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Cargo- and adaptor-specific mechanisms regulate clathrin-mediated endocytosis
Authors:Marcel Mettlen  Dinah Loerke  Defne Yarar  Gaudenz Danuser  Sandra L. Schmid
Affiliation:1.Department of Cell Biology, The Scripps Research Institute, La Jolla, CA 92037;2.Department of Physics and Astronomy, University of Denver, Denver, CO 80208
Abstract:
Clathrin-mediated endocytosis of surface receptors and their bound ligands (i.e., cargo) is highly regulated, including by the cargo itself. One of the possible sources of the observed heterogeneous dynamics of clathrin-coated pits (CCPs) might be the different cargo content. Consistent with this, we show that CCP size and dynamic behavior varies with low density lipoprotein receptor (LDLR) expression levels in a manner dependent on the LDLR-specific adaptors, Dab2 and ARH. In Dab2-mCherry–expressing cells, varying LDLR expression leads to a progressive increase in CCP size and to the appearance of nonterminal endocytic events. In LDLR and ARH-mCherry–expressing cells in addition to an increase in CCP size, turnover of abortive CCPs increases, and the rate of CCP maturation decreases. Altogether, our results underscore the highly dynamic and cargo-responsive nature of CCP assembly and suggest that the observed heterogeneity is, in part, related to compositional differences (e.g., cargo and adaptors) between CCPs.
Keywords:
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