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Exercise-induced BCL2-regulated autophagy is required for muscle glucose homeostasis
Open accessAbstract
Exercise has beneficial effects on human health, including protection against metabolic disorders such as diabetes. However, the cellular mechanisms underlying these effects are incompletely understood. The lysosomal degradation pathway, autophagy, is an intracellular recycling system that functions during basal conditions in organelle and protein quality control. During stress, increased levels of autophagy permit cells to adapt to changing nutritional and energy demands through protein catabolism. Moreover, in animal models, autophagy protects against diseases such as cancer, neurodegenerative disorders, infections, inflammatory diseases, ageing and insulin resistance. Here we show that acute exercise induces autophagy in skeletal and cardiac muscle of fed mice. To investigate the role of exercise-mediated autophagy in vivo, we generated mutant mice that show normal levels of basal autophagy but are deficient in stimulus (exercise- or starvation)-induced autophagy. These mice (termed BCL2 AAA mice) contain knock-in mutations in BCL2 phosphorylation sites (Thr69Ala, Ser70Ala and Ser84Ala) that prevent stimulus-induced disruption of the BCL2-beclin-1 complex and autophagy activation. BCL2 AAA mice show decreased endurance and altered glucose metabolism during acute exercise, as well as impaired chronic exercise-mediated protection against high-fat-diet-induced glucose intolerance. Thus, exercise induces autophagy, BCL2 is a crucial regulator of exercise- (and starvation)-induced autophagy in vivo, and autophagy induction may contribute to the beneficial metabolic effects of exercise.
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“Exercise triggers autophagy by activating ULK1 and dissociating BCL2 from BECN1, thereby disinhibiting the initiation complex [484,485].”
From Autophagy and ALS: mechanistic insights and therapeutic implications (2022) · cites this paper as [485]
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Repertoires of Autophagy in the Pathogenesis of Ocular Diseases
Li, Y., Jiang, Q. L., Cao, G.-F., Yao, J., & Yan, B. (2015) · Cellular Physiology and Biochemistry · doi:10.1159/000373980 · Cited by 16,351
Positional cloning of the mouse obese gene and its human homologue
Zhang, Y., Proenca, R., Maffei, M., Barone, M., Leopold, L., & Friedman, J. M. (1994) · Nature · doi:10.1038/372425a0 · Cited by 13,419
Autophagy in the Pathogenesis of Disease
Levine, B., & Kroemer, G. (2008) · Cell · doi:10.1016/j.cell.2007.12.018 · Cited by 7,069
Self-citationAutophagy and Viruses: Adversaries or Allies?
Dong, X., & Levine, B. (2013) · Journal of Innate Immunity · doi:10.1159/000346388 · Cited by 4,444
Self-citationAntimicrobial Autophagy: A Conserved Innate Immune Response in Drosophila
Moy, R. H., & Cherry, S. R. (2013) · Journal of Innate Immunity · doi:10.1159/000350326 · Cited by 3,551
Induction of autophagy and inhibition of tumorigenesis by beclin 1
Liang, X. H., Jackson, S., Seaman, M., Brown, K., Kempkes, B., Hibshoosh, H., & Levine, B. (1999) · Nature · doi:10.1038/45257 · Cited by 3,347
Self-citationA Novel Serum Protein Similar to C1q, Produced Exclusively in Adipocytes
Scherer, P. E., Williams, S. P., Fogliano, M., Baldini, G., & Lodish, H. F. (1995) · Journal of Biological Chemistry · doi:10.1074/jbc.270.45.26746 · Cited by 3,238
