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p38 Mitogen-Activated Protein Kinase Is the Central Regulator of Cyclic AMP-Dependent Transcription of the Brown Fat Uncoupling Protein 1 Gene
Open accessAbstract
It is well established that catecholamine-stimulated thermogenesis in brown fat requires beta-adrenergic elevations in cyclic AMP (cAMP) to increase expression of the uncoupling protein 1 (UCP1) gene. However, little is known about the downstream components of the signaling cascade or the relevant transcription factor targets thereof. Here we demonstrate that cAMP- and protein kinase A-dependent activation of p38 mitogen-activated protein kinase (MAPK) in brown adipocytes is an indispensable step in the transcription of the UCP1 gene in mice. By phosphorylating activating transcription factor 2 (ATF-2) and peroxisome proliferator-activated receptor gamma (PPARgamma) coativator 1alpha (PGC-1alpha), members of two distinct nuclear factor families, p38 MAPK controls the expression of the UCP1 gene through their respective interactions with a cAMP response element and a PPAR response element that both reside within a critical enhancer motif of the UCP1 gene. Activation of ATF-2 by p38 MAPK additionally serves as the cAMP sensor that increases expression of the PGC-1alpha gene itself in brown adipose tissue. In conclusion, our findings illustrate that by orchestrating the activity of multiple transcription factors, p38 MAPK is a central mediator of the cAMP signaling mechanism of brown fat that promotes thermogenesis.
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“The most well-known condition to induce Ucp1 expression in both humans and rodents is cold, essentially by activating β-adrenergic receptors and the cAMP-dependent protein kinase (PKA)-dependent signaling pathway [38,39].”
From Mitochondrial Uncoupling: A Key Controller of Biological Processes in Physiology and Diseases (2019) · cites this paper as [39]
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Cites
Hybridization of denatured RNA and small DNA fragments transferred to nitrocellulose.
Thomas, P. S. (1980) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.77.9.5201 · Cited by 7,937
Mitogen-Activated Protein Kinase Pathways Mediated by ERK, JNK, and p38 Protein Kinases
Johnson, G. L., & Lapadat, R. (2002) · Science · doi:10.1126/science.1072682 · Cited by 4,295
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
Self-citationA 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
Self-citationLehmann, J. M., Moore, L. B., Smith-Oliver, T. A., Wilkison, W. O., Willson, T. M., & Kliewer, S. A. (1995) · Journal of Biological Chemistry · doi:10.1074/jbc.270.22.12953 · Cited by 3,645
Puigserver, P., & Spiegelman, B. M. (2003) · Endocrine Reviews · doi:10.1210/er.2002-0012 · Cited by 2,076
Self-citationEpac is a Rap1 guanine-nucleotide-exchange factor directly activated by cyclic AMP
de Rooij, J., Zwartkruis, F. J. T., Verheijen, M. H. G., Cool, R. H., Nijman, S. M. B., Wittinghofer, A., & Bos, J. L. (1998) · Nature · doi:10.1038/24884 · Cited by 1,970
Control of hepatic gluconeogenesis through the transcriptional coactivator PGC-1
Yoon, J. C., Puigserver, P., Chen, G., Donovan, J., Wu, Z., Rhee, J., Adelmant, G., Stafford, J., Kahn, C. R., Granner, D. K., et al. (2001) · Nature · doi:10.1038/35093050 · Cited by 1,821
Self-citationTowards a molecular understanding of adaptive thermogenesis
Lowell, B. B., & Spiegelman, B. M. (2000) · Nature · doi:10.1038/35007527 · Cited by 1,630
Self-citationThe p38 signal transduction pathway Activation and function
Ono, K., & Han, J. (2000) · Cellular Signalling · doi:10.1016/s0898-6568(99)00071-6 · Cited by 1,571
Research works printed but not linked: 6
- Badger A. M., 1996, J. Pharmacol. Exp. Ther., 279, 1453
- Cassard-Doulcier A.-M., 1993, Mol. Endocrinol., 7, 497
- Collins S., 1994, Mol. Endocrinol., 8, 518
- Kozak U. C., 1994, Mol. Cell. Biol., 14, 59
- Underwood D. C., 2000, Physiol., 279, L895
