The DOI matches its Crossref record; 233 of the 233 references it cites were found in a registry or an index.
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.
Overview
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
In the citing paper
“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]”
In the citing paper
“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].”
In the citing paper
“enhancing SNS output [19] (3b)”
Citations
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
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
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
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
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
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
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
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
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
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
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
Kanda, H. (2006) · Journal of Clinical Investigation · doi:10.1172/jci26498 · Cited by 2,682
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
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
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
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
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 2,007
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
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 1,924
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
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
CCR2 modulates inflammatory and metabolic effects of high-fat feeding
Weisberg, S. P. (2006) · Journal of Clinical Investigation · doi:10.1172/jci24335c1 · Cited by 1,425
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 1,411
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
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
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 1,270
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 1,229
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
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
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
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
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 1,053
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
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
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
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
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
Lumeng, C. N.-K., DelProposto, J. B., Westcott, D. J., & Saltiel, A. R. (2008) · Diabetes · doi:10.2337/db08-0872 · Cited by 956
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
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 888
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
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 867
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 866
Cawthorn, W. P., & Sethi, J. K. (2007) · FEBS Letters · doi:10.1016/j.febslet.2007.11.051 · Cited by 833
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
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
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
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
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 764
Obesity, Inflammation, Toll-Like Receptor 4 and Fatty Acids
Rogero, M. M., & Calder, P. C. (2018) · Nutrients · doi:10.3390/nu10040432 · Cited by 748
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 741
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
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
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
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 664
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 659
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
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
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
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 615
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 613
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 605
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
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
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
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
Ruan, H., Hacohen, N., Golub, T. R., Parijs, L. V., & Lodish, H. F. (2002) · Diabetes · doi:10.2337/diabetes.51.5.1319 · Cited by 543
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 533
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
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 511
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 504
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. X. (2010) · Science · doi:10.1126/science.1188280 · Cited by 495
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
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
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
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 462
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
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
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
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 455
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
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
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
Adrenergic activation of triiodothyronine production in brown adipose tissue
Silva, J. E., & Larsen, P. R. (1983) · Nature · doi:10.1038/305712a0 · Cited by 401
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 399
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 383
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
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
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 370
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
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 355
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
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 337
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 333
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 327
Adrenergic regulation of innate immunity: a review
Scanzano, A., & Cosentino, M. (2015) · Frontiers in Pharmacology · doi:10.3389/fphar.2015.00171 · Cited by 323
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
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 319
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 318
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 308
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 305
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., 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 302
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
Macrophage recruitment in obese adipose tissue
Bai, Y., & Sun, Q. (2015) · Obesity Reviews · doi:10.1111/obr.12242 · Cited by 287
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
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
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
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
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 271
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 266
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 264
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
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
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 250
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
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
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 238
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
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
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
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
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 228
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 225
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
Bartness, T. J., & Song, C. K. (2007) · Journal of Lipid Research · doi:10.1194/jlr.r700006-jlr200 · Cited by 214
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
Murano, I., Barbatelli, G., Giordano, A., & Cinti, S. (2009) · Journal of Anatomy · doi:10.1111/j.1469-7580.2008.01001.x · Cited by 208
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 207
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
Jiang, H., Ding, X., Cao, Y., Wang, H., & Zeng, W. (2017) · Cell Metabolism · doi:10.1016/j.cmet.2017.08.016 · Cited by 204
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
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 203
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
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
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
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
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
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 182
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
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
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 179
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
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 170
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 169
Fukui, Y., Masui, S., Osada, S., Umesono, K., & Motojima, K. (2000) · Diabetes · doi:10.2337/diabetes.49.5.759 · Cited by 168
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 166
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 164
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
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
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 154
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
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
Park, P., McMullen, M. R., Huang, H., Thakur, V., & Nagy, L. E. (2007) · Journal of Biological Chemistry · doi:10.1074/jbc.m701419200 · Cited by 147
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
Wong, C. K., Cheung, P. F., & Lam, C. W. K. (2007) · European Journal of Immunology · doi:10.1002/eji.200636866 · Cited by 143
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 137
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
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 136
Jiang, Y., Berry, D. C., & Graff, J. M. (2017) · eLife · doi:10.7554/elife.30329 · Cited by 135
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
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
Engin, A. (2017) · Advances in experimental medicine and biology · doi:10.1007/978-3-319-48382-5_13 · Cited by 129
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 126
Monjo, M., Rodríguez, A. M., Palou, A., & Roca, P. (2003) · Endocrinology · doi:10.1210/en.2003-0537 · Cited by 124
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
Niijima, A. (1998) · Journal of the Autonomic Nervous System · doi:10.1016/s0165-1838(98)00109-x · Cited by 121
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 119
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 119
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
Rodríguez, A. M., Monjo, M., Roca, P., & Palou, A. (2002) · Cellular and Molecular Life Sciences · doi:10.1007/pl00012499 · Cited by 117
Hypothalamic AMPK and energy balance
López, M. (2018) · European Journal of Clinical Investigation · doi:10.1111/eci.12996 · Cited by 117
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
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
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 104
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
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
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
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
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
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 90
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 89
Niijima, A. (1999) · Neuroscience Letters · doi:10.1016/s0304-3940(99)00054-3 · Cited by 89
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
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 81
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
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 79
Bell, B. B., Harlan, S. M., Morgan, D., Guo, D., Cui, H.-X., & Rahmouni, K. (2017) · Molecular Metabolism · doi:10.1016/j.molmet.2017.12.006 · Cited by 77
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
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
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
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
Shi, H., & Bartness, T. J. (2005) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.00036.2005 · Cited by 75
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
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
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
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
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 68
Sartipy, P., & Loskutoff, D. J. (2003) · Journal of Biological Chemistry · doi:10.1074/jbc.m306922200 · Cited by 67
Tsiotra, P. C., Pappa, V., Raptis, S., & Tsigos, C. (2000) · Metabolism · doi:10.1053/meta.2000.18519 · Cited by 67
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
Cited by
Sorted by citations
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 490
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 424
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 399
Gonzalez-Gil, A. M., & Elizondo-Montemayor, L. (2020) · Nutrients · doi:10.3390/nu12061899 · Cited by 278
“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 218
Metadata
- 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 › Endocrinology, Diabetes and Metabolism › Adipokines, Inflammation, and Metabolic Diseases
- Health Sciences › Medicine › Physiology (medical) › 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
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review