1998) · Journal of the Autonomic Nervous System · doi:10.1016/s0165-1838(98)00109-x · Cited by 121 · see citing works
Withers, S., Rosei, C. A., Livingstone, D. M., Little, M. C., Aslam, R., Malik, R. A., & Heagerty, A. M. (2011) · Arteriosclerosis Thrombosis and Vascular Biology · doi:10.1161/atvbaha.110.221705 · Cited by 118 · see citing works
Essential role of UCP1 modulating the central effects of thyroid hormones on energy balance
Álvarez-Crespo, M., Csikasz, R. I., Martínez‐Sánchez, N., Diéguez, C., Cannon, B., Nedergaard, J., & López, M. (2016) · Molecular Metabolism · doi:10.1016/j.molmet.2016.01.008 · Cited by 118 · see citing works
Rodríguez, A. M., Monjo, M., Roca, P., & Palou, A. (2002) · Cellular and Molecular Life Sciences · doi:10.1007/pl00012499 · Cited by 117 · see citing works
Hypothalamic AMPK and energy balance
López, M. (2018) · European Journal of Clinical Investigation · doi:10.1111/eci.12996 · Cited by 117 · see citing works
Palin, S., McTernan, P. G., Anderson, L. A., Sturdee, D. W., Barnett, A. H., & Kumar, S. (2003) · Metabolism · doi:10.1053/meta.2003.50088 · Cited by 116 · see citing works
Berthoud, H., Patterson, L. M., Sutton, G. M., Morrison, C. D., & Zheng, H. (2005) · Histochemistry and Cell Biology · doi:10.1007/s00418-005-0761-x · Cited by 113 · see citing works
Leptin receptors in estrogen receptor-containing neurons of the female rat hypothalamus
Diano, S., Kalra, S. P., Sakamoto, H., & Horváth, T. L. (1998) · Brain Research · doi:10.1016/s0006-8993(98)00936-6 · Cited by 107 · see citing works
Suzukawa, M., Nagase, H., Ogahara, I., Han, K., Tashimo, H., Shibui, A., Koketsu, R., Nakae, S., Yamaguchi, M., & Ohta, K. (2011) · The Journal of Immunology · doi:10.4049/jimmunol.1004054 · Cited by 102 · see citing works
Traveling from the hypothalamus to the adipose tissue: The thermogenic pathway
Contreras, C., Nogueiras, R., Diéguez, C., Rahmouni, K., & López, M. (2017) · Redox Biology · doi:10.1016/j.redox.2017.04.019 · Cited by 100 · see citing works
GLP-1/GLP-1R signaling in regulation of adipocyte differentiation and lipogenesis
Chen, J., Zhao, H., Ma, X., Zhang, Y., Lu, S., Wang, Y., Zong, C., Qin, D., Wang, Y., Yingfeng Yang, Y., et al. (2017) · Cellular Physiology and Biochemistry · doi:10.1159/000478872 · Cited by 94 · see citing works
Orexin receptor expression in human adipose tissue: effects of orexin-A and orexin-B
Digby, J. E., Chen, J., Tang, J., Lehnert, H., Matthews, R. N., & Randeva, H. S. (2006) · Journal of Endocrinology · doi:10.1677/joe.1.06886 · Cited by 93 · see citing works
Brain-adipose tissue neural crosstalk
Bartness, T. J., & Song, C. K. (2007) · Physiology & Behavior · doi:10.1016/j.physbeh.2007.04.002 · Cited by 92 · see citing works
Sex Steroid Receptor Expression Profile in Brown Adipose Tissue. Effects of Hormonal Status
Rodriguez-Cuenca, S., Monjo, M., Frontera, M., Gianotti, M., Proenza, A. M., & Roca, P. (2007) · Cellular Physiology and Biochemistry · doi:10.1159/000110448 · Cited by 92 · see citing works
Glucagon‐like peptide‐1(7–36) amide is a new incretin/enterogastrone candidate
Göke, R., Fehmann, H. C., & Göke, B. (1991) · European Journal of Clinical Investigation · doi:10.1111/j.1365-2362.1991.tb01802.x · Cited by 90 · see citing works
Niijima, A. (1999) · Neuroscience Letters · doi:10.1016/s0304-3940(99)00054-3 · Cited by 89 · see citing works
Bell, B., Harlan, S. M., Morgan, D. A., Guo, D., & Rahmouni, K. (2017) · Molecular Metabolism · doi:10.1016/j.molmet.2017.12.006 · Cited by 89 · see citing works
Noh, H., Yu, M. R., Kim, H. J., Lee, J. H., Park, B., Wu, I., Matsumoto, M., & King, G. L. (2017) · Kidney International · doi:10.1016/j.kint.2017.02.013 · Cited by 88 · see citing works
Neuropathy and neural plasticity in the subcutaneous white adipose depot
Blaszkiewicz, M., Willows, J. W., Dubois, A. L., Waible, S., DiBello, K., Lyons, L. L., Johnson, C. P., Paradie, E., Banks, N., Motyl, K., et al. (2019) · PLOS ONE · doi:10.1371/journal.pone.0221766 · Cited by 87 · see citing works
Lipolysis sensation by white fat afferent nerves triggers brown fat thermogenesis
Garretson, J. T., Szymanski, L. A., Schwartz, G. J., Xue, B., Ryu, V., & Bartness, T. J. (2016) · Molecular Metabolism · doi:10.1016/j.molmet.2016.06.013 · Cited by 80 · see citing works
