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Biochemistry & Molecular Biology

The effects of glucose and fatty acids on CXCL10 expression in skeletal muscle cells

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Pages 2448-2457 | Received 09 Apr 2020, Accepted 14 Aug 2020, Published online: 02 Sep 2020

References

  • Pedersen BK. Edward F. Adolph Distinguished Lecture: muscle as an endocrine organ: IL-6 and other myokines. J Appl Physiol. 2009;107(4):1006–1014.
  • Schnyder S, Handschin C. Skeletal muscle as an endocrine organ: PGC-1α, myokines and exercise. Bone. 2015;80:115–125.
  • Fujita H, Nedachi T, Kanzaki M. Accelerated de novo sarcomere assembly by electric pulse stimulation in C2C12 myotubes. Exp Cell Res. 2007;313(9):1853–1865.
  • Nedachi T, Fujita H, Kanzaki M. Contractile C 2 C 12 myotube model for studying exercise-inducible responses in skeletal muscle. Am J Physiol Endocrinol Metab. 2008;295(5):E1191–E1204.
  • Ishiuchi Y, Sato H, Tsujimura K, et al. Skeletal muscle cell contraction reduces a novel myokine, chemokine (C-X-C motif) ligand 10 (CXCL10): potential roles in exercise-regulated angiogenesis. Biosci Biotech Biochem. 2018;82(1):97–105.
  • Sui Y, Potula R, Dhillon N, et al. Neuronal apoptosis is mediated by CXCL10 overexpression in simian human immunodeficiency virus encephalitis. Am J Pathol. 2004;164(5):1557–1566.
  • Loetscher M, Gerber B, Loetscher P, et al. Chemokine receptor specific for IP10 and mig: structure, function, and expression in activated T-lymphocytes. J Exp Med. 1996;184(3):963–969.
  • Sallusto F, Lenig D, Mackay CR, et al. Flexible programs of chemokine receptor expression on human polarized T helper 1 and 2 lymphocytes. J Exp Med. 1998;187(6):875–883.
  • Bodnar RJ, Yates CC, Wells A. IP-10 Blocks Vascular Endothelial Growth Factor-Induced Endothelial Cell Motility and Tube Formation via Inhibition of Calpain. Circ Res. 2006;98(5):617–625.
  • Luster AD, Greenberg SM, Leder LP. The IP-10 chemokine binds to a specific cell surface heparan sulfate site shared with platelet factor 4 and inhibits endothelial cell proliferation. J Exp Med. 1995;182(1):219–231.
  • Luster AD, Cardiff RD, MacLean JA, et al. Delayed wound healing and disorganized neovascularization in transgenic mice expressing the IP-10 chemokine. Proc Assoc Am Physicians. 1998;110(3):183–196.
  • Bodnar RJ, Yates CC, Rodgers ME, et al. IP-10 induces dissociation of newly formed blood vessels. J Cell Sci. 2009;122(12):2064–2077.
  • Waeckel L, Mallat Z, Potteaux S, et al. Impairment in postischemic neovascularization in mice lacking the CXC chemokine receptor 3. Circ Res. 2005;96(5):576–582.
  • Sui Y, Stehno-Bittel L, Li S, et al. CXCL10-induced cell death in neurons: role of calcium dysregulation. Eur J Neurosci. 2006;23(4):957–964.
  • Sato E, Fujimoto J, Tamaya T. Expression of interferon-gamma-inducible protein 10 related to angiogenesis in uterine endometrial cancers. Oncology. 2007;73(3–4):246–251.
  • Crescioli C, Sottili M, Bonini P, et al. Inflammatory response in human skeletal muscle cells: CXCL10 as a potential therapeutic target. Eur J Cell Biol. 2012;91(2):139–149.
  • Antonelli A, Ferrari SM, Corrado A, et al. Extra-ocular muscle cells from patients with Graves‘ ophthalmopathy secrete α (CXCL10) and β (CCL2) chemokines under the influence of cytokines that are modulated by PPARγ. Autoimmune Rev. 2014;13(11):1160–1166.
  • Xu HE, Lambert MH, Montana VG, et al. Molecular Recognition of Fatty Acids by Peroxisome Proliferator–Activated Receptors. Mol Cell. 1999;3(3):397–403.
