Journal
EXPERIMENTAL CELL RESEARCH
Volume 312, Issue 20, Pages 4036-4048Publisher
ELSEVIER INC
DOI: 10.1016/j.yexcr.2006.09.025
Keywords
endocytosis; clathrin; 1-butanol; live-cell imaging; actin; phosphoinositides
Categories
Funding
- NIGMS NIH HHS [P01 GM062566, R01 GM075252, GM 075252, GM62566] Funding Source: Medline
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Assembly of clathrin-coated pits and their maturation into coated vesicles requires coordinated interactions between specific lipids and several structural and regulatory proteins. In the presence of primary alcohols, phospholipase D generates phosphatidylalcohols instead of PA, reducing stimulation of phosphatidyl inositol 5-kinase (PI5K) and hence decreasing formation of phosphoinositide-4,5-biphosphate (PIP2). Using live-cell imaging, we have shown that acute treatment of cells with 1-butanol or other small primary alcohols induces rapid disassembly of coated pits at the plasma membrane and blocks appearance of new ones. Addition of exogenous PIP2 reverses this effect. Coated pits and vesicles reappear synchronously upon removal of 1-butanol; we have used this synchrony to assess the role of actin in coated vesicle assembly. Prolonged inhibition of actin polymerization by latrunculin A or cytochalasin D reduced by similar to 50% the frequency of coated pit formation without affecting maturation into coated vesicles. As in control cells, removal of 1-butanol in the continued presence of an actin depolymerizer led to synchronous appearance of new pits, which matured normally. Thus, remodeling of the actin cytoskeleton is not essential for clathrin-coated vesicle assembly but may indirectly affect the nucleation of clathrin-coated pits. (c) 2006 Elsevier Inc. All rights reserved.
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