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钙黏蛋白 7 和钙黏蛋白 6B 对颅神经轴突的生长、分支和导向具有不同的调控作用。

Cadherin-7 and cadherin-6B differentially regulate the growth, branching and guidance of cranial motor axons.

机构信息

MRC Centre for Developmental Neurobiology, 4th Floor New Hunt's House, Kings College, Guy's Campus, London SE1 1UL, UK.

出版信息

Development. 2010 Mar;137(5):805-14. doi: 10.1242/dev.042457.

Abstract

Cadherin-7 (Cad7) and cadherin-6B (Cad6B) are expressed in early and late phases of cranial motoneuron development, respectively. Cad7 is expressed by cranial motoneurons soon after they are generated, as well as in the environment through which their axons extend. By contrast, Cad6B is expressed by mature cranial motoneurons. We demonstrate in chick that these cadherins play distinct roles in cranial motor axon morphology, branching and projection. Using in vitro approaches, we show that Cad7 enhances motor axon outgrowth, suppresses the formation of multiple axons and restricts interstitial branching, thus promoting the development of a single unbranched axon characteristic of differentiating motoneurons. Conversely, Cad6B in vitro promotes motor axon branching, a characteristic of mature motoneurons. In vivo gain- and loss-of-function experiments for these cadherins yielded phenotypes consistent with this interpretation. In particular, a loss of cadherin-mediated interactions in vivo led to dysregulation of the cranial motoneuron normal branching programme and caused axon navigation defects. We also demonstrate that Cad6B functions via the phosphatidylinositol 3-kinase pathway. Together, these data show that Cad7 and Cad6B differentially regulate cranial motoneuron growth, branching and axon guidance.

摘要

钙黏蛋白-7(Cad7)和钙黏蛋白-6B(Cad6B)分别在颅运动神经元发育的早期和晚期表达。Cad7 在颅运动神经元生成后不久以及其轴突延伸的环境中表达。相比之下,Cad6B 在成熟的颅运动神经元中表达。我们在鸡中证明这些钙黏蛋白在颅运动轴突形态、分支和投射中发挥不同的作用。通过体外方法,我们表明 Cad7 增强运动轴突的生长,抑制多个轴突的形成并限制间质分支,从而促进分化运动神经元特有的单个无分支轴突的发育。相反,Cad6B 在体外促进运动轴突分支,这是成熟运动神经元的特征。这些钙黏蛋白的体内功能获得和功能丧失实验产生的表型与这一解释一致。特别是,体内钙黏蛋白介导的相互作用丧失导致颅运动神经元正常分支程序失调,并导致轴突导航缺陷。我们还证明 Cad6B 通过磷脂酰肌醇 3-激酶途径发挥作用。总之,这些数据表明 Cad7 和 Cad6B 差异调节颅运动神经元的生长、分支和轴突导向。

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