Department of Cell Biology, Harvard Medical School, Boston, Massachusetts 02115, USA; email:
Annu Rev Physiol. 2021 Feb 10;83:153-181. doi: 10.1146/annurev-physiol-031620-094944. Epub 2020 Nov 3.
Cholesterol homeostasis and trafficking are critical to the maintenance of the asymmetric plasma membrane of eukaryotic cells. Disruption or dysfunction of cholesterol trafficking leads to numerous human diseases. ATP-binding cassette (ABC) transporters play several critical roles in this process, and mutations in these sterol transporters lead to disorders such as Tangier disease and sitosterolemia. Biochemical and structural information on ABC sterol transporters is beginning to emerge, with published structures of ABCA1 and ABCG5/G8; these two proteins function in the reverse cholesterol transport pathway and mediate the efflux of cholesterol and xenosterols to high-density lipoprotein and bile salt micelles, respectively. Although both of these transporters belong to the ABC family and mediate the efflux of a sterol substrate, they have many distinct differences. Here, we summarize the current understanding of sterol transport driven by ABC transporters, with an emphasis on these two extensively characterized transporters.
胆固醇稳态和运输对于真核细胞不对称质膜的维持至关重要。胆固醇运输的破坏或功能障碍会导致许多人类疾病。ATP 结合盒 (ABC) 转运蛋白在这一过程中发挥了几个关键作用,这些固醇转运蛋白的突变会导致 Tangier 病和植物固醇血症等疾病。有关 ABC 固醇转运蛋白的生化和结构信息开始出现,已发表的 ABCA1 和 ABCG5/G8 的结构;这两种蛋白质分别在胆固醇逆向转运途径中发挥作用,并介导胆固醇和异固醇向高密度脂蛋白和胆汁盐胶束的外排。尽管这两种转运蛋白都属于 ABC 家族,并且介导固醇底物的外排,但它们有许多明显的差异。在这里,我们总结了 ABC 转运蛋白驱动的固醇运输的最新认识,重点介绍这两种经过广泛表征的转运蛋白。