Department of Chemical Physiology & Biochemistry, Oregon Health & Science University, Portland, OR, USA.
Department of Chemical Physiology & Biochemistry, Oregon Health & Science University, Portland, OR, USA.
Cell Chem Biol. 2021 Jan 21;28(1):88-96.e3. doi: 10.1016/j.chembiol.2020.10.006. Epub 2020 Nov 3.
Pharmacological treatment of pancreatic β cells targeting cannabinoid receptors 1 and 2 (CB1 and CB2) has been shown to result in significant effects on insulin release, possibly by modulating intracellular calcium levels ([Ca]). It is unclear how the interplay of CB1 and CB2 affects insulin secretion. Here, we demonstrate by the use of highly specific receptor antagonists and the recently developed photo-releasable endocannabinoid 2-arachidonoylglycerol that both receptors have counteracting effects on cytosolic calcium oscillations. We further show that both receptors are juxtaposed in a way that increases [Ca] oscillations in silent β cells but dampens them in active ones. This study highlights a functional role of CB1 and CB2 acting in concert as a compensator/attenuator switch for regulating β cell excitability.
靶向大麻素受体 1 和 2(CB1 和 CB2)的胰腺β细胞的药理学治疗已被证明对胰岛素释放有显著影响,这可能是通过调节细胞内钙离子水平([Ca])实现的。目前尚不清楚 CB1 和 CB2 的相互作用如何影响胰岛素分泌。在这里,我们通过使用高度特异性的受体拮抗剂和最近开发的光可释放内源性大麻素 2-花生四烯酸甘油来证明,这两种受体对细胞质钙振荡具有拮抗作用。我们进一步表明,这两种受体以一种增加沉默β细胞中[Ca]振荡但在活跃细胞中抑制它们的方式并置。这项研究强调了 CB1 和 CB2 协同作用作为调节β细胞兴奋性的补偿/衰减开关的功能作用。