- Underwood D. C., 2000, J. Pharmacol. Exp. Ther., 293, 281
Cited by
Sorted by citations
Items 201–300 of 604
Singh, R., Braga, M., Reddy, S. T., Lee, S.-J., Parveen, M., Grijalva, V., Vergnes, L., & Pervin, S. (2017) · Endocrinology · doi:10.1210/en.2016-1607 · Cited by 54
Recent advance in brown adipose physiology and its therapeutic potential
Lee, Y., Jung, Y.-S., & Choi, D. (2014) · Experimental & Molecular Medicine · doi:10.1038/emm.2013.163 · Cited by 56
Muraoka, M., Fukushima, A., Viengchareun, S., Lombès, M., Kishi, F., Miyauchi, A., Kanematsu, M., Doi, J., Kajimura, J., Nakai, R., et al. (2009) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.00024.2009 · Cited by 56
Qiu, Y., Sun, Y., Xu, D., Yang, Y., Liu, X., Wei, Y., Chen, Y., Feng, Z., Li, S., Reyad‐ul‐Ferdous, M., et al. (2018) · EBioMedicine · doi:10.1016/j.ebiom.2018.10.019 · Cited by 53
SIRT3 controls brown fat thermogenesis by deacetylation regulation of pathways upstream of UCP1
Sebaa, R., Johnson, J. R., Pileggi, C. A., Norgren, M., Xuan, J. Y., Sai, Y., Tong, Q., Krystkowiak, I., Bondy‐Chorney, E., Davey, N. E., et al. (2019) · Molecular Metabolism · doi:10.1016/j.molmet.2019.04.008 · Cited by 56
Kumar, N., Liu, D., Wang, H., Robidoux, J., & Collins, S. (2008) · Molecular Endocrinology · doi:10.1210/me.2007-0464 · Cited by 52
Self-citationKaramitri, A., Shore, A., Docherty, K., Speakman, J. R., & Lomax, M. A. (2009) · Journal of Biological Chemistry · doi:10.1074/jbc.m109.021766 · Cited by 51
Brown adipose tissue and novel therapeutic approaches to treat metabolic disorders
Román, S., Agil, A., Perán, M., Alvaro-Galue, E., Ruiz‐Ojeda, F. J., Fernández‐Vázquez, G., & Marchal, J. A. (2014) · Translational research · doi:10.1016/j.trsl.2014.11.002 · Cited by 54
Cypess, A. M., Zhang, H., Schulz, T. J., Huang, T. L., Espinoza, D., Kristiansen, K., Unterman, T. G., & Tseng, Y. (2011) · Endocrinology · doi:10.1210/en.2011-1229 · Cited by 49
Lv, Y., Zhang, S., Liang, X., Zhang, H., Zhi, X., Liu, B., Xu, M., Jiang, C., Shang, J., & Wang, X. (2016) · Journal of Biological Chemistry · doi:10.1074/jbc.m116.735563 · Cited by 53
Long non-coding RNAs regulation in adipogenesis and lipid metabolism: Emerging insights in obesity
Chen, C., Cui, Q., Zhang, X., Luo, X., Liu, Y., Zuo, J., & Peng, Y. (2018) · Cellular Signalling · doi:10.1016/j.cellsig.2018.07.012 · Cited by 53
Beige Fat Maintenance; Toward a Sustained Metabolic Health
Rabiee, A. (2020) · Frontiers in Endocrinology · doi:10.3389/fendo.2020.00634 · Cited by 53
Modular Evolution of PGC-1α in Vertebrates
LeMoine, C. M. R., Lougheed, S. C., & Moyes, C. D. (2010) · Journal of Molecular Evolution · doi:10.1007/s00239-010-9347-x · Cited by 51
Ceddia, R. P., & Collins, S. (2020) · Clinical Science · doi:10.1042/cs20190579 · Cited by 51
Self-citationMa, P.-Y., Li, X., Wang, Y., Lang, D.-Q., Liu, L., Yi, Y., Liu, Q., & Shen, C. (2022) · Pharmacological Research · doi:10.1016/j.phrs.2022.106175 · Cited by 52
Not all fats are created equal: adipose vs. ectopic fat, implication in cardiometabolic diseases
Gaggini, M., Saponaro, C., & Gastaldelli, A. (2015) · Hormone Molecular Biology and Clinical Investigation · doi:10.1515/hmbci-2015-0006 · Cited by 51
Dietary Lactate Supplementation Protects against Obesity by Promoting Adipose Browning in Mice
Yao, Z., Yan, Y., Zheng, X., Wang, M., Zhang, H., Li, H., & Chen, W. (2020) · Journal of Agricultural and Food Chemistry · doi:10.1021/acs.jafc.0c05899 · Cited by 49
GADD45γ regulates the thermogenic capacity of brown adipose tissue
Gantner, M. L., Hazen, B. C., Conkright, J. J., & Kralli, A. (2014) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1406638111 · Cited by 49
SnapShot: Brown and Beige Adipose Thermogenesis
Kissig, M., Shapira, S. N., & Seale, P. (2016) · Cell · doi:10.1016/j.cell.2016.06.038 · Cited by 49
Takeda, Y., Harada, Y., Yoshikawa, T., & Dai, P. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms24021352 · Cited by 49
A New Role for Browning as a Redox and Stress Adaptive Mechanism?