Self-citationPromotion of tumorigenesis by heterozygous disruption of the beclin 1 autophagy gene
Qu, X., Yu, J., Bhagat, G., Furuya, N., Hibshoosh, H., Troxel, A., Rosen, J., Eskelinen, E.-L., Mizushima, N., Ohsumi, Y., et al. (2003) · Journal of Clinical Investigation · doi:10.1172/jci20039 · Cited by 2,311
Self-citationMizushima, N., Yamamoto, A., Matsui, M., Yoshimori, T., & Ohsumi, Y. (2004) · Molecular Biology of the Cell · doi:10.1091/mbc.e03-09-0704 · Cited by 2,105
Frederich, R. C., Hamann, A., Anderson, S., Löllmann, B., Lowell, B. B., & Flier, J. S. (1995) · Nature Medicine · doi:10.1038/nm1295-1311 · Cited by 1,660
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Shi, M., Maique, J., Shaffer, J., Davidson, T. L., Sebti, S., Fernández, Á. F., Zou, Z., Yan, S. X., Levine, B., Moe, O. W., et al. (2020) · The FASEB Journal · doi:10.1096/fj.201902127r · Cited by 20
Self-citationEhrlicher, S. E., Stierwalt, H. D., Miller, B. F., Newsom, S. A., & Robinson, M. M. (2020) · The FASEB Journal · doi:10.1096/fj.201902594rr · Cited by 21
NAF‐1 antagonizes starvation‐induced autophagy through AMPK signaling pathway in cardiomyocytes
Du, X., Xiao, R., Xiao, F., Chen, Y., Hua, F., Yu, S., & Xu, G. (2015) · Cell Biology International · doi:10.1002/cbin.10453 · Cited by 20
Fiedler, L. R., Maifoshie, E., & Schneider, M. D. (2014) · Current topics in developmental biology/Current Topics in Developmental Biology · doi:10.1016/b978-0-12-397920-9.00002-0 · Cited by 20
Autophagy and metabolic aging: Current understanding and future applications
Raza, S. (2024) · Biochimica et Biophysica Acta (BBA) - Molecular Cell Research · doi:10.1016/j.bbamcr.2024.119753 · Cited by 19
Wan, D.-F., Pan, S.-S., Tong, Y.-S., & Huang, Y. (2021) · Frontiers in Physiology · doi:10.3389/fphys.2021.599892 · Cited by 19
Yin, Y., Tan, M., Han, L., Zhang, L., Zhang, Y., Zhang, J., Pan, W., Bai, J., Jiang, T., & Li, H. (2023) · Acta Pharmaceutica Sinica B · doi:10.1016/j.apsb.2023.01.015 · Cited by 19
Autophagy activation by novel inducers prevents BECN2-mediated drug tolerance to cannabinoids
Kuramoto, K., Wang, N., Fan, Y., Zhang, W., Schoenen, F. J., Frankowski, K. J., Marugán, J., Zhou, Y., Huang, S., & He, C. (2016) · Autophagy · doi:10.1080/15548627.2016.1187367 · Cited by 19
Self-citationLi, X., Hou, Y., Wang, X., Zhang, Y., Meng, X., Hu, Y., & Zhang, Y. (2019) · Biological and Pharmaceutical Bulletin · doi:10.1248/bpb.b19-00627 · Cited by 19
Acute Heat Exposure Alters Autophagy Signaling in C2C12 Myotubes
Summers, C. M., & Valentine, R. J. (2020) · Frontiers in Physiology · doi:10.3389/fphys.2019.01521 · Cited by 19
Relationship between insulin sensitivity and gene expression in human skeletal muscle
Parikh, H. M., Elgzyri, T., Alibegovic, A. C., Hiscock, N. J., Ekström, O., Eriksson, K., Vaag, A. A., Groop, L., Ström, K., & Hansson, O. (2021) · BMC Endocrine Disorders · doi:10.1186/s12902-021-00687-9 · Cited by 20
Micro- and Nanosized Substances Cause Different Autophagy-Related Responses
Wang, Y., Zheng, C., Lee, Y., Cheng, Y., Lin, Y., & Chiu, H. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22094787 · Cited by 19
Fang, Q., Liu, X., Ding, J., Zhang, Z., Chen, G., Du, T., Wang, Y., & Xu, R. (2022) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2022/3773415 · Cited by 19
Zheng, D., Bian, Z., Furuya, N., Trejo, J. A. O., Takeda‐Ezaki, M., Takahashi, K., Hiraoka, Y., Mineki, R., Taka, H., Ikeda, S.-I., et al. (2014) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2014.11.118 · Cited by 19
