The DOI matches its Crossref record; 98 of the 98 references it cites were found in a registry or an index.
Contribution of adipogenesis to healthy adipose tissue expansion in obesity
Open accessAbstract
The manner in which white adipose tissue (WAT) expands and remodels directly impacts the risk of developing metabolic syndrome in obesity. Preferential accumulation of visceral WAT is associated with increased risk for insulin resistance, whereas subcutaneous WAT expansion is protective. Moreover, pathologic WAT remodeling, typically characterized by adipocyte hypertrophy, chronic inflammation, and fibrosis, is associated with insulin resistance. Healthy WAT expansion, observed in the "metabolically healthy" obese, is generally associated with the presence of smaller and more numerous adipocytes, along with lower degrees of inflammation and fibrosis. Here, we highlight recent human and rodent studies that support the notion that the ability to recruit new fat cells through adipogenesis is a critical determinant of healthy adipose tissue distribution and remodeling in obesity. Furthermore, we discuss recent advances in our understanding of the identity of tissue-resident progenitor populations in WAT made possible through single-cell RNA sequencing analysis. A better understanding of adipose stem cell biology and adipogenesis may lead to novel strategies to uncouple obesity from metabolic disease.
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?
The cited source says what the claim attributes to it.
In the citing paper
“The distribution of body fat in obesity is closely correlated with metabolic health. The expansion of visceral fat depots increases risks for metabolic disorders, whereas subcutaneous fat depots pose lesser risks or can even offer protection (Vishvanath and Gupta, 2019).”
From Robust single-nucleus RNA sequencing reveals depot-specific cell population dynamics in adipose tissue remodeling during obesity (2025) · cites this paper as Vishvanath and Gupta, 2019
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
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
Adipokines in inflammation and metabolic disease
Ouchi, N., Parker, J. L., Lugus, J. J., & Walsh, K. (2011) · Nature Reviews Immunology · doi:10.1038/nri2921 · Cited by 4,625
Stimulation of adipogenesis in fibroblasts by PPARγ2, a lipid-activated transcription factor
Tontonoz, P., Hu, E., & Spiegelman, B. M. (1994) · Cell · doi:10.1016/0092-8674(94)90006-x · Cited by 3,564
Beige Adipocytes Are a Distinct Type of Thermogenic Fat Cell in Mouse and Human
Wu, J., Boström, P., Sparks, L. M., Li, Y., Choi, J. H., Giang, A.-H., Khandekar, M. J., Virtanen, K. A., Nuutila, P., Schaart, G., et al. (2012) · Cell · doi:10.1016/j.cell.2012.05.016 · Cited by 3,406
What we talk about when we talk about fat
Rosen, E. D., & Spiegelman, B. M. (2014) · Cell · doi:10.1016/j.cell.2013.12.012 · Cited by 2,373
Dynamics of fat cell turnover in humans
Spalding, K. L., Arner, E., Westermark, P. O., Bernard, S., Buchholz, B. A., Bergmann, O., Blomqvist, L., Hoffstedt, J., Näslund, E., Britton, T., et al. (2008) · Nature · doi:10.1038/nature06902 · Cited by 2,357
Adipose tissue remodeling and obesity
Sun, K., Kusminski, C. M., & Scherer, P. E. (2011) · Journal of Clinical Investigation · doi:10.1172/jci45887 · Cited by 1,941
Adipogenesis and metabolic health
Ghaben, A. L., & Scherer, P. E. (2019) · Nature Reviews Molecular Cell Biology · doi:10.1038/s41580-018-0093-z · Cited by 1,395
Barroso, I., Gurnell, M., Crowley, V. E. F., Agostini, M., Schwabe, J. W., Soos, M. A., Maslen, G. L., Williams, T. D. M., Lewis, H., Schafer, A. J., et al. (1999) · Nature · doi:10.1038/47254 · Cited by 1,368
Obesity-associated improvements in metabolic profile through expansion of adipose tissue
Kim, J.-Y., van de Wall, E., Laplante, M., Azzara, A., Trujillo, M. E., Hofmann, S. M., Schraw, T., Durand, J. L., Li, H., Li, G., et al. (2007) · Journal of Clinical Investigation · doi:10.1172/jci31021 · Cited by 1,310 · cited 1×
“These engineered animals are more or equally obese compared with their control littermates, but metabolically healthy (56–59).”
