The DOI matches its Crossref record; 54 of the 54 references it cites were found in a registry or an index.
Obesity induces a phenotypic switch in adipose tissue macrophage polarization
Open accessAbstract
Adipose tissue macrophages (ATMs) infiltrate adipose tissue during obesity and contribute to insulin resistance. We hypothesized that macrophages migrating to adipose tissue upon high-fat feeding may differ from those that reside there under normal diet conditions. To this end, we found a novel F4/80(+)CD11c(+) population of ATMs in adipose tissue of obese mice that was not seen in lean mice. ATMs from lean mice expressed many genes characteristic of M2 or "alternatively activated" macrophages, including Ym1, arginase 1, and Il10. Diet-induced obesity decreased expression of these genes in ATMs while increasing expression of genes such as those encoding TNF-alpha and iNOS that are characteristic of M1 or "classically activated" macrophages. Interestingly, ATMs from obese C-C motif chemokine receptor 2-KO (Ccr2-KO) mice express M2 markers at levels similar to those from lean mice. The antiinflammatory cytokine IL-10, which was overexpressed in ATMs from lean mice, protected adipocytes from TNF-alpha-induced insulin resistance. Thus, diet-induced obesity leads to a shift in the activation state of ATMs from an M2-polarized state in lean animals that may protect adipocytes from inflammation to an M1 proinflammatory state that contributes to insulin resistance.
Overview
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
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
“These cells produce high levels of TNFα, IL-6, and IL-1β, all of which are also observed in increased levels of adipose tissue from insulin resistant individuals.”
From Macrophage polarization: an opportunity for improved outcomes in biomaterials and regenerative medicine (2012) · cites this paper as [70]
In the citing paper
“While the ATMs present in healthy lean adipose tissue are primarily of an M2 phenotype, those that accumulate in the adipose tissue during obesity have a strongly polarized pro-inflammatory, M1 phenotype [63,69–71].”
From Macrophage polarization: an opportunity for improved outcomes in biomaterials and regenerative medicine (2012) · cites this paper as [70]
In the citing paper
“However, two studies that investigated cellular markers of inflammation both reported an anti-inflammatory effect of vitamin D (747,748) .”
From Dietary factors and low-grade inflammation in relation to overweight and obesity (2011) · cites this paper as [747]
In the citing paper
“Using data pooled from thirty-six healthy subjects, twenty-four type 1 diabetics and twenty-six type 1 diabetics with microvascular complications, Devaraj et al. (747) found significant inverse relationships between serum 25(OH)D 3 and CRP concentration, monocyte NF-kB activation and TLR4 expression.”
From Dietary factors and low-grade inflammation in relation to overweight and obesity (2011) · cites this paper as [747]
In the citing paper
“Accordingly, because of their proinflammatory properties, these macrophages are implicated in the pathogenesis of insulin resistance (103, 105, 112, 113).”
From Insulin sensitivity: Modulation by nutrients and inflammation (2008) · cites this paper as [103]
In the citing paper
“The combination of microhypoxia and lipid overload triggers the recruitment of immune cells, such as macrophages in the adipose tissue and their activation ([103](#B103), [129](#B129), [171](#B171)).”
From Mitochondrial fatty acid oxidation in obesity (2013) · cites this paper as [103]
In the citing paper
“Under stimulation by B cells, effector T cells and Th1cells release cytokines such as interferon-γ to further stimulate activation of macrophages and induce a shift in macrophages from an M2-like phenotype to an M1-like phenotype.”
From The Vasculature in Prediabetes (2018) · cites this paper as [83]
In the citing paper
“In obese mice, a shift in the activation state of WAT macrophages from an M2 'alternatively activated' state to an M1 'pro-inflammatory state' was observed in response to diet-induced obesity [47].”
