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首页> 外文期刊>Journal of neuroinflammation >Human oligodendroglial cells express low levels of C1 inhibitor and membrane cofactor protein mRNAs
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Human oligodendroglial cells express low levels of C1 inhibitor and membrane cofactor protein mRNAs

机译:人少突胶质细胞表达低水平的C1抑制剂和膜辅因子蛋白mRNA

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摘要

Background Oligodendrocytes, neurons, astrocytes, microglia, and endothelial cells are capable of synthesizing complement inhibitor proteins. Oligodendrocytes are vulnerable to complement attack, which is particularly observed in multiple sclerosis. This vulnerability may be related to a deficiency in their ability to express complement regulatory proteins. Methods This study compared the expression level of complement inhibitor mRNAs by human oligodendrocytes, astrocytes and microglia using semi-quantitative RT-PCR. Results Semi-quantitative RT-PCR analysis showed that C1 inhibitor (C1-inh) mRNA expression was dramatically lower in oligodendroglial cells compared with astrocytes and microglia. The mRNA expression level of membrane cofactor protein (MCP) by oligodendrocytes was also significantly lower than for other cell types. Conclusion The lower mRNA expression of C1-inh and MCP by oligodendrocytes could contribute to their vulnerability in several neurodegenerative and inflammatory diseases of the central nervous system.
机译:背景技术少突胶质细胞,神经元,星形胶质细胞,小胶质细胞和内皮细胞能够合成补体抑制剂蛋白。少突胶质细胞易受补体攻击,尤其是在多发性硬化症中。此漏洞可能与它们表达补体调节蛋白的能力不足有关。方法采用半定量RT-PCR方法比较人少突胶质细胞,星形胶质细胞和小胶质细胞补体抑制剂mRNA的表达水平。结果半定量RT-PCR分析显示,少突胶质细胞中C1抑制剂(C1-inh)的mRNA表达明显低于星形胶质细胞和小胶质细胞。少突胶质细胞的膜辅因子蛋白(MCP)的mRNA表达水平也明显低于其他细胞类型。结论少突胶质细胞C1-inh和MCP的mRNA表达较低可能是它们在多种中枢神经系统神经退行性和炎性疾病中的易感性。

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