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免疫相关蛋白Serpina3n对大脑发育和髓鞘形成的非必需调节

Dispensable regulation of brain development and myelination by the immune-related protein Serpina3n.

作者信息

Zhu Meina, Wang Yan, Park Joohyun, Titus Annlin, Guo Fuzheng

机构信息

Department of Neurology, School of Medicine, UC Davis; Institute for Pediatric Regenerative Medicine (IPRM), Shriners Hospitals for Children, Sacramento, CA.

出版信息

bioRxiv. 2024 Sep 5:2024.02.06.579239. doi: 10.1101/2024.02.06.579239.

Abstract

Serine protease inhibitor clade A member 3n (Serpina3n) or its human orthologue SERPINA3 is a secretory immune-related molecule produced primarily in the liver and brain under homeostatic conditions and upregulated in response to system inflammation. Yet it remains elusive regarding its cellular identity and physiological significance in the development of the postnatal brain. Here, we reported that oligodendroglial lineage cells are the major cell population expressing Serpina3n protein in the postnatal murine CNS. Using loss-of-function genetic tools, we found that Serpina3n conditional knockout (cKO) from Olig2-expressing cells does not significantly affect cognitive and motor functions in mice. Serpina3n depletion does not appear to interfere with oligodendrocyte differentiation and developmental myelination nor affects the population of other glial cells and neurons . Together, these data suggest that the immune-related molecule Serpina3n plays a minor role, if any, in regulating neural cell development in the postnatal brain under homeostatic conditions. We found that Serpina3n is significantly upregulated in response to oxidative stress, and it potentiates oxidative injury and cell senescence of oligodendrocytes. Our data raise the interest in pursuing its functional significance in the CNS under disease/injury conditions.

摘要

丝氨酸蛋白酶抑制剂A家族成员3n(Serpina3n)或其人类同源物SERPINA3是一种分泌型免疫相关分子,在稳态条件下主要在肝脏和大脑中产生,并在系统炎症反应时上调。然而,其在出生后脑发育中的细胞身份和生理意义仍不清楚。在这里,我们报告少突胶质细胞谱系细胞是出生后小鼠中枢神经系统中表达Serpina3n蛋白的主要细胞群体。使用功能丧失的遗传工具,我们发现从表达Olig2的细胞中条件性敲除(cKO)Serpina3n不会显著影响小鼠的认知和运动功能。Serpina3n的缺失似乎不会干扰少突胶质细胞的分化和发育性髓鞘形成,也不会影响其他神经胶质细胞和神经元的数量。总之,这些数据表明,在稳态条件下,免疫相关分子Serpina3n在调节出生后脑的神经细胞发育中作用甚微(如果有作用的话)。我们发现Serpina3n在氧化应激反应中显著上调,并且它会增强少突胶质细胞的氧化损伤和细胞衰老。我们的数据引发了人们对其在疾病/损伤条件下中枢神经系统中的功能意义的兴趣。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f5a9/11422934/f741b74a0b88/nihpp-2024.02.06.579239v2-f0001.jpg

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