首页> 美国卫生研究院文献>Proceedings of the National Academy of Sciences of the United States of America >PNAS Plus: cTAGE5/MEA6 plays a critical role in neuronal cellular components trafficking and brain development
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PNAS Plus: cTAGE5/MEA6 plays a critical role in neuronal cellular components trafficking and brain development

机译:PNAS Plus:cTAGE5 / MEA6在神经元细胞成分运输和大脑发育中起关键作用

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摘要

Normal neural development is essential for the formation of neuronal networks and brain function. Cutaneous T cell lymphoma-associated antigen 5 (cTAGE5)/meningioma expressed antigen 6 (MEA6) plays a critical role in the secretion of proteins. However, its roles in the transport of nonsecretory cellular components and in brain development remain unknown. Here, we show that cTAGE5/MEA6 is important for brain development and function. Conditional knockout of cTAGE5/MEA6 in the brain leads to severe defects in neural development, including deficits in dendrite outgrowth and branching, spine formation and maintenance, astrocyte activation, and abnormal behaviors. We reveal that loss of cTAGE5/MEA6 affects the interaction between the coat protein complex II (COPII) components, SAR1 and SEC23, leading to persistent activation of SAR1 and defects in COPII vesicle formation and transport from the endoplasmic reticulum to the Golgi, as well as disturbed trafficking of membrane components in neurons. These defects affect not only the transport of materials required for the development of dendrites and spines but also the signaling pathways required for neuronal development. Because mutations in cTAGE5/MEA6 have been found in patients with Fahr’s disease, our study potentially also provides insight into the pathogenesis of this disorder.
机译:正常的神经发育对于神经网络和大脑功能的形成至关重要。皮肤T细胞淋巴瘤相关抗原5(cTAGE5)/脑膜瘤表达抗原6(MEA6)在蛋白质分泌中起关键作用。然而,其在非分泌性细胞成分的运输和大脑发育中的作用仍然未知。在这里,我们表明cTAGE5 / MEA6对大脑发育和功能很重要。大脑中cTAGE5 / MEA6的条件性敲除会导致神经发育的严重缺陷,包括树突生长和分支,脊柱形成和维持,星形胶质细胞活化以及异常行为的缺陷。我们发现,cTAGE5 / MEA6的缺失会影响外壳蛋白复合物II(COPII)组件SAR1和SEC23之间的相互作用,从而导致SAR1的持续活化以及COPII囊泡形成和从内质网向高尔基体运输的缺陷。作为神经元中膜成分的不正常运输。这些缺陷不仅影响树突和棘发育所需的物质运输,而且影响神经元发育所需的信号传导途径。由于已经在Fahr病患者中发现了cTAGE5 / MEA6的突变,因此我们的研究还可能提供对该疾病发病机理的深入了解。

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