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cTAGE5/MEA6 在神经元细胞成分运输和大脑发育中起着关键作用。

cTAGE5/MEA6 plays a critical role in neuronal cellular components trafficking and brain development.

机构信息

State Key Laboratory of Molecular Developmental Biology, Chinese Academy of Sciences Center for Excellence in Brain Science and Intelligence Technology, Institute of Genetics and Developmental Biology, Chinese Academy of Sciences, 100101 Beijing, China.

University of Chinese Academy of Sciences, 100101 Beijing, China.

出版信息

Proc Natl Acad Sci U S A. 2018 Oct 2;115(40):E9449-E9458. doi: 10.1073/pnas.1804083115. Epub 2018 Sep 17.

Abstract

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 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.

摘要

正常的神经发育对于神经元网络的形成和大脑功能至关重要。皮肤 T 细胞淋巴瘤相关抗原 5(cTAGE5)/脑膜瘤表达抗原 6(MEA6)在蛋白质分泌中发挥着关键作用。然而,其在非分泌细胞成分的运输以及在大脑发育中的作用尚不清楚。在这里,我们展示了 cTAGE5/MEA6 对于大脑发育和功能的重要性。在大脑中条件性敲除 会导致神经发育严重缺陷,包括树突生长和分支、棘突形成和维持、星形胶质细胞激活以及异常行为缺陷。我们揭示了 cTAGE5/MEA6 的缺失会影响 COPII 成分 SAR1 和 SEC23 之间的相互作用,导致 SAR1 的持续激活和 COPII 囊泡从内质网到高尔基体形成和运输的缺陷,以及神经元中膜成分的运输紊乱。这些缺陷不仅影响树突和棘突发育所需物质的运输,还影响神经元发育所需的信号通路。由于在 Fahr 病患者中发现了 cTAGE5/MEA6 的突变,我们的研究也为该疾病的发病机制提供了潜在的见解。

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