氨基类固醇U73122促进少突胶质细胞的生成和髓鞘的形成。

IF 6.9 1区 医学 Q1 CHEMISTRY, MULTIDISCIPLINARY Acta Pharmacologica Sinica Pub Date : 2024-03-01 Epub Date: 2023-11-07 DOI:10.1038/s41401-023-01183-7
Shi-Hao Cui, Na Suo, Ying Yang, Xuan Wu, Shi-Meng Guo, Xin Xie
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引用次数: 0

摘要

少突胶质细胞(OLs)是包裹神经元轴突并在中枢神经系统(CNS)中形成髓鞘的神经胶质细胞。在发育和髓鞘修复过程中,OLs与少突胶质细胞前体细胞(OPCs)分化,而在多发性硬化症(MS)等脱髓鞘疾病的后一种情况下,这通常是不够的。据报道,许多因素调节OPC向OL的分化,包括许多G蛋白偶联受体(GPCR)。为了寻找GPCR下游可能参与OPC分化的途径,我们发现U73122,一种磷酸肌醇特异性磷脂酶C(PI-PLC)抑制剂,在实验性自身免疫性脑脊髓炎模型中显著促进OPC向OL的分化和髓鞘再生。出乎意料的是,缺乏PI-PLC抑制活性的U73122的紧密类似物U73343也促进了OL分化,而另一种报道的PI-PLC抑制剂依地福辛没有这种作用,这表明U73122和U73343独立于PLC增强OPC分化。尽管U73122和U73343的结构与17β-雌二醇非常相似,并且这两种化合物都激活雌激素受体Erα和Erβ,但疗效和效力都很低,但进一步的研究表明,这些化合物不通过Erα或Erβ促进OPC分化。RNA-Seq和生物信息学分析表明U73122和U73343可能调节胆固醇的生物合成。进一步的研究表明,在OPC培养中,这两种化合物都增加了14-脱氢酶原缩醇,这是一种据报道可以促进OPC分化的类固醇。总之,氨基类固醇U73122和U73343通过调节胆固醇生物合成途径促进OPC对OL的产生和髓鞘的形成。
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The aminosteroid U73122 promotes oligodendrocytes generation and myelin formation.

Oligodendrocytes (OLs) are glial cells that ensheath neuronal axons and form myelin in the central nervous system (CNS). OLs are differentiated from oligodendrocyte precursor cells (OPCs) during development and myelin repair, which is often insufficient in the latter case in demyelinating diseases such as multiple sclerosis (MS). Many factors have been reported to regulate OPC-to-OL differentiation, including a number of G protein-coupled receptors (GPCRs). In an effort to search pathways downstream of GPCRs that might be involved in OPC differentiation, we discover that U73122, a phosphoinositide specific phospholipase C (PI-PLC) inhibitor, dramatically promotes OPC-to-OL differentiation and myelin regeneration in experimental autoimmune encephalomyelitis model. Unexpectedly, U73343, a close analog of U73122 which lacks PI-PLC inhibitory activity also promotes OL differentiation, while another reported PI-PLC inhibitor edelfosine does not have such effect, suggesting that U73122 and U73343 enhance OPC differentiation independent of PLC. Although the structures of U73122 and U73343 closely resemble 17β-estradiol, and both compounds do activate estrogen receptors Erα and Erβ with low efficacy and potency, further study indicates that these compounds do not act through Erα and/or Erβ to promote OPC differentiation. RNA-Seq and bioinformatic analysis indicate that U73122 and U73343 may regulate cholesterol biosynthesis. Further study shows both compounds increase 14-dehydrozymostenol, a steroid reported to promote OPC differentiation, in OPC culture. In conclusion, the aminosteroids U73122 and U73343 promote OPC-to-OL generation and myelin formation by regulating cholesterol biosynthesis pathway.

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来源期刊
Acta Pharmacologica Sinica
Acta Pharmacologica Sinica 医学-化学综合
CiteScore
15.10
自引率
2.40%
发文量
4365
审稿时长
2 months
期刊介绍: APS (Acta Pharmacologica Sinica) welcomes submissions from diverse areas of pharmacology and the life sciences. While we encourage contributions across a broad spectrum, topics of particular interest include, but are not limited to: anticancer pharmacology, cardiovascular and pulmonary pharmacology, clinical pharmacology, drug discovery, gastrointestinal and hepatic pharmacology, genitourinary, renal, and endocrine pharmacology, immunopharmacology and inflammation, molecular and cellular pharmacology, neuropharmacology, pharmaceutics, and pharmacokinetics. Join us in sharing your research and insights in pharmacology and the life sciences.
期刊最新文献
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