Jeanson, Y., Carrière, A., & Casteilla, L. (2015) · Frontiers in Endocrinology · doi:10.3389/fendo.2015.00158 · Cited by 49
p38α blocks brown adipose tissue thermogenesis through p38δ inhibition
Matesanz, N., Nikolić, I., Leiva, M., Pulgarín-Alfaro, M., Santamans, A. M., Bernardo, E., Mora, A., Herrera‐Melle, L., Rodríguez, E., Beiroa, D., et al. (2018) · PLoS Biology · doi:10.1371/journal.pbio.2004455 · Cited by 46
Zhao, Y., Li, X., Yang, L., Eckel‐Mahan, K. L., Tong, Q., Gu, X., Kolonin, M. G., & Sun, K. (2018) · Molecular and Cellular Biology · doi:10.1128/mcb.00242-18 · Cited by 45
Carper, D., Coué, M., Nascimento, E. B. M., Barquissau, V., Lagarde, D., Pestourie, C., Laurens, C., Vily‐Petit, J., Soty, M., Monbrun, L., et al. (2020) · Cell Reports · doi:10.1016/j.celrep.2020.108075 · Cited by 47
Cold-Inducible Klf9 Regulates Thermogenesis of Brown and Beige Fat
Fan, H., Zhang, Y., Zhang, J., Yao, Q., Song, Y., Shen, Q., Lin, J., Gao, Y., Wang, X., Zhang, L., et al. (2020) · Diabetes · doi:10.2337/db19-1153 · Cited by 46
Watanabe, M., Yamamoto, T., Mori, C., Okada, N., Yamazaki, N., Kajimoto, K., Kataoka, M., & Shinohara, Y. (2008) · Biological and Pharmaceutical Bulletin · doi:10.1248/bpb.31.775 · Cited by 46
Eddy, S. F., & Storey, K. B. (2007) · Cell Biochemistry and Function · doi:10.1002/cbf.1416 · Cited by 50
Gill, J. A., & Merrill, M. A. L. (2017) · Current Zoology · doi:10.1093/eep/dvx009 · Cited by 48
Shi, F., & Collins, S. (2017) · Hormone Molecular Biology and Clinical Investigation · doi:10.1515/hmbci-2017-0062 · Cited by 46
Self-citationDietary polyphenols turn fat “brown”: A narrative review of the possible mechanisms
Hu, J., Wang, Z., Tan, B. K., & Christian, M. (2020) · Trends in Food Science & Technology · doi:10.1016/j.tifs.2020.01.013 · Cited by 47
ER-resident sensor PERK is essential for mitochondrial thermogenesis in brown adipose tissue
Kato, H., Okabe, K., Miyake, M., Hattori, K., Fukaya, T., Tanimoto, K., Shi, B., Mizuguchi, M., Torii, S., Arakawa, S., et al. (2020) · Life Science Alliance · doi:10.26508/lsa.201900576 · Cited by 46
The Stress Axis in Obesity and Diabetes Mellitus: An Update
Gianotti, L., Belcastro, S., D’Agnano, S., & Tassone, F. (2021) · Endocrines · doi:10.3390/endocrines2030031 · Cited by 49
Inosine: novel activator of brown adipose tissue and energy homeostasis
Pfeifer, A., Mikhael, M., & Niemann, B. (2023) · Trends in Cell Biology · doi:10.1016/j.tcb.2023.04.007 · Cited by 45
Cho, Y., Kim, S., Kim, P.-K., Jo, M. J., Park, S.-E., Choi, Y., Jung, S. M., & Kang, H. J. (2025) · Biomolecules · doi:10.3390/biom15020291 · Cited by 49
Cao, L., Li, Y. S., Smirnov, A., Voshtani, R., Wang, T., Shao, C., Candi, E., Melino, G., Shi, Y., & Fang, J. (2025) · Cell & Bioscience · doi:10.1186/s13578-025-01519-2 · Cited by 52
Rouble, A. N., Tessier, S. N., & Storey, K. B. (2014) · Molecular and Cellular Biochemistry · doi:10.1007/s11010-014-2070-y · Cited by 43
Regulation of metabolism by cGMP
