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胰岛素分泌细胞中的胞质游离钙离子及其被分离细胞器的调节。

Cytosolic free Ca2+ in insulin secreting cells and its regulation by isolated organelles.

作者信息

Prentki M, Wollheim C B

出版信息

Experientia. 1984 Oct 15;40(10):1052-60. doi: 10.1007/BF01971451.

Abstract

The role of Ca2+ in secretagogue-induced insulin release is documented not only by the measurements of 45Ca fluxes in pancreatic islets, but also, by direct monitoring of cytosolic free Ca2+, [Ca2+]i. As demonstrated, using the fluorescent indicator quin 2, glyceraldehyde, carbamylcholine and alanine raise [Ca2+]i in the insulin secreting cell line RINm5F, whereas glucose has a similar effect in pancreatic islet cells. The regulation of cellular Ca2+ homeostasis by organelles from a rat insulinoma, was investigated with a Ca2+ selective electrode. The results suggest that both the endoplasmic reticulum and the mitochondria participate in this regulation, albeit at different Ca2+ concentrations. By contrast, the secretory granules do not appear to be involved in the short-term regulation of [Ca2+]i. Evidence is presented that inositol 1,4,5-trisphosphate, which is shown to mobilize Ca2+ from the endoplasmic reticulum, is acting as an intracellular mediator in the stimulation of insulin release.

摘要

钙离子(Ca2+)在促分泌剂诱导的胰岛素释放中的作用不仅通过测量胰岛中的45Ca通量得以证实,还通过直接监测细胞质游离钙离子浓度([Ca2+]i)得以体现。如研究所示,使用荧光指示剂喹啉2时,甘油醛、氨甲酰胆碱和丙氨酸可提高胰岛素分泌细胞系RINm5F中的[Ca2+]i,而葡萄糖对胰岛细胞有类似作用。利用钙离子选择性电极研究了大鼠胰岛素瘤细胞器对细胞钙离子稳态的调节。结果表明,内质网和线粒体均参与了这一调节,尽管作用的钙离子浓度不同。相比之下,分泌颗粒似乎未参与[Ca2+]i的短期调节。有证据表明,肌醇1,4,5-三磷酸可从内质网中动员钙离子,它作为细胞内介质参与刺激胰岛素释放。

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