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Mitochondrial remodeling in adipose tissue associated with obesity and treatment with rosiglitazone.
Open accessAbstract
Adipose tissue plays a central role in the control of energy homeostasis through the storage and turnover of triglycerides and through the secretion of factors that affect satiety and fuel utilization. Agents that enhance insulin sensitivity, such as rosiglitazone, appear to exert their therapeutic effect through adipose tissue, but the precise mechanisms of their actions are unclear. Rosiglitazone changes the morphological features and protein profiles of mitochondria in 3T3-L1 adipocytes. To examine the relevance of these effects in vivo, we studied white adipocytes from ob/ob mice during the development of obesity and after treatment with rosiglitazone. The levels of approximately 50% of gene transcripts encoding mitochondrial proteins were decreased with the onset of obesity. About half of those genes were upregulated after treatment with rosiglitazone, and this was accompanied by an increase in mitochondrial mass and changes in mitochondrial structure. Functionally, adipocytes from rosiglitazone-treated mice displayed markedly enhanced oxygen consumption and significantly increased palmitate oxidation. These data reveal mitochondrial remodeling and increased energy expenditure in white fat in response to rosiglitazone treatment in vivo and suggest that enhanced lipid utilization in this tissue may affect whole-body energy homeostasis and insulin sensitivity.
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“White adipocyte mitochondrial content is decreased in both rodent and human obesity (177, 188 -191) and correlates with insulin resistance that accompanies obesity.”
From The role of mitochondria in the pathogenesis of type 2 diabetes (2010) · cites this paper as [177]
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“Administration of thiazolidinediones induces changes in mitochondrial content and remodeling in white adipocytes concomitantly with an improvement in insulin sensitivity (170, 173, 177, 190, 194 -198).”
From The role of mitochondria in the pathogenesis of type 2 diabetes (2010) · cites this paper as [177]
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“Higher mitochondrial density and even UCP1 can be induced in response to pharmacological or genetic alterations of white adipocytes (170 -177), suggesting that white adipose tissue could potentially be induced to acquire more oxidative metabolic phenotypes, promoting increased fuel consumption and thus energy expenditure.”
From The role of mitochondria in the pathogenesis of type 2 diabetes (2010) · cites this paper as [177]
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“Conversely, both genetic and dietinduced obesity result in decreased mitochondrial density and OXPHOS activity in adipose tissue (127, 177, 189 -191), potentially contributing to adipose tissue dysfunction and exacerbation of insulin resistance.”
From The role of mitochondria in the pathogenesis of type 2 diabetes (2010) · cites this paper as [177]
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Cites
Mootha, V. K., Lindgren, C. M., Eriksson, K.-F., Subramanian, A., Sihag, S., Lehar, J., Puigserver, P., Carlsson, E., Ridderstråle, M., Laurila, E., et al. (2003) · Nature Genetics · doi:10.1038/ng1180 · Cited by 10,197