From Adipose tissue transcriptomic signature highlights the pathological relevance of extracellular matrix in human obesity (2008) · cites this paper as [47]
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
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
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
The chemokine system in diverse forms of macrophage activation and polarization
MANTOVANI, A., SICA, A., SOZZANI, S., ALLAVENA, P., VECCHI, A., & LOCATI, M. (2004) · Trends in Immunology · doi:10.1016/j.it.2004.09.015 · Cited by 6,534
Alternative activation of macrophages
Gordon, S. (2003) · Nature Reviews Immunology · doi:10.1038/nri978 · Cited by 6,189
MANTOVANI, A., SOZZANI, S., LOCATI, M., ALLAVENA, P., & SICA, A. (2002) · Trends in Immunology · doi:10.1016/s1471-4906(02)02302-5 · Cited by 5,528
Monocyte and macrophage heterogeneity
Gordon, S., & Taylor, P. R. (2005) · Nature Reviews Immunology · doi:10.1038/nri1733 · Cited by 5,190
Inflammation and insulin resistance
Shoelson, S. E. (2006) · Journal of Clinical Investigation · doi:10.1172/jci29069 · Cited by 4,769
Blood Monocytes Consist of Two Principal Subsets with Distinct Migratory Properties
Geissmann, F., Jung, S., & Littman, D. R. (2003) · Immunity · doi:10.1016/s1074-7613(03)00174-2 · Cited by 3,504
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
Kanda, H. (2006) · Journal of Clinical Investigation · doi:10.1172/jci26498 · Cited by 2,682
Research works printed but not linked: 3
- Barzilai, 1999, Am. J. Physiol., 277, E291
- Juge-Aubry, 2005, Cytokine., 29, 270
- Lumeng, 2006, Diabetes.
Cited by
Sorted by citations
Items 901–1,000 of 1,050
Kim, B., Farruggia, C., Ku, C. S., Pham, T. X., Yang, Y. J., Bae, M., Wegner, C., Farrell, N., Harness, E., Park, Y., et al. (2016) · The Journal of Nutritional Biochemistry · doi:10.1016/j.jnutbio.2016.01.006 · Cited by 112
miR-155 Deletion in Female Mice Prevents Diet-Induced Obesity
Gaudet, A. D., Fonken, L. K., Gushchina, L. V., Aubrecht, T. G., Maurya, S. K., Periasamy, M., Nelson, R. J., & Popovich, P. G. (2016) · Scientific Reports · doi:10.1038/srep22862 · Cited by 115
Neutrophils Actively Contribute to Obesity-Associated Inflammation and Pathological Complications
Uribe‐Querol, E., & Rosales, C. (2022) · Cells · doi:10.3390/cells11121883 · Cited by 122
Adipose tissue inflammation in aging
Mau, T., & Yung, R. (2018) · Experimental Gerontology · doi:10.1016/j.exger.2017.10.014 · Cited by 110
Adipose tissue changes in obesity and the impact on metabolic function
Sam, S., & Mazzone, T. (2014) · Translational research · doi:10.1016/j.trsl.2014.05.008 · Cited by 113
Zizzo, G., & Cohen, P. (2015) · Journal of Inflammation · doi:10.1186/s12950-015-0081-4 · Cited by 94
Immune cells in adipose tissue: Key players in metabolic disorders
Lolmède, K., Duffaut, C., Zakaroff‐Girard, A., & Bouloumié, A. (2011) · Diabetes & Metabolism · doi:10.1016/j.diabet.2011.03.002 · Cited by 122
Leptin–cytokine crosstalk in breast cancer
Newman, G. W., & Gonzalez-Perez, R. R. (2013) · Molecular and Cellular Endocrinology · doi:10.1016/j.mce.2013.03.025 · Cited by 112
G protein-coupled receptors as targets for anti-diabetic therapeutics
Oh, D. Y., & Olefsky, J. M. (2016) · Nature Reviews Drug Discovery · doi:10.1038/nrd.2015.4 · Cited by 110