Leptin-sensitive sensory nerves innervate white fat
Murphy, K. T., Schwartz, G. J., Nguyen, N. L. T., Mendez, J. M., Ryu, V., & Bartness, T. J. (2013) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.00021.2013 · Cited by 78 · see citing works
Acedo, S. C., Gambero, S., Cunha, F. G. P., Lorand-Metze, I. G. H., & Gambero, A. (2013) · In Vitro Cellular & Developmental Biology - Animal · doi:10.1007/s11626-013-9629-x · Cited by 76 · see citing works
SF1-Specific AMPKα1 Deletion Protects Against Diet-Induced Obesity
Seoane‐Collazo, P., Roa, J., Rial‐Pensado, E., Liñares‐Pose, L., Beiroa, D., Ruíz-Pino, F., López-González, T., Morgan, D. A., Pardavila, J. Á., Sanchez-Tapia, M. J., et al. (2018) · Diabetes · doi:10.2337/db17-1538 · Cited by 76 · see citing works
de Souza, F. S. J., Nasif, S., López-Leal, R., Levi, D. H., Low, M. J., & Rubinsten, M. (2011) · European Journal of Pharmacology · doi:10.1016/j.ejphar.2010.10.114 · Cited by 75 · see citing works
Rubio, A., Raasmaja, A., Maia, A. L., Kim, K. R., & Silva, J. E. (1995) · Endocrinology · doi:10.1210/endo.136.8.7628360 · Cited by 75 · see citing works
Reduced Rearing Temperature Augments Responses in Sympathetic Outflow to Brown Adipose Tissue
Morrison, S. F., Ramamurthy, S., & Young, J. B. (2000) · Journal of Neuroscience · doi:10.1523/jneurosci.20-24-09264.2000 · Cited by 75 · see citing works
Shi, H., & Bartness, T. J. (2005) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.00036.2005 · Cited by 75 · see citing works
Cross-talk between orexins (hypocretins) and the neuroendocrine axes (hypothalamic–pituitary axes)
López, M., Tena‐Sempere, M., & Diéguez, C. (2009) · Frontiers in Neuroendocrinology · doi:10.1016/j.yfrne.2009.07.001 · Cited by 74 · see citing works
Norepinephrine Inhibits Human Natural Killer Cell Activity in Vitro
Takamoto, T., Hori, Y., Koga, Y., Toshima, H., Hara, A., & YOKOYAMA, M. M. (1991) · International Journal of Neuroscience · doi:10.3109/00207459108987189 · Cited by 70 · see citing works
Grisanti, L. A., Traynham, C. J., Repas, A. A., Gao, E., Koch, W. J., & Tilley, D. G. (2016) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1611023114 · Cited by 69 · see citing works
Sympathetic innervation of the interscapular brown adipose tissue in mouse
François, M., Torres, H., Huesing, C., Zhang, R., Saurage, C., Lee, N., Qualls‐Creekmore, E., Yu, S., Morrison, C. D., Burk, D. H., et al. (2019) · Annals of the New York Academy of Sciences · doi:10.1111/nyas.14119 · Cited by 69 · see citing works
Sartipy, P., & Loskutoff, D. J. (2003) · Journal of Biological Chemistry · doi:10.1074/jbc.m306922200 · Cited by 67 · see citing works
Tsiotra, P. C., Pappa, V., Raptis, S., & Tsigos, C. (2000) · Metabolism · doi:10.1053/meta.2000.18519 · Cited by 67 · see citing works
Perivascular adipose tissue: An unique fat compartment relevant for the cardiometabolic syndrome
Siegel-Axel, D. I., & Häring, H. (2016) · Reviews in Endocrine and Metabolic Disorders · doi:10.1007/s11154-016-9346-3 · Cited by 67 · see citing works
Adrenergic regulation of cellular plasticity in brown, beige/brite and white adipose tissues
Ramseyer, V. D., & Granneman, J. G. (2016) · Adipocyte · doi:10.1080/21623945.2016.1145846 · Cited by 67 · see citing works
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Reactive Oxygen Species in Macrophages: Sources and Targets
Canton, M., Sánchez‐Rodríguez, R., Spera, I., Venegas, F. C., Favia, M., Viola, A., & Castegna, A. (2021) · Frontiers in Immunology · doi:10.3389/fimmu.2021.734229 · Cited by 463 · see citing works
Roles and mechanisms of exosomal non-coding RNAs in human health and diseases
Li, C., Ni, Y., Xu, H., Xiang, Q., Zhao, Y. Q., Zhan, J., He, J., Li, S., & Liu, Y. (2021) · Signal Transduction and Targeted Therapy · doi:10.1038/s41392-021-00779-x · Cited by 407 · see citing works
Brestoff, J. R., Wilen, C. B., Moley, J. R., Li, Y., Zou, W., Malvin, N. P., Rowen, M. N., Saunders, B. T., Ma, H., Mack, M. R., et al. (2020) · Cell Metabolism · doi:10.1016/j.cmet.2020.11.008 · Cited by 393 · see citing works
Gonzalez-Gil, A. M., & Elizondo-Montemayor, L. (2020) · Nutrients · doi:10.3390/nu12061899 · Cited by 278 · see citing works
“It has been shown to directly increase GLP-1 in mice [73] and to stimulate SNS, increasing WAT lipolysis and “browning” and BAT thermogenesis [19].”