Brown Adipose Tissue: Function and Physiological Significance
CANNON, B., & NEDERGAARD, J. (2004) · Physiological Reviews · doi:10.1152/physrev.00015.2003 · Cited by 6,433
Wu, Z., Puigserver, P., Andersson, U., Zhang, C., Adelmant, G., Mootha, V., Troy, A., Cinti, S., Lowell, B., Scarpulla, R. C., et al. (1999) · Cell · doi:10.1016/s0092-8674(00)80611-x · Cited by 4,139
A Cold-Inducible Coactivator of Nuclear Receptors Linked to Adaptive Thermogenesis
Puigserver, P., Wu, Z., Park, C. W., Graves, R., Wright, M., & Spiegelman, B. M. (1998) · Cell · doi:10.1016/s0092-8674(00)81410-5 · Cited by 3,864
Mitochondrial dysfunction in the elderly: possible role in insulin resistance
Petersen, K. F., Befroy, D., Dufour, S., Dziura, J., Ariyan, C., Rothman, D. L., DiPietro, L., Cline, G. W., & Shulman, G. I. (2003) · Science · doi:10.1126/science.1082889 · Cited by 2,107
Patti, M. E., Butte, A. J., Crunkhorn, S., Cusi, K., Berria, R., Kashyap, S., Miyazaki, Y., Kohane, I., Costello, M., Saccone, R., et al. (2003) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1032913100 · Cited by 1,952
Transcriptional regulatory circuits controlling mitochondrial biogenesis and function
Kelly, D. P., & Scarpulla, R. C. (2004) · Genes & Development · doi:10.1101/gad.1177604 · Cited by 1,243
Minireview: The Adipocyte—At the Crossroads of Energy Homeostasis, Inflammation, and Atherosclerosis
Rajala, M. W., & Scherer, P. E. (2003) · Endocrinology · doi:10.1210/en.2003-0580 · Cited by 1,204
Okuno, A., Tamemoto, H., Kazuuki, T. O. B. E., Ueki, K., Mori, Y., Iwamoto, K., Umesono, K., Akanuma, Y., Fujiwara, T., Horikoshi, H., et al. (1998) · Journal of Clinical Investigation · doi:10.1172/jci1235 · Cited by 995
Miyazaki, Y., Mahankali, A., Matsuda, M., Mahankali, S., Hardies, J., Cusi, K., Mandarino, L. J., & DeFronzo, R. A. (2002) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/jcem.87.6.8567 · Cited by 726
Cited by
Sorted by citations
Items 301–400 of 623
Schrauwen‐Hinderling, V. B., Mensink, M., Hesselink, M. K. C., Sels, J.-P. J. E., Kooi, M. E., & Schrauwen, P. (2008) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/jc.2008-0267 · Cited by 42
Xie, X., Yi, Z., Sinha, S., Madan, M., Bowen, B. P., Langlais, P. R., Ma, D., Mandarino, L. J., & Meyer, C. (2016) · Obesity · doi:10.1002/oby.21528 · Cited by 42
Stress turns on the heat: Regulation of mitochondrial biogenesis and UCP1 by ROS in adipocytes
Palacios-Ortega, S., Chouchani, E. T., & Boudina, S. (2016) · Adipocyte · doi:10.1080/21623945.2016.1273298 · Cited by 42
Mitochondrial DNA: An Up‐and‐coming Actor in White Adipose Tissue Pathophysiology
Villarroya, J., Giralt, M., & Villarroya, F. (2009) · Obesity · doi:10.1038/oby.2009.152 · Cited by 41
Targeting the mitochondria to augment myocardial protection
SCHWARTZ, D., & Sack, M. N. (2008) · Current Opinion in Pharmacology · doi:10.1016/j.coph.2007.12.008 · Cited by 41
Das, S., Mukhuty, A., Mullen, G. P., & Rudolph, M. C. (2024) · International Journal of Molecular Sciences · doi:10.3390/ijms25126681 · Cited by 43
Storey, S. M., McIntosh, A. L., Subramanian, S., Moon, K. C., & Atshaves, B. P. (2011) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.00109.2011 · Cited by 40
Bhaskaran, S., Unnikrishnan, A., Ranjit, R., Qaisar, R., Pharaoh, G. A., Matyi, S., Kinter, M. T., & Deepa, S. S. (2017) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2017.04.028 · Cited by 40
Liver X receptors as regulators of metabolism
