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Filopodia are required for cortical neurite initiation
被引:243
作者:
Dent, Erik W.
Kwiatkowski, Adam V.
Mebane, Leslie M.
Philippar, Ulrike
Barzik, Melanie
Rubinson, Douglas A.
Gupton, Stephanie
Van Veen, J. Edward
Furman, Craig
Zhang, Jiangyang
Alberts, Arthur S.
Mori, Susumu
Gertler, Frank B.
机构:
[1] MIT, Dept Biol, Cambridge, MA 02139 USA
[2] Johns Hopkins Univ, Sch Med, Dept Radiol, Div Nucl Magnet Resonance Res, Baltimore, MD 21205 USA
[3] Van Andel Res Inst, Lab Cell Struct & Signal Integrat, Grand Rapids, MI 49503 USA
[4] Univ Wisconsin, Dept Anat, Madison, WI 53706 USA
[5] Stanford Univ, Dept Sci Biol, Stanford, CA 94305 USA
关键词:
D O I:
10.1038/ncb1654
中图分类号:
Q2 [细胞生物学];
学科分类号:
071009 ;
090102 ;
摘要:
Extension of neurites from a cell body is essential to form a functional nervous system; however, the mechanisms underlying neuritogenesis are poorly understood. Ena/VASP proteins regulate actin dynamics and modulate elaboration of cellular protrusions. We recently reported that cortical axon-tract formation is lost in Ena/VASP-null mice and Ena/VASP-null cortical neurons lack filopodia and fail to elaborate neurites. Here, we report that neuritogenesis in Ena/VASP-null neurons can be rescued by restoring filopodia formation through ectopic expression of the actin nucleating protein mDia2. Conversely, wildtype neurons in which filopodia formation is blocked fail to elaborate neurites. We also report that laminin, which promotes the formation of filopodia-like actin-rich protrusions, rescues neuritogenesis in Ena/VASP-deficient neurons. Therefore, filopodia formation is a key prerequisite for neuritogenesis in cortical neurons. Neurite initiation also requires microtubule extension into filopodia, suggesting that interactions between actin-filament bundles and dynamic microtubules within filopodia are crucial for neuritogenesis.
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页码:1347 / U28
页数:19
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