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大麻素调节胰腺β细胞中Bcl-2和细胞周期蛋白D2的表达。

Cannabinoids Regulate Bcl-2 and Cyclin D2 Expression in Pancreatic β Cells.

作者信息

Kim Jihye, Lee Kyung Jin, Kim Jung Seok, Rho Jun Gi, Shin Jung Jae, Song Woo Keun, Lee Eun Kyung, Egan Josephine M, Kim Wook

机构信息

Department of Molecular Science and Technology, Ajou University, Suwon, 16499, South Korea.

Department of Convergence Medicine, Asan Institute for Life Sciences, University of Ulsan College of Medicine, Asan Medical Center, Seoul, 05505, Korea.

出版信息

PLoS One. 2016 Mar 11;11(3):e0150981. doi: 10.1371/journal.pone.0150981. eCollection 2016.

Abstract

Recent reports have shown that cannabinoid 1 receptors (CB1Rs) are expressed in pancreatic β cells, where they induce cell death and cell cycle arrest by directly inhibiting insulin receptor activation. Here, we report that CB1Rs regulate the expression of the anti-apoptotic protein Bcl-2 and cell cycle regulator cyclin D2 in pancreatic β cells. Treatment of MIN6 and βTC6 cells with a synthetic CB1R agonist, WIN55,212-2, led to a decrease in the expression of Bcl-2 and cyclin D2, in turn inducing cell cycle arrest in G0/G1 phase and caspase-3-dependent apoptosis. Additionally, genetic deletion and pharmacological blockade of CB1Rs after injury in mice led to increased levels of Bcl-2 and cyclin D2 in pancreatic β cells. These findings provide evidence for the involvement of Bcl-2 and cyclin D2 mediated by CB1Rs in the regulation of β-cell survival and growth, and will serve as a basis for developing new therapeutic interventions to enhance β-cell function and growth in diabetes.

摘要

最近的报告显示,大麻素1受体(CB1Rs)在胰腺β细胞中表达,在那里它们通过直接抑制胰岛素受体激活来诱导细胞死亡和细胞周期停滞。在此,我们报告CB1Rs调节胰腺β细胞中抗凋亡蛋白Bcl-2和细胞周期调节因子细胞周期蛋白D2的表达。用合成的CB1R激动剂WIN55,212-2处理MIN6和βTC6细胞,导致Bcl-2和细胞周期蛋白D2的表达降低,进而诱导细胞周期停滞在G0/G1期并引发caspase-3依赖性凋亡。此外,小鼠受伤后CB1Rs的基因缺失和药物阻断导致胰腺β细胞中Bcl-2和细胞周期蛋白D2水平升高。这些发现为CB1Rs介导的Bcl-2和细胞周期蛋白D2参与β细胞存活和生长的调节提供了证据,并将作为开发新的治疗干预措施以增强糖尿病患者β细胞功能和生长的基础。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f768/4788443/dbaaa8bbf5e6/pone.0150981.g001.jpg

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