Program in Neuroscience and Behavioral Disorder, Duke-NUS Graduate Medical School, Singapore, Singapore.
PLoS One. 2013 Jun 10;8(6):e65572. doi: 10.1371/journal.pone.0065572. Print 2013.
Class 3 semaphorins are well-known axonal guidance cues during the embryonic development of mammalian nervous system. However, their activity on postnatally differentiated neurons in neurogenic regions of adult brains has not been characterized. We found that silencing of semaphorin receptors neuropilins (NRP) 1 or 2 in neural progenitors at the adult mouse dentate gyrus resulted in newly differentiated neurons with shorter dendrites and simpler branching in vivo. Tyrosine phosphorylation (Tyr 397) and serine phosphorylation (Ser 732) of FAK were essential for these effects. Semaphorin 3A and 3F mediate serine phosphorylation of FAK through the activation of Cdk5. Silencing of either Cdk5 or FAK in newborn neurons phenocopied the defects in dendritic development seen upon silencing of NRP1 or NRP2. Furthermore, in vivo overexpression of Cdk5 or FAK rescued the dendritic phenotypes seen in NRP1 and NRP2 deficient neurons. These results point to a novel role for class 3 semaphorins in promoting dendritic growth and branching during adult hippocampal neurogenesis through the activation of Cdk5-FAK signaling pathway.
3 类信号素是哺乳动物神经系统胚胎发育过程中著名的轴突导向信号。然而,它们在成年大脑神经发生区域中已分化神经元上的活性尚未被描述。我们发现,在成年小鼠齿状回的神经祖细胞中沉默神经纤毛蛋白(NRP)1 或 2 受体,会导致体内新分化的神经元的树突变短,分支更简单。FAK 的酪氨酸磷酸化(Tyr397)和丝氨酸磷酸化(Ser732)对于这些效应是必需的。信号素 3A 和 3F 通过激活 Cdk5 介导 FAK 的丝氨酸磷酸化。在新生神经元中沉默 Cdk5 或 FAK,可模拟沉默 NRP1 或 NRP2 时观察到的树突发育缺陷。此外,体内过表达 Cdk5 或 FAK 可挽救 NRP1 和 NRP2 缺陷神经元中观察到的树突表型。这些结果表明,3 类信号素通过激活 Cdk5-FAK 信号通路,在成年海马神经发生过程中促进树突生长和分支,发挥了新的作用。