Pfeifer, A., Kilić, A., & Hoffmann, L. S. (2013) · Pharmacology & Therapeutics · doi:10.1016/j.pharmthera.2013.06.001 · Cited by 47
Time of day determines postexercise metabolism in mouse adipose tissue
Pendergrast, L. A., Lundell, L. S., Ehrlich, A. M., Ashcroft, S. P., Schönke, M., Basse, A. L., Krook, A., Treebak, J. T., Dollet, L., & Zierath, J. R. (2023) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2218510120 · Cited by 42
Neural circuits of long-term thermoregulatory adaptations to cold temperatures and metabolic demands
Mota, C. M. D., & Madden, C. J. (2024) · Nature reviews. Neuroscience · doi:10.1038/s41583-023-00785-8 · Cited by 42
G Protein-coupled Receptor 40 (GPR40) and Peroxisome Proliferator-activated Receptor γ (PPARγ)
Wang, S., Awad, K. S., Elinoff, J. M., Dougherty, E. J., Ferreyra, G. A., Wang, J. Y., Cai, R., Sun, J., Ptasinska, A., & Danner, R. L. (2015) · Journal of Biological Chemistry · doi:10.1074/jbc.m115.638924 · Cited by 44
Haas, B., Schlinkert, P., Mayer, P. E., & Eckstein, N. (2012) · Diabetology & Metabolic Syndrome · doi:10.1186/1758-5996-4-43 · Cited by 43
Ngoc, H. L., Shin, S., Tu, T. H., Kim, C.-S., Kang, J., Goto, T., Teruo, K., Han, S. N., & Yu, R. (2012) · Journal of Agricultural and Food Chemistry · doi:10.1021/jf303548k · Cited by 41
“Browning” of adipose tissue – regulation and therapeutic perspectives
Peschechera, A., & Eckel, J. (2013) · Archives of Physiology and Biochemistry · doi:10.3109/13813455.2013.796995 · Cited by 42
Metabolic benefits of inhibition of p38α in white adipose tissue in obesity
Zhang, S., Cao, H., Li, Y., Jing, Y., Liu, S., Cheng, Y., Wang, H., Yu, S., Peng, C., Hui, L., et al. (2018) · PLoS Biology · doi:10.1371/journal.pbio.2004225 · Cited by 41
Nutritional and non-nutritional agents that stimulate white adipose tissue browning
Concha, F., Prado, G., Quezada, J. U. C., Ramı́rez, A., Bravo, N., Flores, C., Herrera, J. J., Lopez, N., Uribe, D., Duarte-Silva, L., et al. (2019) · Reviews in Endocrine and Metabolic Disorders · doi:10.1007/s11154-019-09495-y · Cited by 41
Lee, S. J., Kim, S. H., Park, K. M., Lee, J. H., & Park, J. (2016) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2016.08.011 · Cited by 40
Brown and beige adipose tissues: phenotype and metabolic potential in mice and men
Chechi, K., Lichtenbelt, W. D. V. M., & Richard, D. (2017) · Journal of Applied Physiology · doi:10.1152/japplphysiol.00021.2017 · Cited by 40
Tian, S., Zhao, H., & Song, H. (2022) · Critical Reviews in Food Science and Nutrition · doi:10.1080/10408398.2022.2148090 · Cited by 42
Xenobiotic-induced TNF-α expression and apoptosis through the p38 MAPK signaling pathway
Frigo, D. E., Vigh, K. A., Struckhoff, A. P., Elliott, S. G., Beckman, B. S., Burow, M. E., & McLachlan, J. A. (2004) · Toxicology Letters · doi:10.1016/j.toxlet.2004.09.008 · Cited by 39
Antioxidant and anti-inflammatory effects of exercise: role of redox signaling
Ji, L. L., & Zhang, Y. (2013) · Free Radical Research · doi:10.3109/10715762.2013.844341 · Cited by 40
