Targeting of the F-actin-binding protein drebrin by the microtubule plus-tip protein EB3 is required for neuritogenesis

被引:195
作者
Geraldo, Sara [1 ]
Khanzada, Umme K. [1 ]
Parsons, Maddy [2 ]
Chilton, John K. [1 ]
Gordon-Weeks, Phillip R. [1 ]
机构
[1] Kings Coll London, MRC Ctr Dev Neurobiol, London SE1 1UL, England
[2] Kings Coll London, Randall Div Cell & Mol Biophys, London SE1 1UL, England
基金
英国医学研究理事会; 英国惠康基金;
关键词
D O I
10.1038/ncb1778
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Interactions between dynamic microtubules and actin filaments (F-actin) underlie a range of cellular processes including cell polarity and motility. In growth cones, dynamic microtubules are continually extending into selected filopodia, aligning alongside the proximal ends of the F-actin bundles. This interaction is essential for neuritogenesis and growth-cone pathfinding. However, the molecular components mediating the interaction between microtubules and filopodial F-actin have yet to be determined. Here we show that drebrin, an F-actin-associated protein, binds directly to the microtubule-binding protein EB3. In growth cones, this interaction occurs specifically when drebrin is located on F-actin in the proximal region of filopodia and when EB3 is located at the tips of microtubules invading filopodia. When this interaction is disrupted, the formation of growth cones and the extension of neurites are impaired. We conclude that drebrin targets EB3 to coordinate F-actin-microtubule interactions that underlie neuritogenesis.
引用
收藏
页码:1181 / 1189
页数:9
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