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EphA4 在体内维持出生后和成年神经干细胞的未分化状态。

EphA4 preserves postnatal and adult neural stem cells in an undifferentiated state in vivo.

机构信息

Department of Clinical Neurobiology, Heidelberg University Medical Center, 69120 Heidelberg, Germany.

出版信息

J Cell Sci. 2011 Apr 15;124(Pt 8):1268-79. doi: 10.1242/jcs.076059.

Abstract

In the postnatal brain, new neurons continue to be generated in two neurogenic areas, the subventricular zone of the lateral ventricles (SVZ) and the subgranular zone of the hippocampus. There is evidence that ephrins and their Eph receptors belong to a signaling network that regulates neurogenesis. On the basis of previous data, we have identified Eph receptor A4 (EphA4) as a potential regulator of neurogenesis. We showed by immunohistochemistry that in adult neurogenic niches EphA4 is expressed only by neural stem cells (NSCs). Using in vitro and in vivo assays, we demonstrated that EphA4 expression maintains NSCs in an undifferentiated state. Specifically, in neurosphere cultures Epha4 knockdown resulted in a decrease of NSC proliferation and premature differentiation. In postnatal and adult brain, Epha4 knockdown caused a decrease in NSCs in the SVZ, eventually resulting in a reduced number of postnatally generated neuroblasts. Both in vitro and in vivo effects were rescued by co-infection with a modified EphA4 that was resistant to Epha4 shRNA.

摘要

在出生后的大脑中,新的神经元继续在两个神经发生区域中产生,即侧脑室的室下区(SVZ)和海马的颗粒下区。有证据表明,ephrin 及其 Eph 受体属于调节神经发生的信号网络。基于先前的数据,我们确定 Eph 受体 A4(EphA4)是神经发生的潜在调节剂。我们通过免疫组织化学染色表明,在成年神经发生龛中 EphA4 仅由神经干细胞(NSCs)表达。通过体外和体内实验,我们证明 EphA4 表达使 NSCs 保持未分化状态。具体而言,在神经球培养物中,Epha4 敲低导致 NSC 增殖减少和过早分化。在出生后和成年大脑中,Epha4 敲低导致 SVZ 中的 NSCs 减少,最终导致出生后产生的神经母细胞数量减少。体外和体内的作用都可以通过共感染具有抗 EphA4 shRNA 抗性的修饰 EphA4 来挽救。

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