Swimming Differentially Affects T2DM-Induced Skeletal Muscle ER Stress and Mitochondrial Dysfunction Related to MAM

References

• Rieusset J. Mitochondria and endoplasmic reticulum: mitochondria-endoplasmic reticulum interplay in type 2 diabetes pathophysiology. Int J Biochem Cell Biol. 2011;43(9):1257–1262. doi:10.1016/j.biocel.2011.05.006
   PubMedGoogle Scholar
• Gispen WH, Biessels GJ. Cognition and synaptic plasticity in diabetes mellitus. Trends Neurosci. 2000;23(11):542–549. doi:10.1016/S0166-2236(00)01656-8
   PubMed Web of Science ®Google Scholar
• Karlsson HK, Zierath JR. Insulin signaling and glucose transport in insulin resistant human skeletal muscle. Cell Biochem Biophys. 2007;48(2–3):103–113. doi:10.1007/s12013-007-0030-9
   PubMed Web of Science ®Google Scholar
• Patti ME, Butte AJ, Crunkhorn S, et al. Coordinated reduction of genes of oxidative metabolism in humans with insulin resistance and diabetes: potential role of PGC1 and NRF1. Proc Natl Acad Sci U S A. 2003;100(14):8466–8471. doi:10.1073/pnas.1032913100
   PubMed Web of Science ®Google Scholar
• Greco AV, Tataranni PA, Mingrone G, et al. Daily energy metabolism in patients with type 1 diabetes mellitus. J Am Coll Nutr. 1995;14(3):286–291. doi:10.1080/07315724.1995.10718509
   PubMed Web of Science ®Google Scholar
• Brandenburg SL, Reusch JE, Bauer TA, et al. Effects of exercise training on oxygen uptake kinetic responses in women with type 2 diabetes. Diabetes Care. 1999;22(10):1640–1646. doi:10.2337/diacare.22.10.1640
   PubMedGoogle Scholar
• Davidsen PK, Gallagher IJ, Hartman JW, et al. High responders to resistance exercise training demonstrate differential regulation of skeletal muscle microRNA expression. J Appl Physiol (1985). 2011;110(2):309–317. doi:10.1152/japplphysiol.00901.2010
   PubMedGoogle Scholar
• Nishikawa T, Kukidome D, Sonoda K, et al. Impact of mitochondrial ROS production in the pathogenesis of insulin resistance. Diabetes Res Clin Pract. 2007;77(Suppl 1):S161–S164. doi:10.1016/j.diabres.2007.01.071
   PubMedGoogle Scholar
• Nishikawa T, Edelstein D, Du XL, et al. Normalizing mitochondrial superoxide production blocks three pathways of hyperglycaemic damage. Nature. 2000;404(6779):787–790. doi:10.1038/35008121
   PubMed Web of Science ®Google Scholar
• Baur JA, Pearson KJ, Price NL, et al. Resveratrol improves health and survival of mice on a high-calorie diet. Nature. 2006;444(7117):337–342. doi:10.1038/nature05354
   PubMed Web of Science ®Google Scholar
• Deldicque L. Endoplasmic reticulum stress in human skeletal muscle: any contribution to sarcopenia? Front Physiol. 2013;4:236. doi:10.3389/fphys.2013.00236
   PubMedGoogle Scholar
• Giorgi C, De Stefani D, Bononi A, et al. Structural and functional link between the mitochondrial network and the endoplasmic reticulum. Int J Biochem Cell Biol. 2009;41(10):1817–1827. doi:10.1016/j.biocel.2009.04.010
   PubMedGoogle Scholar
• Lowell BB, Shulman GI. Mitochondrial dysfunction and type 2 diabetes. Science. 2005;307(5708):384–387. doi:10.1126/science.1104343