BackgroundAdipose tissue at single-cell resolution
Maniyadath, B., Zhang, Q., Gupta, R. K., & Mandrup, S. (2023) · Cell Metabolism · doi:10.1016/j.cmet.2023.02.002 · Cited by 207 · see citing works
Dietary regulation in health and disease
Wu, Q., Gao, Z., Yu, X., & Wang, P. (2022) · Signal Transduction and Targeted Therapy · doi:10.1038/s41392-022-01104-w · Cited by 182 · see citing works
Liao, B., Qiao, J., & Pang, Y. (2021) · Frontiers in Endocrinology · doi:10.3389/fendo.2021.667422 · Cited by 175 · see citing works
Neuropeptide Y Is an Immunomodulatory Factor: Direct and Indirect
Chen, W.-C., Liu, Y., Liu, W.-F., Zhou, Y., He, H., & Lin, S. (2020) · Frontiers in Immunology · doi:10.3389/fimmu.2020.580378 · Cited by 136 · see citing works
Martínez-Sánchez, N., Sweeney, O., Sidarta-Oliveira, D., Caron, A., Stanley, S., & Domingos, A. (2022) · Neuron · doi:10.1016/j.neuron.2022.10.017 · Cited by 105 · see citing works
de Frel, D. L., Atsma, D. E., Pijl, H., Seidell, J. C., Leenen, P. J. M., Dik, W. A., & van Rossum, E. F. C. (2020) · Frontiers in Nutrition · doi:10.3389/fnut.2020.597600 · Cited by 121 · see citing works
Cancer-Associated Adipocytes in Breast Cancer: Causes and Consequences
Rybińska, I., Mangano, N., Tagliabue, E., & Triulzi, T. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22073775 · Cited by 106 · see citing works
Li, Y., Yun, K., & Mu, R. (2020) · Lipids in Health and Disease · doi:10.1186/s12944-020-01342-3 · Cited by 89 · see citing works
Xie, H., Heier, C., Meng, X., Bakiri, L., Pototschnig, I., Tang, Z., Schauer, S., Baumgartner, V. J., Grabner, G. F., Schabbauer, G., et al. (2022) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2112840119 · Cited by 83 · see citing works
Campolim, C. M., Weissmann, L., Ferreira, C. K. D. O., Zordão, O. P., Dornellas, A. P. S., de Castro, G., Zanotto, T. M., Boico, V. F., Quaresma, P. G. F., Lima, R. P. A., et al. (2020) · Scientific Reports · doi:10.1038/s41598-020-67040-3 · Cited by 76 · see citing works
Exercise and adrenergic regulation of immunity
Simpson, R. J., Boßlau, T. K., Weyh, C., Niemiro, G. M., Batatinha, H., Smith, K. A., & Krüger, K. (2021) · Brain Behavior and Immunity · doi:10.1016/j.bbi.2021.07.010 · Cited by 76 · see citing works
New Insights into Adipose Tissue Macrophages in Obesity and Insulin Resistance
Cai, Z., Huang, Y., & He, B. (2022) · Cells · doi:10.3390/cells11091424 · Cited by 70 · see citing works
Vascularized adipocyte organoid model using isolated human microvessel fragments
Strobel, H. A., Gerton, T. J., & Hoying, J. B. (2021) · Biofabrication · doi:10.1088/1758-5090/abe187 · Cited by 68 · see citing works
Leyrolle, Q., Cserjési, R., Mulders, M. D. G. H., Zamariola, G., Hiel, S., Gianfrancesco, M. A., Rodriguez, J., Portheault, D., Amadieu, C., Leclercq, S., et al. (2020) · Clinical Nutrition · doi:10.1016/j.clnu.2020.09.025 · Cited by 69 · see citing works
Vitamin D alleviates non-alcoholic fatty liver disease via restoring gut microbiota and metabolism
Zhang, X., Chen, L., Yang, J., Zhao, S.-S., Jin, S., Ao, N., Yang, J., Liu, H., & Du, J. (2023) · Frontiers in Microbiology · doi:10.3389/fmicb.2023.1117644 · Cited by 66 · see citing works
Physiological role of cytokines in the regulation of mammalian metabolism
Baat, A. D., Trinh, B., Ellingsgaard, H., & Donath, M. Y. (2023) · Trends in Immunology · doi:10.1016/j.it.2023.06.002 · Cited by 58 · see citing works
Is Adipose Tissue Inflammation the Culprit of Obesity‐Associated Comorbidities?