The glycoprotein follistatin-like 1 promotes brown adipose thermogenesis
Fang, D., Shi, X., Lu, T., Ruan, H., & Gao, Y. (2019) · Metabolism · doi:10.1016/j.metabol.2019.05.008 · Cited by 40
Irisin regulates thermogenesis and lipolysis in 3T3-L1 adipocytes
Vliora, M., Grillo, E., Corsini, M., Ravelli, C., Nintou, E., Karligiotou, E., Flouris, A. D., & Mitola, S. M. F. (2022) · Biochimica et Biophysica Acta (BBA) - General Subjects · doi:10.1016/j.bbagen.2022.130085 · Cited by 39
Wu, J., & Spiegelman, B. M. (2014) · Diabetes · doi:10.2337/db13-1586 · Cited by 39
Self-citationBordicchia, M., Pocognoli, A., D’Anzeo, M., Siquini, W., Minardi, D., Muzzonigro, G., Dessı̀-Fulgheri, P., & Sarzani, R. (2013) · Journal of Hypertension · doi:10.1097/hjh.0000000000000024 · Cited by 38
Sensing the Environment Through Sestrins: Implications for Cellular Metabolism
Parmigiani, A., & Budanov, A. V. (2016) · International review of cytology · doi:10.1016/bs.ircmb.2016.05.003 · Cited by 40
Epigenetic Regulation of the Thermogenic Adipose Program
Sambeat, A., Gulyaeva, О. N., Dempersmier, J. M., & Sul, H. S. (2016) · Trends in Endocrinology and Metabolism · doi:10.1016/j.tem.2016.09.003 · Cited by 40
Complementary Roles of Estrogen-Related Receptors in Brown Adipocyte Thermogenic Function
Gantner, M. L., Hazen, B. C., Eury, E., Brown, E. L., & Kralli, A. (2016) · Endocrinology · doi:10.1210/en.2016-1767 · Cited by 43
Natural Bioactive Compounds as Potential Browning Agents in White Adipose Tissue
Choi, Y., & Yu, L. (2021) · Pharmaceutical Research · doi:10.1007/s11095-021-03027-7 · Cited by 39
Saez-Lopez, C., Villena, J. A., Simó, R., & Selva, D. M. (2020) · The Journal of Nutritional Biochemistry · doi:10.1016/j.jnutbio.2020.108480 · Cited by 38
miR-199a-3p regulates brown adipocyte differentiation through mTOR signaling pathway
Gao, Y., Cao, Y., Cui, X., Wang, X., Zhou, Y., Huang, F., Wang, X., Wen, J., Xie, K., Xu, P., et al. (2018) · Molecular and Cellular Endocrinology · doi:10.1016/j.mce.2018.05.005 · Cited by 37
Role of PGC-1α in muscle function and aging
Kang, C., & Ji, L. L. (2013) · Journal of sport and health science/Journal of Sport and Health Science · doi:10.1016/j.jshs.2013.03.005 · Cited by 37
Meng, W., Liang, X., Chen, H., Luo, H., Bai, J., Li, G., Zhang, Q., Xiao, T., He, S., Zhang, Y., et al. (2017) · Diabetes · doi:10.2337/db16-0886 · Cited by 36
The kinase p38 Regulates Peroxisome Proliferator Activated Receptor-γ in Human Trophoblasts
Schild, R. L., Sonnenberg-Hirche, C., Schaiff, W. T., Bildirici, İ., Nelson, D. M., & Sadovsky, Y. (2005) · Placenta · doi:10.1016/j.placenta.2005.01.012 · Cited by 36
Feng, H., Kang, C., Dickman, J. R., Koenig, R. T., Awoyinka, I., Zhang, Y., & Ji, L. L. (2012) · Experimental Physiology · doi:10.1113/expphysiol.2012.069286 · Cited by 35
Rajan, A., Shi, H., & Xue, B. (2018) · Scientific Reports · doi:10.1038/s41598-018-31560-w · Cited by 36
Can Brown Fat Win the Battle Against White Fat?