Background
Flagged first, then by citations
Cited by
Sorted by citations
Adipose-tissue plasticity in health and disease
Sakers, A. P., Siqueira, M. K. D., Seale, P., & Villanueva, C. J. (2022) · Cell · doi:10.1016/j.cell.2021.12.016 · Cited by 1,124
Causes, consequences, and treatment of metabolically unhealthy fat distribution
Stefan, N. (2020) · The Lancet Diabetes & Endocrinology · doi:10.1016/s2213-8587(20)30110-8 · Cited by 566
Lipid and glucose metabolism in white adipocytes: pathways, dysfunction and therapeutics
Morigny, P., Boucher, J., Arner, P., & Langin, D. (2021) · Nature Reviews Endocrinology · doi:10.1038/s41574-021-00471-8 · Cited by 560
Signaling pathways in obesity: mechanisms and therapeutic interventions
Wen, X., Zhang, B., Wu, B., Xiao, H., Li, Z., Li, R., Xu, X., & Li, T. (2022) · Signal Transduction and Targeted Therapy · doi:10.1038/s41392-022-01149-x · Cited by 490
Sárvári, A. K., Hauwaert, E. L. V., Markussen, L. K., Gammelmark, E., Marcher, A.-B., Ebbesen, M. F., Nielsen, R., Brewer, J. R., Madsen, J. G. S., & Mandrup, S. (2020) · Cell Metabolism · doi:10.1016/j.cmet.2020.12.004 · Cited by 377
Obese visceral fat tissue inflammation: from protective to detrimental?
Kolb, H. (2022) · BMC Medicine · doi:10.1186/s12916-022-02672-y · Cited by 399
White adipose tissue dysfunction in obesity and aging
Reyes-Farias, M., Fos-Domenech, J., Serra, D., Herrero, L., & Sánchez-Infantes, D. (2021) · Biochemical Pharmacology · doi:10.1016/j.bcp.2021.114723 · Cited by 250
White adipocyte dysfunction and obesity-associated pathologies in humans
Hagberg, C. E., & Spalding, K. L. (2023) · Nature Reviews Molecular Cell Biology · doi:10.1038/s41580-023-00680-1 · Cited by 236
Obesity I: Overview and molecular and biochemical mechanisms
Lustig, R. H., Collier, D., Kassotis, C., Roepke, T. A., Kim, M. J., Blanc, E., Barouki, R., Bansal, A., Cave, M. C., Chatterjee, S., et al. (2022) · Biochemical Pharmacology · doi:10.1016/j.bcp.2022.115012 · Cited by 203
PARPs in lipid metabolism and related diseases
Szántó, M., Gupte, R., Kraus, W. L., Pacher, P., & Bai, P. (2021) · Progress in Lipid Research · doi:10.1016/j.plipres.2021.101117 · Cited by 181
Metabolically healthy obesity: from epidemiology and mechanisms to clinical implications
Schulze, M. B., & Stefan, N. (2024) · Nature Reviews Endocrinology · doi:10.1038/s41574-024-01008-5 · Cited by 211
Tang, S., Yao, L., Ruan, J., Kang, J., Cao, Y., Nie, X., Lan, W., Zhu, Z., Han, W., Liu, Y., et al. (2024) · Science Translational Medicine · doi:10.1126/scitranslmed.adf4590 · Cited by 173
ECM formation and degradation during fibrosis, repair, and regeneration
Mayorca-Guiliani, A. E., Leeming, D. J., Henriksen, K., Mortensen, J. H., Nielsen, S. H., Anstee, Q. M., Sanyal, A. J., Karsdal, M. A., & Schuppan, D. (2025) · npj Metabolic Health and Disease · doi:10.1038/s44324-025-00063-4 · Cited by 176
Contreras, O., Rossi, F. M. V., & Théret, M. (2021) · Skeletal Muscle · doi:10.1186/s13395-021-00265-6 · Cited by 163
Innate Immune Cells in the Adipose Tissue in Health and Metabolic Disease