Caputo, T., Gilardi, F., & Desvergne, B. (2017) · FEBS Letters · doi:10.1002/1873-3468.12742 · Cited by 112
Poret, J. M., Souza‐Smith, F. M., Marcell, S. J., Gaudet, D. A., Tzeng, T. H., Braymer, H. D., Harrison‐Bernard, L. M., & Primeaux, S. D. (2017) · International Journal of Obesity · doi:10.1038/ijo.2017.280 · Cited by 112
Weinstock, A., Brown, E. J., Garabedian, M. L., Pena, S., Sharma, M., Lafaille, J. J., Moore, K. J., & Fisher, E. A. A. (2019) · Immunometabolism · doi:10.20900/immunometab20190008 · Cited by 110
Yuan, X., Yuan, W., Ding, L., Ming, S., Luo, L., Wan, Y., Oh, J., Zhou, Y., Bian, L., & Deng, D. Y. B. (2021) · Biomaterials · doi:10.1016/j.biomaterials.2021.121190 · Cited by 111
Mauer, J., Chaurasia, B., Plum, L., Quast, T., Hampel, B., Blüher, M., Kolanus, W., Kahn, C. R., & Brüning, J. C. (2010) · PLoS Genetics · doi:10.1371/journal.pgen.1000938 · Cited by 111
Disabled homolog 2 controls macrophage phenotypic polarization and adipose tissue inflammation
Adamson, S. E., Griffiths, R., Moravec, R., Senthivinayagam, S., Montgomery, G., Chen, W., Han, J., Sharma, P. R., Mullins, G. R., Gorski, S. A., et al. (2016) · Journal of Clinical Investigation · doi:10.1172/jci79590 · Cited by 98
B‐1a lymphocytes attenuate insulin resistance
Shen, L., Chng, M. H. Y., Alonso, M. N., Yuan, R., Winer, D. A., & Engleman, E. G. (2015) · Diabetes · doi:10.2337/db14-0554 · Cited by 109
Adipose tissue, diet and aging
Zamboni, M. M., Rossi, A. P., Fantin, F., Zamboni, G. A., Chirumbolo, S., Zoico, E., & Mazzali, G. (2013) · Mechanisms of Ageing and Development · doi:10.1016/j.mad.2013.11.008 · Cited by 115
Relation of Abdominal Fat Depots to Systemic Markers of Inflammation in Type 2 Diabetes
Sam, S., Haffner, S., Davidson, M., D'Agostino, R., Feinstein, S., Kondos, G., Perez, A. T., & Mazzone, T. (2009) · Diabetes Care · doi:10.2337/dc08-1856 · Cited by 120
M2 Macrophage Polarization Mediates Anti-inflammatory Effects of Endothelial Nitric Oxide Signaling
Lee, W. J., Tateya, S., Cheng, A. M., Rizzo, N. O., Wang, N. F., Handa, P., Wilson, C. L., Clowes, A. W., Sweet, I. R., Bomsztyk, K., et al. (2015) · Diabetes · doi:10.2337/db14-1668 · Cited by 109
Zheng, C., Yang, Q., Xu, C., Shou, P., Cao, J., Jiang, M., Chen, Q., Cao, G., Han, Y., Li, F., et al. (2015) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1500396113 · Cited by 115
Metabolically Healthy Obesity—Heterogeneity in Definitions and Unconventional Factors
Brandão, I., Martins, M. J., & Monteiro, R. (2020) · Metabolites · doi:10.3390/metabo10020048 · Cited by 117
Role of NLRP3 Inflammasome Activation in Obesity-Mediated Metabolic Disorders
Wani, K., AlHarthi, H., Alghamdi, A. A., Sabico, S., & Al‐Daghri, N. M. (2021) · International Journal of Environmental Research and Public Health · doi:10.3390/ijerph18020511 · Cited by 118
Zeyda, M., Gollinger, K., Kriehuber, E., Kiefer, F. W., Neuhofer, A., & Stulnig, T. M. (2010) · International Journal of Obesity · doi:10.1038/ijo.2010.103 · Cited by 114
Luche, É., Cousin, B., Garidou, L., Sérino, M., Waget, A., Barreau, C., André, M., Valet, P., Courtney, M., Casteilla, L., et al. (2013) · Molecular Metabolism · doi:10.1016/j.molmet.2013.06.005 · Cited by 115
Immune Cell Crosstalk in Obesity: A Key Role for Costimulation?