Korach-André, M., & Gustafsson, J.-Α. (2015) · BioMolecular Concepts · doi:10.1515/bmc-2015-0007 · Cited by 40
Reddy, N. L., Tan, B. K., Barber, T. M., & Randeva, H. S. (2014) · BMC Obesity · doi:10.1186/s40608-014-0013-5 · Cited by 40
The Crosstalk between Gut Microbiota and White Adipose Tissue Mitochondria in Obesity
Colangeli, L., Marcillo, D. I. E., Simonelli, V., Iorio, E., Rinaldi, T. G., Sbraccia, P., Fortini, P., & Guglielmi, V. (2023) · Nutrients · doi:10.3390/nu15071723 · Cited by 40
Exercise as a tool to mitigate metabolic disease
Esteves, J. V. D. C., & Stanford, K. I. (2024) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.00144.2024 · Cited by 39
The Warburg effect: The hacked mitochondrial-nuclear communication in cancer
Jiang, H., & Ye, J. (2025) · Seminars in Cancer Biology · doi:10.1016/j.semcancer.2025.03.006 · Cited by 40
Ebaid, G. M. X., Seiva, F. R. F., Rocha, K. K. H. R., Souza, G. A., & Novelli, E. L. B. (2010) · Nutrition Journal · doi:10.1186/1475-2891-9-46 · Cited by 39
Gondret, F., Louveau, I., Mourot, J., Duclos, M. J. M. J., Lagarrigue, S., Gilbert, H., & van Milgen, J. J. (2014) · Journal of Animal Science · doi:10.2527/jas.2014-7995 · Cited by 39
Okamoto, Y., Higashiyama, H., Rong, J. X., McVey, M. J., Kinoshita, M., Asano, S., & Hansen, M. K. (2007) · Experimental and Molecular Pathology · doi:10.1016/j.yexmp.2007.02.007 · Cited by 38
Pires, K. M. P., Ilkun, O. L., Barroso, M. V., & Boudina, S. (2013) · Obesity · doi:10.1002/oby.20465 · Cited by 38
Systems biology of adipose tissue metabolism: regulation of growth, signaling and inflammation
Manteiga, S., Choi, K., Jayaraman, A., & Lee, K. (2013) · WIREs Systems Biology and Medicine · doi:10.1002/wsbm.1213 · Cited by 38
Mcilroy, G. D., Tammireddy, S. R., Maskrey, B. H., Grant, L., Doherty, M. K., Watson, D. G., Delibegović, M., Whitfield, P. D., & Mody, N. (2015) · Biochemical Pharmacology · doi:10.1016/j.bcp.2015.11.017 · Cited by 38
Formation and activation of thermogenic fat
Wu, J., Jun, H., & McDermott, J. R. (2015) · Trends in Genetics · doi:10.1016/j.tig.2015.03.003 · Cited by 37
Genetic & epigenetic approach to human obesity.
Rao, K. R., Lal, N., & Giridharan, N. V. (2014) · Europe PMC (PubMed Central) · Cited by 37
A systems perspective on brown adipogenesis and metabolic activation
Pradhan, R., Zachara, M., & Deplancke, B. (2017) · Obesity Reviews · doi:10.1111/obr.12512 · Cited by 37
Tamucci, K. A., Namwanje, M., Fan, L., & Qiang, L. (2017) · Protein & Cell · doi:10.1007/s13238-017-0434-2 · Cited by 39
Exercise-inducible factors to activate lipolysis in adipocytes
Hashimoto, T., Sato, K., & Iemitsu, M. (2013) · Journal of Applied Physiology · doi:10.1152/japplphysiol.00427.2013 · Cited by 37
Unraveling Biochemical Pathways Affected by Mitochondrial Dysfunctions Using Metabolomic Approaches
Demine, S., Reddy, N., Renard, P., Raes, M. J., & Arnould, T. (2014) · Metabolites · doi:10.3390/metabo4030831 · Cited by 37
To, A. W. M., Ribé, E. M., Chuang, T. T., Schroeder, J. E., & Lovestone, S. (2011) · PLoS ONE · doi:10.1371/journal.pone.0016991 · Cited by 37
Fluorescence imaging of interscapular brown adipose tissue in living mice
Rice, D. R., White, A. G., Leevy, W. M., & Smith, B. D. (2015) · Journal of Materials Chemistry B · doi:10.1039/c4tb01914h · Cited by 37
Measuring Respiratory Activity of Adipocytes and Adipose Tissues in Real Time
