KU Leuven, Center for Human Genetics and Leuven Institute for Neurodegenerative Diseases, 3000 Leuven, Belgium.
J Cell Sci. 2013 Mar 1;126(Pt 5):1268-77. doi: 10.1242/jcs.122440. Epub 2013 Jan 23.
Expression of amyloid precursor protein (APP) and its two paralogues, APLP1 and APLP2 during brain development coincides with key cellular events such as neuronal differentiation and migration. However, genetic knockout and shRNA studies have led to contradictory conclusions about their role during embryonic brain development. To address this issue, we analysed in depth the role of APLP2 during neurogenesis by silencing APLP2 in vivo in an APP/APLP1 double knockout mouse background. We find that under these conditions cortical progenitors remain in their undifferentiated state much longer, displaying a higher number of mitotic cells. In addition, we show that neuron-specific APLP2 downregulation does not impact the speed or position of migrating excitatory cortical neurons. In summary, our data reveal that APLP2 is specifically required for proper cell cycle exit of neuronal progenitors, and thus has a distinct role in priming cortical progenitors for neuronal differentiation.
淀粉样前体蛋白(APP)及其两个旁系同源物 APLP1 和 APLP2 在大脑发育过程中的表达与关键的细胞事件(如神经元分化和迁移)相吻合。然而,基因敲除和 shRNA 研究对它们在胚胎大脑发育过程中的作用得出了相互矛盾的结论。为了解决这个问题,我们在 APP/APLP1 双敲除小鼠背景下,通过体内沉默 APLP2 对 APLP2 在神经发生过程中的作用进行了深入分析。我们发现,在这些条件下,皮质祖细胞保持未分化状态的时间更长,有丝分裂细胞的数量更多。此外,我们还表明,神经元特异性的 APLP2 下调并不影响兴奋性皮质神经元的迁移速度或位置。总之,我们的数据表明,APLP2 是皮质祖细胞正常细胞周期退出所必需的,因此在启动皮质祖细胞向神经元分化方面具有独特的作用。