Nicotinamide: Oversight of Metabolic Dysfunction Through SIRT1, mTOR, and Clock Genes
Maiese, K. (2020) · Current Neurovascular Research · doi:10.2174/1567202617999201111195232 · Cited by 20
Oh, S. J., & Lee, M. (2022) · Journal of Korean Medical Science · doi:10.3346/jkms.2022.37.e276 · Cited by 18
Liu, Z., Lu, T., Qian, R., Wang, Z., Qi, R., & Zhang, Z. (2024) · International Journal of Nanomedicine · doi:10.2147/ijn.s455407 · Cited by 18
Klionsky, D. J., & Saltiel, A. R. (2012) · Cell Metabolism · doi:10.1016/j.cmet.2012.02.008 · Cited by 18
Noncoding RNAs in exercise-induced cardio-protection for chronic heart failure
Ma, S., & Liao, Y. (2019) · EBioMedicine · doi:10.1016/j.ebiom.2019.07.051 · Cited by 18
Intracellular pH Regulation of Skeletal Muscle in the Milieu of Insulin Signaling
Posa, D. K., & Baba, S. P. (2020) · Nutrients · doi:10.3390/nu12102910 · Cited by 19
Bostancıklıoğlu, M., Demiryürek, Ş., Cengiz, B., Demi̇r, T., Öztuzcu, S., Aras, M. H., Özsevik, A. S., Usumez, A., Ergün, S., Özbal, H. K., et al. (2015) · Lasers in Medical Science · doi:10.1007/s10103-015-1727-4 · Cited by 18
Liu, W., & Zhao, J. (2014) · Saudi Journal of Biological Sciences · doi:10.1016/j.sjbs.2014.01.005 · Cited by 18
McCormick, J. J., King, K. E., Dokładny, K., & Mermier, C. M. (2019) · Canadian Journal of Diabetes · doi:10.1016/j.jcjd.2019.04.005 · Cited by 19
A crosstalk between autophagy and apoptosis in intracerebral hemorrhage
Wang, M., Chen, X., Li, S., Wang, L., Tang, H., Pu, Y., Zhang, D., Fang, B., & Bai, X. (2024) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2024.1445919 · Cited by 18
Ma, Z., Qi, J., Gao, L., & Zhang, J. (2020) · International Heart Journal · doi:10.1536/ihj.19-443 · Cited by 17
Rao, A., Clayton, P., & Briskey, D. R. (2021) · Journal of Human Nutrition and Dietetics · doi:10.1111/jhn.12936 · Cited by 17
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Claude‐Taupin, A., Codogno, P., & Dupont, N. (2021) · Journal of Cell Science · doi:10.1242/jcs.258589 · Cited by 17
Song, Y., Yang, H., Kim, J., Lee, Y., Kim, S., Do, I., & Park, C. (2023) · Molecular Metabolism · doi:10.1016/j.molmet.2023.101806 · Cited by 17
Treadmill exercise induces murine cardiac allograft survival and generates regulatory T cell
Uchiyama, M., Jin, X., Yin, E., Shimokawa, T., & Niimi, M. (2014) · Transplant International · doi:10.1111/tri.12491 · Cited by 17
A bird’s-eye view of autophagy
Starokadomskyy, P., & Dmytruk, K. V. (2013) · Autophagy · doi:10.4161/auto.24544 · Cited by 17
Pompeani, N., Rybalka, E., Latchman, H. K., Murphy, R. M., Croft, K. D., & Hayes, A. (2014) · Journal of Negative Results in BioMedicine · doi:10.1186/s12952-014-0019-z · Cited by 17
Distinct surveillance pathway for immunopathology during acute infection via autophagy and SR-BI
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Thongrod, S., Wanichanon, C., Kankuan, W., Siangcham, T., Phadngam, S., Morani, F., Isidoro, C., & Sobhon, P. (2018) · Frontiers in Physiology · doi:10.3389/fphys.2018.00613 · Cited by 17
Yu, W., Zha, W., Hu, P., Wang, Q., Zhang, S., & Ren, J. T. (2019) · Current Pharmaceutical Design · doi:10.2174/1381612825666190708221539 · Cited by 17
Liu, W., Fu, R., Wang, Z., Liu, S., Tang, C., Li, L., & Yin, D. (2019) · Journal of Neuropathology & Experimental Neurology · doi:10.1093/jnen/nlz106 · Cited by 17
