Programs in Cell Biology, Developmental and Stem Cell Biology, and Neurosciences and Mental Health, Hospital for Sick Children, Toronto, Ontario M5G 1X8, Canada.
J Neurosci. 2013 Jul 31;33(31):12569-85. doi: 10.1523/JNEUROSCI.1251-13.2013.
The molecular mechanisms that regulate adult neural precursor cell (NPC) survival, and thus maintain adult neurogenesis, are not well defined. Here, we investigate the role of p63, a p53 family member, in adult NPC function in mice. Conditional ablation of p63 in adult NPCs or p63 haploinsufficiency led to reduced numbers of NPCs and newborn neurons in the neurogenic zones of the hippocampus and lateral ventricles and in the olfactory bulb. These reductions were attributable to enhanced apoptosis of NPCs and newborn neurons and were rescued by inhibition of caspase activity, p53, or the p53 apoptotic effector PUMA (p53-upregulated modulator of apoptosis). Moreover, these cellular deficits were functionally important because they led to perturbations in hippocampus-dependent memory formation. These results indicate that p63 regulates the numbers of adult NPCs and adult-born neurons as well as neural stem cell-dependent cognitive functions, and that it does so, at least in part, by inhibiting p53-dependent cell death.
调节成人神经前体细胞 (NPC) 存活的分子机制,从而维持成人神经发生,尚未完全明确。在这里,我们研究了 p63(p53 家族成员之一)在小鼠成年 NPC 功能中的作用。条件性敲除成年 NPC 中的 p63 或 p63 杂合不足导致海马和侧脑室神经发生区以及嗅球中的 NPC 和新生神经元数量减少。这些减少归因于 NPC 和新生神经元的凋亡增加,并且通过抑制半胱天冬酶活性、p53 或 p53 凋亡效应物 PUMA(p53 上调凋亡调节剂)得到挽救。此外,这些细胞缺陷具有功能重要性,因为它们导致海马依赖性记忆形成的扰动。这些结果表明,p63 调节成年 NPC 和成年神经元的数量以及神经干细胞依赖性认知功能,并且它至少部分通过抑制 p53 依赖性细胞死亡来实现这一点。