Turner, L., Wanasinghe, A. I., Brunori, P., & Santosa, S. (2025) · Obesity Reviews · doi:10.1111/obr.13956 · Cited by 58 · see citing works
Luo, D., Xie, Q., Chen, C., Mu, K., Wang, Z., Gu, S., & Xue, W. (2023) · International Journal of Biological Macromolecules · doi:10.1016/j.ijbiomac.2023.123820 · Cited by 47 · see citing works
The sympathetic nervous system in heart failure revisited
Triposkiadis, F. K., Briasoulis, Α., Kitai, T., Magouliotis, D. E., Athanasiou, T., Skoularigis, J. S., & Xanthopoulos, A. V. (2023) · Heart Failure Reviews · doi:10.1007/s10741-023-10345-y · Cited by 42 · see citing works
Seth, M., Biswas, R., Ganguli, S., Chakrabarti, N., & Chaudhuri, A. G. (2020) · Physiology International · doi:10.1556/2060.2020.00038 · Cited by 44 · see citing works
Neuroimmunometabolism: A New Pathological Nexus Underlying Neurodegenerative Disorders
Mitra, S., Banik, A., Saurabh, S., Maulik, M., & Khatri, S. (2022) · Journal of Neuroscience · doi:10.1523/jneurosci.0998-21.2022 · Cited by 44 · see citing works
Metabolic Syndrome and psoriatic arthritis: considerations for the clinician
Caso, F., Chimenti, M. S., Navarini, L., Ruscitti, P., Peluso, R., Girolimetto, N., PUENTE, A. D., Giacomelli, R., Scarpa, R., & Costa, L. (2020) · Expert Review of Clinical Immunology · doi:10.1080/1744666x.2020.1740593 · Cited by 41 · see citing works
Mast cells as important regulators in the development of psoriasis
Zhou, X., Chen, K., & Zhang, J.-A. (2022) · Frontiers in Immunology · doi:10.3389/fimmu.2022.1022986 · Cited by 39 · see citing works
Zhang, N., Wáng, Q., Lin, F., Zheng, B.-D., Huang, Y., Yang, Y., Xue, C., Xiao, M., & Ye, J. (2022) · Carbohydrate Polymers · doi:10.1016/j.carbpol.2022.119903 · Cited by 37 · see citing works
Interaction between IgA and gut microbiota and its role in controlling metabolic syndrome
Guo, J., Han, X., Huang, W., You, Y., & Zhan, J. (2020) · Obesity Reviews · doi:10.1111/obr.13155 · Cited by 37 · see citing works
The role of circadian clock in regulating cell functions: implications for diseases
Lin, Y., He, L., Cai, Y., Wang, X., Wang, S., & Li, F. (2024) · MedComm · doi:10.1002/mco2.504 · Cited by 35 · see citing works
Gart, E., Salic, K., Morrison, M. C., Caspers, M. P. M., van Duyvenvoorde, W., Heijnk, M., Giera, M. A., Bobeldijk‐Pastorova, I., Keijer, J., Storsve, A. B., et al. (2021) · Nutrients · doi:10.3390/nu13082836 · Cited by 35 · see citing works
Zhou, Q., Wang, Y., Lu, Z., Wang, B., Li, L., You, M., Wang, L., Cao, T., Zhao, Y., Li, Q., et al. (2023) · Obesity · doi:10.1002/oby.23707 · Cited by 35 · see citing works
Liver disease in obesity and underweight: the two sides of the coin. A narrative review
Risi, R., Tuccinardi, D., Mariani, S., Lubrano, C., Manfrini, S., Donini, L. M., & Watanabe, M. (2020) · Eating and Weight Disorders - Studies on Anorexia Bulimia and Obesity · doi:10.1007/s40519-020-01060-w · Cited by 33 · see citing works
Psychological intervention to treat distress: An emerging frontier in cancer prevention and therapy
Yang, M., Zhang, Z., Nice, E. C., Wang, C., Zhang, W., & Huang, C. (2021) · Biochimica et Biophysica Acta (BBA) - Reviews on Cancer · doi:10.1016/j.bbcan.2021.188665 · Cited by 33 · see citing works
Ren, W., Hua, M.-L., Cao, F., & Zeng, W.-W. (2023) · Advancement of science · doi:10.1002/advs.202306128 · Cited by 31 · see citing works
Shinjyo, N., & Kita, K. (2021) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2021.765217 · Cited by 29 · see citing works
Annunziata, C., Pirozzi, C., Lama, A., Senzacqua, M., Comella, F., Bordin, A., Monnolo, A., Pelagalli, A., Ferrante, M. C., Mollica, M. P., et al. (2022) · Pharmaceutics · doi:10.3390/pharmaceutics14020338 · Cited by 28 · see citing works
