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异常神经节苷脂功能以支持失调的髓鞘形成、胰岛素信号和细胞因子表达:是否存在联系和治疗空间?

Aberrant Ganglioside Functions to Underpin Dysregulated Myelination, Insulin Signalling, and Cytokine Expression: Is There a Link and a Room for Therapy?

机构信息

Neuroplast BV, 6222 NK Maastricht, The Netherlands.

Laboratory of Psychiatric Neurobiology, Institute of Molecular Medicine and Department of Normal Physiology, Sechenov First Moscow State Medical University, 119048 Moscow, Russia.

出版信息

Biomolecules. 2022 Oct 7;12(10):1434. doi: 10.3390/biom12101434.

DOI:10.3390/biom12101434
PMID:36291644
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9599472/
Abstract

Gangliosides are molecules widely present in the plasma membranes of mammalian cells, participating in a variety of processes, including protein organization, transmembrane signalling and cell adhesion. Gangliosides are abundant in the grey matter of the brain, where they are critically involved in postnatal neural development and function. The common precursor of the majority of brain gangliosides, GM3, is formed by the sialylation of lactosylceramide, and four derivatives of its a- and b-series, GM1, GD1a, GD1b and GT1b, constitute 95% of all the brain gangliosides. Impairments in ganglioside metabolism due to genetic abnormalities of GM-synthases are associated with severe neurological disorders. Apart from that, the latest genome-wide association and translational studies suggest a role of genes involved in brain ganglioside synthesis in less pervasive psychiatric disorders. Remarkably, the most recent animal studies showed that abnormal ganglioside functions result in dysregulated neuroinflammation, aberrant myelination and altered insulin receptor signalling. At the same time, these molecular features are well established as accompanying developmental psychiatric disorders such as attention-deficit hyperactivity disorder (ADHD) and autism spectrum disorders (ASD). This led us to hypothesize a role of deficient ganglioside function in developmental neuropsychiatric disorders and warrants further gene association clinical studies addressing this question. Here, we critically review the literature to discuss this hypothesis and focus on the recent studies on ST3GAL5-deficient mice. In addition, we elaborate on the therapeutic potential of various anti-inflammatory remedies for treatment of developmental neuropsychiatric conditions related to aberrant ganglioside functions.

摘要

神经节苷脂广泛存在于哺乳动物细胞膜的血浆中,参与多种过程,包括蛋白质组织、跨膜信号传递和细胞黏附。神经节苷脂在大脑灰质中含量丰富,在出生后神经发育和功能中起着关键作用。大多数脑神经节苷脂的常见前体 GM3 是由乳糖基神经酰胺的唾液酸化形成的,其 a 系列和 b 系列的四个衍生物 GM1、GD1a、GD1b 和 GT1b,构成了所有脑神经节苷脂的 95%。GM-合酶遗传异常导致神经节苷脂代谢受损与严重神经障碍有关。除此之外,最新的全基因组关联和转化研究表明,参与脑神经节苷脂合成的基因在不那么普遍的精神疾病中发挥作用。值得注意的是,最近的动物研究表明,异常的神经节苷脂功能导致神经炎症失调、髓鞘异常和胰岛素受体信号改变。与此同时,这些分子特征已被确立为伴随发育性精神疾病,如注意缺陷多动障碍(ADHD)和自闭症谱系障碍(ASD)的特征。这使我们假设神经节苷脂功能缺陷在发育性神经精神疾病中的作用,并需要进一步进行基因关联的临床研究来解决这个问题。在这里,我们批判性地回顾了文献,讨论了这一假设,并重点介绍了最近关于 ST3GAL5 缺陷型小鼠的研究。此外,我们详细阐述了各种抗炎疗法在治疗与异常神经节苷脂功能相关的发育性神经精神疾病方面的治疗潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2810/9599472/61a6a810dff5/biomolecules-12-01434-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2810/9599472/2b2e90bcee6d/biomolecules-12-01434-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2810/9599472/61a6a810dff5/biomolecules-12-01434-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2810/9599472/2b2e90bcee6d/biomolecules-12-01434-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2810/9599472/61a6a810dff5/biomolecules-12-01434-g002.jpg

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