Loss of beta-arrestin2 mediates pancreatic-islet dysfunction in mice
文献类型：期刊论文
| 作者 | Zhang, ML; Zhu, YX; Mu, KD; Li, L; Lu, JX; Zhao, J; Huang, XY; Wang, C; Jia, WP |
| 刊名 | BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS
 |
| 出版日期 | 2013 |
| 卷号 | 435期号:3页码:345-349 |
| 关键词 | beta-Arrestin2 Insulin secretion Hyperglycemic clamp Exocytosis |
| 通讯作者 | Wang, C (reprint author), Shanghai Jiao Tong Univ, Affiliated Peoples Hosp 6, Dept Endocrinol & Metab, 600 Yishan Rd, Shanghai 200233, Peoples R China.,wangchen@sjtu.edu.cn ; wpjia@sjtu.edu.cn |
| 英文摘要 | Insulin resistance and defective insulin secretion are two major factors contributing to the pathogenesis of type 2 diabetes. beta-Arrestin2 is known to interact with numerous signaling molecules. Our previous study demonstrated that beta-arrestin2 regulates insulin sensitivity in both skeletal muscle and liver, yet its role in insulin secretion remains elusive. In this study, we found that beta-arrestin2 was abundantly expressed in mouse pancreatic beta cells, while its expression was significantly decreased in obese and diabetic mouse models. Hyperglycemic clamp study showed that the acute and late phase of insulin secretion were impaired in beta-arrestin2 knockout mice. Ex vivo study showed that beta-arrestin2 deficient pancreatic islets exhibited blunted glucose-stimulated insulin secretion. Further analysis demonstrated the number of docked insulin granules in beta-arrestin2 deficient islets was markedly decreased compared to wild-type islets, while insulin content and beta cell mass remained unchanged. Our study establishes a new role for beta-arrestin2 in beta-cell functions, and suggests that the down regulation of beta-arrestin2 may contribute to impaired insulin secretion in type 2 diabetes. (C) 2013 Elsevier Inc. All rights reserved. |
| 学科主题 | Biochemistry & Molecular Biology; Biophysics |
| 类目[WOS] | Biochemistry & Molecular Biology ; Biophysics |
| 关键词[WOS] | STIMULATED INSULIN-SECRETION ; BETA-CELL DYSFUNCTION ; GENE-EXPRESSION ; IN-VITRO ; RECEPTOR ; GLUCOSE ; RESISTANCE ; MOUSE ; ARRESTINS ; RELEASE |
| 收录类别 | SCI |
| 语种 | 英语 |
| WOS记录号 | WOS:000320904900004 |
| 版本 | 出版稿 |
| 源URL | [http://202.127.25.143/handle/331003/355]  |
| 专题 | 上海生化细胞研究所_上海生科院生化细胞研究所 |
| 推荐引用方式 GB/T 7714 | Zhang, ML,Zhu, YX,Mu, KD,et al. Loss of beta-arrestin2 mediates pancreatic-islet dysfunction in mice[J]. BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS,2013,435(3):345-349. |
| APA | Zhang, ML.,Zhu, YX.,Mu, KD.,Li, L.,Lu, JX.,...&Jia, WP.(2013).Loss of beta-arrestin2 mediates pancreatic-islet dysfunction in mice.BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS,435(3),345-349. |
| MLA | Zhang, ML,et al."Loss of beta-arrestin2 mediates pancreatic-islet dysfunction in mice".BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS 435.3(2013):345-349. |
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