Michailidou, Z., Gomez-Salazar, M. A., & Alexaki, V. I. (2021) · Journal of Innate Immunity · doi:10.1159/000515117 · Cited by 143
Shamsi, F., Piper, M. E., Ho, L., Huang, T. L., Gupta, A., Streets, A., Lynes, M. D., & Tseng, Y. (2021) · Nature Metabolism · doi:10.1038/s42255-021-00373-z · Cited by 123
Abildgaard, J., Ploug, T., Al-Saoudi, E., Wagner, T., Thomsen, C., Ewertsen, C., Bzorek, M., Pedersen, B. K., Pedersen, A. T., & Lindegaard, B. (2021) · Scientific Reports · doi:10.1038/s41598-021-94189-2 · Cited by 116
Peikert, A., Vaduganathan, M., Claggett, B. L., Kulac, I. J., Litwin, S. E., Zile, M. R., Desai, A. S., Jhund, P. S., Butt, J. H., Lam, C. S. P., et al. (2025) · European Heart Journal · doi:10.1093/eurheartj/ehaf057 · Cited by 126
Adipose Tissue: Understanding the Heterogeneity of Stem Cells for Regenerative Medicine
Ong, W. K., Chakraborty, S., & Sugii, S. (2021) · Biomolecules · doi:10.3390/biom11070918 · Cited by 112
Cardiovascular protection by SGLT2 inhibitors – Do anti-inflammatory mechanisms play a role?
Elrakaybi, A., Laubner, K., Zhou, Q., Hug, M. J., & Seufert, J. (2022) · Molecular Metabolism · doi:10.1016/j.molmet.2022.101549 · Cited by 118
Sastourné-Arrey, Q., Mathieu, M., Contreras, X., Monferran, S., Bourlier, V., Gil‐Ortega, M., Murphy, E. E., Laurens, C., Varin, A., Guissard, C., et al. (2023) · Nature Communications · doi:10.1038/s41467-022-35524-7 · Cited by 96
Gut Microbial-Derived Short Chain Fatty Acids: Impact on Adipose Tissue Physiology
May, K. S., & den Hartigh, L. J. (2023) · Nutrients · doi:10.3390/nu15020272 · Cited by 100
The regulation of PKA signaling in obesity and in the maintenance of metabolic health
London, E., & Stratakis, C. A. (2022) · Pharmacology & Therapeutics · doi:10.1016/j.pharmthera.2022.108113 · Cited by 99
Pathologic HIF1α signaling drives adipose progenitor dysfunction in obesity
Shao, M., Hepler, C., Zhang, Q., Shan, B., Vishvanath, L., Henry, G. H., Zhao, S., An, Y., Wu, Y., Strand, D. W., et al. (2021) · Cell stem cell · doi:10.1016/j.stem.2020.12.008 · Cited by 87
Self-citationProgress in Understanding Metabolic Syndrome and Knowledge of Its Complex Pathophysiology
Jha, B. K., Sherpa, M. L., Imran, M., Mohammed, Y., Jha, L. A., Paudel, K. R., & Jha, S. K. (2023) · Diabetology · doi:10.3390/diabetology4020015 · Cited by 111
Obesity: pathophysiology and therapeutic interventions
Kong, Y., Yang, H., Nie, R., Zhang, X., Zuo, F., Zhang, H., & Nian, X. (2025) · Molecular Biomedicine · doi:10.1186/s43556-025-00264-9 · Cited by 89
Adipose Tissue Macrophage Polarization in Healthy and Unhealthy Obesity
Ruggiero, A. D., Key, C.-C. C., & Kavanagh, K. (2021) · Frontiers in Nutrition · doi:10.3389/fnut.2021.625331 · Cited by 93
Szántó, M., & Bai, P. (2020) · Genes & Development · doi:10.1101/gad.334284.119 · Cited by 91
PKA functions in metabolism and resistance to obesity: lessons from mouse and human studies
London, E., Bloyd, M., & Stratakis, C. A. (2020) · Journal of Endocrinology · doi:10.1530/joe-20-0035 · Cited by 94
Regulatory mechanisms of the early phase of white adipocyte differentiation: an overview
