4.4 Article

Clathrin hub expression affects early endosome distribution with minimal impact on receptor sorting and recycling

期刊

MOLECULAR BIOLOGY OF THE CELL
卷 12, 期 9, 页码 2790-2799

出版社

AMER SOC CELL BIOLOGY
DOI: 10.1091/mbc.12.9.2790

关键词

-

资金

  1. NIAID NIH HHS [AI45865] Funding Source: Medline
  2. NIDDK NIH HHS [DK27083, R37 DK027083, R01 DK027083] Funding Source: Medline
  3. NIGMS NIH HHS [GM57657] Funding Source: Medline
  4. Wellcome Trust Funding Source: Medline

向作者/读者索取更多资源

Clathrin-coated vesicles execute receptor-mediated endocytosis at the plasma membrane. However, a role for clathrin in later endocytic trafficking processes, such as receptor sorting and recycling or maintaining the organization of the endocytic pathway, has not been thoroughly characterized. The existence of clathrin-coated buds on endosomes suggests that clathrin might mediate later endocytic trafficking events. To investigate the function of clathrin-coated buds on endosomal membranes, endosome function and distribution were analyzed in a HeLa cell line that expresses the dominant-negative clathrin inhibitor Hub in an inducible manner. As expected, Hub expression reduced receptor-mediated endocytosis at the plasma membrane. Hub expression also induced a perinuclear aggregation of early endosome antigen 1-positive early endosomes, such that sorting and recycling endosomes were found tightly concentrated in the perinuclear region. Despite the dramatic redistribution of endosomes, Hub expression did not affect the overall kinetics of receptor sorting or recycling. These data show that clathrin function is necessary to maintain proper cellular distribution of early endosomes but does not play a prominent role in sorting and recycling events. Thus, clathrin's role on endosomal membranes is to influence organelle localization and is distinct from its role in trafficking pathways at the plasma membrane and trans-Golgi network.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.4
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据