Palmitate reduces starvation-induced ER stress by inhibiting ER-phagy in hypothalamic cells
Lim, Y., Kim, S., & Kim, E. (2021) · Molecular Brain · doi:10.1186/s13041-021-00777-8 · Cited by 18
Morales-Scholz, M. G., Wette, S. G., Stokie, J. R., Tepper, B. T., Swinton, C., Hamilton, D. L., Dwyer, K. M., Murphy, R. M., Howlett, K. F., & Shaw, C. S. (2022) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.00015.2022 · Cited by 17
Role of skeletal muscle autophagy in high-fat-diet–induced obesity and exercise
Herrenbruck, A. R., & Bollinger, L. M. (2019) · Nutrition Reviews · doi:10.1093/nutrit/nuz044 · Cited by 18
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Ding, W., Feng, H., Li, W., Liao, H.-H., & Tang, Q. (2020) · Frontiers in Pharmacology · doi:10.3389/fphar.2020.587438 · Cited by 17
Gao, B., Wang, L., Gong, J., Zhu, Z., Liu, Q., Han, Y., & Wang, H. (2025) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2025.1579208 · Cited by 16
Human skeletal muscle methylome after low-carbohydrate energy-balanced exercise
Gorski, P. P., Turner, D. C., Iraki, J., Morton, J. P., Sharples, A. P., & Areta, J. L. (2023) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.00029.2023 · Cited by 17
Dai, Y., Zhou, S., Lin, Q., Zhao, P., Zhao, J., Xu, D., Wu, C., Li, M., Zeng, X., & Wang, Q. (2023) · Frontiers in Endocrinology · doi:10.3389/fendo.2023.1126661 · Cited by 16
McCormick, J. J., McManus, M. K., King, K. E., Goulet, N., & Kenny, G. P. (2023) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.00163.2023 · Cited by 16
Martinez‐Canton, M., Galván-Álvarez, V., Gallego-Selles, Á., Gelabert‐Rebato, M., García-Gonzalez, E., González, J. J., Martín-Rincón, M., & Calbet, J. A. L. (2024) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2024.07.012 · Cited by 17
Irisin reduces senile osteoporosis by inducing osteocyte mitophagy through Ampk activation
Li, H., Luo, D., Xie, W., Ye, W., Chen, J., Alberton, P., Zhang, M., Feng, E., Docheva, D., & Lin, D. (2024) · iScience · doi:10.1016/j.isci.2024.111042 · Cited by 19
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Dagon, Y., Mantzoros, C. S., & Kim, Y. (2015) · Metabolism · doi:10.1016/j.metabol.2015.03.002 · Cited by 16
Rocha‐Rodrigues, S., Gonçalves, I. O., Beleza, J., Ascensão, A. A. M. R., & Magalhães, J. (2017) · European Journal of Nutrition · doi:10.1007/s00394-017-1500-5 · Cited by 16
Das, G. C., & Hollinger, F. B. (2012) · Virology · doi:10.1016/j.virol.2012.07.003 · Cited by 16
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Sun, H. B. (2013) · Journal of Exercise Sports & Orthopedics · doi:10.15226/2374-6904/1/1/00104 · Cited by 16
Smiles, W. J., Conceição, M. S., Telles, G. D., Chacon‐Mikahil, M. P. T., Cavaglieri, C. R., VECHIN, F. C., Libardi, C. A., Hawley, J. A., & CAMERA, D. M. (2017) · European Journal of Applied Physiology · doi:10.1007/s00421-016-3530-8 · Cited by 16
The Nuclear Receptor Nor-1 Is a Pleiotropic Regulator of Exercise-Induced Adaptations
Pearen, M. A., & Muscat, G. E. O. (2018) · Exercise and Sport Sciences Reviews · doi:10.1249/jes.0000000000000143 · Cited by 16
Burgeiro, A., Fonseca, A. C., Espinoza, D., Carvalho, L., Lourenço, N., Antunes, M., & Carvalho, E. (2018) · Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease · doi:10.1016/j.bbadis.2018.03.025 · Cited by 16
Endospanin-2 enhances skeletal muscle energy metabolism and running endurance capacity
