Rajagopal Senthilkumar, Fields Blanche L, Kamatchi Ganesan L
Department of Zoology, Nizam College, Osmania University, Hyderabad, 500001, Andhra Pradesh, India.
Endocrine. 2014 Nov;47(2):463-71. doi: 10.1007/s12020-013-0149-y. Epub 2014 Jan 23.
Voltage-gated calcium (Cav) channels and protein kinase C (PKC) isozymes are involved in insulin secretion. In addition, Cavβ, one of the auxiliary subunits of Cav channels, also regulates the secretion of insulin as knockout of Cavβ3 (β3(-/-)) subunits in mice led to efficient glucose homeostasis and increased insulin levels. We examined whether other types of Cavβ subunits also have similar properties. In this regard, we used small interfering RNA (siRNA) of these subunits (20 μg each) to down-regulate them and examined blood glucose, serum insulin and PKC translocation in isolated pancreatic β cells of mice. While the down-regulation of Cavβ2 and β3 subunits increased serum insulin levels and caused efficient glucose homeostasis, the down-regulation of Cavβ1 and β4 subunits failed to affect both these parameters. Examination of PKC isozymes in the pancreatic β-cells of Cavβ2- or β3 siRNA-injected mice showed that three PKC isozymes, viz., PKC α, βII and θ, translocated to the membrane. This suggests that when present, Cavβ2 and β3 subunits inhibited PKC activation. Among these three isozymes, only PKCα siRNA inhibited insulin and increased glucose concentrations. It is possible that the activation of PKCs βII and θ is not sufficient for the release of insulin and PKCα is the mediator of insulin secretion under the control of Cavβ subunits. Since Cavβ subunits are present intracellularly, it is possible that they (1) inhibited the translocation of PKC isozymes to the membrane and (2) decreased the interaction between Cav channels and PKC isozymes and thus the secretion of insulin.
电压门控钙(Cav)通道和蛋白激酶C(PKC)同工酶参与胰岛素分泌。此外,Cav通道的辅助亚基之一Cavβ也调节胰岛素分泌,因为小鼠中Cavβ3(β3(-/-))亚基的敲除导致有效的葡萄糖稳态和胰岛素水平升高。我们研究了其他类型的Cavβ亚基是否也具有类似特性。在这方面,我们使用这些亚基的小干扰RNA(siRNA)(各20μg)来下调它们,并检测小鼠分离的胰腺β细胞中的血糖、血清胰岛素和PKC易位。虽然下调Cavβ2和β3亚基可提高血清胰岛素水平并导致有效的葡萄糖稳态,但下调Cavβ1和β4亚基未能影响这两个参数。对注射Cavβ2或β3 siRNA的小鼠胰腺β细胞中的PKC同工酶进行检测发现,三种PKC同工酶,即PKCα、βII和θ,易位至细胞膜。这表明,当存在时,Cavβ2和β3亚基会抑制PKC激活。在这三种同工酶中,只有PKCα siRNA抑制胰岛素分泌并提高葡萄糖浓度。有可能PKCβII和θ的激活不足以释放胰岛素,而PKCα是在Cavβ亚基控制下胰岛素分泌的介质。由于Cavβ亚基存在于细胞内,它们有可能(1)抑制PKC同工酶向细胞膜的易位,以及(2)减少Cav通道与PKC同工酶之间的相互作用,从而减少胰岛素分泌。