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疟原虫感染红细胞中“新渗透途径”的膜片钳分析

Patch-clamp analysis of the "new permeability pathways" in malaria-infected erythrocytes.

作者信息

Huber Stephan M, Duranton Christophe, Lang Florian

机构信息

Department of Physiology, Eberhard-Karls-University, D-72076 Tübingen, Germany.

出版信息

Int Rev Cytol. 2005;246:59-134. doi: 10.1016/S0074-7696(05)46003-9.

Abstract

The intraerythrocytic amplification of the malaria parasite Plasmodium falciparum induces new pathways of solute permeability in the host cell's membrane. These pathways play a pivotal role in parasite development by supplying the parasite with nutrients, disposing of the parasite's metabolic waste and organic osmolytes, and adapting the host's electrolyte composition to the parasite's needs. The "new permeability pathways" allow the fast electrogenic diffusion of ions and thus can be analyzed by patch-clamp single-channel or whole-cell recording. By employing these techniques, several ion-channel types with different electrophysiological profiles have been identified in P. falciparum-infected erythrocytes; they have also been identified in noninfected cells. This review discusses a possible contribution of these channels to the new permeability pathways on the one hand and their supposed functions in noninfected erythrocytes on the other.

摘要

恶性疟原虫在红细胞内的增殖会诱导宿主细胞膜出现新的溶质通透途径。这些途径在寄生虫发育过程中起着关键作用,为寄生虫提供营养物质、排出寄生虫的代谢废物和有机渗透溶质,并使宿主的电解质组成适应寄生虫的需求。“新的通透途径”允许离子进行快速的电致扩散,因此可以通过膜片钳单通道或全细胞记录进行分析。通过运用这些技术,在感染恶性疟原虫的红细胞中已鉴定出几种具有不同电生理特征的离子通道类型;在未感染的细胞中也已鉴定出这些通道。本综述一方面讨论了这些通道对新通透途径的可能贡献,另一方面讨论了它们在未感染红细胞中的假定功能。

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