Audano, M., Pedretti, S., Caruso, D., Crestani, M., Fabiani, E. D., & Mitro, N. (2022) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-022-04169-6 · Cited by 89
The Role of Autophagy in White Adipose Tissue Function: Implications for Metabolic Health
Clemente‐Postigo, M., Tinahones, A., Bekay, R. E., Malagón, M. M., & Tinahones, F. J. (2020) · Metabolites · doi:10.3390/metabo10050179 · Cited by 78
Modeling Adipogenesis: Current and Future Perspective
Bahmad, H. F., Daouk, R., Azar, J. H., Sapudom, J., Teo, J. C. M., Abou-Kheir, W. G., & Al‐Sayegh, M. (2020) · Cells · doi:10.3390/cells9102326 · Cited by 74
Zhao, G., Tian, Z., Tian, T., Zhu, Z.-P., Zhao, W.-J., Tian, H., Cheng, X., Hu, F., Hu, M., Tian, S., et al. (2021) · Cell Metabolism · doi:10.1016/j.cmet.2021.05.014 · Cited by 73
Fischer, A. W., Jaeckstein, M. Y., Gottschling, K., Heine, M., Sass, F., Mangels, N., Schlein, C., Worthmann, A., Bruns†, O. T., Yuan, Y., et al. (2020) · Cell Metabolism · doi:10.1016/j.cmet.2020.12.001 · Cited by 70
Nelson, M. E., Madsen, S., Cooke, K. C., Fritzen, A. M., Thorius, I. H., Masson, S. W. C., Carroll, L., Weiss, F. C., Seldin, M. M., Potter, M., et al. (2022) · Cell Metabolism · doi:10.1016/j.cmet.2021.12.013 · Cited by 61
The regulation of adipocyte growth in white adipose tissue
Li, Q., & Spalding, K. L. (2022) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2022.1003219 · Cited by 72
Review article: prognostic significance of body composition abnormalities in patients with cirrhosis
Ebadi, M., Bhanji, R. A., Tandon, P., Mazurak, V. C., Baracos, V. E., & Montaño‐Loza, A. J. (2020) · Alimentary Pharmacology & Therapeutics · doi:10.1111/apt.15927 · Cited by 68
Adipose tissue fibrosis: the unwanted houseguest invited by obesity
Gliniak, C. M., Pedersen, L., & Scherer, P. E. (2023) · Journal of Endocrinology · doi:10.1530/joe-23-0180 · Cited by 82
Adipotropic effects of heavy metals and their potential role in obesity
Tinkov, A. A., Aschner, M., Ke, T., Ferrer, B., Zhou, J., Chang, J., Santamarı́a, A., Chao, J. C.-J., Aaseth, J., & Skalny, A. V. (2021) · Faculty Reviews · doi:10.12703/r/10-32 · Cited by 70
The pathobiology of perivascular adipose tissue (PVAT), the fourth layer of the blood vessel wall
Hillock-Watling, C., & Gotlieb, A. I. (2022) · Cardiovascular Pathology · doi:10.1016/j.carpath.2022.107459 · Cited by 65
Leptin Increases Hepatic Triglyceride Export via a Vagal Mechanism in Humans
Metz, M., Beghini, M., Wolf, P. S., Pfleger, L., Hackl, M. T., Bastian, M., Freudenthaler, A., Harreiter, J., Zeyda, M., Baumgartner-Parzer, S. M., et al. (2022) · Cell Metabolism · doi:10.1016/j.cmet.2022.09.020 · Cited by 65
The role of adipose tissue dysfunction in hepatic insulin resistance and T2D
Sancar, G., & Birkenfeld, A. L. (2024) · Journal of Endocrinology · doi:10.1530/joe-24-0115 · Cited by 69
Porro, S., Genchi, V. A., Cignarelli, A., Natalicchio, A., Laviola, L., Giorgino, F., & Perrini, S. (2020) · Journal of Endocrinological Investigation · doi:10.1007/s40618-020-01446-8 · Cited by 64