Bugge, A. K., Dib, L. H., & Collins, S. (2014) · Methods in enzymology on CD-ROM/Methods in enzymology · doi:10.1016/b978-0-12-800280-3.00013-x · Cited by 37
Ryu, M. J., Kim, S. J., Choi, M. J., Kim, Y. K., Lee, M. H., Lee, S. E., Chung, H. K., Jung, S. B., Kim, H. J., Kim, K. S., et al. (2013) · Molecules and Cells · doi:10.1007/s10059-012-2257-1 · Cited by 36
Fat tissues, the brite and the dark sides
Chen, Y., Pan, R., & Pfeifer, A. (2016) · Pflügers Archiv - European Journal of Physiology · doi:10.1007/s00424-016-1884-8 · Cited by 36
ANGPTL6 expression is coupled with mitochondrial OXPHOS function to regulate adipose FGF21
Kang, S., Yi, H., Choi, M. J., Ryu, M. J., Jung, S.-B., Chung, H. K., Chang, J. Y., Kim, Y. K., Lee, S. E., Kim, H. W., et al. (2017) · Journal of Endocrinology · doi:10.1530/joe-16-0549 · Cited by 36
Jackisch, L., Murphy, A. M., Kumar, S., Randeva, H. S., Tripathi, G., & McTernan, P. G. (2020) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/clinem/dgaa258 · Cited by 36
Chang, T., Zimmerley, M., Quinn, K. P., Lamarre, I., Kaplan, D. L., Beaurepaire, E., & Georgakoudi, I. (2013) · Biomaterials · doi:10.1016/j.biomaterials.2013.07.066 · Cited by 36
Intermittent fasting up-regulates Fsp27/Cidec gene expression in white adipose tissue
Karbowska, J., & Kochan, Z. (2011) · Nutrition · doi:10.1016/j.nut.2011.06.009 · Cited by 36
BNIP3 is essential for mitochondrial bioenergetics during adipocyte remodelling in mice
Choi, J. W., Jo, A., Kim, M., Park, H. S., Chung, S. S., Kang, S., & Park, K. S. (2015) · Diabetologia · doi:10.1007/s00125-015-3836-9 · Cited by 36
Coêlho, M. S., de Lima, C. L., Royer, C., da Silva, J. B., Oliveira, F. C. B., Christ, C. G., Pereira, S. A., Báo, S. N., de Lima, M. D. C. A., Pitta, M. G. D. R., et al. (2016) · PLoS ONE · doi:10.1371/journal.pone.0154310 · Cited by 36
Xie, X., Sinha, S., Yi, Z., Langlais, P. R., Madan, M., Bowen, B. P., Willis, W. T., & Meyer, C. (2017) · International Journal of Obesity · doi:10.1038/ijo.2017.192 · Cited by 36
Fu, Y.-Y., Zhang, M., Turner, N., Zhang, L.-N., Dong, T.-C., Gu, M., Leslie, S. J., Li, J.-Y., Nan, F.-J., & Li, J. (2013) · Diabetologia · doi:10.1007/s00125-013-2987-9 · Cited by 35
Mitochondrial stress protein HSP60 regulates ER stress-induced hepatic lipogenesis
Xiao, T., Liang, X., Liu, H., Zhang, F., Meng, W., & Hu, F. (2020) · Journal of Molecular Endocrinology · doi:10.1530/jme-19-0207 · Cited by 35
Mitochondrial DNA Content in Human Omental Adipose Tissue
Lindinger, A., Peterli, R., Peters, T. T. A., Kern, B. E., von Flüe, M., Calame‐Christe, M., Hoch, M., Eberlé, A. N., & Lindinger, P. W. (2009) · Obesity Surgery · doi:10.1007/s11695-009-9987-3 · Cited by 35
Oort, P. J., Knotts, T. A., Grino, M., Naour, N., Bastard, J.-P., Clément, K., Ninkina, N. N., Buchman, V. L., Permana, P. A., Luo, X., et al. (2008) · Journal of Nutrition · doi:10.1093/jn/138.5.841 · Cited by 35
Nogiec, C., Burkart, A., Dreyfuss, J. M., Lerin, C., Kasif, S., & Patti, M.-E. (2015) · Molecular Metabolism · doi:10.1016/j.molmet.2014.12.012 · Cited by 34
Esterson, Y. B., Zhang, K., Koppaka, S., Kehlenbrink, S., Kishore, P., Raghavan, P., Maginley, S. R., Carey, M., & Hawkins, M. (2013) · Journal of Investigative Medicine · doi:10.2310/jim.0000000000000017 · Cited by 34
MicroRNAs as regulators of mitochondrial dysfunction and obesity
Murri, M., & el Azzouzi, H. (2018) · American Journal of Physiology-Heart and Circulatory Physiology · doi:10.1152/ajpheart.00691.2017 · Cited by 34