Neural innervation in adipose tissue, gut, pancreas, and liver
Sun, M., Wan, Y., Shi, M., Meng, Z., & Zeng, W. (2023) · Life Metabolism · doi:10.1093/lifemeta/load022 · Cited by 28 · see citing works
Kukucka, T., Ferencová, N., Višňovcová, Z., Ondrejka, I., Hrtánek, I., Kovacova, V., Macejova, A., Mlyncekova, Z., & Tonhajzerová, I. (2024) · International Journal of Molecular Sciences · doi:10.3390/ijms25084511 · Cited by 27 · see citing works
Dodd, J. M., Louise, J., Deussen, A. R., Mitchell, M., & Poston, L. (2024) · BMC Medicine · doi:10.1186/s12916-024-03410-2 · Cited by 26 · see citing works
Leptin Elicits In Vivo Eosinophil Migration and Activation: Key Role of Mast Cell-Derived PGD2
Amorim, N., Souza-Almeida, G., Luna-Gomes, T., Bozza, P. T., Canetti, C. D. A., Diaz, B. L., Maya‐Monteiro, C. M., & Bandeira‐Melo, C. (2020) · Frontiers in Endocrinology · doi:10.3389/fendo.2020.572113 · Cited by 25 · see citing works
Macrophage beta2-adrenergic receptor is dispensable for the adipose tissue inflammation and function
Petkevicius, K., Bidault, G., Virtue, S., Newland, S. A., Dale, M., Dugourd, A. J. F., Sáez-Rodríguez, J., Mallat, Z., & Vidal‐Puig, A. (2021) · Molecular Metabolism · doi:10.1016/j.molmet.2021.101220 · Cited by 24 · see citing works
HDAC1 inhibits beige adipocyte-mediated thermogenesis through histone crotonylation of Pgc1a/Ucp1
Tian, D., Zeng, X., Gong, Y., Yin, Z., Zhang, J., & Wu, Z. (2023) · Cellular Signalling · doi:10.1016/j.cellsig.2023.110875 · Cited by 25 · see citing works
Immunity and the carotid body: implications for metabolic diseases
Conde, S. V., Sacramento, J. F., & Martins, F. O. (2020) · Bioelectronic Medicine · doi:10.1186/s42234-020-00061-5 · Cited by 25 · see citing works
The regulatory role of adipocyte mitochondrial homeostasis in metabolism-related diseases
Song, H., Zhang, X., Wang, J., Wu, Y., Xiong, T., Shen, J., Lin, R., Xiao, T., & Lin, W. (2023) · Frontiers in Physiology · doi:10.3389/fphys.2023.1261204 · Cited by 22 · see citing works
Amo-Aparicio, J., Dinarello, C. A., & Lopez-Vales, R. (2024) · Neural Regeneration Research · doi:10.4103/1673-5374.391330 · Cited by 25 · see citing works
Landgraaf, R. G., Bloem, M. N., Fumagalli, M., Benninga, M. A., de Lorijn, F., & Nieuwdorp, M. (2023) · Frontiers in Endocrinology · doi:10.3389/fendo.2023.1236370 · Cited by 21 · see citing works
Wu, L., Fang, Q., Wang, M., Wang, Y., Zhu, X., Fang, Z., Lu, F., Xu, B., Jin, R., Han, H., et al. (2022) · Frontiers in Endocrinology · doi:10.3389/fendo.2022.954428 · Cited by 20 · see citing works
A Tale of Three Systems: Toward a Neuroimmunoendocrine Model of Obesity
O’Brien, C. J. O., Haberman, E. R., & Domingos, A. I. (2021) · Annual Review of Cell and Developmental Biology · doi:10.1146/annurev-cellbio-120319-114106 · Cited by 18 · see citing works
Neuro-immune-metabolism: The tripod system of homeostasis
Deshpande, D., Fuchs, L., & Klose, C. S. N. (2021) · Immunology Letters · doi:10.1016/j.imlet.2021.10.001 · Cited by 19 · see citing works
Immune Cell Regulation of White Adipose Progenitor Cell Fate
Altun, I., Yan, X., & Ussar, S. (2022) · Frontiers in Endocrinology · doi:10.3389/fendo.2022.859044 · Cited by 18 · see citing works
Schroeder, K., Dumenci, L., Sarwer, D. B., Noll, J. G., Henry, K., Suglia, S. F., Forke, C. M., & Wheeler, D. C. (2022) · International Journal of Environmental Research and Public Health · doi:10.3390/ijerph19137819 · Cited by 18 · see citing works
Li, Q., Byun, J., Choi, J., Park, J.-W., Lee, J., & Oh, Y. (2024) · ACS Nano · doi:10.1021/acsnano.3c06001 · Cited by 19 · see citing works
Neuroimmune regulation of white adipose tissues