Seijkens, T. T. P., Kusters, P. J. H., Chatzigeorgiou, A., Chavakis, T., & Lutgens, E. (2014) · Diabetes · doi:10.2337/db14-0272 · Cited by 108
Tissue Immunometabolism: Development, Physiology, and Pathobiology
Man, K., Kutyavin, V. I., & Chawla, A. (2016) · Cell Metabolism · doi:10.1016/j.cmet.2016.08.016 · Cited by 108
The complex relationship between obesity and neurodegenerative diseases: an updated review
Neto, A., Fernandes, A. M. A., & Barateiro, A. P. (2023) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2023.1294420 · Cited by 120
Sebastian, B. M., Roychowdhury, S., Tang, H., Hillian, A. D., Feldstein, A. E., Stahl, G. L., Takahashi, K., & Nagy, L. E. (2011) · Journal of Biological Chemistry · doi:10.1074/jbc.m111.254201 · Cited by 107
Inoue, M., Tanabe, H., Matsumoto, A., Takagi, M., Umegaki, K., Amagaya, S., & Takahashi, J. (2012) · Biochemical Pharmacology · doi:10.1016/j.bcp.2012.05.021 · Cited by 110
γδ T cells promote inflammation and insulin resistance during high fat diet-induced obesity in mice
Mehta, P., Nuotio-Antar, A. M., & Smith, C. W. (2014) · Journal of Leukocyte Biology · doi:10.1189/jlb.3a0414-211rr · Cited by 111
Interplay of extracellular matrix and leukocytes in lung inflammation
Wight, T. N., Frevert, C. W., Debley, J. S., Reeves, S. R., Parks, W. C., & Ziegler, S. F. (2016) · Cellular Immunology · doi:10.1016/j.cellimm.2016.12.003 · Cited by 105
Perivascular Adipose Tissue as a Relevant Fat Depot for Cardiovascular Risk in Obesity
da Costa, R. M., Neves, K. B., Tostes, R. C., & Lobato, N. S. (2018) · Frontiers in Physiology · doi:10.3389/fphys.2018.00253 · Cited by 108
Jayaraj, R. L., Azimullah, S., & Beiram, R. (2019) · Saudi Journal of Biological Sciences · doi:10.1016/j.sjbs.2019.12.028 · Cited by 107
Exaggerated effects of particulate matter air pollution in genetic type II diabetes mellitus
Liu, C., Bai, Y., Xu, X., Sun, L., Wang, A., Wang, T.-Y., Maurya, S. K., Periasamy, M., Morishita, M., Harkema, J. R., et al. (2014) · Particle and Fibre Toxicology · doi:10.1186/1743-8977-11-27 · Cited by 107
Kapellos, T. S., & Iqbal, A. J. (2016) · Mediators of Inflammation · doi:10.1155/2016/6591703 · Cited by 109
Yao, M., Zhang, W., Ma, W., Liu, Q., Xing, L., & Zhao, G.-F. (2019) · Experimental & Molecular Medicine · doi:10.1038/s12276-019-0255-x · Cited by 107
Role of Caspase-1 in the Pathogenesis of Inflammatory-Associated Chronic Noncommunicable Diseases
Molla, M. D., Akalu, Y., Geto, Z., Dagnew, B., Ayelign, B., & Shibabaw, T. (2020) · Journal of Inflammation Research · doi:10.2147/jir.s277457 · Cited by 119
Visceral Adiposity and Cancer: Role in Pathogenesis and Prognosis
Crudele, L., Piccinin, E., & Moschetta, A. (2021) · Nutrients · doi:10.3390/nu13062101 · Cited by 114
Brown adipose tissue-derived MaR2 contributes to cold-induced resolution of inflammation
Sugimoto, S., Mena, H. A., Sansbury, B. E., Kobayashi, S., Tsuji, T., Wang, C., Yin, X., Huang, T. L., Kusuyama, J., Kodani, S. D., et al. (2022) · Nature Metabolism · doi:10.1038/s42255-022-00590-0 · Cited by 119
Interferon regulatory factor 7 deficiency prevents diet-induced obesity and insulin resistance
Wang, X., Zhang, R., Zhang, S., Deng, S., Jiang, D., Zhong, J., Yang, L. C., Wang, T., Hong, S., Guo, S., et al. (2013) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.00505.2012 · Cited by 110
Fat in flames: influence of cytokines and pattern recognition receptors on adipocyte lipolysis
Grant, R. W., & Stephens, J. M. (2015) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.00053.2015 · Cited by 109
