Control of growth cone motility and neurite outgrowth by SPIN90

被引:9
作者
Kim, Seon-Myung [1 ]
Bae, Jeomil [1 ]
Cho, In Ha [1 ]
Choi, Kyu Yeong [2 ]
Park, Yeon Jung [1 ]
Ryu, Jin Hee [1 ]
Chun, Jang-Soo [1 ]
Song, Woo Keun [1 ]
机构
[1] Gwangju Inst Sci & Technol, Sch Life Sci, Cell Dynam & Bioimaging Res Ctr, Kwangju 500712, South Korea
[2] Natl Inst Neurol Disorders & Stroke, NIH, Bethesda, MD 20892 USA
基金
新加坡国家研究基金会;
关键词
Hippocampal; Growth cone; Neurite outgrowth; F-actin; SPIN90; knockout; DIP; WISH; CYTOSKELETAL DYNAMICS; MICROTUBULE BEHAVIOR; ACTIN CYTOSKELETON; BINDING PROTEINS; ARP2/3; COMPLEX; N-WASP; FILOPODIA; CDC42; MECHANISMS; ESTABLISHMENT;
D O I
10.1016/j.yexcr.2011.06.018
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
SPIN90 is an F-actin binding protein thought to play important roles in regulating cytoskeletal dynamics. It is known that SPIN90 is expressed during the early stages of neuronal development, but details of its localization and function in growth cones have not been fully investigated. Our immunocytochemical data show that SPIN90 is enriched throughout growth cones and neuronal shafts in young hippocampal neurons. We also found that its localization correlates with and depends upon the presence of F-actin. Detailed observation of primary cultures of hippocampal neurons revealed that SPIN90 knockout reduces both growth cone areas and in the numbers of filopodia, as compared to wild-type neurons. In addition, total neurite length, the combined lengths of the longest (axonal) and shorter (dendritic) neurites, was smaller in SPIN90 knockout neurons than wild-type neurons. Finally, Cdc42 activity was down-regulated in SPIN90 knockout neurons. Taken together, our findings suggest that SPIN90 plays critical roles in controlling growth cone dynamics and neurite outgrowth. (C) 2011 Elsevier Inc. All rights reserved.
引用
收藏
页码:2276 / 2287
页数:12
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