   PubMed Web of Science ®Google Scholar
• Bonnard C, Durand A, Peyrol S, et al. Mitochondrial dysfunction results from oxidative stress in the skeletal muscle of diet-induced insulin-resistant mice. J Clin Invest. 2008;118(2):789–800. doi:10.1172/JCI32601
   PubMed Web of Science ®Google Scholar
• Kekuda R, Prasad PD, Fei YJ, et al. Cloning and functional expression of the human type 1 sigma receptor (hSigmaR1). Biochem Biophys Res Commun. 1996;229(2):553–558. doi:10.1006/bbrc.1996.1842
   PubMed Web of Science ®Google Scholar
• Hanner M, Moebius FF, Flandorfer A, et al. Purification, molecular cloning, and expression of the mammalian sigma1-binding site. Proc Natl Acad Sci U S A. 1996;93(15):8072–8077. doi:10.1073/pnas.93.15.8072
   PubMed Web of Science ®Google Scholar
• Su TP, Hayashi T, Maurice T, et al. The sigma-1 receptor chaperone as an inter-organelle signaling modulator. Trends Pharmacol Sci. 2010;31(12):557–566. doi:10.1016/j.tips.2010.08.007
   PubMed Web of Science ®Google Scholar
• Kourrich S, Su TP, Fujimoto M, et al. The sigma-1 receptor: roles in neuronal plasticity and disease[J]. Trends Neurosci. 2012;35(12):762–771. doi:10.1016/j.tins.2012.09.007
   PubMed Web of Science ®Google Scholar
• Harding HP, Ron D. Endoplasmic reticulum stress and the development of diabetes: a review. Diabetes. 2002;51(Suppl 3):S455–S461. doi:10.2337/diabetes.51.2007.S455
   PubMedGoogle Scholar
• Deldicque L, Cani PD, Philp A, et al. The unfolded protein response is activated in skeletal muscle by high-fat feeding: potential role in the downregulation of protein synthesis. Am J Physiol Endocrinol Metab. 2010;299(5):E695–E705. doi:10.1152/ajpendo.00038.2010
   PubMedGoogle Scholar
• Verfaillie T, Salazar M, Velasco G, et al. Linking ER stress to autophagy: potential implications for cancer therapy. Int J Cell Biol. 2010;2010:930509. doi:10.1155/2010/930509
   PubMedGoogle Scholar
• Gething MJ. Role and regulation of the ER chaperone BiP. Semin Cell Dev Biol. 1999;10(5):465–472. doi:10.1006/scdb.1999.0318
   PubMedGoogle Scholar
• Ron D, Walter P. Signal integration in the endoplasmic reticulum unfolded protein response. Nat Rev Mol Cell Biol. 2007;8(7):519–529. doi:10.1038/nrm2199
   PubMed Web of Science ®Google Scholar
• Araki E, Oyadomari S, Mori M. Endoplasmic reticulum stress and diabetes mellitus. Intern Med. 2003;42(1):7–14. doi:10.2169/internalmedicine.42.7
   PubMed Web of Science ®Google Scholar
• Rao RV, Peel A, Logvinova A, et al. Coupling endoplasmic reticulum stress to the cell death program: role of the ER chaperone GRP78. FEBS Lett. 2002;514(2–3):122–128. doi:10.1016/S0014-5793(02)02289-5
   PubMed Web of Science ®Google Scholar
• Joseph AM, Pilegaard H, Litvintsev A, et al. Control of gene expression and mitochondrial biogenesis in the muscular adaptation to endurance exercise. Essays Biochem. 2006;42:13–29. doi:10.1042/bse0420013
   PubMed Web of Science ®Google Scholar
• Coffey VG, Hawley JA. The molecular bases of training adaptation. Sports Med. 2007;37(9):737–763. doi:10.2165/00007256-200737090-00001
