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直视氯离子通道:贝斯特蛋白、脂褐质沉积症与视网膜变性。

Looking chloride channels straight in the eye: bestrophins, lipofuscinosis, and retinal degeneration.

作者信息

Hartzell Criss, Qu Zhiqiang, Putzier Ilva, Artinian Liana, Chien Li-Ting, Cui Yuanyuan

机构信息

Department of Cell Biology, The Center for Neurodegenerative Disease, Emory University School of Medicine, Atlanta, Georgia, USA.

出版信息

Physiology (Bethesda). 2005 Oct;20:292-302. doi: 10.1152/physiol.00021.2005.

Abstract

Recent evidence suggests that Cl(-) ion channels are important for retinal integrity. Bestrophin Cl(-) channel mutations in humans are genetically linked to a juvenile form of macular degeneration, and disruption of some ClC Cl(-) channels in mice leads to retinal degeneration. In both cases, accumulation of lipofuscin pigment is a key feature of the cellular degeneration. Because Cl(-) channels regulate the ionic environment inside organelles in the endosomal-lysosomal pathway, retinal degeneration may result from defects in lysosomal trafficking or function.

摘要

最近的证据表明,氯离子通道对视网膜完整性很重要。人类中Bestrophin氯离子通道突变与青少年型黄斑变性存在遗传关联,而小鼠中某些ClC氯离子通道的破坏会导致视网膜变性。在这两种情况下,脂褐素色素的积累都是细胞变性的关键特征。由于氯离子通道调节内体-溶酶体途径中细胞器内的离子环境,视网膜变性可能是由溶酶体运输或功能缺陷引起的。

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