Beals, J. W., Smith, G. I., Shankaran, M., Fuchs, A. G., Schweitzer, G. G., Yoshino, J., Field, T., Matthews, M. D., Nyangau, E., Morozov, D., et al. (2021) · Hepatology · doi:10.1002/hep.31822 · Cited by 64
Al-Ghadban, S. I., Diaz, Z. T., Singer, H. J., Mert, K. B., & Bunnell, B. A. (2020) · Cells · doi:10.3390/cells9020430 · Cited by 58
Adetunji, C. O., Michael, O. S., Rathee, S., Singh, K. R., Ajayi, O. O., Adetunji, J. B., Ojha, A., Singh, J., & Singh, R. P. (2021) · Materials Today Advances · doi:10.1016/j.mtadv.2021.100198 · Cited by 62
Zhang, J., Yi, C., Han, J., Ming, T., Zhou, J., Lu, C., Li, Y., & Su, X. (2020) · Food Science & Nutrition · doi:10.1002/fsn3.1941 · Cited by 59
Dpp4+ interstitial progenitor cells contribute to basal and high fat diet-induced adipogenesis
Stefkovich, M. L., Traynor, S., Cheng, L., Merrick, D., & Seale, P. (2021) · Molecular Metabolism · doi:10.1016/j.molmet.2021.101357 · Cited by 58
Adult-Onset Diseases in Low Birth Weight Infants: Association with Adipose Tissue Maldevelopment
Nakano, Y. (2019) · Journal of Atherosclerosis and Thrombosis · doi:10.5551/jat.rv17039 · Cited by 60
Wu, S.-C., Lo, Y.-M., Lee, J., Chen, C., Chen, T.-W., Liu, H., Lian, W.-N., Hua, K., Liao, C., Lin, W.-J., et al. (2022) · Nature Communications · doi:10.1038/s41467-022-31825-z · Cited by 56
The Potential to Fight Obesity with Adipogenesis Modulating Compounds
Zhao, J., Zhou, A., & Qi, W. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms23042299 · Cited by 55
Scheidl, T. B., Brightwell, A. L., Easson, S., & Thompson, J. A. (2023) · BMC Medicine · doi:10.1186/s12916-023-02730-z · Cited by 61
Research advances in the anti-inflammatory effects of SGLT inhibitors in type 2 diabetes mellitus
Zhang, R., Xie, Q., Lu, X., Fan, R., & Tong, N. (2024) · Diabetology & Metabolic Syndrome · doi:10.1186/s13098-024-01325-9 · Cited by 63
Insulin Resistance Is Cheerfully Hitched with Hypertension
Sinha, S., & Haque, M. (2022) · Life · doi:10.3390/life12040564 · Cited by 65
Song, T., Yang, Y., Jiang, S., & Peng, J. (2020) · Advanced Science · doi:10.1002/advs.202001563 · Cited by 52
Novel insights into adipose tissue heterogeneity
Wang, T., Sharma, A. K., & Wolfrum, C. (2021) · Reviews in Endocrine and Metabolic Disorders · doi:10.1007/s11154-021-09703-8 · Cited by 51
Chao, Y.-Q., Jiang, Y., Zhong, M., Wei, K., Hu, C., Qin, Y., Zuo, Y., Yang, L., Shen, Z., & Zou, C. (2021) · Cell & Bioscience · doi:10.1186/s13578-021-00581-w · Cited by 54
Primary cilia-dependent lipid raft/caveolin dynamics regulate adipogenesis
Yamakawa, D., Katoh, D., Kasahara, K., Shiromizu, T., Matsuyama, M., Matsuda, C., Maeno, Y., Watanabe, M., Nishimura, Y., & Inagaki, M. (2021) · Cell Reports · doi:10.1016/j.celrep.2021.108817 · Cited by 49
Honecker, J., Ruschke, S., Seeliger, C., Laber, S., Strobel, S., Pröll, P., Nellåker, C., Lindgren, C. M., Kulozik, U., Ecker, J., et al. (2022) · EBioMedicine · doi:10.1016/j.ebiom.2022.104020 · Cited by 48
Takeda, Y., Harada, Y., Yoshikawa, T., & Dai, P. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms24021352 · Cited by 49
Sarcopenia and cachexia: molecular mechanisms and therapeutic interventions