   PubMed Web of Science ®Google Scholar
• Deldicque L, Cani PD, Delzenne NM, et al. Endurance training in mice increases the unfolded protein response induced by a high-fat diet. J Physiol Biochem. 2013;69(2):215–225. doi:10.1007/s13105-012-0204-9
   PubMedGoogle Scholar
• Lara-Riegos JC, Ortiz-Lopez MG, Pena-Espinoza BI, et al. Diabetes susceptibility in Mayas: evidence for the involvement of polymorphisms in HHEX, HNF4alpha, KCNJ11, PPARgamma, CDKN2A/2B, SLC30A8, CDC123/CAMK1D, TCF7L2, ABCA1 and SLC16A11 genes. Gene. 2015;565(1):68–75. doi:10.1016/j.gene.2015.03.065
   PubMedGoogle Scholar
• Sun Y, Cui D, Zhang Z, et al. Attenuated oxidative stress following acute exhaustive swimming exercise was accompanied with modified gene expression profiles of apoptosis in the skeletal muscle of mice. Oxid Med Cell Longev. 2016;2016:8381242. doi:10.1155/2016/8381242
   PubMedGoogle Scholar
• Rasmussen HN, Andersen AJ, Rasmussen UF. Optimization of preparation of mitochondria from 25–100 mg skeletal muscle. Anal Biochem. 1997;252(1):153–159. doi:10.1006/abio.1997.2304
   PubMedGoogle Scholar
• Sun Y, Qi Z, He Q, et al. The effect of treadmill training and N-acetyl-l-cysteine intervention on biogenesis of cytochrome c oxidase (COX). Free Radic Biol Med. 2015;87:326–335. doi:10.1016/j.freeradbiomed.2015.06.035
   PubMed Web of Science ®Google Scholar
• Romanello V, Scalabrin M, Albiero M, et al. Inhibition of the fission machinery mitigates OPA1 Impairment in adult skeletal muscles. Cells. 2019;8(6):597. doi:10.3390/cells8060597
   PubMedGoogle Scholar
• Silva RE, Motori E, Bruser C, et al. Mitochondrial fusion is required for regulation of mitochondrial DNA replication. PLoS Genet. 2019;15(6):e1008085. doi:10.1371/journal.pgen.1008085
   PubMedGoogle Scholar
• Martinez J, Tarallo D, Martinez-Palma L, et al. Mitofusins modulate the increase in mitochondrial length, bioenergetics and secretory phenotype in therapy-induced senescent melanoma cells. Biochem J. 2019;476(17):2463–2486. doi:10.1042/BCJ20190405
   PubMedGoogle Scholar
• Dhananjaya D, Hung KY, Tarn WY. RBM4 modulates radial migration via alternative splicing of Dab1 during cortex development. Mol Cell Biol. 2018;38(12):e00007–18.
   PubMedGoogle Scholar
• Karbowski M, Norris KL, Cleland MM, et al. Role of Bax and Bak in mitochondrial morphogenesis. Nature. 2006;443(7112):658–662. doi:10.1038/nature05111
   PubMed Web of Science ®Google Scholar
• Zhang Z, Sliter DA, Bleck C, et al. Fis1 deficiencies differentially affect mitochondrial quality in skeletal muscle. Mitochondrion. 2019;49:217–226. doi:10.1016/j.mito.2019.09.005
   PubMedGoogle Scholar
• Sun Y, Cui D, Zhang Z, et al. Voluntary wheel exercise alters the levels of miR-494 and miR-696 in the skeletal muscle of C57BL/6 mice. Comp Biochem Physiol B Biochem Mol Biol. 2016;202:16–22. doi:10.1016/j.cbpb.2016.07.002
   PubMedGoogle Scholar
• Fujimaki S, Kuwabara T. Diabetes-induced dysfunction of mitochondria and stem cells in skeletal muscle and the nervous system. Int J Mol Sci. 2017;18(10):2147.