  • Hueso L, Ortega R, Selles F, et al. Upregulation of angiostatic chemokines IP-10/CXCL10 and I-TAC/CXCL11 in human obesity and their implication for adipose tissue angiogenesis. Int J Obes (Lond). 2018;42(8):1406–1417.
  • Hohos NM, Cho KJ, Swindle DC, et al. High-fat diet exposure, regardless of induction of obesity, is associated with altered expression of genes critical to normal ovulatory function. Mol Cell Endocrinol. 2018;470:199–207.
  • Liu P, Lin H, Xu Y, et al. Frataxin-Mediated PINK1-Parkin-Dependent Mitophagy in Hepatic steatosis: the Protective Effects of Quercetin. Mol Nutr Food Res. 2018;62(16):e1800164.
  • Augusto V, Padovani CR, Campos GER. Skeletal muscle fiber types in C57BL6J mice. Braz J morphol Sci. 2004;21(2):89–94.
  • Ariga M, Yoneyama Y, Fukushima T, et al. Glucose deprivation attenuates sortilin levels in skeletal muscle cells. Endocr J. 2017;64(3):255–268.
  • Chen X, Xu S, Wei S, et al. Comparative Proteomic Study of Fatty Acid-treated Myoblasts Reveals Role of Cox-2 in Palmitate-induced Insulin Resistance. Sci Rep. 2016;6(1):21454.
  • Coll T, Palomer X, Blanco-Vaca F, et al. Cyclooxygenase 2 Inhibition Exacerbates Palmitate-Induced Inflammation and Insulin Resistance in Skeletal Muscle Cells. Endocrinology. 2010;151(2):537–548.
  • Nieto-Vazquez I, Fernàndez-Veledo S, de Alvaro C, et al. Dual role of interleukin-6 in regulating insulin sensitivity in murine skeletal muscle. Diabetes. 2008;57(12):3211–3221.
  • Boström P, Wu J, Jedrychowski MP, et al. A PGC1-α-dependent myokine that drives brown-fat-like development of white fat and thermogenesis. Nature. 2012;481(7382):463–468.
  • Peterson JM, Pizza FX. Cytokines derived from cultured skeletal muscle cells after mechanical strain promote neutrophil chemotaxis in vitro. J Appl Physiol (1985). 2009;106(1):130–137.
  • Glund S, Deshmukh A, Long YC, et al. Interleukin-6 directly increases glucose metabolism in resting human skeletal muscle. Diabetes. 2007;56(6):1630–1637.
  • Høier B, Olsen K, Nyberg M, et al. Contraction-induced secretion of VEGF from skeletal muscle cells is mediated by adenosine. Am J Physiol Heart Circ Physiol. 2010;299(3):857–862.
  • Kivelä R, Silvennoinen M, Touvra A-M, et al. Effects of experimental type 1 diabetes and exercise training on angiogenic gene expression and capillarization in skeletal muscle. Faseb J. 2006;20(9):1570–1572.
  • Kondo H, Fujino H, Murakami S, et al. Low-intensity running exercise enhances the capillary volume and pro-angiogenic factors in the soleus muscle of type 2 diabetic rats. Muscle Nerve. 2015;51(3):391–399.
  • Basic VT, Jacobsen A, Sirsjö A, et al. TNF stimulation induces VHL overexpression and impairs angiogenic potential in skeletal muscle myocytes. Int J Mol Med. 2014;34(1):228–236.
  • Kikuchi R, Nakamura K, MacLauchlan S, et al. An antiangiogenic isoform of VEGF-A contributes to impaired vascularization in peripheral artery disease. Nat Med. 2014;20(12):1464–1471.
  • Kishlyansky M, Vojnovic J, Roudier E, et al. Striated muscle angio-adaptation requires changes in Vasohibin-1 expression pattern. Biochem Biophys Res Commun. 2010;399(3):359–364.
  • Jobin J, Maltais F, Doyon J-F, et al. Chronic obstructive pulmonary disease: capillarity and fiber-type characteristics of skeletal muscle. J Cardiopulm Rehabil. 1998;18(6):432–437.
  • Yoshimatsu G, Kunnathodi F, Saravanan PB, et al. Pancreatic β-Cell–Derived IP-10/CXCL10 Isletokine Mediates Early Loss of Graft Function in Islet Cell Transplantation. Diabetes. 2017;66(11):2857–2867.
  • You N, Li J, Huang X, et al. COMMD7 activates CXCL10 production by regulating NF-κB and the production of reactive oxygen species.. Mol Med Rep. 2018;17(5):6784–6788.
