Cell Dynamics and Bioimaging Research Center, School of Life Sciences, Gwangju Institute of Science and Technology, Gwangju, Republic of Korea.
Exp Cell Res. 2011 Oct 1;317(16):2276-87. doi: 10.1016/j.yexcr.2011.06.018. Epub 2011 Jul 7.
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.
SPIN90 是一种 F- 肌动蛋白结合蛋白,被认为在调节细胞骨架动力学方面发挥着重要作用。已知 SPIN90 在神经元发育的早期阶段表达,但它在生长锥中的定位和功能的细节尚未被充分研究。我们的免疫细胞化学数据显示,SPIN90 在年轻海马神经元的生长锥和神经元轴突中广泛富集。我们还发现,它的定位与 F- 肌动蛋白的存在相关,并依赖于 F- 肌动蛋白的存在。对海马神经元原代培养物的详细观察表明,与野生型神经元相比,SPIN90 敲除减少了生长锥的面积和丝状伪足的数量。此外,SPIN90 敲除神经元的总神经突长度(最长(轴突)和较短(树突)神经突的总和长度)小于野生型神经元。最后,SPIN90 敲除神经元中的 Cdc42 活性下调。总之,我们的研究结果表明,SPIN90 在控制生长锥动力学和神经突生长中发挥着关键作用。