Qian, X., Meng, X., Zhang, S., & Zeng, W. (2021) · FEBS Journal · doi:10.1111/febs.16213 · Cited by 16 · see citing works
Paniskaki, K., Konik, M., Anft, M., Heidecke, H., Meister, T. L., Pfaender, S., Krawczyk, A., Zettler, M., Jäger, J., Gaeckler, A., et al. (2023) · Frontiers in Microbiology · doi:10.3389/fmicb.2023.1196721 · Cited by 17 · see citing works
Zhang, F., Qiao, W., Wei, J., Tao, Z., Chen, C., Wu, Y., Lin, M., Ng, K. M. C., Zhang, L., Yeung, K., et al. (2024) · Nature Communications · doi:10.1038/s41467-024-45436-3 · Cited by 18 · see citing works
Adipose tissue–gut microbiome crosstalk in inflammation and thermogenesis
Mauney, E. E., Wibowo, M. C., Tseng, Y., & Kostic, A. D. (2024) · Trends in Endocrinology and Metabolism · doi:10.1016/j.tem.2024.10.004 · Cited by 17 · see citing works
The autonomic nervous system in the regulation of glucose and lipid metabolism
Wangler, S., Jarczok, M. N., Ennis, M., Herhaus, B., Wagner, R., Sehgal, R., & Heni, M. (2026) · Nature Reviews Endocrinology · doi:10.1038/s41574-025-01221-w · Cited by 17 · see citing works
Gene-Environment interactions and stochastic variations in the Gero-Exposome.
Finch, C., & Haghani, A. (2021) · The journals of gerontology. Series A, Biological sciences and medical sciences · doi:10.1093/gerona/glab045 · Cited by 15 · see citing works
An, Z., Wang, H., & Mokadem, M. (2021) · Frontiers in Neuroscience · doi:10.3389/fnins.2021.770690 · Cited by 16 · see citing works
Mechanisms and pathophysiology of SARS-CoV-2 infection of the adipose tissue
Moser, J., Emous, M., Heeringa, P., & Rodenhuis‐Zybert, I. A. (2023) · Trends in Endocrinology and Metabolism · doi:10.1016/j.tem.2023.08.010 · Cited by 16 · see citing works
Becker, M., Kälin, S., Neubig, A. H., Lauber, M., Opaleva, D., Hipp, H., Salb, V. K., Ott, V. B., Legutko, B., Kälin, R. E., et al. (2025) · Nature Communications · doi:10.1038/s41467-025-57918-z · Cited by 17 · see citing works
Gu, M., Feng, Y., Chen, Y., Fan, S., & Huang, C. (2023) · Phytotherapy Research · doi:10.1002/ptr.7770 · Cited by 15 · see citing works
Lambert, G. W., Patel, M., & Lambert, É. (2025) · Metabolites · doi:10.3390/metabo15050286 · Cited by 14 · see citing works
Crosstalk between adipose tissue and the microbiota-gut-brain axis in metabolic diseases
Yu, Z.-W., Wang, Y., Yu, Z. H., Lu, M., & Xu, B. (2022) · International Journal of Biological Sciences · doi:10.7150/ijbs.68786 · Cited by 14 · see citing works
Komaravolu, R. K., Mehta-D’souza, P., Conner, T., Allen, M. T., Lumry, J., Batushansky, A., Pezant, N. P., Montgomery, C. G., & Griffin, T. M. (2024) · Osteoarthritis and Cartilage · doi:10.1016/j.joca.2024.03.109 · Cited by 13 · see citing works
Ameka, M., & Hasty, A. H. (2020) · Immunometabolism · doi:10.20900/immunometab20200034 · Cited by 12 · see citing works
Immunometabolic regulation of adipose tissue resident immune cells
Davanzo, G. G., Castro, G., & Moraes‐Vieira, P. M. (2021) · Current Opinion in Pharmacology · doi:10.1016/j.coph.2021.03.004 · Cited by 13 · see citing works
Thakur, P., Baraskar, K., Shrivastava, V. K., & Medhi, B. (2024) · Brain Research · doi:10.1016/j.brainres.2024.149176 · Cited by 12 · see citing works
Chi, Z., Jia, Q., Yang, H., Ren, H., Jin, C., He, J., Wuri, N., Sui, Z., Zhang, J., Mengke, B., et al. (2024) · BMC Genomics · doi:10.1186/s12864-024-10913-y · Cited by 12 · see citing works
Huo, R., Zhang, M., Zhang, Y., Bai, X., Zhang, Y., & Guo, X. (2022) · Frontiers in Nutrition · doi:10.3389/fnut.2022.871556 · Cited by 12 · see citing works
Inulin reduces liver triacylglycerol by increasing lipid droplet lipolysis in fat-loaded mice
Chen, B., Shi, Y., Zhang, K., Chang, Y., Fu, P., Liu, P., & Zhang, S. (2022) · Food Research International · doi:10.1016/j.foodres.2022.112226 · Cited by 12 · see citing works
