Rutgers University, Department of Molecular Biology and Biochemistry, Piscataway, NJ, 08854, USA.
Rutgers University, Department of Molecular Biology and Biochemistry, Piscataway, NJ, 08854, USA.
Curr Opin Cell Biol. 2020 Aug;65:86-95. doi: 10.1016/j.ceb.2020.02.018. Epub 2020 Apr 1.
It is widely recognized that after endocytosis, internalized cargo is delivered to endosomes that act as sorting stations. The limiting membrane of endosomes contain specialized subregions, or microdomains, that represent distinct functions of the endosome, including regions competing for cargo capture leading to degradation or recycling. Great progress has been made in defining the endosomal protein coats that sort cargo in these domains, including Retromer that recycles transmembrane cargo, and ESCRT (endosomal sorting complex required for transport) that degrades transmembrane cargo. In this review, we discuss recent work that is beginning to unravel how such coat complexes contribute to the creation and maintenance of endosomal microdomains. We highlight data that indicates that adjacent microdomains do not act independently but rather interact to cross-regulate. We posit that these interactions provide an agile means for the cell to adjust sorting in response to extracellular signals and intracellular metabolic cues.
人们普遍认为,内吞作用后,内化的货物被递送到作为分拣站的内体。内体的限制膜包含专门的亚区或微区,代表内体的不同功能,包括竞争货物捕获的区域,导致降解或回收。在定义这些区域中分拣货物的内体蛋白衣被方面已经取得了很大进展,包括回收跨膜货物的Retromer 和降解跨膜货物的 ESCRT(内体分选复合物必需的运输)。在这篇综述中,我们讨论了最近开始揭示这些衣被复合物如何有助于内体微区的形成和维持的工作。我们强调的数据表明,相邻的微区不是独立作用的,而是相互作用以交叉调节。我们假设这些相互作用为细胞提供了一种灵活的方式,以响应细胞外信号和细胞内代谢线索来调整分拣。