Wang, T., Zhou, D., & Hong, Z. (2025) · MedComm · doi:10.1002/mco2.70030 · Cited by 46
The pivotal role of Nrf2 activators in adipocyte biology
Annie-Mathew, A. S., Prem-Santhosh, S., Jayasuriya, R., Ganesh, G., Ramkumar, K. M., & Sarada, D. V. L. (2021) · Pharmacological Research · doi:10.1016/j.phrs.2021.105853 · Cited by 49
MHO or MUO? White adipose tissue remodeling
Zhao, J. Y., Li, Z., Ma, K. L., Hao, R., & Li, M. (2024) · Obesity Reviews · doi:10.1111/obr.13691 · Cited by 49
Slc25a5 regulates adipogenesis by modulating ERK signaling in OP9 cells
Zhu, S., Wang, W., Zhang, J., Ji, S., Jing, Z., & Chen, Y. Q. (2022) · Cellular & Molecular Biology Letters · doi:10.1186/s11658-022-00314-y · Cited by 43
Adipose Tissue Dynamics: Cellular and Lipid Turnover in Health and Disease
Palacios‐Marin, I., Serra, D., Jiménez‐Chillarón, J. C., Herrero, L., & Todorčević, M. (2023) · Nutrients · doi:10.3390/nu15183968 · Cited by 47
PPARγ Acetylation Orchestrates Adipose Plasticity and Metabolic Rhythms
He, Y., Taub, A., Yu, L., Yao, Y., Zhang, R., Zahr, T., Aaron, N., LeSauter, J., Fan, L., Liu, L., et al. (2022) · Advanced Science · doi:10.1002/advs.202204190 · Cited by 40
Autophagy: a molecular switch to regulate adipogenesis and lipolysis
Sekar, M., & Thirumurugan, K. (2022) · Molecular and Cellular Biochemistry · doi:10.1007/s11010-021-04324-w · Cited by 41
Grancieri, M., Verediano, T. A., Sant'Ana, C. T., de Assis, A., Toledo, R. L., de Mejia, E. G., & Martino, H. S. D. (2022) · PharmaNutrition · doi:10.1016/j.phanu.2022.100298 · Cited by 37
Primary Cilia Are Critical Regulators of White Adipose Tissue Expansion
Hilgendorf, K. I. (2021) · Frontiers in Physiology · doi:10.3389/fphys.2021.769367 · Cited by 36
Divoux, A., Erdős, E., Whytock, K. L., Osborne, T. F., & Smith, S. R. (2022) · Cells · doi:10.3390/cells11050848 · Cited by 40
Significance of Adipose Tissue Maintenance in Patients Undergoing Hemodialysis
Okuno, S. (2021) · Nutrients · doi:10.3390/nu13061895 · Cited by 36
Yang, Y., Qi, J.-J., Jiang, S.-Y., & Ye, L. (2023) · Journal of Ethnopharmacology · doi:10.1016/j.jep.2023.117251 · Cited by 37
Okabe, K., Nawaz, A., Nishida, Y., Yaku, K., Usui, I., Tobe, K., & Nakagawa, T. (2020) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2020.586179 · Cited by 36
Effect of Antarctic krill phospholipid (KOPL) on high fat diet-induced obesity in mice
Xiang, X., Zhou, X., Wang, W., Zhou, Y., Zhou, X., Deng, S., Zheng, B., & Wen, Z. (2021) · Food Research International · doi:10.1016/j.foodres.2021.110456 · Cited by 36
Liu, Y., Wang, M., Deng, T., Liu, R., Ning, T., Bai, M., Ying, G., Zhang, H., & Ba, Y. (2022) · Cancer Biology and Medicine · doi:10.20892/j.issn.2095-3941.2021.0220 · Cited by 37
Effects of exercise intensity on white adipose tissue browning and its regulatory signals in mice
Tanimura, R., Kobayashi, L., Shirai, T., & Takemasa, T. (2022) · Physiological Reports · doi:10.14814/phy2.15205 · Cited by 36
Adipose and non-adipose perspectives of plant derived natural compounds for mitigation of obesity
