Involvement of Notch1 inhibition in serum-stimulated glia and oligodendrocyte differentiation from human mesenchymal stem cells.

IF 1.7 Q4 CELL BIOLOGY
Stem Cells and Cloning-Advances and Applications Pub Date : 2010-11-23 eCollection Date: 2010-01-01 DOI:10.2147/SCCAA.S14388
Yi-Jang Lee, Shih-Chieh Hung, Mien-Sheng Chu
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引用次数: 1

Abstract

The use of in vitro oligodendrocyte differentiation for transplantation of stem cells to treat demyelinating diseases is an important consideration. In this study, we investigated the effects of serum on glia and oligodendrocyte differentiation from human mesenchymal stem cells (KP-hMSCs). We found that serum deprivation resulted in a reversible downregulation of glial- and oligodendrocyte-specific markers. Serum stimulated expression of oligodendrocyte markers, such as galactocerebroside, as well as Notch1 and JAK1 transcripts. Inhibition of Notch1 activation by the Notch inhibitor, MG132, led to enhanced expression of a serum-stimulated oligodendrocyte marker. This marker was undetectable in serum-deprived KP-hMSCs treated with MG132, suggesting that inhibition of Notch1 function is additive to serum-stimulated oligodendrocyte differentiation. Furthermore, a dominant-negative mutant RBP-J protein also inhibited Notch1 function and led to upregulation of oligodendrocyte-specific markers. Our results demonstrate that serum-stimulated oligodendrocyte differentiation is enhanced by the inhibition of Notch1-associated functions.

Abstract Image

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Abstract Image

Notch1抑制参与血清刺激的胶质细胞和少突胶质细胞从人间充质干细胞分化。
利用体外少突胶质细胞分化进行干细胞移植治疗脱髓鞘疾病是一个重要的考虑因素。在这项研究中,我们研究了血清对人间充质干细胞(KP-hMSCs)胶质细胞和少突胶质细胞分化的影响。我们发现血清剥夺导致胶质细胞和少突胶质细胞特异性标记物的可逆下调。血清刺激少突胶质细胞标记物的表达,如半乳糖脑苷,以及Notch1和JAK1转录物。Notch抑制剂MG132抑制Notch1的激活,导致血清刺激的少突胶质细胞标记物的表达增强。在MG132处理的血清缺失的KP-hMSCs中检测不到该标记物,这表明Notch1功能的抑制与血清刺激的少突胶质细胞分化有关。此外,显性阴性突变体RBP-J蛋白也抑制Notch1功能,导致少突胶质细胞特异性标记物上调。我们的研究结果表明,血清刺激的少突胶质细胞分化通过抑制notch1相关功能而增强。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
6.50
自引率
0.00%
发文量
10
审稿时长
16 weeks
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