Department of Cell Biology, The Scripps Research Institute, La Jolla, CA 92037, USA.
J Cell Biol. 2010 Dec 27;191(7):1381-93. doi: 10.1083/jcb.201008117.
Clathrin-mediated endocytosis (CME) is the major pathway for concentrative uptake of receptors and receptor-ligand complexes (cargo). Although constitutively internalized cargos are known to accumulate into maturing clathrin-coated pits (CCPs), whether and how cargo recruitment affects the initiation and maturation of CCPs is not fully understood. Previous studies have addressed these issues by analyzing the global effects of receptor overexpression on CME or CCP dynamics. Here, we exploit a refined approach using expression of a biotinylated transferrin receptor (bTfnR) and controlling its local clustering using mono- or multivalent streptavidin. We show that local clustering of bTfnR increased CCP initiation. By tracking cargo loading in individual CCPs, we found that bTfnR clustering preceded clathrin assembly and confirmed that bTfnR-containing CCPs mature more efficiently than bTfnR-free CCPs. Although neither the clustering nor the related changes in cargo loading altered the rate of CCP maturation, bTfnR-containing CCPs exhibited significantly longer lifetimes than other CCPs within the same cell. Together these results demonstrate that cargo composition is a key source of the differential dynamics of CCPs.
网格蛋白介导的内吞作用(CME)是受体和受体-配体复合物(货物)浓缩摄取的主要途径。虽然已知组成性内化的货物会积累到成熟的网格蛋白包被小窝(CCP)中,但货物募集是否以及如何影响 CCP 的起始和成熟尚不完全清楚。以前的研究通过分析受体过表达对 CME 或 CCP 动力学的全局影响来解决这些问题。在这里,我们利用一种改良的方法,使用生物素化转铁蛋白受体(bTfnR)的表达,并使用单或多价链霉亲和素来控制其局部聚集。我们表明,bTfnR 的局部聚集增加了 CCP 的起始。通过在单个 CCP 中跟踪货物加载,我们发现 bTfnR 聚集先于网格蛋白组装,并证实 bTfnR 包含的 CCP 比 bTfnR 不含的 CCP 成熟更有效率。尽管聚集或相关的货物加载变化都不会改变 CCP 的成熟速度,但 bTfnR 包含的 CCP 的寿命明显长于同一细胞内的其他 CCP。这些结果表明货物组成是 CCP 动力学差异的关键来源。