Maxfield Frederick R, Iaea David B, Pipalia Nina H
Department of Biochemistry, Weill Cornell Medical College, 1300 York Avenue, New York, NY 10065, USA.
Biochem Cell Biol. 2016 Dec;94(6):499-506. doi: 10.1139/bcb-2015-0154. Epub 2016 Jan 28.
Cholesterol plays an important role in determining the biophysical properties of membranes in mammalian cells, and the concentration of cholesterol in membranes is tightly regulated. Cholesterol moves among membrane organelles by a combination of vesicular and nonvesicular transport pathways, but the details of these transport pathways are not well understood. In this review, we discuss the mechanisms for nonvesicular sterol transport with an emphasis on the role of STARD4, a small, soluble, cytoplasmic sterol transport protein. STARD4 can rapidly equilibrate sterol between membranes, especially membranes with anionic lipid headgroups. We also discuss the sterol transport in late endosomes and lysosomes, which is mediated by a soluble protein, NPC2, and a membrane protein, NPC1. Homozygous mutations in these proteins lead to a lysosomal lipid storage disorder, Niemann-Pick disease type C. Many of the disease-causing mutations in NPC1 are associated with degradation of the mutant NPC1 proteins in the endoplasmic reticulum. Several histone deacetylase inhibitors have been found to rescue the premature degradation of the mutant NPC1 proteins, and one of these is now in a small clinical trial.
胆固醇在决定哺乳动物细胞膜的生物物理特性方面发挥着重要作用,并且细胞膜中胆固醇的浓度受到严格调控。胆固醇通过囊泡运输和非囊泡运输途径的组合在膜细胞器之间移动,但这些运输途径的细节尚未完全清楚。在本综述中,我们讨论非囊泡甾醇运输的机制,重点是STARD4的作用,STARD4是一种小的、可溶性的细胞质甾醇运输蛋白。STARD4可以在膜之间迅速平衡甾醇,尤其是具有阴离子脂质头部基团的膜。我们还讨论了晚期内体和溶酶体中的甾醇运输,这是由一种可溶性蛋白NPC2和一种膜蛋白NPC1介导的。这些蛋白的纯合突变会导致溶酶体脂质贮积病,即C型尼曼-匹克病。NPC1中的许多致病突变与内质网中突变NPC1蛋白的降解有关。已发现几种组蛋白脱乙酰酶抑制剂可挽救突变NPC1蛋白的过早降解,其中一种目前正在进行小型临床试验。