Borah, A. K., Sharma, P., Singh, A., Kalita, K. J., Saha, S., & Borah, J. C. (2021) · Journal of Ethnopharmacology · doi:10.1016/j.jep.2021.114410 · Cited by 35
Distinct functional properties of murine perinatal and adult adipose progenitor subpopulations
Zhang, Q., Shan, B., Guo, L., Shao, M., Vishvanath, L., Elmquist, G., Xu, L., & Gupta, R. K. (2022) · Nature Metabolism · doi:10.1038/s42255-022-00613-w · Cited by 35
Self-citationFate of Adipose Progenitor Cells in Obesity-Related Chronic Inflammation
Pyrina, I., Chung, K., Michailidou, Z., Koutsilieris, M., Chavakis, T., & Chatzigeorgiou, A. (2020) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2020.00644 · Cited by 35
Asc-1 regulates white versus beige adipocyte fate in a subcutaneous stromal cell population
Suwandhi, L., Altun, I., Karlina, R., Miok, V., Wiedemann, T., Fischer, D. S., Walzthoeni, T., Lindner, C., Böttcher, A., Heinzmann, S. S., et al. (2021) · Nature Communications · doi:10.1038/s41467-021-21826-9 · Cited by 34
Macchi, C., Moregola, A., Greco, M. F., Svecla, M., Bonacina, F., Dhup, S., Dadhich, R. K., Audano, M., Sonveaux, P., Mauro, C., et al. (2022) · iScience · doi:10.1016/j.isci.2022.104435 · Cited by 34
Li, Y., Chen, Q., Wang, T., Ji, Z., Regmi, S., Tong, H., Ju, J., & Wang, A. (2025) · Journal of Nanobiotechnology · doi:10.1186/s12951-025-03432-9 · Cited by 33
Adipogenic progenitors in different organs: Pathophysiological implications
Favaretto, F., Bettini, S., Busetto, L., Milan, G., & Vettor, R. (2021) · Reviews in Endocrine and Metabolic Disorders · doi:10.1007/s11154-021-09686-6 · Cited by 35
Deconstructing Adipose Tissue Heterogeneity One Cell at a Time
Duerre, D. J., & Galmozzi, A. (2022) · Frontiers in Endocrinology · doi:10.3389/fendo.2022.847291 · Cited by 35
Interaction mechanisms between major depressive disorder and non-alcoholic fatty liver disease
Shao, Q., Wu, Y., Ji, J., Xu, T., Yu, Q., Ma, C., Liao, X., Cheng, F., & Wang, X. (2021) · Frontiers in Psychiatry · doi:10.3389/fpsyt.2021.711835 · Cited by 32
Fisk, H. L., Childs, C. E., Miles, E. A., Ayres, R., Noakes, P. S., Paras-Chavez, C., Kuda, O., Kopecký, J., Antoun, E., Lillycrop, K. A., et al. (2021) · Clinical Science · doi:10.1042/cs20201060 · Cited by 32
Cadmium: An Emerging Role in Adipose Tissue Dysfunction
Attia, S. M., Kavitha, V., Shanmugakonar, M., Das, S. C., & Al‐Naemi, H. A. (2021) · Exposure and Health · doi:10.1007/s12403-021-00427-3 · Cited by 33
Tung, Y., Liang, Z.-R., Yang, M., Ho, C., & Pan, M. (2022) · Food & Function · doi:10.1039/d1fo03356e · Cited by 34
Zhang, Q., Li, R., Wang, L., Zhang, T., Qian, D., Tang, D., He, C., Wu, C., & Li, A. (2022) · Frontiers in Pharmacology · doi:10.3389/fphar.2022.1089558 · Cited by 33
Benvie, A. M., Lee, D., Steiner, B. M., Xue, S., Jiang, Y., & Berry, D. C. (2023) · Nature Communications · doi:10.1038/s41467-023-37386-z · Cited by 28
Petito, G., Cioffi, F., Magnacca, N., de Lange, P., Senese, R., & Lanni, A. (2023) · Pharmaceuticals · doi:10.3390/ph16040572 · Cited by 35
Zhang, Q., He, C., Wang, L., Qian, D., Tang, D., Jiang, S., Chen, W., Wu, C., & Peng, W. (2023) · Phytomedicine · doi:10.1016/j.phymed.2023.155113 · Cited by 31
