Skrzypski M, Khajavi N, Mergler S, Szczepankiewicz D, Kołodziejski P A, Metzke D, Wojciechowicz T, Billert M, Nowak K W, Strowski M Z
Department of Hepatology and Gastroenterology & the Interdisciplinary Centre of Metabolism: Endocrinology, Diabetes and Metabolism, Charité-University Medicine Berlin, 13353 Berlin, Germany; Department of Animal Physiology and Biochemistry,Poznań University of Life Sciences, 60-637Poznań, Poland.
Institute for Experimental Pediatric Endocrinology, Charite-University-Medicine Berlin, 13353Berlin, Germany.
Biochim Biophys Acta. 2015 Dec;1853(12):3202-10. doi: 10.1016/j.bbamcr.2015.09.012. Epub 2015 Sep 16.
Transient receptor potential channel vanilloid type 6 (TRPV6) is a non-selective cation channel with high permeability for Ca²⁺ ions. So far, the role of TRPV6 in pancreatic beta cells is unknown. In the present study, we characterized the role of TRPV6 in controlling calcium signaling, cell proliferation as well as insulin expression, and secretion in experimental INS-1E beta cell model. TRPV6 protein production was downregulated using siRNA by approx. 70%, as detected by Western blot. Intracellular free Ca²⁺ ([Ca²⁺]i) was measured by fluorescence Ca²⁺ imaging using fura-2. Calcineurin/NFAT signaling was analyzed using a NFAT reporter assay as well as a calcineurin activity assay. TRPV6 downregulation resulted in impaired cellular calcium influx. Its downregulation also reduced cell proliferation and decreased insulin mRNA expression. These changes were companied by the inhibition of the calcineurin/NFAT signaling. In contrast, insulin exocytosis was not affected by TRPV6 downregulation. In conclusion, this study demonstrates for the first time the expression of TRPV6 in INS-1E cells and rat pancreatic beta cells and describes its role in modulating calcium signaling, beta cell proliferation and insulin mRNA expression. In contrast, TRPV6 fails to influence insulin secretion.
瞬时受体电位香草酸亚型6(TRPV6)是一种对Ca²⁺离子具有高通透性的非选择性阳离子通道。到目前为止,TRPV6在胰腺β细胞中的作用尚不清楚。在本研究中,我们在实验性INS-1Eβ细胞模型中,对TRPV6在控制钙信号传导、细胞增殖以及胰岛素表达和分泌方面的作用进行了表征。通过Western印迹检测,使用小干扰RNA(siRNA)使TRPV6蛋白表达下调了约70%。使用fura-2通过荧光钙成像测量细胞内游离钙([Ca²⁺]i)。使用NFAT报告基因检测以及钙调神经磷酸酶活性检测分析钙调神经磷酸酶/NFAT信号传导。TRPV6下调导致细胞钙内流受损。其下调还降低了细胞增殖并减少了胰岛素mRNA表达。这些变化伴随着钙调神经磷酸酶/NFAT信号传导的抑制。相比之下,胰岛素胞吐作用不受TRPV6下调的影响。总之,本研究首次证明了TRPV6在INS-1E细胞和大鼠胰腺β细胞中的表达,并描述了其在调节钙信号传导、β细胞增殖和胰岛素mRNA表达中的作用。相比之下,TRPV6不影响胰岛素分泌。