Control of growth cone motility and neurite outgrowth by SPIN90 |
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Authors: | Seon-Myung Kim Jeomil Bae In Ha Cho Kyu Yeong Choi Yeon Jung Park Jin Hee Ryu Jang-Soo Chun Woo Keun Song |
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Affiliation: | aCell Dynamics and Bioimaging Research Center, School of Life Sciences, Gwangju Institute of Science and Technology, Gwangju 500-712, Republic of Korea;bNational Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, MD 20892, USA |
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Abstract: | 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. |
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Keywords: | Abbreviations: DIV, days in vitro KO, knockout GFP, green fluorescent protein GST, glutathione S transferase PBD, p21 binding-domain |
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