   PubMedGoogle Scholar
• Ju JS, Jeon SI, Park JY, et al. Autophagy plays a role in skeletal muscle mitochondrial biogenesis in an endurance exercise-trained condition. J Physiol Sci. 2016;66(5):417–430. doi:10.1007/s12576-016-0440-9
   PubMedGoogle Scholar
• Sliter DA, Martinez J, Hao L, et al. Parkin and PINK1 mitigate STING-induced inflammation. Nature. 2018;561(7722):258–262. doi:10.1038/s41586-018-0448-9
   PubMed Web of Science ®Google Scholar
• Ding H, Jiang N, Liu H, et al. Response of mitochondrial fusion and fission protein gene expression to exercise in rat skeletal muscle. Biochim Biophys Acta. 2010;1800(3):250–256. doi:10.1016/j.bbagen.2009.08.007
   PubMedGoogle Scholar
• Youle RJ, van der Bliek AM. Mitochondrial fission, fusion, and stress. Science. 2012;337(6098):1062–1065. doi:10.1126/science.1219855
   PubMed Web of Science ®Google Scholar
• Twig G, Elorza A, Molina AJ, et al. Fission and selective fusion govern mitochondrial segregation and elimination by autophagy. EMBO J. 2008;27(2):433–446. doi:10.1038/sj.emboj.7601963
   PubMed Web of Science ®Google Scholar
• Zhang T, Qi Z, Wang H, et al. Adeno-associated virus-mediated knockdown of SLC16A11 improves glucose tolerance and hepatic insulin signaling in high fat diet-fed mice. Exp Clin Endocrinol Diabetes. 2019
   Google Scholar
• Liu R, Jin P, Yu L, et al. Impaired mitochondrial dynamics and bioenergetics in diabetic skeletal muscle. PLoS One. 2014;9(3):e92810. doi:10.1371/journal.pone.0092810
   PubMed Web of Science ®Google Scholar
• Yamano K, Fogel AI, Wang C, et al. Mitochondrial Rab GAPs govern autophagosome biogenesis during mitophagy. Elife. 2014;3:e1612. doi:10.7554/eLife.01612
   PubMed Web of Science ®Google Scholar
• Shen Q, Yamano K, Head BP, et al. Mutations in Fis1 disrupt orderly disposal of defective mitochondria. Mol Biol Cell. 2014;25(1):145–159. doi:10.1091/mbc.e13-09-0525
   PubMed Web of Science ®Google Scholar
• Joseph AM, Joanisse DR, Baillot RG, et al. Mitochondrial dysregulation in the pathogenesis of diabetes: potential for mitochondrial biogenesis-mediated interventions. Exp Diabetes Res. 2012;2012:642038. doi:10.1155/2012/642038
   PubMedGoogle Scholar
• Chen H, Chomyn A, Chan DC. Disruption of fusion results in mitochondrial heterogeneity and dysfunction. J Biol Chem. 2005;280(28):26185–26192. doi:10.1074/jbc.M503062200
   PubMed Web of Science ®Google Scholar
• Tubbs E, Chanon S, Robert M, et al. Disruption of mitochondria-associated endoplasmic reticulum membrane (MAM) integrity contributes to muscle insulin resistance in mice and humans. Diabetes. 2018;67(4):636–650. doi:10.2337/db17-0316
   PubMedGoogle Scholar
• Sasi U, Sindhu G, Raj PS, et al. Mitochondria associated membranes (MAMs): emerging drug targets for diabetes. Curr Med Chem. 2019
   Google Scholar
• Ogborn DI, Mckay BR, Crane JD, et al. The unfolded protein response is triggered following a single, unaccustomed resistance-exercise bout. Am J Physiol Regul Integr Comp Physiol. 2014;307(6):R664–R669. doi:10.1152/ajpregu.00511.2013
   PubMedGoogle Scholar
• Cnop M, Foufelle F, Velloso LA. Endoplasmic reticulum stress, obesity and diabetes. Trends Mol Med. 2012;18(1):59–68. doi:10.1016/j.molmed.2011.07.010
   PubMed Web of Science ®Google Scholar
• Tabas I, Ron D. Integrating the mechanisms of apoptosis induced by endoplasmic reticulum stress. Nat Cell Biol. 2011;13(3):184–190. doi:10.1038/ncb0311-184
   PubMed Web of Science ®Google Scholar