The flux of energy in critical illness and the obesity paradox
Jaitovich, A., & Hall, J. B. (2025) · Physiological Reviews · doi:10.1152/physrev.00029.2024 · Cited by 34
Huang, X., Wang, Y., & Xiang, Y. (2022) · EBioMedicine · doi:10.1016/j.ebiom.2022.104263 · Cited by 32
Thermogenic adipose tissue in energy regulation and metabolic health
Xue, S., Lee, D. P. H., & Berry, D. C. (2023) · Frontiers in Endocrinology · doi:10.3389/fendo.2023.1150059 · Cited by 31
The Impact of Obesity on Inflammatory Bowel Disease
Kaazan, P., Seow, W., Yong, S., Heilbronn, L. K., & Segal, J. P. (2023) · Biomedicines · doi:10.3390/biomedicines11123256 · Cited by 32
Zhu, Q., Wang, D., Liang, F., Tong, X., Liang, Z., Wang, X., Chen, Y., & Mo, D. (2022) · Journal of Biological Chemistry · doi:10.1016/j.jbc.2022.102309 · Cited by 32
Insights into the Anti-Adipogenic and Anti-Inflammatory Potentialities of Probiotics against Obesity
Kober, A. K. M. H., Saha, S., Ayyash, M. M., Namai, F., Nishiyama, K., Yoda, K., Villena, J., & Kitazawa, H. (2024) · Nutrients · doi:10.3390/nu16091373 · Cited by 31
The Collision of Meta-Inflammation and SARS-CoV-2 Pandemic Infection
Huizinga, G. P., Singer, B. H., & Singer, K. (2020) · Endocrinology · doi:10.1210/endocr/bqaa154 · Cited by 28
Di, W., Amdanee, N., Zhang, W., & Zhou, Y. (2020) · Life Sciences · doi:10.1016/j.lfs.2020.118464 · Cited by 28
Metadata
- Authors
- Vishvanath, L., & Gupta, R. K.
- Affiliations
- The University of Texas at Dallas (US)
- Touchstone (China) (CN)
- Corresponding author
- Gupta, Rana K.
- Venue
- Journal of Clinical Investigation
- Published
- 2019-10-01
- Volume
- 129
- Issue
- 10
- Pages
- 4022-4031
- ISSN
- 0021-9738 (ISSN-L)
- 1558-8238
- PMC
- PMC6763245
- OpenAlex
- W2978642359
- Cited by
- 558
- References
- 98
- Citations by year
- 2026: 77 · 2025: 72 · 2024: 89 · 2023: 92 · 2022: 98 · 2021: 85 · 2020: 43 · 2019: 2
- FWCI
- 8.39
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Locations
- Journal of Clinical Investigation (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Funders
- National Institute of Diabetes and Digestive and Kidney Diseases (R01DK119163, R56DK119163)
- Topics
- Health Sciences › Medicine › Endocrinology, Diabetes and Metabolism › Adipokines, Inflammation, and Metabolic Diseases
- Health Sciences › Medicine › Physiology (medical) › Adipose Tissue and Metabolism
- Health Sciences › Medicine › Cardiology and Cardiovascular Medicine › Cardiovascular Disease and Adiposity
- Keywords
- adipogenesis, obesity, metabolically healthy obesity, adipose tissue remodeling, visceral adipose tissue, subcutaneous adipose tissue, insulin resistance, adipocyte hypertrophy, adipose tissue inflammation, adipose tissue fibrosis, adipose-derived stem cells, single-cell RNA sequencing
- MeSH terms
- RNA-Seq, Animals, Energy Metabolism, Humans, Insulin Resistance, Obesity, Risk Factors, Stem Cells, Metabolic Syndrome, Adipogenesis, Mice, Adipose Tissue, White, Adipocytes, White, Single-Cell Analysis
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