Late endosomal membranes rich in lysobisphosphatidic acid regulate cholesterol transport

被引:539
作者
Kobayashi, T
Beuchat, MH
Lindsay, M
Frias, S
Palmiter, RD
Sakuraba, H
Parton, RG
Gruenberg, J
机构
[1] Univ Geneva, Dept Biochem, CH-1211 Geneva 4, Switzerland
[2] Univ Washington, Dept Biochem, Seattle, WA 98195 USA
[3] Tokyo Metropolitan Inst Med Sci, Dept Clin Genet, Bunkyo Ku, Tokyo 113, Japan
[4] Univ Washington, Howard Hughes Med Inst, Seattle, WA 98195 USA
[5] Univ Queensland, Dept Physiol & Pharmacol, St Lucia, Qld 4072, Australia
[6] Univ Queensland, Ctr Microscopy & Microanal, Ctr Mol & Cellular Biol, St Lucia, Qld 4072, Australia
基金
英国医学研究理事会;
关键词
D O I
10.1038/10084
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The fate of free cholesterol released after endocytosis of low-density lipoproteins remains obscure. Here we report that late endosomes have a pivotal role in intracellular cholesterol transport. We find that in the genetic disease Niemann-Pick type C (NPC), and in drug-treated cells that mimic NPC, cholesterol accumulates in late endosomes and sorting of the lysosomal enzyme receptor is impaired. Our results show that the characteristic network of lysobisphosphatidic acid-rich membranes contained within multivesicular late endosomes regulates cholesterol transport, presumably by acting as a collection and distribution device. The results also suggest that similar endosomal defects accompany the anti-phospholipid syndrome and NPC.
引用
收藏
页码:113 / 118
页数:6
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