Ernsberger, U., Deller, T., & Rohrer, H. (2021) · Cell and Tissue Research · doi:10.1007/s00441-021-03548-y · Cited by 12 · see citing works
Macrophages Can Drive Sympathetic Excitability in the Early Stages of Hypertension
Neely, O. C., Domingos, A. I., & Paterson, D. J. (2022) · Frontiers in Cardiovascular Medicine · doi:10.3389/fcvm.2021.807904 · Cited by 12 · see citing works
Exploring the multifaceted role of obesity in breast cancer progression
Kakkat, S., Suman, P., Herrera, E. A. T., Singh, S., Chakroborty, D., & Sarkar, C. (2024) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2024.1408844 · Cited by 11 · see citing works
Huang, S. S. Y., Makhlouf, M., AbouMoussa, E. H., Segura, M. L. R. T., Mathew, L. S., Wang, K., Leung, M. C., Chaussabel, D., Logan, D. W., Scialdone, A., et al. (2020) · Molecular Metabolism · doi:10.1016/j.molmet.2020.101038 · Cited by 11 · see citing works
Quan, Q., Kim, E. J., Kim, S., Kim, Y. K., Chung, M. H., Tian, Y.-D., Shin, C.-Y., Lee, D. H., & Chung, J. H. (2024) · Journal of Investigative Dermatology · doi:10.1016/j.jid.2024.03.012 · Cited by 10 · see citing works
Rheumatic diseases and metabolism: where centre and periphery meet
López, M., & Gualillo, O. (2024) · Nature Reviews Rheumatology · doi:10.1038/s41584-024-01178-6 · Cited by 11 · see citing works
Risi, R., Amendolara, R., Pantano, A. L., Fassino, V., D’Onofrio, L., Coraggio, L., Luverà, D., Masi, D., Watanabe, M., Gnessi, L., et al. (2025) · Cardiovascular Diabetology · doi:10.1186/s12933-025-02635-6 · Cited by 10 · see citing works
Lu, M., Yu, Z.-W., Yang, X., Yang, Z., Xu, T., Yu, Z., Jing, X., An, L., Zhang, J., & Xu, B. (2025) · Adipocyte · doi:10.1080/21623945.2025.2524638 · Cited by 10 · see citing works
High-Risk Obesity Phenotypes: Target for Multimorbidity Prevention at the ROFEMI Study
Carretero‐Gómez, J., Pérez-Martínez, P., Seguí‐Ripoll, J. M., Carrasco-Sánchez, F. J., Martínez, N. L., Pérez, E. F., Hernández, O. P., Ordoñez, M. G., Martín‐González, C., Vigueras-Pérez, J., et al. (2022) · Journal of Clinical Medicine · doi:10.3390/jcm11164644 · Cited by 10 · see citing works
Bo, B., Guo, A., Kaila, S. J., Hao, Z., Zhang, H., Wei, J., & Yao, Y. (2023) · Frontiers in Physiology · doi:10.3389/fphys.2023.1170324 · Cited by 8 · see citing works
Yu, Z.-W., Zhang, T., Yang, X., Xu, B., Yu, Z. H., An, L., Xu, T., Jing, X., Wang, Y., & Lu, M. (2024) · Diabetes Obesity and Metabolism · doi:10.1111/dom.15735 · Cited by 8 · see citing works
Shao, J., Li, C., Bai, L., Ni, X., Ge, S., Zhang, J., & Zhao, H. (2022) · Heliyon · doi:10.1016/j.heliyon.2022.e09482 · Cited by 8 · see citing works
TLR4 in POMC neurons regulates thermogenesis in a sex-dependent manner
Li, Y., Zhu, S., Du, D., Li, Q., Xie, K., Chen, L., Feng, X., Wu, X., Sun, Z., Zhou, J., et al. (2023) · Journal of Lipid Research · doi:10.1016/j.jlr.2023.100368 · Cited by 8 · see citing works
Sarwer, D. B., Schroeder, K., Fischbach, S. R., Atwood, S. M., & Heinberg, L. J. (2024) · Obesity Surgery · doi:10.1007/s11695-024-07597-4 · Cited by 7 · see citing works
A New Era, New Risks: The Cardio-Oncology Perspective on Immunotherapy in Non-Small Cell Lung Cancer
Tarantini, L., Gallucci, G., Inno, A., Camerini, A., Canale, M. L., Larocca, M., Zanelli, F., Pagano, M., Alberti, G., Ciammella, P., et al. (2025) · Cancers · doi:10.3390/cancers17213443 · Cited by 7 · see citing works
Gong, J., Wei, F., Wu, T., Zhang, N., Zhang, Y., Cui, Z., & Ge, J. (2025) · Journal of Translational Medicine · doi:10.1186/s12967-025-06834-3 · Cited by 7 · see citing works
Boulet, N., Luijten, I. H. N., Cannon, B., & Nedergaard, J. (2020) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.00352.2020 · Cited by 7 · see citing works