Santander, A. M., López-Ocejo, O., Casas, O., Agostini, T., Sanchez, L., Lamas-Basulto, E., Carrió, R., Cleary, M. P., Gonzalez-Perez, R. R., & Torroella‐Kouri, M. (2015) · Cancers · doi:10.3390/cancers7010143 · Cited by 110
Adipose tissue macrophages and their polarization in health and obesity
Catrysse, L., & Loo, G. (2018) · Cellular Immunology · doi:10.1016/j.cellimm.2018.03.001 · Cited by 111
Sharma, M., Boytard, L., Hadi, T., Koelwyn, G. J., Simon, R., Ouimet, M. I., Seifert, L., Spiro, W., Yan, B., Hutchison, S. B., et al. (2020) · Scientific Reports · doi:10.1038/s41598-020-62272-9 · Cited by 105
The Effects of Obesity on Anti-Cancer Immunity and Cancer Immunotherapy
Woodall, M. J., Neumann, S., Campbell, K., Pattison, S. T., & Young, S. L. (2020) · Cancers · doi:10.3390/cancers12051230 · Cited by 110
ER stress and inflammation crosstalk in obesity
Ajoolabady, A., Lebeaupin, C., Wu, N. N., Kaufman, R. J., & Ren, J. T. (2022) · Medicinal Research Reviews · doi:10.1002/med.21921 · Cited by 110
Fujisaka, S., Usui, I., Kanatani, Y., Ikutani, M., Takasaki, I., Tsuneyama, K., Tabuchi, Y., Bukhari, A., Yamazaki, Y., Suzuki, H., et al. (2011) · Endocrinology · doi:10.1210/en.2010-1312 · Cited by 105
Endocannabinoids and the Control of Energy Homeostasis
Kunos, G., Osei‐Hyiaman, D., Liu, J., Godlewski, G., & Bátkai, S. (2008) · Journal of Biological Chemistry · doi:10.1074/jbc.r800012200 · Cited by 112
Ni, Y., Nagashimada, M., Zhan, L., Nagata, N., Kobori, M., Sugiura, M., Ogawa, K., Kaneko, S., & Ota, T. (2015) · Endocrinology · doi:10.1210/en.2014-1776 · Cited by 104
Metabolic Inflammation-Differential Modulation by Dietary Constituents
Lyons, C. L., Kennedy, E. B., & Roche, H. M. (2016) · Nutrients · doi:10.3390/nu8050247 · Cited by 106
Jayabalan, N., Nair, S., Nuzhat, Z., Rice, G. E., Zuñiga, F. A., Sobrevía, L., Leiva, A., Sanhueza, C., Gutiérrez, J., Lappas, M., et al. (2017) · Frontiers in Endocrinology · doi:10.3389/fendo.2017.00239 · Cited by 106
Katsimbri, P., Korakas, E., Kountouri, A., Ikonomidis, I., Tsougos, E., Vlachos, D., Papadavid, E., Raptis, A. E., & Lambadiari, V. (2021) · Antioxidants · doi:10.3390/antiox10020157 · Cited by 114
Adipocytes, Innate Immunity and Obesity: A Mini-Review
Blaszczak, A. M., Jalilvand, A., & Hsueh, W. A. (2021) · Frontiers in Immunology · doi:10.3389/fimmu.2021.650768 · Cited by 109
Arteriolar Function in Visceral Adipose Tissue Is Impaired in Human Obesity
Farb, M. G., Ganley-Leal, L. M., Mott, M. M., Liang, Y., Ercan, B., Widlansky, M. E., Bigornia, S., Fiscale, A. J., Apovian, C. M., Carmine, B. J., et al. (2011) · Arteriosclerosis Thrombosis and Vascular Biology · doi:10.1161/atvbaha.111.235846 · Cited by 102
Talbot, N. A., Wheeler-Jones, C. P. D., & Cleasby, M. E. (2014) · Molecular and Cellular Endocrinology · doi:10.1016/j.mce.2014.06.010 · Cited by 105
Ichioka, M., Suganami, T., Tsuda, N., Shirakawa, I., Hirata, Y., Satoh‐Asahara, N., Shimoda, Y., Tanaka, M., Kim-Saijo, M., Miyamoto, Y., et al. (2011) · Diabetes · doi:10.2337/db10-0864 · Cited by 104
The role of adipose tissue in mediating the beneficial effects of dietary fish oil
Puglisi, M. J., Hasty, A. H., & Saraswathi, V. (2010) · The Journal of Nutritional Biochemistry · doi:10.1016/j.jnutbio.2010.07.003 · Cited by 108
Lipin-2 Reduces Proinflammatory Signaling Induced by Saturated Fatty Acids in Macrophages
Valdearcos, M., Esquinas, E., Meana, C., Peña, L., Gil‐de‐Gómez, L., Balsinde, J., & Balboa, M. A. (2012) · Journal of Biological Chemistry · doi:10.1074/jbc.m112.342915 · Cited by 102
