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补体系统在发育和疾病中的神经突触消除作用。

Complement System in Neural Synapse Elimination in Development and Disease.

机构信息

Program in Cellular and Molecular Medicine, Boston Children's Hospital, Boston, MA, United States.

Program in Cellular and Molecular Medicine, Boston Children's Hospital, Boston, MA, United States.

出版信息

Adv Immunol. 2017;135:53-79. doi: 10.1016/bs.ai.2017.06.004. Epub 2017 Jul 31.

Abstract

Recent discoveries implicate the classical complement cascade in normal brain development and in disease. Complement proteins C1q, C3, and C4 participate in synapse elimination, tagging inappropriate synaptic connections between neurons for removal by phagocytic microglia that exist in a special, highly phagocytic state during the synaptic pruning period. Several neurodevelopmental disorders, such as schizophrenia and autism, are thought to be caused by an imbalance in synaptic pruning, and recent studies suggest that dysregulation of complement could promote this synaptic pruning imbalance. Moreover, in the mature brain, complement can be aberrantly activated in early stages of neurodegenerative diseases to stimulate synapse loss. Similar pathways can also be activated in response to inflammation, as in West Nile Virus infection or in lupus, where peripheral inflammation can promote microglia-mediated synapse loss. Whether synapse loss in disease is a true reactivation of developmental synaptic pruning programs remains unclear; nonetheless, complement proteins represent potential therapeutic targets for both neurodevelopmental and neurodegenerative diseases.

摘要

最近的发现表明经典补体级联反应在正常大脑发育和疾病中发挥作用。补体蛋白 C1q、C3 和 C4 参与突触消除,标记神经元之间不合适的突触连接,以便由吞噬小胶质细胞清除,吞噬小胶质细胞在突触修剪期处于特殊的、高度吞噬状态。几种神经发育障碍,如精神分裂症和自闭症,被认为是由突触修剪失衡引起的,最近的研究表明,补体失调可能会促进这种突触修剪失衡。此外,在成熟的大脑中,补体在神经退行性疾病的早期阶段可能会异常激活,从而刺激突触丧失。类似的途径也可以在炎症反应中被激活,如西尼罗河病毒感染或狼疮中,外周炎症可以促进小胶质细胞介导的突触丧失。在疾病中,突触丧失是否是发育性突触修剪程序的真正再激活仍不清楚;尽管如此,补体蛋白代表了神经发育和神经退行性疾病的潜在治疗靶点。

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