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衰变加速因子(CD55)表达上调赋予新生神经细胞更强的补体抗性。

Up-regulated expression of decay-accelerating factor (CD55) confers increased complement resistance to sprouting neural cells.

作者信息

Zhang K Z, Junnikkala S, Erlander M G, Guo H, Westberg J A, Meri S, Andersson L C

机构信息

Department of Pathology, Haartman Institute, University of Helsinki, Finland.

出版信息

Eur J Immunol. 1998 Apr;28(4):1189-96. doi: 10.1002/(SICI)1521-4141(199804)28:04<1189::AID-IMMU1189>3.0.CO;2-D.

DOI:10.1002/(SICI)1521-4141(199804)28:04<1189::AID-IMMU1189>3.0.CO;2-D
PMID:9565358
Abstract

We studied gene expression in relation to induced neural differentiation in a human neural crest-derived cell line, Paju. Messenger RNA isolated before and after treatment with phorbol 12-myristate 13-acetate was analyzed by differential display reverse transcription PCR. A strongly up-regulated expression of decay-accelerating factor (DAF, CD55) was found to parallel the induced neural sprouting while the expression of two other complement regulatory proteins (CD59/protectin, CD46/membrane cofactor protein) remained unaltered during neural differentiation. The increased membrane expression of DAF, which was also seen on neural processes and growth cones, conferred elevated resistance to complement-mediated lysis. Our findings suggest that in sprouting neurons DAF expression is up-regulated to provide additional complement resistance to pathfinding axons/dendrites invading new environment. It is also suggested that membrane expression of DAF may constitute a marker of growing and regenerating neurons.

摘要

我们研究了人神经嵴衍生细胞系Paju中与诱导神经分化相关的基因表达。用佛波酯12 - 肉豆蔻酸酯13 - 乙酸酯处理前后分离的信使核糖核酸通过差异显示逆转录聚合酶链反应进行分析。发现衰变加速因子(DAF,CD55)的强烈上调表达与诱导的神经芽生平行,而另外两种补体调节蛋白(CD59 /保护素,CD46 /膜辅因子蛋白)的表达在神经分化过程中保持不变。DAF在膜上的表达增加,这在神经突起和生长锥上也可见,赋予了对补体介导的溶解的更高抗性。我们的研究结果表明,在发芽神经元中,DAF表达上调,为侵入新环境的寻路轴突/树突提供额外的补体抗性。还表明,DAF的膜表达可能构成生长和再生神经元的标志物。

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Up-regulated expression of decay-accelerating factor (CD55) confers increased complement resistance to sprouting neural cells.衰变加速因子(CD55)表达上调赋予新生神经细胞更强的补体抗性。
Eur J Immunol. 1998 Apr;28(4):1189-96. doi: 10.1002/(SICI)1521-4141(199804)28:04<1189::AID-IMMU1189>3.0.CO;2-D.
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Regulation of CD59 expression on K562 cells: effects of phorbol myristate acetate, cross-linking antibody and non-lethal complement attack.K562细胞上CD59表达的调控:佛波酯、交联抗体和非致死性补体攻击的影响
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Decay-accelerating factor is a component of subendothelial extracellular matrix in vitro, and is augmented by activation of endothelial protein kinase C.衰变加速因子是体外内皮下细胞外基质的一个组成部分,并通过内皮蛋白激酶C的激活而增加。
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引用本文的文献

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The regulation of the CNS innate immune response is vital for the restoration of tissue homeostasis (repair) after acute brain injury: a brief review.中枢神经系统固有免疫反应的调节对于急性脑损伤后组织内环境稳定(修复)的恢复至关重要:简要综述。
Int J Inflam. 2010 Aug 9;2010:151097. doi: 10.4061/2010/151097.
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Herpes simplex virus 1 infected neuronal and skin cells differ in their susceptibility to complement attack.单纯疱疹病毒1感染的神经元细胞和皮肤细胞对补体攻击的敏感性不同。
Immunology. 2002 Jul;106(3):404-11. doi: 10.1046/j.1365-2567.2002.01421.x.
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CD59 blocks not only the insertion of C9 into MAC but inhibits ion channel formation by homologous C5b-8 as well as C5b-9.
CD59不仅能阻止C9插入膜攻击复合物(MAC),还能抑制同源的C5b - 8以及C5b - 9形成离子通道。
J Physiol. 2002 Mar 1;539(Pt 2):537-45. doi: 10.1113/jphysiol.2001.013381.
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Spontaneous classical pathway activation and deficiency of membrane regulators render human neurons susceptible to complement lysis.自发的经典途径激活和膜调节因子的缺乏使人类神经元易受补体溶解作用的影响。
Am J Pathol. 2000 Sep;157(3):905-18. doi: 10.1016/S0002-9440(10)64604-4.
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High expression of stanniocalcin in differentiated brain neurons.脑分化神经元中鲽鱼钙蛋白的高表达。
Am J Pathol. 1998 Aug;153(2):439-45. doi: 10.1016/S0002-9440(10)65587-3.