Elattar, S., & Ande, S. (2015) · Journal of Cellular Physiology · doi:10.1002/jcp.24986 · Cited by 37
Kraemer, A. I., & Handschin, C. (2019) · International Journal of Molecular Sciences · doi:10.3390/ijms20215449 · Cited by 34
Thermogenesis and Energy Metabolism in Brown Adipose Tissue in Animals Experiencing Cold Stress
Zhang, X., Jin, X., Jiang, M., Phillips, C. J. C., & Shi, B. (2025) · International Journal of Molecular Sciences · doi:10.3390/ijms26073233 · Cited by 42
IRE1α-XBP1 is a novel branch in the transcriptional regulation of Ucp1 in brown adipocytes
Asada, R., Kanemoto, S., Matsuhisa, K., Hino, K., Cui, M., Cui, X., Kaneko, M., & Imaizumi, K. (2015) · Scientific Reports · doi:10.1038/srep16580 · Cited by 36
Perm1 regulates cardiac energetics as a downstream target of the histone methyltransferase Smyd1
Oka, S., Sabry, A. D., Horiuchi, A. K., Cawley, K. M., O’Very, S., Zaitsev, M. A., Shankar, T. S., Byun, J., Mukai, R., Xu, X., et al. (2020) · PLoS ONE · doi:10.1371/journal.pone.0234913 · Cited by 34
Conjugated Linoleic Acid Induces Uncoupling Protein 1 in White Adipose Tissue of ob/ob Mice
Wendel, A. A., Purushotham, A., Liu, L., & Belury, M. A. (2009) · Lipids · doi:10.1007/s11745-009-3348-9 · Cited by 33
Effects of growth hormone on uncoupling protein 1 in white adipose tissues in obese mice
Hayashi, M., Futawaka, K., Koyama, R., Fan, Y., Matsushita, M., Hirao, A., Fukuda, Y., Nushida, A., Nezu, S., Tagami, T., et al. (2017) · Growth Hormone & IGF Research · doi:10.1016/j.ghir.2017.10.006 · Cited by 33
Barceló-Batllori, S., Kalko, S. G., Esteban, Y., Moreno, S., Carmona, M. C., & Gomis, R. (2007) · Molecular & Cellular Proteomics · doi:10.1074/mcp.m700198-mcp200 · Cited by 33
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
α-Cedrene protects rodents from high-fat diet-induced adiposity via adenylyl cyclase 3
Tong, T., Yu, R., & Park, T. (2018) · International Journal of Obesity · doi:10.1038/s41366-018-0176-0 · Cited by 34
Araiz, C., Yan, A., Bettedi, L., Samuelson, I., Virtue, S., McGavigan, A. K., Dani, C., Vidal‐Puig, A., & Foukas, L. C. (2019) · Nature Communications · doi:10.1038/s41467-019-09514-1 · Cited by 36
Joubert, R., Métayer, S., Swennen, Q., Sibut, V., Crochet, S., Cailleau-Audouin, E., Buyse, J. G., Decuypere, E., Wrutniak‐Cabello, C., Cabello, G., et al. (2009) · Domestic Animal Endocrinology · doi:10.1016/j.domaniend.2009.08.002 · Cited by 38
Baan, B., van Dam, H., van der Zon, G. C. M., Maassen, J. A., & Ouwens, D. M. (2006) · Molecular Endocrinology · doi:10.1210/me.2005-0289 · Cited by 33
Shi, F., & Collins, S. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms241411497 · Cited by 34
Self-citationItaconate alleviates diet-induced obesity via activation of brown adipocyte thermogenesis
Yu, Z., Li, X., Quan, Y., Chen, J., Liu, J., Zheng, N., Liu, S., Wang, Y., Liu, W., Qiu, C., et al. (2024) · Cell Reports · doi:10.1016/j.celrep.2024.114142 · Cited by 32
Subramani, J., Kundumani‐Sridharan, V., & Das, K. C. (2020) · Aging · doi:10.18632/aging.104071 · Cited by 31