Loss of P2X7 receptor function dampens whole body energy expenditure and fatty acid oxidation
Giacovazzo, G., Apolloni, S., & Coccurello, R. (2018) · Purinergic Signalling · doi:10.1007/s11302-018-9610-y · Cited by 34
Tang, C., Zhao, H., Kong, L., Meng, F., Zhou, L., Lu, Z., & Lu, Y. (2023) · Journal of Agricultural and Food Chemistry · doi:10.1021/acs.jafc.2c05670 · Cited by 34
Mitochondrial Dynamics in Drug-Induced Liver Injury
Ramachandran, A., Umbaugh, D. S., & Jaeschke, H. (2021) · Livers · doi:10.3390/livers1030010 · Cited by 34
Priyanka, A., Anusree, S. S., Nisha, V. M., & Raghu, K. G. (2014) · BioFactors · doi:10.1002/biof.1175 · Cited by 33
Mitochondria in the pathogenesis of diabetes: a proteomic view
Chen, X., Wei, S., & Yang, F. (2012) · Protein & Cell · doi:10.1007/s13238-012-2043-4 · Cited by 33
Huang, C., Chiang, W.-D., Pai, P., & Lin, W. (2014) · Journal of Functional Foods · doi:10.1016/j.jff.2014.11.027 · Cited by 33
Townsend, L. K., Knuth, C. M., & Wright, D. C. (2017) · Physiological Reports · doi:10.14814/phy2.13247 · Cited by 33
Caldwell, S. H., Patrie, J. T., Brunt, E. M., Redick, J. A., Davis, C. A., Park, S. H., & Neuschwander‐Tetri, B. A. (2007) · Hepatology · doi:10.1002/hep.21813 · Cited by 33
Khoo, N. K. H., Mo, L., Zharikov, S. I., Kamga, C., Quesnelle, K. M., Golin-Bisello, F., Li, L., Wang, Y., & Shiva, S. (2014) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2014.02.009 · Cited by 32
Kobayashi, M., Uta, S., Otsubo, M., Deguchi, Y., Tagawa, R., Mizunoe, Y., Nakagawa, Y., Shimano, H., & Higami, Y. (2020) · Nutrients · doi:10.3390/nu12072054 · Cited by 32
Deng, T., Sieglaff, D. H., Zhang, A., Lyon, C. J., Ayers, S. D., Čvoro, A., Gupte, A. A., Xia, X., Baxter, J. D., Webb, P., et al. (2011) · Journal of Biological Chemistry · doi:10.1074/jbc.m111.251926 · Cited by 32
Sakellariou, P., Valente, A., Carrillo, A. E., Metsios, G. S., Nadolnik, L. I., Jamurtas, A. Z., Koutedakis, Y., Boguszewski, C. L., Andrade, C. M. B., Svensson, P., et al. (2016) · Medical Hypotheses · doi:10.1016/j.mehy.2016.05.006 · Cited by 31
Zamora, M., Pardo, R., & Villena, J. A. (2015) · Biochemical Pharmacology · doi:10.1016/j.bcp.2015.06.032 · Cited by 32
Benton, C. R., Koonen, D. P. Y., Calles-Escandón, J., Tandon, N. N., Glatz, J. F. C., Luiken, J. J. F. P., Heikkila, J. J., & Bonen, A. (2006) · The Journal of Physiology · doi:10.1113/jphysiol.2006.106013 · Cited by 32
Mitoflash altered by metabolic stress in insulin-resistant skeletal muscle
Ding, Y., Fang, H., Shang, W. H., Xiao, Y., Sun, T., Hou, N., Pan, L., Sun, X., Ma, Q., Zhou, J., et al. (2015) · Journal of Molecular Medicine · doi:10.1007/s00109-015-1278-y · Cited by 31
AMPK/Mitochondria in Metabolic Diseases
Bullón, P., Marín‐Aguilar, F., & Román-Malo, L. (2016) · Proceedings of the Fourth International Symposium on Polarization Phenomena in Nuclear Reactions · doi:10.1007/978-3-319-43589-3_6 · Cited by 31
Effects and Mechanism of Chlorogenic Acid on Weight Loss
Zhong, Y., Ding, Y., Li, L., Ge, M., Guangguo, B., Yang, H., Dai, J., & Zhang, L. (2020) · Current Pharmaceutical Biotechnology · doi:10.2174/1389201021666200318124922 · Cited by 31
Sphingosine 1-Phosphate Regulates Obesity and Glucose Homeostasis
Kajita, K., Ishii, I., Mori, I., Asano, M., Fuwa, M., & Morita, H. (2024) · International Journal of Molecular Sciences · doi:10.3390/ijms25020932 · Cited by 31
