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Regulation of Chandelier Cell Cartridge and Bouton Development via DOCK7-Mediated ErbB4 Activation

机译:通过DOCK7介导的ErbB4激活调节枝形吊灯细胞和Bouton发育

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摘要

Chandelier cells (ChCs), typified by their unique axonal morphology, are the most distinct interneurons present in cortical circuits. Via their distinctive axonal terminals, called cartridges, these cells selectively target the axon initial segment of pyramidal cells and control action potential initiation; however, the mechanisms that govern the characteristic ChC axonal structure have remained elusive. Here, by employing an in utero electroporation-based method that enables genetic labeling and manipulation of ChCs in vivo, we identify DOCK7, a member of the DOCK180 family, as a molecule essential for ChC cartridge and bouton development. Furthermore, we present evidence that DOCK7 functions as a cytoplasmic activator of the schizophrenia-associated ErbB4 receptor tyrosine kinase and that DOCK7 modulates ErbB4 activity to control ChC cartridge and bouton development. Thus, our findings define DOCK7 and ErbB4 as key components of a pathway that controls the morphological differentiation of ChCs, with implications for the pathogenesis of schizophrenia.
机译:以其独特的轴突形态为代表的枝形吊灯细胞(ChCs)是存在于皮质回路中的最独特的中间神经元。这些细胞通过其独特的轴突末端(称为子弹头),选择性地靶向锥体细胞的轴突起始节段并控制动作电位的启动。然而,控制特征性ChC轴突结构的机制仍然难以捉摸。在这里,通过采用基于子宫内电穿孔的方法,可以对体内ChCs进行基因标记和操作,我们将DOCK180家族的一个成员DOCK7鉴定为ChC药筒和胸腺发育必不可少的分子。此外,我们目前提供证据,DOCK7充当精神分裂症相关的ErbB4受体酪氨酸激酶的胞质激活剂,DOCK7调节ErbB4活性以控制ChC弹药筒和胸腺发育。因此,我们的发现将DOCK7和ErbB4定义为控制ChCs形态分化的途径的关键组成部分,对精神分裂症的发病机制有影响。

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