Effects of genistein on insulin pathway-related genes in mouse differentiated myoblast C2C12 cell line: evidence for two independent modes of action
Abstract
Introduction. Genistein (plant isoflavone) is a well-known anti-cancer drug with estrogenic-like properties. Genistein also regulates sugar and lipid metabolism; thus, it has anti-diabetic properties. The aim of the study was to evaluate in vitro effects of genistein on glucose transport, fatty acids oxidation, activation of PKB, and expression of genes related to insulin pathway in differentiated myoblast C2C12 mouse cell line.
Material and methods. Differentiated myoblast C2C12 mouse cell line was used to assess the effects of different genistein concentrations on glucose transport and fatty acids oxidation measured by radioactivity technique, activation of PKB, and expression of selected genes related to insulin signaling pathway (IR-a, IR-b, IRS-1, PKB, GLUT-4, PP2A, SH-PTP2) at the mRNA and protein levels. Cells were incubated with various concentrations of genistein under standard conditions for 0–48 hours.
Results. Genistein in low concentrations (0.1–1 μM) significantly increased glucose transport and decreased fatty acids oxidation in C2C12 cells after 48 h of incubation. High concentration of genistein (50 μM) had the opposite effect. Genistein stimulated PKB phosphorylation during the first 5–10 minutes of incubation. There was no significant impact on the protein expression of selected genes (IR-a, IR-b, IRS-1, PKB, GLUT-4, PP2A-Ca, ER-a and ER-b) after 48 h treatment. We observed inverse correlation between genistein concentration and the expression of SH-PTP2 protein. Genistein affected the expression pattern of mRNAs for genes related to the insulin pathway, however, not the expression of the encoded proteins.
Conclusions. The results of this study showed that depending on the concentration and time of incubation genistein significantly affects glucose and lipid metabolism and at low concentration modifies expression pattern
of a few genes in C2C12 cells.
Keywords: genisteinC2C12 cell lineglucose transportinsulin pathway proteinsfatty acids oxidation
References
- Wang M, Gao XJ, Zhao WW, et al. Opposite effects of genistein on the regulation of insulin-mediated glucose homeostasis in adipose tissue. Br J Pharmacol. 2013; 170(2): 328–340.
- He FJ, Chen JQ. Consumption of soybean, soy foods, soy isoflavones and breast cancer incidence: Differences between Chinese women and women in Western countries and possible mechanisms. Food Science and Human Wellness. 2013; 2(3-4): 146–161.
- Talaei M, Pan An. Role of phytoestrogens in prevention and management of type 2 diabetes. World J Diabetes. 2015; 6(2): 271–283.
- Fu Z, Gilbert ER, Liu D. Regulation of insulin synthesis and secretion and pancreatic Beta-cell dysfunction in diabetes. Curr Diabetes Rev. 2013; 9(1): 25–53.
- Miller BR, Nguyen H, Hu CJH, et al. New and emerging drugs and targets for type 2 diabetes: reviewing the evidence. Am Health Drug Benefits. 2014; 7(8): 452–463.
- Behloul N, Wu G. Genistein: a promising therapeutic agent for obesity and diabetes treatment. Eur J Pharmacol. 2013; 698(1-3): 31–38.
- Gilbert ER, Liu D. Anti-diabetic functions of soy isoflavone genistein: mechanisms underlying its effects on pancreatic β-cell function. Food Funct. 2013; 4(2): 200–212.
- Fu Z, Zhang W, Zhen W, et al. Genistein induces pancreatic beta-cell proliferation through activation of multiple signaling pathways and prevents insulin-deficient diabetes in mice. Endocrinology. 2010; 151(7): 3026–3037.
- Fu Z, Liu D. Long-term exposure to genistein improves insulin secretory function of pancreatic beta-cells. Eur J Pharmacol. 2009; 616(1-3): 321–327.
- You F, Li Q, Jin G, et al. Genistein protects against Aβ induced apoptosis of PC12 cells through JNK signaling and modulation of Bcl-2 family messengers. BMC Neurosci. 2017; 18(1): 12.
- Lee SJ, Kim HE, Choi SE, et al. Involvement of Ca2+/calmodulin kinase II (CaMK II) in genistein-induced potentiation of leucine/glutamine-stimulated insulin secretion. Mol Cells. 2009; 28(3): 167–174.
- Liu D, Zhen W, Yang Z, et al. Genistein acutely stimulates insulin secretion in pancreatic beta-cells through a cAMP-dependent protein kinase pathway. Diabetes. 2006; 55(4): 1043–1050.
- Uifălean A, Schneider S, Ionescu C, et al. Soy Isoflavones and Breast Cancer Cell Lines: Molecular Mechanisms and Future Perspectives. Molecules. 2015; 21(1): E13.
- Murata M, Midorikawa K, Koh M, et al. Genistein and daidzein induce cell proliferation and their metabolites cause oxidative DNA damage in relation to isoflavone-induced cancer of estrogen-sensitive organs. Biochemistry. 2004; 43(9): 2569–2577.
- Moore AB, Castro L, Yu L, et al. Stimulatory and inhibitory effects of genistein on human uterine leiomyoma cell proliferation are influenced by the concentration. Hum Reprod. 2007; 22(10): 2623–2631.