Perspective on a pathogenesis and treatment of Alzheimer's disease
Roses, A. D., & Saunders, A. M. (2006) · Alzheimer s & Dementia · doi:10.1016/j.jalz.2005.12.001 · Cited by 30
Dual PPAR α/γ Agonists: Promises and Pitfalls in Type 2 Diabetes
Ahmed, I., Furlong, K., Flood, J. J., Treat, V., & Goldstein, B. J. (2007) · American Journal of Therapeutics · doi:10.1097/01.mjt.0000212890.82339.8d · Cited by 30
Glycerolipid Cycling in Thermogenesis, Energy Homeostasis, Signaling, and Diseases
Poursharifi, P., Madiraju, S. R. M., Oppong, A. K., Kajimura, S., Nolan, C. J., Blondin, D. P., & Prentki, M. (2025) · Physiological Reviews · doi:10.1152/physrev.00024.2024 · Cited by 29
IL-6 Is Not Necessary for the Regulation of Adipose Tissue Mitochondrial Content
Wan, Z., Perry, C. G. R., MacDonald, T. L., Chan, C. B., Holloway, G. P., & Wright, D. C. (2012) · PLoS ONE · doi:10.1371/journal.pone.0051233 · Cited by 29
McKie, G. L., & Wright, D. C. (2020) · Biochemical Journal · doi:10.1042/bcj20190466 · Cited by 29
Obesity Pharmacotherapy: Current Perspectives and Future Directions
Misra, M. (2013) · Current Cardiology Reviews · doi:10.2174/157340313805076322 · Cited by 29
RBM43 controls PGC1α translation and a PGC1α-STING signaling axis
Dumesic, P. A., Wilensky, S. E., Bose, S., Vranken, J. G. V., Gygi, S. P., & Spiegelman, B. M. (2025) · Cell Metabolism · doi:10.1016/j.cmet.2025.01.013 · Cited by 28
Politis‐Barber, V., Brunetta, H. S., Paglialunga, S., Petrick, H. L., & Holloway, G. P. (2020) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.00028.2020 · Cited by 28
Molecular pathways regulating the formation of brown‐like adipocytes in white adipose tissue
Fu, J., Li, Z., Zhang, H., Mao, Y., Wang, A., Wang, X., Zou, Z., & Zhang, X. (2014) · Diabetes/Metabolism Research and Reviews · doi:10.1002/dmrr.2600 · Cited by 29
Hydrogel-based engineering of beige adipose tissue
Vaicik, M. K., Morse, M. C., Blagajcevic, A., Rios, J., Larson, J. C., Yang, F., Cohen, R., Papavasiliou, G., & Brey, E. M. (2015) · Journal of Materials Chemistry B · doi:10.1039/c5tb00952a · Cited by 29
A novel peptide that improves metabolic parameters without adverse central nervous system effects
Reckziegel, P., Festuccia, W. T., Britto, L. R. G., Jang, K. L. L., Romão, C. M., Heimann, J. C., Fogaça, M. V., Rodrigues, N. S., da Silva, N. R., Guimarães, F. S., et al. (2017) · Scientific Reports · doi:10.1038/s41598-017-13690-9 · Cited by 28
Pardo, R., Vilà, M., Cervela, L., de Marco, M., Gama-Pérez, P., González-Franquesa, A., Statuto, L., Vilallonga, R., Simó, R., Garcia-Roves, P. M., et al. (2019) · The FASEB Journal · doi:10.1096/fj.201800310r · Cited by 27
Petrick, H. L., Foley, K. P., Zlitni, S., Brunetta, H. S., Paglialunga, S., Miotto, P. M., Politis‐Barber, V., O’Dwyer, C., Philbrick, D. J., Fullerton, M. D., et al. (2020) · Function · doi:10.1093/function/zqaa013 · Cited by 27
Proteomics in the characterization of adipose dysfunction in obesity
Brockman, D. A., & Chen, X. (2012) · Adipocyte · doi:10.4161/adip.19129 · Cited by 27
Organization of nuclear architecture during adipocyte differentiation
Charó, N. L., Ceschan, M. I. R., Galigniana, N. M., Toneatto, J., & Piwien‐Pilipuk, G. (2016) · Nucleus · doi:10.1080/19491034.2016.1197442 · Cited by 27
Krautbauer, S., Eisinger, K., Neumeier, M., Hader, Y., Buettner, R., Schmid, P. M., Aslanidis, C., & Buechler, C. (2014) · PLoS ONE · doi:10.1371/journal.pone.0086866 · Cited by 26