Lancel, S., Hesselink, M. K. C., Woldt, E., Rouillé, Y., Dorchies, E., Delhaye, S., Duhem, C., Thorel, Q., Mayeuf-Louchart, A., Pourcet, B., et al. (2018) · JCI Insight · doi:10.1172/jci.insight.98081 · Cited by 17
PGC-1α in exercise and fasting-induced regulation of hepatic UPR in mice
Kristensen, C. M., Olsen, M. A., Jessen, H., Brandt, N., Nøhr-Meldgaard, J., & Pilegaard, H. (2018) · Pflügers Archiv - European Journal of Physiology · doi:10.1007/s00424-018-2159-3 · Cited by 16
Liu, W., Xia, Y., Kuang, H., Wang, Z., Liu, S., Tang, C., & Yin, D. (2019) · Gerontology · doi:10.1159/000500742 · Cited by 16
Qi, Z., & Ding, S. (2012) · PPAR Research · doi:10.1155/2012/348245 · Cited by 16
Packer, M. (2025) · Circulation · doi:10.1161/circulationaha.125.075568 · Cited by 16
Self-citationExercise attenuates the hallmarks of aging: Novel perspectives
Qiu, Y., Fernández‐Garcia, B., Lehmann, H. I., Li, G., Kroemer, G., López-Otín, C., & Xiao, J. (2025) · Journal of sport and health science/Journal of Sport and Health Science · doi:10.1016/j.jshs.2025.101108 · Cited by 16
Modeling to Link Regional Myocardial Work, Metabolism and Blood Flows
Bassingthwaighte, J. B., Beard, D. A., Carlson, B. E., Dash, R. K., & Vinnakota, K. C. (2012) · Annals of Biomedical Engineering · doi:10.1007/s10439-012-0613-5 · Cited by 15
Survival-apoptosis associated signaling in GNE myopathy-cultured myoblasts
Harazi, A., Chaouat, M., Shlomai, Z., Levitzki, R., Becker‐Cohen, M., Sadeh, M., Dabby, R., Ben‐Bassat, H., & Mitrani‐Rosenbaum, S. (2014) · Journal of Receptors and Signal Transduction · doi:10.3109/10799893.2014.956755 · Cited by 15
Liang, Y., Huang, X., Zhang, Z., Deng, K., An, S., Gao, X., Wang, Z., Liu, Z., Wang, F., Liu, D., et al. (2020) · Archives of Animal Nutrition · doi:10.1080/1745039x.2020.1820806 · Cited by 15
The Role of Autophagy Modulated by Exercise in Cancer Cachexia
Gunadi, J. W., Welliangan, A. S., Soetadji, R. S., Jasaputra, D. K., & Lesmana, R. (2021) · Life · doi:10.3390/life11080781 · Cited by 16
Ma, G., Liu, Y., Zhang, Q., Zhang, B.-G., Zhao, N. O., Wang, Q.-L., & Wang, X. (2014) · Hepatology International · doi:10.1007/s12072-014-9529-5 · Cited by 15
Mechanism and Physiological Significance of Growth Factor-Related Autophagy
Li, T. Y., Lin, S., & Lin, S. (2013) · Physiology · doi:10.1152/physiol.00023.2013 · Cited by 16
Hong, Y. H., Yang, C., Betik, A. C., Lee, R. S., & McConell, G. K. (2016) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.00513.2015 · Cited by 15
Tarawan, V. M., Gunadi, J. W., Setiawan, S., Lesmana, R., Goenawan, H., Meilina, D. E., Sipayung, J. A., Wargasetia, T. L., Widowati, W., Limyati, Y., et al. (2019) · Europe PMC (PubMed Central) · Cited by 15
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Sopariwala, D. H., Yadav, V., Badin, P.-M., Likhite, N., Sheth, M., Lorca, S., Vila, I. K., Kim, E. R., Tong, Q., Song, M. S., et al. (2017) · Scientific Reports · doi:10.1038/s41598-017-10238-9 · Cited by 14
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Kuramoto, K., & He, C. (2022) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2022.844481 · Cited by 16
Self-citationRole of adiponectin in osteoarthritis
Feng, X., Xiao, J., & Bai, L. (2022) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2022.992764 · Cited by 15
Gut Microbiome Regulation of Autophagic Flux and Neurodegenerative Disease Risks
Shoubridge, A. P., Fourrier, C., Choo, J. M., Proud, C. G., Sargeant, T. J., & Rogers, G. B. (2021) · Frontiers in Microbiology · doi:10.3389/fmicb.2021.817433 · Cited by 15
