Loss of membrane cholesterol influences lysosomal permeability to potassium ions and protons

被引:49
作者
Deng, Dong [2 ]
Jiang, Nan [3 ]
Hao, Shu-jing [1 ,4 ]
Sun, Hui [2 ]
Zhang, Guo-jiang [1 ]
机构
[1] Chinese Acad Sci, Inst Biophys, Beijing 100101, Peoples R China
[2] NE Normal Univ, Sch Life Sci, Changchun 130024, Peoples R China
[3] Capital Normal Univ, Beijing 100037, Peoples R China
[4] Acad Sinica, Grad Sch, Beijing 100039, Peoples R China
来源
BIOCHIMICA ET BIOPHYSICA ACTA-BIOMEMBRANES | 2009年 / 1788卷 / 02期
基金
中国国家自然科学基金;
关键词
Lysosome; Cholesterol; Ion permeability; Membrane fluidity; Methyl-beta-cyclodextrin (M beta CD); RAT-LIVER; PHYSICAL STATE; DESTABILIZATION; TRANSLOCATION; FLUORESCENCE; MECHANISM; APOPTOSIS; AUTOPHAGY; TRANSPORT; STEROLS;
D O I
10.1016/j.bbamem.2008.11.018
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Cholesterol is an essential component of lysosomal membranes. In this study, we investigated the effects of membrane cholesterol on the permeability of rat liver lysosomes to K+ and H+, and the organelle stability. Through the measurements of lysosomal beta-hexosaminidase free activity, membrane potential, membrane fluidity, intra-lysosomal pH, and lysosomal proton leakage, we established that methyl-beta-cyclodextrin (M beta CD)-produced loss of membrane cholesterol could increase the lysosomal permeability to both potassium ions and protons, and fluidize the lysosomal membranes. As a result, potassium ions entered the lysosomes through K+/H+ exchange, which produced osmotic imbalance across the membranes and osmotically destabilized the lysosomes. In addition, treatment of the lysosomes with M beta CD caused leakage of the lysosomal protons and raised the intra-lysosomal pH. The results indicate that membrane cholesterol plays important roles in the maintenance of the lysosomal limited permeability to K+ and H+. Loss of this membrane sterol is critical for the organelle acidification and stability. (c) 2008 Elsevier B.V. All rights reserved.
引用
收藏
页码:470 / 476
页数:7
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