Objective:The aim of this study is to clarify ERS and the expression level of WFS1 in IUGR newborn rats,further exploring the molecular basis related to T2DM,which may provide a new therapy for preventing IUGR from leading to T2DM. Methods:The pregnant rats in the IUGR group were fed 50% calorie restriction from gestational day 14 until term. Immunohistochemistry,RT-PCR,transmission electron microscope and western blot were applied. Results:①The expressions of WFS1 and GRP78 in the pancreas and islets of IUGR rats were increased(P < 0.05,n=10). ② Electron microscope showed that the endoplasmic reticulums in the pancreas of newborn IUGR rats were swollen and fused. ③Glucose-regulated protein 78(GRP78/Bip)and CHOP were significantly elevated in the pancreas and islets of IUGR. Conclusion:This study demonstrated that WFS1 might play roles in maintaining islet structure and function in IUGR rats,maybe partly via UPR.
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DAI Chengting, YUAN Yi, LI Yihui, YUAN Qingxin. The effects of WFS1 on pancreatic islet β cell function in rats born with intrauterine growth retardation[J].,2020,(5):658-662.