Nebivolol stimulates mitochondrial biogenesis in 3T3-L1 adipocytes
Huang, C., Chen, D., Xie, Q., Yang, Y., & Shen, W. (2013) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2013.07.055 · Cited by 26
On the role of macrophages in the control of adipocyte energy metabolism
Keuper, M. (2019) · Endocrine Connections · doi:10.1530/ec-19-0016 · Cited by 26
Yang, X., Wu, F., Li, L., Lynch, E. C., Xie, L., Zhao, Y. Q., Fang, K., Li, J., Luo, J., Xu, L., et al. (2020) · Phytotherapy Research · doi:10.1002/ptr.6800 · Cited by 26
LXRα fuels fatty acid-stimulated oxygen consumption in white adipocytes
Dib, L. H., Bugge, A. K., & Collins, S. (2013) · Journal of Lipid Research · doi:10.1194/jlr.m043422 · Cited by 26
Kim, H., Ryoo, Z. Y., Choi, S. U., & Lee, S. (2015) · Gene · doi:10.1016/j.gene.2015.03.077 · Cited by 25
Goedecke, J. H., Mendham, A. E., Clamp, L. D., Nankam, P. A. N., Smidt, M. F.-D., Phiri, L., Micklesfield, L. K., Keswell, D., Woudberg, N. J., Lecour, S., et al. (2018) · JMIR Research Protocols · doi:10.2196/resprot.9098 · Cited by 25
Emerging role of protein kinase C in energy homeostasis: A brief overview
Mehta, K. D. (2014) · World Journal of Diabetes · doi:10.4239/wjd.v5.i3.385 · Cited by 25
Pioglitazone treatment restores in vivo muscle oxidative capacity in a rat model of diabetes
Wessels, B., Čiapaitė, J., van den Broek, N. M. A., Houten, S. M., Nicolay, K., & Prompers, J. J. (2014) · Diabetes Obesity and Metabolism · doi:10.1111/dom.12388 · Cited by 25
Role of NCoR1 in mitochondrial function and energy metabolism
de Lima, T. I., Valentim, R. R., Araújo, H. N., de Oliveira, A. G., Favero‐Santos, B. C., Menezes, E. S., Araújo, R. M. D. S., & Silveira, L. R. (2018) · Cell Biology International · doi:10.1002/cbin.10973 · Cited by 25
Brunetta, H. S., Politis‐Barber, V., Petrick, H. L., Dennis, K. M. J. H., Kirsh, A. J., Barbeau, P., Nunes, E. A., & Holloway, G. P. (2020) · The Journal of Physiology · doi:10.1113/jp279455 · Cited by 25
Mitoproteome Plasticity of Rat Brown Adipocytes in Response to Cold Acclimation
Navet, R., Mathy, G., Douette, P., Dobson, R., Leprince, P., Pauw, E. D., Sluse‐Goffart, C. M., & Sluse, F. E. (2006) · Journal of Proteome Research · doi:10.1021/pr060064u · Cited by 25
PPARα and PPARγ Regulation of Liver and Adipose Proteins in Obese and Dyslipidemic Rodents
Lanne, B., Dahllöf, B., Lindahl, C., Ebefors, K., Kanmert, I., von Bahr, H., Miliotis, T., Nyström, A., Arnerup, G., Paulsons, I., et al. (2006) · Journal of Proteome Research · doi:10.1021/pr060004o · Cited by 25
Aydemir, D., Sarayloo, E., & Ulusu, N. N. (2019) · Journal of Medical Biochemistry · doi:10.2478/jomb-2019-0041 · Cited by 24
Phthalate exposure causes browning-like effects on adipocytes in vitro and in vivo
Hsu, J.-W., Nien, C.-Y., Yeh, S., Tsai, F., Chen, H., Lee, T., Chen, S. L., Kao, Y.-H., & Tsou, T. (2020) · Food and Chemical Toxicology · doi:10.1016/j.fct.2020.111487 · Cited by 24
Castro, É., Vieira, T. S., Oliveira, T. E., Ortiz‐Silva, M., Andrade, M. L., Tomazelli, C. A., Peixoto, Á. S., Sobrinho, C. R., Moreno, M. F., Gilio, G. R., et al. (2021) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.00587.2020 · Cited by 25
Wang, Y., Katayama, A., Terami, T., Han, X., Nunoue, T., Zhang, D., Teshigawara, S., Eguchi, J., Nakatsuka, A., Murakami, K., et al. (2015) · Metabolism · doi:10.1016/j.metabol.2015.02.004 · Cited by 24