Mitochondrial Kinases and the Role of Mitochondrial Protein Phosphorylation in Health and Disease
Kotrasová, V., Keresztesová, B., Ondrovičová, G., Bauer, J., Havalová, H., Pevala, V., Kutějová, E., & Kunová, N. (2021) · Life · doi:10.3390/life11020082 · Cited by 35
Ma, D., Wu, T., Qu, Y., Yang, J., Cai, L., Li, X., & Wang, Y. (2023) · Lipids in Health and Disease · doi:10.1186/s12944-022-01770-3 · Cited by 32
Farmer, S. R., & Auwerx, J. H. (2004) · Obesity Reviews · doi:10.1111/j.1467-789x.2004.00157.x · Cited by 32
A two-way street - cellular metabolism and myofibroblast contraction
Noom, A., Sawitzki, B., Knaus, P., & Duda, G. N. (2024) · npj Regenerative Medicine · doi:10.1038/s41536-024-00359-x · Cited by 31
Chu, P., Wang, S., Yu, W., Wang, A., Zong, Y., Yin, S., Zhao, C., & Wang, T. (2023) · Aquaculture · doi:10.1016/j.aquaculture.2023.740155 · Cited by 34
GSK3 is a negative regulator of the thermogenic program in brown adipocytes
Markussen, L. K., Winther, S., Wicksteed, B. L., & Hansen, J. B. (2018) · Scientific Reports · doi:10.1038/s41598-018-21795-y · Cited by 32
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Metadata
- Authors
- Cao, W., Daniel, K. W., Robidoux, J., Puigserver, P., Medvedev, A. V., Bai, X., Floering, L. M., Spiegelman, B. M., & Collins, S.
- Affiliations
- Duke University (US)
- Harvard University (US)
- Corresponding author
- Collins, Sheila
- ORCID
- Venue
- Molecular and Cellular Biology
- Publisher
- Informa UK Limited
- Published
- 2004-04-01
- Volume
- 24
- Issue
- 7
- Pages
- 3057-3067
- ISSN
- 0270-7306 (ISSN-L)
- 1098-5549
- PMC
- PMC371122
- OpenAlex
- W2162186867
- Cited by
- 605
- References
- 46
- Citations by year
- 2026: 17 · 2025: 33 · 2024: 36 · 2023: 29 · 2022: 28 · 2021: 46 · 2020: 51 · 2019: 28 · 2018: 29 · 2017: 29 · 2016: 37 · 2015: 27 · 2014: 26 · 2013: 34 · 2012: 26
- FWCI
- 10.31
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- Molecular and Cellular Biology (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Funders
- National Institutes of Health (DK54477)
- National Institute of Diabetes and Digestive and Kidney Diseases (R01-DK-54024, R01 DK54477, R01DK054024, R01DK053092, R01DK054477)
- 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 › Metabolism, Diabetes, and Cancer
- Keywords
- p38 MAPK, UCP1, brown adipocytes, thermogenesis, cAMP signaling, protein kinase A, ATF2, PGC-1α, PPAR response element, cAMP response element, enhancers, catecholamine signaling, beta-adrenergic signaling
- MeSH terms
- Uncoupling Protein 1, Cyclic AMP, Animals, Adipose Tissue, Brown, Carrier Proteins, Cells, Cultured, Cold Temperature, Enhancer Elements, Genetic, Enzyme Activation, Enzyme Inhibitors, Gene Expression Regulation, Humans, Ion Channels, Membrane Proteins, Mice, Inbred C57BL, Random Allocation, Transcription Factors, Transcription, Genetic, Uncoupling Agents, Signal Transduction, Adipocytes, Mitogen-Activated Protein Kinases, Thermogenesis, Mitochondrial Proteins, p38 Mitogen-Activated Protein Kinases, Mice
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