Ding, M., Li, Q. F., Yin, G., Liu, J. L., Jan, X. Y., Huang, T., Li, A. C., & Zheng, L. (2022) · PLoS ONE · doi:10.1371/journal.pone.0262471 · Cited by 14
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Seyrek, K., Wohlfromm, F., Espe, J., & Lavrik, I. N. (2022) · Biochemical Journal · doi:10.1042/bcj20210676 · Cited by 15
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Halma, M. T. J., Marik, P. E., & Saleeby, Y. M. (2024) · Endocrine and Metabolic Science · doi:10.1016/j.endmts.2024.100163 · Cited by 14
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Kroemer, G., & Galluzzi, L. (2016) · Oncotarget · doi:10.18632/oncotarget.13892 · Cited by 15
Moberg, M., Hendo, G., Jakobsson, M., Mattsson, C. M., Ekblom‐Bak, E., Flockhart, M., Pontén, M., Söderlund, K., & Ekblom, B. T. (2017) · Physiological Reports · doi:10.14814/phy2.13518 · Cited by 14
Ablation of Bax and Bak protects skeletal muscle against pressure-induced injury
Tam, B. T., Yu, A. P., Tam, E. W., Monks, D. A., Wang, X. P., Pei, X. M., Koh, S. P., Sin, T. K., Law, H., Ugwu, F. N., et al. (2018) · Scientific Reports · doi:10.1038/s41598-018-21853-5 · Cited by 14
Periodized low protein-high carbohydrate diet confers potent, but transient, metabolic improvements
Li, Z., Rasmussen, M. L., Li, J., Henríquez‐Olguín, C., Knudsen, J. R., Madsen, A. B., Sanchez-Quant, E., Kleinert, M., & Jensen, T. E. (2018) · Molecular Metabolism · doi:10.1016/j.molmet.2018.08.008 · Cited by 15
Bednarczyk, M., Szeja, N., Łętowski, D., Waniczek, D., Dzięgielewska-Gęsiak, S., & Muc‐Wierzgoń, M. (2024) · Nutrients · doi:10.3390/nu16234003 · Cited by 13
Muscle PGC ‐1α in exercise and fasting‐induced regulation of hepatic UPR in mice
Kristensen, C. M., Jessen, H., Ringholm, S., & Pilegaard, H. (2018) · Acta Physiologica · doi:10.1111/apha.13158 · Cited by 14
Møller, A. B., Voss, T. S., Vendelbo, M. H., Pedersen, S. B., Møller, N., & Jessen, N. (2018) · Journal of Applied Physiology · doi:10.1152/japplphysiol.00490.2018 · Cited by 13
Bardi, E., Majerczak, J., Zoladz, J. A., Tyrankiewicz, U., Skórka, T., Chłopicki, S., Jabłońska, M., Bar, A., Jasiński, K., Buso, A., et al. (2019) · Physiological Reports · doi:10.14814/phy2.14161 · Cited by 13
Heparan sulfate controls skeletal muscle differentiation and motor functions
Yokoyama, M., Matsuzawa, T., Yoshikawa, T., Nunomiya, A., Yamaguchi, Y., & Yanai, K. (2020) · Biochimica et Biophysica Acta (BBA) - General Subjects · doi:10.1016/j.bbagen.2020.129707 · Cited by 13
Keeping the beat against time: Mitochondrial fitness in the aging heart
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Targeting autophagy drug discovery: Targets, indications and development trends
Jiang, M., Wu, W., Xiong, Z., Ye, Z., Ye, Z., & Wu, Z. (2024) · European Journal of Medicinal Chemistry · doi:10.1016/j.ejmech.2023.116117 · Cited by 13
Audzeyenka, I., Rogacka, D., Piwkowska, A., Rychłowski, M., Bierła, J. B., Czarnowska, E., Angielski, S., & Jankowski, M. (2016) · The International Journal of Biochemistry & Cell Biology · doi:10.1016/j.biocel.2016.03.015 · Cited by 13
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Qi, M., Geng, H., Geng, N., Cui, Y., Qi, C., Cheng, G., Song, K., Hu, L., Liu, Y., Liu, J., et al. (2022) · Journal of Dairy Research · doi:10.1017/s0022029922000243 · Cited by 13
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Li, Y., Xue, L., Wang, F., Wang, Y., Sun, Y., Niu, Z., Liu, S., Yan, Y., Shen, S., Zhang, K., et al. (2025) · Cell chemical biology · doi:10.1016/j.chembiol.2025.10.007 · Cited by 12
