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Expression of TMEM16A and SLC4A4 in Human Pancreatic Islets

机译:TMEM16A和SLC4A4在人胰岛中的表达

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Background/aims Stimulation of insulin release by D-glucose is accompanied by Clsup-/sup and HCOsub3/subsup-/sup efflux from pancreatic islet cells. The efflux of these anions may involve volume-regulated anion channels, including possibly TMEM16A, and the Nasup+/sup-HCOsub3/subsup-/sup-cotransporter SLC4A4. The present study was designed to explore the expression of both TMEM16A and SLC4A4 in human pancreatic islets. Methods Pancreases were obtained from human cadaveric donors. Immunodetection of TMEM16A and SLC4A4 was performed by immunohistochemistry on sections of fixed pancreas, while real-time PCR for the study of corresponding gene expression was performed on RNA extracted from both total pancreatic pieces and isolated pancreatic islets. Results RT-PCR yielded lower levels of SLC4A4 in isolated islets than in the total pancreas, whilst a mirror image prevailed for TMEM16A mRNA. Immunohistochemistry of human pancreas, however, indicated comparable immunostaining of SLC4A4 in insulin-producing cells and exocrine pancreatic cells, whilst that of TMEM16A appeared less pronounced in insulin-producing cells than in exocrine cells. Conclusion The present findings support the view that, in humans like in rodent, the regulation of anion fluxes in insulin-producing cells may involve both SLC4A4 and TMEM16A.
机译:背景/目的D-葡萄糖刺激胰岛素释放伴随有胰岛细胞的Cl -和HCO 3 -外排。这些阴离子的流出可能涉及体积调节的阴离子通道,可能包括TMEM16A,以及Na + -HCO 3 --共转运蛋白SLC4A4。本研究旨在探讨TMEM16A和SLC4A4在人胰岛中的表达。方法从人尸体供体中获取胰腺。 TMEM16A和SLC4A4的免疫检测是通过免疫组织化学法在固定的胰腺切片上进行的,而实时PCR技术则是对从总胰腺碎片和分离的胰岛中提取的RNA进行相应基因表达的研究。结果RT-PCR在分离的胰岛中产生的SLC4A4水平低于总胰岛中的水平,而TMEM16A mRNA普遍存在镜像。然而,人胰腺的免疫组织化学表明,在产生胰岛素的细胞和外分泌胰腺细胞中,SLC4A4的免疫染色相当,而在产生胰岛素的细胞中,TMEM16A的免疫染色不如在外分泌细胞中明显。结论本发现支持这样的观点,即在人类中,例如在啮齿动物中,胰岛素产生细胞中阴离子通量的调节可能涉及SLC4A4和TMEM16A。

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