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失活蛋白磷酸酶 2A 会破坏端脑神经脊龛中放射状胶质祖细胞的保留,从而损害皮质发育过程中晚期产生的神经元。

Loss of PP2A Disrupts the Retention of Radial Glial Progenitors in the Telencephalic Niche to Impair the Generation for Late-Born Neurons During Cortical Development†.

机构信息

State Key Laboratory of Pharmaceutical Biotechnology, MOE Key Laboratory of Model Animal for Disease Study, Model Animal Research Center, Institute for Brain Sciences, Nanjing University, Nanjing 210061, China.

Department of Anesthesiology, The Second Affiliated Changzhou People's Hospital of Nanjing Medical University, Changzhou 213000, China.

出版信息

Cereb Cortex. 2020 Jun 1;30(7):4183-4196. doi: 10.1093/cercor/bhaa042.

Abstract

Telencephalic radial glial progenitors (RGPs) are retained in the ventricular zone (VZ), the niche for neural stem cells during cortical development. However, the underlying mechanism is not well understood. To study whether protein phosphatase 2A (PP2A) may regulate the above process, we generate Ppp2cα conditional knockout (cKO) mice, in which PP2A catalytic subunit α (PP2Acα) is inactivated in neural progenitor cells in the dorsal telencephalon. We show that RGPs are ectopically distributed in cortical areas outside of the VZ in Ppp2cα cKO embryos. Whereas deletion of PP2Acα does not affect the proliferation of RGPs, it significantly impairs the generation of late-born neurons. We find complete loss of apical adherens junctions (AJs) in the ventricular membrane in Ppp2cα cKO cortices. We observe abundant colocalization for N-cadherin and PP2Acα in control AJs. Moreover, in vitro analysis reveals direct interactions of N-cadherin to PP2Acα and to β-catenin. Overall, this study not only uncovers a novel function of PP2Acα in retaining RGPs into the VZ but also demonstrates the impact of PP2A-dependent retention of RGPs on the generation for late-born neurons.

摘要

端脑放射状胶质祖细胞(RGPs)在皮质发育过程中保留在脑室区(VZ),即神经干细胞的龛位。然而,其潜在机制尚不清楚。为了研究蛋白磷酸酶 2A(PP2A)是否可能调节上述过程,我们生成了 Ppp2cα 条件性敲除(cKO)小鼠,其中 PP2A 催化亚基α(PP2Acα)在背侧端脑中的神经祖细胞中失活。我们发现,在 Ppp2cα cKO 胚胎中,RGPs 异位分布在 VZ 以外的皮质区域。虽然 PP2Acα 的缺失不影响 RGPs 的增殖,但它显著损害了晚期神经元的生成。我们发现 Ppp2cα cKO 皮质中的脑室膜上完全丧失了顶端黏附连接(AJs)。我们观察到在对照 AJs 中,N-钙黏蛋白和 PP2Acα 大量共定位。此外,体外分析显示 N-钙黏蛋白与 PP2Acα 和β-连环蛋白之间存在直接相互作用。总的来说,这项研究不仅揭示了 PP2Acα 在将 RGPs 保留在 VZ 中的新功能,还证明了 PP2A 依赖性 RGPs 保留对晚期神经元生成的影响。

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