Emerging Role of Mast Cells and Macrophages in Cardiovascular and Metabolic Diseases
Xu, J., & Shi, G. (2012) · Endocrine Reviews · doi:10.1210/er.2011-0013 · Cited by 105
Mancini, S. J., White, A. D., Bijland, S., Rutherford, C. L., Graham, D., Richter, E. A., Viollet, B., Touyz, R. M., Palmer, T. M., & Salt, I. P. (2016) · Molecular and Cellular Endocrinology · doi:10.1016/j.mce.2016.11.010 · Cited by 106
Functions of omega-3 fatty acids and FFA4 (GPR120) in macrophages
Im, D. (2015) · European Journal of Pharmacology · doi:10.1016/j.ejphar.2015.03.094 · Cited by 104
The obesity-breast cancer link: a multidisciplinary perspective
Devericks, E. N., Carson, M. S., McCullough, L. E., Coleman, M. F., & Hursting, S. D. (2022) · Cancer and Metastasis Reviews · doi:10.1007/s10555-022-10043-5 · Cited by 119
Unbalanced M1/M2 Phenotype of Peripheral Blood Monocytes in Obese Diabetic Patients
Satoh, N., Shimatsu, A., Himeno, A., Sasaki, Y., Yamakage, H., Yamada, K., Suganami, T., & Ogawa, Y. (2009) · Diabetes Care · doi:10.2337/dc09-1315 · Cited by 103
Alternatively Activated Macrophages in Types 1 and 2 Diabetes
Espinoza-Jiménez, A., Peón, A. N., & Terrazas, L. I. (2012) · Mediators of Inflammation · doi:10.1155/2012/815953 · Cited by 109
Toll-like receptors and macrophage activation in atherosclerosis
Seneviratne, A. N., Sivagurunathan, B., & Monaco, C. G. (2011) · Clinica Chimica Acta · doi:10.1016/j.cca.2011.08.021 · Cited by 106
New therapeutic approaches for the treatment of obesity
Saltiel, A. R. (2016) · Science Translational Medicine · doi:10.1126/scitranslmed.aad1811 · Cited by 102
Self-citationCimini, F. A., Barchetta, I., Carotti, S., Bertoccini, L., Baroni, M. G., Vespasiani-Gentilucci, U., Cavallo, M.-G., & Morini, S. (2017) · World Journal of Gastroenterology · doi:10.3748/wjg.v23.i19.3407 · Cited by 101
Insulin Resistance in the Defense against Obesity
Saltiel, A. R. (2012) · Cell Metabolism · doi:10.1016/j.cmet.2012.03.001 · Cited by 105
Self-citationSatoh, M., Andoh, Y., Clingan, C. S., Ogura, H., Fujii, S., Eshima, K., Nakayama, T., Taniguchi, M., Hirata, N., Ishimori, N., et al. (2012) · PLoS ONE · doi:10.1371/journal.pone.0030568 · Cited by 103
Chavakis, T., Chmelař, J., & Chung, K. (2013) · Thrombosis and Haemostasis · doi:10.1160/th12-09-0703 · Cited by 106
Adipose tissue inflammation in glucose metabolism
Kammoun, H. L., Kraakman, M. J., & Febbraio, M. A. (2013) · Reviews in Endocrine and Metabolic Disorders · doi:10.1007/s11154-013-9274-4 · Cited by 101
Deletion of Cd39/Entpd1 Results in Hepatic Insulin Resistance
Enjyoji, K., Kotani, K., Thukral, C., Blumel, B., Sun, X., Wu, Y., Imai, M., Friedman, D. J., Csizmadia, E., Bleibel, W., et al. (2008) · Diabetes · doi:10.2337/db07-1265 · Cited by 101
NLRP3 Inflammasome Activation in Adipose Tissues and Its Implications on Metabolic Diseases
Wu, K. K.-L., Cheung, S. W. M., & Cheng, K. K. Y. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21114184 · Cited by 105
Pasquarelli-do-Nascimento, G., Braz-de-Melo, H. A., Faria, S. S., Santos, I. D. O., Kobinger, G., & Magalhães, K. G. (2020) · Frontiers in Endocrinology · doi:10.3389/fendo.2020.00530 · Cited by 103
Resident tissue macrophages: Key coordinators of tissue homeostasis beyond immunity
Zhao, J., Andreev, I., & Silva, H. M. (2024) · Science Immunology · doi:10.1126/sciimmunol.add1967 · Cited by 109
Lipid-associated macrophages between aggravation and alleviation of metabolic diseases