Intercellular mitochondria transfer: a new perspective for the treatment of metabolic diseases
Hu, X., Duan, T., Wu, Z., Xiong, Y., & Cao, Z. (2021) · Acta Biochimica et Biophysica Sinica · doi:10.1093/abbs/gmab052 · Cited by 7 · see citing works
Modena, D. A. O., Soares, C. D., Martignago, C. C. S., Almeida, S., Cazzo, E., & Chaim, É. A. (2022) · Journal of Cosmetic and Laser Therapy · doi:10.1080/14764172.2022.2109677 · Cited by 7 · see citing works
Xu, Y., Jia, X., Zhang, W. Y., Xie, Q., Zhu, M., Zhao, Z., Hao, J., Li, H., Du, J., Liu, Y., et al. (2023) · Frontiers in Nutrition · doi:10.3389/fnut.2023.1242157 · Cited by 7 · see citing works
Díaz‐Castro, J., Reyes-Olavarría, D., Toledano, J. M., Puche-Juárez, M., Garcia-Vega, J. E., Ochoa, J. J., & Moreno‐Fernández, J. (2024) · Clinical Nutrition · doi:10.1016/j.clnu.2024.02.024 · Cited by 6 · see citing works
da Silva, A. A., Rocha‐Gomes, A., Reis, Í. G., Leal, P. E. D. P. T., Lessa, M. R., Pinto, N. A. V. D., Riul, T. R., & Villela, D. C. (2023) · Journal of Neuroimmunology · doi:10.1016/j.jneuroim.2023.578237 · Cited by 5 · see citing works
ON THE BIOLOGICAL ROLE OF LEPTIN
Chaulin, A. M., & Grigoryeva, J. (2021) · Научное обозрение Биологические науки (Scientific Review Biological Sciences) · doi:10.17513/srbs.1222 · Cited by 5 · see citing works
Wang, K., Wang, Y.-Y., Wu, L.-L., Jiang, L., Hu, Y., Xiao, X., & Wang, Y. (2022) · Endocrinology · doi:10.1210/endocr/bqac062 · Cited by 5 · see citing works
Zhang, M., Wang, H., Li, X., Shu, S., Piao, J., Yue, X., Zhao, S., Li, M., Jin, X., Nan, Y., et al. (2025) · The FASEB Journal · doi:10.1096/fj.202502147r · Cited by 4 · see citing works
The biological basis of disease recurrence in psoriasis
Carmona‐Rocha, E., & Puig, L. (2023) · Italian Journal of Dermatology and Venereology · doi:10.23736/s2784-8671.23.07583-7 · Cited by 4 · see citing works
Schroeder, K., Dumenci, L., Day, S. E., Konty, K., Noll, J. G., Henry, K., Suglia, S. F., Wheeler, D. C., Argenio, K. L., & Sarwer, D. B. (2024) · Childhood Obesity · doi:10.1089/chi.2024.0215 · Cited by 3 · see citing works
The interplay between the adrenergic system and obesity: a systematic review
Araújo, B., Leite, F., & Ribeiro, L. V. P. T. (2025) · International Journal of Obesity · doi:10.1038/s41366-025-01924-0 · Cited by 2 · see citing works
- Authors
- Larabee, C. M., Neely, O. C., & Domingos, A. I.
- Affiliations
- University of Oxford (GB)
- Howard Hughes Medical Institute (US)
- Corresponding author
- Domingos, Ana I.
- Venue
- Nature Reviews Endocrinology
- Published
- 2019-11-27
- Volume
- 16
- Issue
- 1
- Pages
- 30-43
- ISSN
- 1759-5029 (ISSN-L)
- 1759-5037
- OpenAlex
- W2989580600
- Cited by
- 123
- References
- 233
- Citations by year
- 2026: 4 · 2025: 14 · 2024: 21 · 2023: 24 · 2022: 22 · 2021: 21 · 2020: 17
- FWCI
- 2.19
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Nature Reviews Endocrinology (publishedVersion)
- PubMed (publishedVersion)
- Funders
- Wellcome Trust (208576/Z/17/Z)
- Topics
- Health Sciences › Medicine › Epidemiology › Adipokines, Inflammation, and Metabolic Diseases
- Health Sciences › Medicine › Physiology › Adipose Tissue and Metabolism
- Life Sciences › Neuroscience › Endocrine and Autonomic Systems › Regulation of Appetite and Obesity
- Keywords
- obesity, neuroimmunology, immunometabolism, adipose tissue, sympathetic nervous system, leptin, norepinephrine, innate immune cells, adrenergic signaling, adipose tissue macrophages, metabolic homeostasis
- MeSH terms
- Animals, Energy Metabolism, Humans, Macrophages, Obesity, Neuroimmunomodulation, Adipocytes
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