V1bR enhances glucose-stimulated insulin secretion by paracrine production of glucagon which activates GLP-1 receptor
文献类型:期刊论文
作者 | Yun, Ying1,2,3; Guo, Shimeng2; Xie, Xin1,2,3![]() |
刊名 | CELL AND BIOSCIENCE
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出版日期 | 2024-08-31 |
卷号 | 14期号:1页码:11 |
关键词 | Arginine vasopressin Insulin Glucagon V1bR GLP-1R Islets Diabetes |
DOI | 10.1186/s13578-024-01288-4 |
通讯作者 | Xie, Xin(xxie@simm.ac.cn) |
英文摘要 | BackgroundArginine vasopressin (AVP) has been reported to regulate insulin secretion and glucose homeostasis in the body. Previous study has shown that AVP and its receptor V1bR modulate insulin secretion via the hypothalamic-pituitary-adrenal axis. AVP has also been shown to enhance insulin secretion in islets, but the exact mechanism remains unclear.ResultsIn our study, we unexpectedly discovered that AVP could only stimulates insulin secretion from islets, but not beta cells, and AVP-induced insulin secretion could be blocked by V1bR selective antagonist. Single-cell transcriptome analysis identified that V1bR is only expressed by the alpha cells. Further studies indicated that activation of the V1bR stimulates the alpha cells to secrete glucagon, which then promotes glucose-dependent insulin secretion from beta cells in a paracrine way by activating GLP-1R but not GCGR on these cells.ConclusionsOur study revealed a crosstalk between alpha and beta cells initiated by AVP/V1bR and mediated by glucagon/GLP-1R, providing a mechanism to develop new glucose-controlling therapies targeting V1bR. |
WOS关键词 | VASOPRESSIN RECEPTOR ; ARGININE-VASOPRESSIN ; BETA ; RELEASE ; CELLS ; ANTAGONIST ; PHYSIOLOGY ; OXYTOCIN ; STRESS ; ISLETS |
资助项目 | National Natural Science Foundation of China[82121005] ; National Natural Science Foundation of China[82304579] ; National Natural Science Foundation of China[82330113] ; Taishan Scholars Program |
WOS研究方向 | Biochemistry & Molecular Biology |
语种 | 英语 |
WOS记录号 | WOS:001302496500001 |
出版者 | BMC |
源URL | [http://119.78.100.183/handle/2S10ELR8/313077] ![]() |
专题 | 新药研究国家重点实验室 |
通讯作者 | Xie, Xin |
作者单位 | 1.Univ Chinese Acad Sci, Hangzhou Inst Adv Study, Sch Pharmaceut Sci & Technol, Hangzhou 310024, Peoples R China 2.Chinese Acad Sci, Shanghai Inst Mat Med, Natl Ctr Drug Screening, State Key Lab Drug Res, 189 Guo Shou Jing Rd, Shanghai 201203, Peoples R China 3.Bohai Rim Adv Res Inst Drug Discovery, Shandong Lab Yantai Drug Discovery, Yantai, Peoples R China |
推荐引用方式 GB/T 7714 | Yun, Ying,Guo, Shimeng,Xie, Xin. V1bR enhances glucose-stimulated insulin secretion by paracrine production of glucagon which activates GLP-1 receptor[J]. CELL AND BIOSCIENCE,2024,14(1):11. |
APA | Yun, Ying,Guo, Shimeng,&Xie, Xin.(2024).V1bR enhances glucose-stimulated insulin secretion by paracrine production of glucagon which activates GLP-1 receptor.CELL AND BIOSCIENCE,14(1),11. |
MLA | Yun, Ying,et al."V1bR enhances glucose-stimulated insulin secretion by paracrine production of glucagon which activates GLP-1 receptor".CELL AND BIOSCIENCE 14.1(2024):11. |
入库方式: OAI收割
来源:上海药物研究所
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