Xu, R., Vujić, N., Bianco, V., Reinisch, I., Kratky, D., Krstić, J., & Prokesch, A. (2024) · Trends in Endocrinology and Metabolism · doi:10.1016/j.tem.2024.04.009 · Cited by 108
Mechanism of ER Stress and Inflammation for Hepatic Insulin Resistance in Obesity
Kim, O., Jun, W., & Lee, J. (2015) · Annals of Nutrition and Metabolism · doi:10.1159/000440905 · Cited by 103
Psoriatic disease—from skin to bone
Ritchlin, C. T. (2007) · Nature Clinical Practice Rheumatology · doi:10.1038/ncprheum0670 · Cited by 102
Grant, W. F., Gillingham, M. B., Batra, A. K., Fewkes, N. M., Comstock, S. M., Takahashi, D. L., Braun, T. P., Grove, K. L., Friedman, J. E., & Marks, D. L. (2011) · PLoS ONE · doi:10.1371/journal.pone.0017261 · Cited by 101
Alliin, a Garlic (Allium sativum) Compound, Prevents LPS-Induced Inflammation in 3T3-L1 Adipocytes
Quintero-Fabián, S., Ortuño‐Sahagún, D., Vázquez‐Carrera, M., & López-Roa, R. I. (2013) · Mediators of Inflammation · doi:10.1155/2013/381815 · Cited by 101
Visceral fat accumulation is an indicator of adipose tissue macrophage infiltration in women
Michaud, A., Drolet, R., Noël, S., Paris, G., & Tchernof, A. (2011) · Metabolism · doi:10.1016/j.metabol.2011.10.004 · Cited by 105
The role of GM-CSF in adipose tissue inflammation
Kim, D., Sandoval, D. A., Reed, J. A. H., Matter, E. K., Tolod, E. G., Woods, S. C., & Seeley, R. J. (2008) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.00061.2008 · Cited by 105
Adipocyte SIRT1 controls systemic insulin sensitivity by modulating macrophages in adipose tissue
Hui, X. H., Zhang, M., Gu, P., Li, K., Gao, Y. Z., Wu, D., Wang, Y., & Xu, A. (2017) · EMBO Reports · doi:10.15252/embr.201643184 · Cited by 99
Inflammation, dysregulated metabolism and aromatase in obesity and breast cancer
Zahid, H., Simpson, E. R., & Brown, K. A. (2016) · Current Opinion in Pharmacology · doi:10.1016/j.coph.2016.11.003 · Cited by 101
Kimball, A., Joshi, A., Carson, W. F., Boniakowski, A. E., Schaller, M. A., Allen, R., Bermick, J., Davis, F. M., Henke, P. K., Burant, C., et al. (2017) · Diabetes · doi:10.2337/db17-0194 · Cited by 105
Pesticides-induced energy metabolic disorders
He, B., Ni, Y., Jin, Y., & Fu, Z. (2020) · The Science of The Total Environment · doi:10.1016/j.scitotenv.2020.139033 · Cited by 100
Obesity and chronic inflammation crosslinking
Artemniak-Wojtowicz, D., Kucharská, A., & Pyrżak, B. (2021) · Central European Journal of Immunology · doi:10.5114/ceji.2020.103418 · Cited by 106
Cai, X., Hu, J., Wen, W., Wang, J., Wang, M., Liu, S., Zhu, Q., Hong, J., Dang, Y., Yao, X., et al. (2022) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2022/4914791 · Cited by 101
Bassaganya-Riera, J., Misyak, S. A., Guri, A. J., & Hontecillas, R. (2009) · Cellular Immunology · doi:10.1016/j.cellimm.2009.04.003 · Cited by 101
Paik, J., Fierce, Y., Treuting, P. M., Brabb, T., & Maggio‐Price, L. (2013) · Journal of Nutrition · doi:10.3945/jn.113.174615 · Cited by 102
Neuropeptide Y Is Produced by Adipose Tissue Macrophages and Regulates Obesity-Induced Inflammation
Singer, K., Morris, D. L., Oatmen, K. E., Wang, T., DelProposto, J. L., Mergian, T. A., Cho, K. W., & Lumeng, C. N.-K. (2013) · PLoS ONE · doi:10.1371/journal.pone.0057929 · Cited by 100
Self-citationAdipose Tissue Remodeling as Homeostatic Inflammation
Itoh, M., Suganami, T., Hachiya, R., & Ogawa, Y. (2011) · International Journal of Inflammation · doi:10.4061/2011/720926 · Cited by 107
Interactions between adipose tissue and the immune system in health and malnutrition
