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缝隙连接细胞中最大氯离子通道的钙离子敏感性。

Ca2+ sensitivity of the maxi chloride channel in interstitial cells of Cajal.

机构信息

Department of Medicine, Farncombe Family Digestive Health Research Institute, McMaster University, Hamilton, ON, Canada.

出版信息

Neurogastroenterol Motil. 2012 May;24(5):e221-34. doi: 10.1111/j.1365-2982.2012.01881.x. Epub 2012 Feb 1.

Abstract

BACKGROUND

Interstitial cells of Cajal (ICC) associated with the myenteric plexus of the small intestine express maxi chloride channels. Our aim was to investigate whether or not these channels would be activated by increases in intracellular Ca(2+) , as that would strengthen evidence for their potential role in ICC pacemaking. A further aim was to examine whether inwardly and outwardly rectifying maxi chloride currents signify different channels.

METHODS

We used Fluo-4 AM Ca(2+) imaging and patch clamp electrophysiology (cell-attached and inside-out) on isolated ICC in short term culture.

KEY RESULTS

Increasing intracellular Ca(2+) by three functionally distinct mechanisms (blocking sarcoplasmic reticulum Ca(2+) refilling, creating membrane Ca(2+) pores and a solution designed to block plasmalemmal Ca(2+) extrusion) was followed by inwardly rectifying maxi chloride channel activation assessed in the cell-attached configuration. Furthermore, in the inside-out configuration, increased outwardly rectifying maxi-chloride channel activity followed an increase in Ca(2+) to 2 mmol L(-1) at the cytoplasmic face of the channel.

CONCLUSIONS & INFERENCES: Increase in intracellular Ca(2+) will activate the maxi chloride channels. Maxi chloride currents are inwardly rectifying in the cell-attached patch clamp configuration under physiological conditions and are outwardly rectifying in the inside-out configuration. The same channel is responsible for both currents. Ca(2+) does not appear to regulate the rectification.

摘要

背景

与小肠肌间神经丛相关的 Cajal 间质细胞(ICC)表达最大氯通道。我们的目的是研究这些通道是否会被细胞内 Ca(2+)的增加激活,因为这将加强它们在 ICC 起搏中的潜在作用的证据。另一个目的是检查内向和外向整流的最大氯电流是否表示不同的通道。

方法

我们使用 Fluo-4 AM Ca(2+)成像和短期培养的分离 ICC 的膜片钳电生理学(细胞贴附和内面向外)。

主要结果

通过三种功能上不同的机制(阻断肌浆网 Ca(2+)再填充、形成膜 Ca(2+)孔和一种旨在阻断质膜 Ca(2+)外排的溶液)增加细胞内 Ca(2+)后,在细胞贴附配置中评估了内向整流的最大氯通道激活。此外,在膜片钳内面向外配置中,随着 Ca(2+)在通道细胞质侧增加到 2 mmol L(-1),外向整流的最大氯通道活性增加。

结论和推论

细胞内 Ca(2+)的增加将激活最大氯通道。在生理条件下,最大氯电流在细胞贴附膜片钳配置中呈内向整流,而在膜片钳内面向外配置中呈外向整流。同一通道负责两种电流。Ca(2+)似乎不会调节整流。

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