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脑源性神经营养因子在中枢髓鞘形成中的三十年研究:从生物学到治疗

Thirty years of BDNF study in central myelination: From biology to therapy.

作者信息

Xiao Junhua

机构信息

School of Health Sciences, Swinburne University of Technology, Hawthorn, Victoria, Australia.

School of Allied Health, La Trobe University, Bundoora, Victoria, Australia.

出版信息

J Neurochem. 2023 Nov;167(3):321-336. doi: 10.1111/jnc.15968. Epub 2023 Sep 25.

DOI:10.1111/jnc.15968
PMID:37747083
Abstract

Being the highest expressed neurotrophin in the mammalian brain, the brain-derived neurotrophic factor (BDNF) is essential to neural development and plasticity in both health and diseases. Following the discovery of BDNF by Yves-Alain Barde in 1982, the main feature of BDNF's activity in myelination was first described by Cellerino et al. in 1997. Since then, genetic manipulation of the BDNF-encoding gene and its receptors in murine models has revealed the contribution of BDNF to the myelinating process in the central nervous system (CNS). The series of BDNF or receptor mouse mutants as well as the BDNF polymorphism in humans have provided new insights into the roles that BDNF signaling plays in myelination in a complex manner. 2024 marks the 30th year of BDNF's research in myelination. Here, we share our perspective on the 30-year history of BDNF in the field of CNS myelination from phenotyping to therapeutic development, focusing on genetic evidence regarding the mechanism by which BDNF regulates myelin formation and repair in the CNS. This review also discusses the current hypotheses of BDNF's action on CNS myelination: axonal- and oligodendroglial-driven mechanisms, which may be ultimately activity-dependent. Last, this review raises the challenges and opportunities of developing BDNF-based therapies for neurodegenerative diseases, opening unanswered questions for future investigation.

摘要

脑源性神经营养因子(BDNF)是哺乳动物大脑中表达量最高的神经营养因子,对健康和疾病状态下的神经发育及可塑性至关重要。1982年伊夫 - 阿兰·巴德发现BDNF后,1997年塞莱里诺等人首次描述了BDNF在髓鞘形成中的主要活性特征。从那时起,在小鼠模型中对BDNF编码基因及其受体进行基因操作,揭示了BDNF对中枢神经系统(CNS)髓鞘形成过程的作用。一系列BDNF或受体小鼠突变体以及人类中的BDNF多态性,为BDNF信号以复杂方式在髓鞘形成中所起的作用提供了新的见解。2024年是BDNF在髓鞘形成研究的第30年。在此,我们分享对BDNF在CNS髓鞘形成领域30年历史的看法,从表型分析到治疗开发,重点关注BDNF调节CNS髓鞘形成和修复机制的遗传学证据。本综述还讨论了BDNF对CNS髓鞘形成作用的当前假说:轴突驱动和少突胶质细胞驱动机制,这可能最终依赖于活性。最后,本综述提出了开发基于BDNF的神经退行性疾病疗法的挑战和机遇,为未来研究留下了未解决的问题。

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