Dugani Chandrasagar B, Paquin Annie, Fujitani Masashi, Kaplan David R, Miller Freda D
Developmental and Stem Cell Biology Program, Hospital for Sick Children, Toronto, Ontario M5G 1L7, Canada.
J Neurosci. 2009 May 20;29(20):6710-21. doi: 10.1523/JNEUROSCI.5878-08.2009.
The molecular mechanisms that regulate survival of embryonic neural precursors are still relatively ill-defined. Here, we have asked whether the p53 family member p63 plays any role during this developmental window, focusing on the embryonic cerebral cortex. We show that genetic knockdown of p63 either in culture or in the embryonic telencephalon causes apoptosis of cortical precursors and newly born cortical neurons, and that this can be rescued by expression of DeltaNp63, but not TAp63 isoforms. This cortical precursor apoptosis is the consequence of deregulated p53 activity, since both basal precursor apoptosis and that induced by loss of p63 are rescued by coincident genetic silencing of p53. Finally, we demonstrate that the third p53 family member, DeltaNp73, does not regulate survival of cortical precursor cells, but that it collaborates with DeltaNp63 to ensure the survival of newly born cortical neurons. Thus, the balance of DeltaNp63 versus p53 determines the life versus death of embryonic cortical precursors, a role that these p53 family members may well play in other populations of developing and/or adult neural precursors.
调节胚胎神经前体细胞存活的分子机制仍相对不明确。在此,我们探讨了p53家族成员p63在这个发育阶段是否发挥作用,重点研究胚胎大脑皮层。我们发现,无论是在培养环境中还是在胚胎端脑中,p63基因敲低都会导致皮层前体细胞和新生皮层神经元凋亡,而这种凋亡可通过DeltaNp63的表达来挽救,但TAp63亚型则不能。这种皮层前体细胞凋亡是p53活性失调的结果,因为基础前体细胞凋亡以及由p63缺失诱导的凋亡都可通过同时对p53进行基因沉默来挽救。最后,我们证明第三个p53家族成员DeltaNp73并不调节皮层前体细胞的存活,但它与DeltaNp63协同作用以确保新生皮层神经元的存活。因此,DeltaNp63与p53之间的平衡决定了胚胎皮层前体细胞的生死,这些p53家族成员在其他发育中和/或成体神经前体细胞群体中可能也发挥着类似作用。