Cummings, S. R., Hong, N., & Cohen, A. A. (2025) · Aging Cell · doi:10.1111/acel.70292 · Cited by 12
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Kwon, I., Kim, K. S., & Lee, Y. (2024) · Physical Activity and Nutrition · doi:10.20463/pan.2024.0013 · Cited by 12
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Guo, R., Yu, Q., Liong, E. C., Fung, M., & Tipoe, G. L. (2020) · PubMed · doi:10.14670/hh-18-204 · Cited by 12
Wang, P., Li, C. G., Zhou, X., Cui, D., Ouyang, T., Chen, W., & Ding, S. (2022) · Clinical and Experimental Pharmacology and Physiology · doi:10.1111/1440-1681.13632 · Cited by 12
Metadata
- Authors
- He, C., Bassik, M. C., Moresi, V., Sun, K., Wei, Y., Zou, Z., An, Z., Loh, J., Fisher, J., Sun, Q., Korsmeyer, S., Packer, M., May, H. I., Hill, J. A., Virgin, H. W., Gilpin, C., Xiao, G., Bassel-Duby, R., Scherer, P. E., & Levine, B.
- Affiliations
- The University of Texas Southwestern Medical Center (US)
- Dana-Farber Cancer Institute (US)
- Howard Hughes Medical Institute (US)
- Washington University in St. Louis (US)
- Corresponding author
- Levine, Beth
- ORCID
- Venue
- Nature
- Published
- 2012-01-18
- Volume
- 481
- Issue
- 7382
- Pages
- 511-515
- ISSN
- 0028-0836 (ISSN-L)
- 1476-4687
- PMC
- PMC3518436
- OpenAlex
- W2082476985
- Cited by
- 1,136
- References
- 36
- Citations by year
- 2026: 40 · 2025: 47 · 2024: 49 · 2023: 55 · 2022: 64 · 2021: 90 · 2020: 93 · 2019: 76 · 2018: 93 · 2017: 99 · 2016: 94 · 2015: 112 · 2014: 82 · 2013: 80 · 2012: 61
- FWCI
- 79.93
- Type
- journal article
- Language
- en
- Update notices
- erratum (2013-11-06)
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- Nature (publishedVersion)
- PubMed (publishedVersion)
- Europe PMC (PubMed Central) (acceptedVersion)
- PubMed Central (acceptedVersion)
- RePEc: Research Papers in Economics (submittedVersion)
- IRIS Research product catalog (Sapienza University of Rome) (submittedVersion)
- Funders
- Howard Hughes Medical Institute
- National Heart, Lung, and Blood Institute (R0I HL090842, R0I HL080244, R01HL090842)
- National Cancer Institute (R01CA112023, R01CA109618, P30CA142543)
- National Institute of Allergy and Infectious Diseases (R01AI084887, R0I AI084887)
- National Institute of Diabetes and Digestive and Kidney Diseases (RCI DK086629, R01DK055758, 1P01 DK0887761, RC1DK086629, P01DK088761)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Autophagy in Disease and Therapy
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Metabolism, Diabetes, and Cancer
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Muscle Physiology and Disorders
- Keywords
- Bcl-2, Bcl-2 phosphorylation, skeletal muscle, myocardium, glucose metabolism, impaired glucose tolerance, high-fat diet, endurance, starvation-induced autophagy, exercise metabolism, diabetes protection
- MeSH terms
- Beclin-1, Animals, Autophagy, Cells, Cultured, Dietary Fats, Physical Exertion, Food Deprivation, Glucose, Glucose Tolerance Test, Homeostasis, Male, Mice, Transgenic, Mutation, Myocardium, Phosphorylation, Physical Conditioning, Animal, Physical Endurance, Protein Binding, Proto-Oncogene Proteins, Running, Glucose Intolerance, Muscle, Skeletal, Proto-Oncogene Proteins c-bcl-2, Leptin, Apoptosis Regulatory Proteins, Mice, Adiponectin, Gene Knock-In Techniques
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