Wensveen, F. M., Marinović, S., Šestan, M., Wensveen, T. T., & Polić, B. (2015) · Seminars in Immunology · doi:10.1016/j.smim.2015.10.006 · Cited by 103
Adipose tissue dysfunction and hypertriglyceridemia: mechanisms and management
van de Woestijne, A. P., Monajemi, H., Kalkhoven, E., & Visseren, F. L. J. (2011) · Obesity Reviews · doi:10.1111/j.1467-789x.2011.00900.x · Cited by 100
Hybrid nanoparticles improve targeting to inflammatory macrophages through phagocytic signals
Bagalkot, V., Badgeley, M. A., Kampfrath, T., Deiuliis, J. A., Rajagopalan, S., & Maiseyeu, A. (2015) · Journal of Controlled Release · doi:10.1016/j.jconrel.2015.09.027 · Cited by 99
The obesity-related pathology and Th17 cells
Endo, Y., Yokote, K., & Nakayama, T. (2016) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-016-2399-3 · Cited by 102
Nuclear receptors linking metabolism, inflammation, and fibrosis in nonalcoholic fatty liver disease
Puengel, T., Liu, H., Guillot, A., Heymann, F., Tacke, F., & Peiseler, M. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms23052668 · Cited by 95
Role of the gut in visceral fat inflammation and metabolic disorders
Lam, Y. Y., Mitchell, A. J., Holmes, A. J., Denyer, G. S., Gummesson, A., Caterson, I. D., Hunt, N. H., & Storlien, L. H. (2011) · Obesity · doi:10.1038/oby.2011.68 · Cited by 97
Zhou, J., Xu, G., Ma, S., Li, F., Yuan, M., Xu, H., & Huang, K. (2015) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2015.10.054 · Cited by 97
Lasselin, J., Magne, E., Beau, C., Ledaguenel, P., Dexpert, S., Aubert, A., Layé, S., & Capuron, L. (2014) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/jc.2013-2673 · Cited by 96
Metadata
- Authors
- Lumeng, C. N., Bodzin, J. L., & Saltiel, A. R.
- Affiliations
- University of Michigan (US)
- Corresponding author
- Saltiel, Alan R.
- Venue
- Journal of Clinical Investigation
- Published
- 2007-01-02
- Volume
- 117
- Issue
- 1
- Pages
- 175-184
- ISSN
- 0021-9738 (ISSN-L)
- PMC
- PMC1716210
- OpenAlex
- W2145697808
- Cited by
- 4,664
- References
- 54
- Citations by year
- 2026: 157 · 2025: 214 · 2024: 227 · 2023: 224 · 2022: 256 · 2021: 324 · 2020: 320 · 2019: 304 · 2018: 290 · 2017: 322 · 2016: 296 · 2015: 290 · 2014: 286 · 2013: 319 · 2012: 226
- FWCI
- 92.09
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Locations
- Journal of Clinical Investigation (publishedVersion)
- Europe PMC (PubMed Central) (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Funders
- University of Michigan
- National Institutes of Health (HD028820)
- National Institute of Diabetes and Digestive and Kidney Diseases (R01DK60591, R01DK060591)
- Eunice Kennedy Shriver National Institute of Child Health and Human Development (T32HD007513, K12HD028820)
- Topics
- Health Sciences › Medicine › Endocrinology, Diabetes and Metabolism › Adipokines, Inflammation, and Metabolic Diseases
- Life Sciences › Immunology and Microbiology › Immunology › Immune cells in cancer
- Health Sciences › Medicine › Physiology (medical) › Adipose Tissue and Metabolism
- Keywords
- obesity, adipose tissue macrophages, macrophage polarization, M1/M2 macrophages, insulin resistance, diet-induced obesity, CCR2, IL-10, TNF-α, adipocyte inflammation, high-fat diet, M2 macrophages
- MeSH terms
- Adipose Tissue, Animals, Base Sequence, Biological Transport, Energy Intake, Deoxyglucose, Dietary Fats, Disease Models, Animal, Macrophages, Male, Mice, Inbred C57BL, Mice, Obese, Obesity, 3T3 Cells, DNA Primers, Reverse Transcriptase Polymerase Chain Reaction, Mice
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