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PAQR9 regulates glucose homeostasis in diabetic mice and modulates insulin secretion in beta cells in vitro under stress conditions.
論文作者 Li, Zixuan; Lin, Yijun; Zhuo, Shixuan; Chen, Jinzhu; Chen, Lingling; Wang, Shuying; Chen, Yan
期刊/會議名稱 Molecular and cellular endocrinology
論文年度 2023
論文類別 Journal Article; Research Support, Non-U.S. Gov't
摘要 Copyright ? 2023 Elsevier B.V. All rights reserved.Progesterone and adipoQ receptor 9 (PAQR9) is an endoplasmic reticulum (ER)-localized membrane protein that is involved in protein quality control of ER by interacting with BAG6. One of the physiological functions of PAQR9 is regulation of fasting-induced ketogenesis and fatty acid oxidation in the liver via modulating protein degradation of PPARalpha. However, it is currently unknown whether or not PAQR9 impacts glucose homeostasis. We addressed this question using a Paqr9-deleted mouse model in which type 1 diabetes was induced by streptozotocin injection and type 2 diabetes was induced by high-fat diet (HFD) with streptozotocin injection. Paqr9 deletion improved hyperglycemia and glucose tolerance in both of the diabetic mouse models. In the pancreatic islets, Paqr9 deletion reduced apoptosis of beta cells in type 2 diabetic mice. Paqr9 deletion also reduced HFD-induced hepatic steatosis and adiposity of white adipose tissue. In Min6 cells, overexpression of DUF3538 domain of BAG6 to block the interaction of PAQR9 with BAG6 was able to enhance glucose-stimulated insulin secretion upon treatment with inflammatory factors or thapsigargin, an ER stress inducer. Thapsigargin-induced ER stress markers were also reduced by overexpression of DUF3538 domain. Collectively, these results indicate that PAQR9 has a modulatory role in glucose homeostasis, associated with regulation on insulin secretion of beta cells in vitro under stress conditions.
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