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一种新的测定 Na,K-ATPase 活性的方法:在完整的胰腺β细胞中的应用。

A new approach for determination of Na,K-ATPase activity: application to intact pancreatic β-cells.

机构信息

Department of Chemistry, University of Évora, Rua Romao Ramalho, 59, 7000 757 Évora, Portugal.

出版信息

In Vitro Cell Dev Biol Anim. 2010 Jan;46(1):7-10. doi: 10.1007/s11626-009-9243-0.

Abstract

It has been postulated that a decrease in Na,KATPase- mediated ion gradients may be a contributing mechanism to insulin secretion. However, the precise role of the Na,K-ATPase in pancreatic β-cell membrane depolarization and insulin secretion signalling have been difficult to evaluate, mostly because data reporting changes in enzymatic activity have been obtained in cell homogenates or membrane preparations, lacking intact intracellular signalling pathways. The aim of this work was to develop a method to characterize Na,K-ATPase activity in intact pancreatic β-cells that will allow the investigation of putative Na,K-ATPase activity regulation by glucose and its possible role in insulin secretion signalling. This work demonstrates for the first time that it is possible to determine Na,K-ATPase activity in intact pancreatic β-cells and that this is a suitable method for the study of the mechanisms involved in the Na,K-ATPase regulation and eventually its relevance for insulin secretion signalling.

摘要

有人假设,Na,KATPase 介导的离子梯度的降低可能是导致胰岛素分泌的一个机制。然而,Na,K-ATPase 在胰腺β细胞膜去极化和胰岛素分泌信号中的确切作用一直难以评估,这主要是因为报告酶活性变化的数据是在细胞匀浆或膜制剂中获得的,缺乏完整的细胞内信号通路。本工作的目的是开发一种方法来描述完整的胰腺β细胞中 Na,K-ATPase 的活性,这将允许研究葡萄糖对 Na,K-ATPase 活性的可能调节作用及其在胰岛素分泌信号中的作用。本工作首次证明,在完整的胰腺β细胞中测定 Na,K-ATPase 活性是可能的,并且这是研究 Na,K-ATPase 调节机制及其与胰岛素分泌信号相关性的一种合适方法。

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