Miura Yuki, Kanaho Yasunori
Department of Physiological Chemistry, Faculty of Medicine and Graduate School of Comprehensive Human Sciences, University of Tsukuba, 1-1-1 Tennodai, Tsukuba 305-8578, Japan; Ph.D. Program in Human Biology, School of Integrative and Global Majors, University of Tsukuba, 1-1-1 Tennodai, Tsukuba 305-8578, Japan.
Department of Physiological Chemistry, Faculty of Medicine and Graduate School of Comprehensive Human Sciences, University of Tsukuba, 1-1-1 Tennodai, Tsukuba 305-8578, Japan.
Biochem Biophys Res Commun. 2017 Nov 18;493(2):1089-1094. doi: 10.1016/j.bbrc.2017.09.076. Epub 2017 Sep 15.
The GTPase-activating protein (GAP) specific to the small GTPase Arf6, ACAP3, is known to regulate morphogenesis of neurons in vitro. However, physiological significance of ACAP3 in the brain development in vivo remains unclear. Here, we show that ACAP3 is involved in neuronal migration in the developing cerebral cortex of mice. Knockdown of ACAP3 in the developing cortical neurons of mice in utero significantly abrogated neuronal migration in the cortical layer, which was restored by ectopic expression of wild type of ACAP3, but not by its GAP-inactive mutant. Furthermore, morphological changes of neurons during migration in the cortical layer were impeded in ACAP3-knocked-down cortical neurons. These results provide evidence that ACAP3 plays a crucial role in migration of cortical neurons by regulating their morphological change during development of cerebral cortex.
已知小GTP酶Arf6特异性的GTP酶激活蛋白(GAP)即ACAP3,可在体外调节神经元的形态发生。然而,ACAP3在体内大脑发育中的生理意义仍不清楚。在此,我们表明ACAP3参与小鼠发育中的大脑皮质的神经元迁移。在子宫内对小鼠发育中的皮质神经元敲低ACAP3,可显著消除皮质层中的神经元迁移,野生型ACAP3的异位表达可恢复这种迁移,但GAP失活突变体则不能。此外,在ACAP3敲低的皮质神经元中,皮质层神经元迁移过程中的形态变化受到阻碍。这些结果证明,ACAP3在大脑皮质发育过程中通过调节皮质神经元的形态变化,在其迁移中起关键作用。