Yu, J., Yu, B., He, J., Zheng, P., Mao, X., Han, G., & Chen, D. (2014) · PLoS ONE · doi:10.1371/journal.pone.0112628 · Cited by 24
CD14 Deficiency Impacts Glucose Homeostasis in Mice through Altered Adrenal Tone
Young, J. L., Mora, A., Cerny, A., Czech, M., Woda, B. A., Kurt‐Jones, E. A., Finberg, R. W., & Corvera, S. (2012) · PLoS ONE · doi:10.1371/journal.pone.0029688 · Cited by 24
Self-citationXie, S., Li, Y., Teng, W., Du, ., Li, Y., & Sun, B. (2019) · Nutrients · doi:10.3390/nu11071640 · Cited by 24
Triglyceride-lowering Effect of Respiratory Uncoupling in White Adipose Tissue
Rossmeisl, M., Kovar, J., Syrovy, I., Flachs, P., Bobkova, D., Kolar, F., Poledne, R., & Kopecky, J. (2005) · Obesity Research · doi:10.1038/oby.2005.96 · Cited by 23
Overexpression of NYGGF4 (PID1) induces mitochondrial impairment in 3T3-L1 adipocytes
Zhao, Y., Zhang, C., Chen, X., Gao, C., Ji, C., Chen, F., Zhu, C., Zhu, J., Wang, J., Qian, L., et al. (2010) · Molecular and Cellular Biochemistry · doi:10.1007/s11010-010-0398-5 · Cited by 23
Inter-organ regulation of adipose tissue browning
Wang, S., & Yang, X. (2016) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-016-2420-x · Cited by 23
Metadata
- Authors
- Wilson-Fritch, L., Nicoloro, S., Chouinard, M., Lazar, M. A., Chui, P. C., Leszyk, J., Straubhaar, J., Czech, M. P., & Corvera, S.
- Affiliations
- University of Massachusetts Chan Medical School (US)
- University of Pennsylvania (US)
- Corresponding author
- Corvera, Silvia
- Venue
- Journal of Clinical Investigation
- Published
- 2004-11-01
- Volume
- 114
- Issue
- 9
- Pages
- 1281-1289
- ISSN
- 0021-9738 (ISSN-L)
- PMC
- PMC524228
- OpenAlex
- W2022473709
- Cited by
- 616
- References
- 32
- Citations by year
- 2026: 4 · 2025: 13 · 2024: 21 · 2023: 19 · 2022: 23 · 2021: 17 · 2020: 34 · 2019: 22 · 2018: 28 · 2017: 32 · 2016: 32 · 2015: 36 · 2014: 42 · 2013: 44 · 2012: 33
- FWCI
- 15.62
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Locations
- Journal of Clinical Investigation (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- The Journal of the American Medical Association (JAMA) Network (American Medical Association) (submittedVersion)
- Funders
- National Institutes of Health
- National Institute of Diabetes and Digestive and Kidney Diseases (DK60837-02)
- Topics
- Health Sciences › Medicine › Physiology (medical) › Adipose Tissue and Metabolism
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Peroxisome Proliferator-Activated Receptors
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Mitochondrial Function and Pathology
- Keywords
- mitochondrial remodeling, adipose tissue, obesity, rosiglitazone, white adipocytes, ob/ob mice, insulin sensitivity, energy homeostasis, mitochondrial mass, mitochondrial structure, oxygen consumption, palmitate oxidation, lipid utilization, 3T3-L1 adipocytes, mitochondrial gene expression
- MeSH terms
- Rosiglitazone, Adipose Tissue, Animals, Blood Glucose, Fatty Acids, Insulin, Mice, Inbred C57BL, Mice, Obese, Mice, Transgenic, Microscopy, Fluorescence, Mitochondria, Obesity, Oxygen, RNA, Messenger, Mass Spectrometry, Time Factors, Vasodilator Agents, Blotting, Northern, Blotting, Western, Adipocytes, RNA, Complementary, Chaperonin 60, Palmitic Acid, Oligonucleotide Array Sequence Analysis, 3T3-L1 Cells, Thiazolidinediones, PPAR gamma, Mice
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