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黄芪多糖通过诱导少突胶质细胞从脱髓鞘模型中的神经干细胞分化来增强髓鞘再生。

Remyelination is enhanced by Astragalus polysaccharides through inducing the differentiation of oligodendrocytes from neural stem cells in cuprizone model of demyelination.

机构信息

Institute of Clinical Immunology, Yue-Yang Hospital of Integrative Medicine, Shanghai University of Traditional Chinese Medicine, Shanghai 200437, PR China.

Institute of Clinical Immunology, Yue-Yang Hospital of Integrative Medicine, Shanghai University of Traditional Chinese Medicine, Shanghai 200437, PR China; Doctoral Program of Acupuncture & Oriental Medicine, The Atlantic Institute of Oriental Medicine, FL 33301, USA.

出版信息

Brain Res. 2021 Jul 15;1763:147459. doi: 10.1016/j.brainres.2021.147459. Epub 2021 Mar 30.

Abstract

Demyelination is the hallmark of multiple sclerosis (MS). Promoting remyelination is an important strategy to treat MS. Our previous study showed that Astragalus polysaccharides (APS), the main bioactive component of Astragalus membranaceus, could prevent demyelination in experimental autoimmune encephalomyelitis mice. To investigate the effects of APS on remyelination and the underlying mechanisms, in this study we set up a cuprizone-induced demyelination model in mice and treated them with APS. It was found that APS relieved the neurobehavioral dysfunctions caused by demyelination, and efficaciously facilitated remyelination in vivo. In order to determine whether the mechanism of enhancing remyelination was associated with the differentiation of neural stem cells (NSCs), biomarkers of NSCs, astrocytes, oligodendrocytes and neurons were measured in the corpus callosum tissues of mice through Real-time PCR, Western blot and immunohistochemistry assays. Data revealed that APS suppressed the stemness of NSCs, reduced the differentiation of NSCs into astrocytes, and promoted the differentiation into oligodendrocytes and neurons. This phenomenon was confirmed in the differentiation model of C17.2 NSCs cultured in vitro. Since Sonic hedgehog signaling pathway has been proven to be crucial to the differentiation of NSCs into oligodendrocytes, we examined expression levels of the key molecules in this pathway in vivo and in vitro, and eventually found APS activated this signaling pathway. Together, our results demonstrated that APS probably activated Sonic hedgehog signaling pathway first, then induced NSCs to differentiate into oligodendrocytes and promoted remyelination, which suggested that APS might be a potential candidate in treating MS.

摘要

脱髓鞘是多发性硬化症(MS)的标志。促进髓鞘再生是治疗 MS 的重要策略。我们之前的研究表明,黄芪多糖(APS)是黄芪的主要生物活性成分,可预防实验性自身免疫性脑脊髓炎小鼠的脱髓鞘。为了研究 APS 对髓鞘再生的影响及其潜在机制,本研究在小鼠中建立了铜诱导的脱髓鞘模型,并给予 APS 治疗。结果发现,APS 缓解了脱髓鞘引起的神经行为功能障碍,并有效地促进了体内髓鞘再生。为了确定增强髓鞘再生的机制是否与神经干细胞(NSCs)的分化有关,通过实时 PCR、Western blot 和免疫组织化学检测,测量了小鼠胼胝体组织中的 NSCs、星形胶质细胞、少突胶质细胞和神经元的生物标志物。数据显示,APS 抑制了 NSCs 的干性,减少了 NSCs 向星形胶质细胞的分化,并促进了向少突胶质细胞和神经元的分化。这一现象在体外培养的 C17.2 NSCs 分化模型中得到了证实。由于 Sonic hedgehog 信号通路已被证明对 NSCs 分化为少突胶质细胞至关重要,我们在体内和体外检查了该通路中的关键分子的表达水平,最终发现 APS 激活了该信号通路。总之,我们的结果表明,APS 可能首先激活 Sonic hedgehog 信号通路,然后诱导 NSCs 分化为少突胶质细胞并促进髓鞘再生,这表明 APS 可能是治疗 MS 的潜在候选药物。

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