Role of lipids and actin in the formation of clathrin-coated pits

被引:110
作者
Boucrot, Emmanuel
Saffarian, Saveez
Massol, Ramiro
Kirchhausen, Tomas
Ehrlich, Marcelo
机构
[1] Harvard Univ, Sch Med, Dept Cell Biol, Boston, MA 02115 USA
[2] Harvard Univ, Sch Med, CBR Inst Biomed Res, Boston, MA 02115 USA
[3] Tel Aviv Univ, Dept Cell Res & Immunol, IL-69978 Tel Aviv, Israel
关键词
endocytosis; clathrin; 1-butanol; live-cell imaging; actin; phosphoinositides;
D O I
10.1016/j.yexcr.2006.09.025
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
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.
引用
收藏
页码:4036 / 4048
页数:13
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