- Choi EJ, Jung JY, Kim GH. Genistein inhibits the proliferation and differentiation of MCF-7 and 3T3-L1 cells via the regulation of ERα expression and induction of apoptosis. Exp Ther Med. 2014; 8(2): 454–458.
- Yu JY, Lee JJ, Lim Y, et al. Genistein inhibits rat aortic smooth muscle cell proliferation through the induction of p27kip1. J Pharmacol Sci. 2008; 107(1): 90–98.
- Kayisli UA, Guzeloglu-Kayisli O, Guzel E, et al. Genistein inhibits cell proliferation and stimulates apoptosis in human coronary artery endothelial cells. Gynecol Obstet Invest. 2013; 75(4): 235–242.
- Wang X, Clubbs EA, Bomser JA. Genistein modulates prostate epithelial cell proliferation via estrogen- and extracellular signal-regulated kinase-dependent pathways. J Nutr Biochem. 2006; 17(3): 204–210.
- Shafiee G, Saidijam M, Tavilani H, et al. Genistein Induces Apoptosis and Inhibits Proliferation of HT29 Colon Cancer Cells. Int J Mol Cell Med. 2016; 5(3): 178–191.
- LOWRY OH, ROSEBROUGH NJ, FARR AL, et al. Protein measurement with the Folin phenol reagent. J Biol Chem. 1951; 193(1): 265–275.
- Manning NJ, Olpin SE, Pollitt RJ, et al. A comparison of [9,10-3H]palmitic and [9,10-3H]myristic acids for the detection of defects of fatty acid oxidation in intact cultured fibroblasts. Journal of Inherited Metabolic Disease. 1990; 13(1): 58–68.
- Gil-Izquierdo A, Penalvo JL, Gil JI, et al. Soy isoflavones and cardiovascular disease epidemiological, clinical and -omics perspectives. Curr Pharm Biotechnol. 2012; 13(5): 624–631.
- Ramdath DD, Padhi EMT, Sarfaraz S, et al. Beyond the Cholesterol-Lowering Effect of Soy Protein: A Review of the Effects of Dietary Soy and Its Constituents on Risk Factors for Cardiovascular Disease. Nutrients. 2017; 9(4).
- Cederroth CR, Vinciguerra M, Gjinovci A, et al. Dietary phytoestrogens activate AMP-activated protein kinase with improvement in lipid and glucose metabolism. Diabetes. 2008; 57(5): 1176–1185.
- Tanigawa T, Shibata R, Kondo K, et al. Soybean β-Conglycinin Prevents Age-Related Hearing Impairment. PLOS ONE. 2015; 10(9): e0137493.
- Ng WWH, Keung W, Xu YC, et al. Genistein potentiates protein kinase A activity in porcine coronary artery. Mol Cell Biochem. 2008; 311(1-2): 37–44.
- Lewicki S, Lewicka A, Kalicki B, et al. Chromium III ions imitate the estradiol influence on expression of insulin pathway related genes and proteins in mouse myocytes cell line C2C12. Trace Elements and Electrolytes. 2016; 33(01): 28–34.
- Jou SB, Huang CC, Liu IM, et al. Activation of alpha1A-adrenoceptors by genistein at concentrations lower than that to inhibit tyrosine kinase in cultured C2C12 cells. Planta Med. 2004; 70(7): 610–614.
- Nomura M, Takahashi T, Nagata N, et al. Inhibitory Mechanisms of Flavonoids on Insulin-Stimulated Glucose Uptake in MC3T3-G2/PA6 Adipose Cells. Biological & Pharmaceutical Bulletin. 2008; 31(7): 1403–1409.
- Bazuine M, van den Broek PJA, Maassen JA. Genistein directly inhibits GLUT4-mediated glucose uptake in 3T3-L1 adipocytes. Biochem Biophys Res Commun. 2005; 326(2): 511–514.
- Smith RM, Tiesinga JJ, Shah N, et al. Genistein inhibits insulin-stimulated glucose transport and decreases immunocytochemical labeling of GLUT4 carboxyl-terminus without affecting translocation of GLUT4 in isolated rat adipocytes: additional evidence of GLUT4 activation by insulin. Arch Biochem Biophys. 1993; 300(1): 238–246.
- Germain M, Pezzolesi MG, Sandholm N, et al. SORBS1 gene, a new candidate for diabetic nephropathy: results from a multi-stage genome-wide association study in patients with type 1 diabetes. Diabetologia. 2015; 58(3): 543–548.
- Rui L. Energy metabolism in the liver. Compr Physiol. 2014; 4(1): 177–197.
- Lee DS, Lee SH. Genistein, a soy isoflavone, is a potent alpha-glucosidase inhibitor. FEBS Lett. 2001; 501(1): 84–86.
- Chen WF, Wong MS. Genistein enhances insulin-like growth factor signaling pathway in human breast cancer (MCF-7) cells. J Clin Endocrinol Metab. 2004; 89(5): 2351–2359.
- Ponnusamy S, Tran QT, Harvey I, et al. Pharmacologic activation of estrogen receptor β increases mitochondrial function, energy expenditure, and brown adipose tissue. FASEB J. 2017; 31(1): 266–281.
- Hamilton D, Minze L, Kumar T, et al. Estrogen receptor alpha activation enhances mitochondrial function and systemic metabolism in high-fat-fed ovariectomized mice. Physiological Reports. 2016; 4(17): e12913.