  • Hancock CR, Han D-H, Chen M, et al. High-fat diets cause insulin resistance despite an increase in muscle mitochondria. Proc Natl Acad Sci USA. 2008;105(22):7815–7820.
  • Anderson EJ, Lustig ME, Boyle KE, Anderson EJ, Lusting ME, Boyle KE, et al. Mitochondrial H2O2 emission and cellular redox state link excess fat intake to insulin resistance in both rodents and humans. J Clin Invest. 2009;119(3):573–581.
  • Pinho RA, Sepa-Kishi DM, Bikopoulos G, et al. High-fat diet induces skeletal muscle oxidative stress in a fiber type-dependent manner in rats. Free Radic Biol Med. 2017;110:381–389.
  • Bjursell M, Gerdin A-K, Lelliott CJ, et al. Acutely reduced locomotor activity is a major contributor to Western diet-induced obesity in mice. Am J Physiol Endocrinol Metab. 2008;294(2):E251‐E260.
  • Shimada A, Morimoto J, Kodama K, et al. Elevated Serum IP-10 Levels Observed in Type 1 Diabetes. Diabetes Care. 2001;24(3):510–515.
  • Suzuki R, Shimada A, Maruyama, et al. T-cell function in anti-GAD65+diabetes with residual β-cell function. J Autoimmun. 2003;20(1):83–90.
  • Satrom KM, Ennis K, Sweis BM, et al. Neonatal hyperglycemia induces CXCL10/CXCR3 signaling and microglial activation and impairs long-term synaptogenesis in the hippocampus and alters behavior in rats. J Neuroinflammation. 2018;15(1):82.
  • Devaraj S, Jialal I. Increased secretion of IP-10 from monocytes under hyperglycemia is via the TLR2 and TLR4 pathway. Cytokine. 2009;47(1):6–10.
  • Rachek LI. Free fatty acids and skeletal muscle insulin resistance. Prog Mol Biol Transl Sci. 2014;121:267–292.
  • Dupont J, Dedeyne L, Dalle S, et al. The role of omega-3 in the prevention and treatment of sarcopenia. Aging Clin Exp Res. 2019;31(6):825–836.
  • Lipina C, Hundal HS. Lipid modulation of skeletal muscle mass and function. J Cachexia Sarcopenia Muscle. 2017;8(2):190–201.
  • Corcoran MP, Lamon-Fava S, Fielding RA. Skeletal muscle lipid deposition and insulin resistance: effect of dietary fatty acids and exercise.. Am J Clin Nutr. 2007;85(3):662–677.
  • Woodworth-Hobbs ME, Hudson MB, Rahnert JA, et al. Docosahexaenoic acid prevents palmitate-induced activation of proteolytic systems in C2C12 myotubes. J Nutr Biochem. 2014;25(8):868–874.
  • Perry BD, Rahnert JA, Xie Y, et al. Palmitate-induced ER stress and inhibition of protein synthesis in cultured myotubes does not require Toll-like receptor 4. PLoS One. 2018;13(1):e0191313.
  • Taheripak G, Bakhtiyari S, Rajabibazl M, et al. Protein tyrosine phosphatase 1B inhibition ameliorates palmitate-induced mitochondrial dysfunction and apoptosis in skeletal muscle cells. Free Radic Biol Med. 2013;65:1435–1446.
  • Kalinkovich A, Livshits G. Sarcopenic obesity or obese sarcopenia: A cross talk between age-associated adipose tissue and skeletal muscle inflammation as a main mechanism of the pathogenesis. Ageing Res Rev. 2017;35:200–221.
  • Gomes JL, Fernandes T, Soci UP, et al. Obesity Downregulates MicroRNA-126 Inducing Capillary Rarefaction in Skeletal Muscle: effects of Aerobic Exercise Training. Oxid Med Cell Longev. 2017;2415246. (Article ID).
  • Nwadozi E, Roudier E, Rullman E, et al. Endothelial FoxO proteins impair insulin sensitivity and restrain muscle angiogenesis in response to a high-fat diet. Faseb J. 2016;30(9):3039–3052.
  • Yang J, Richmond A. The Angiostatic Activity of Interferon-Inducible Protein-10/CXCL10 In Human Melanoma Depends on Binding to CXCR3 but Not to Glycosaminoglycan. Mol Ther. 2004;9(6):846–855.

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