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补体调节蛋白在人自然杀伤细胞亚群上的表达。

Expression of complement regulatory proteins on human natural killer cell subsets.

作者信息

Wang Lin, Halliday Deborah, Johnson Peter M, Christmas Stephen E

机构信息

Division of Immunology, School of Infection and Host Defence, University of Liverpool, Liverpool, UK.

出版信息

Immunol Lett. 2007 Oct 15;112(2):104-9. doi: 10.1016/j.imlet.2007.07.005. Epub 2007 Aug 9.

Abstract

The cell surface complement regulatory (CReg) proteins CD46, CD55 and CD59 are widely distributed on human leucocytes and protect against complement-mediated damage. To investigate heterogeneity in CReg protein expression by human natural killer (NK) cells, levels were assessed on resting and activated NK cell subsets identified phenotypically on the basis of expression of CD56 and CD158 markers. Levels of all three CReg proteins on CD56+ cells were lower than on T cells (p<0.05). Freshly isolated CD56(bright) cells expressed higher levels of CD55 than CD56dim cells (p<0.05). CD158a+ cells expressed significantly lower levels of both CD46 and CD59, and CD158e+ cells expressed significantly lower levels of CD46, than CD158a(-) CD158e(-) cells, respectively (both p<0.05). Stimulation with PHA did not significantly alter NK cell surface CReg protein levels whereas, following culture with IL-2, CD46 and CD59 were decreased on both CD56bright and CD56dim subsets (p<0.05). In the case of CD59, this was independent of T cells. Only CD46 was significantly downregulated on CD158b+ (GL183+) and CD158e (NKB1+) subsets (p<0.05). However, culture in IL-15 significantly increased levels of all three CReg proteins. These observations that CReg proteins are downregulated on certain NK cell subsets following activation with IL-2 are opposite to previous findings for other leucocyte subpopulations. Activated NK cells may instead use other strategies for protection against complement-mediated damage in a local inflammatory response.

摘要

细胞表面补体调节(CReg)蛋白CD46、CD55和CD59广泛分布于人类白细胞上,可防止补体介导的损伤。为了研究人类自然杀伤(NK)细胞CReg蛋白表达的异质性,对基于CD56和CD158标志物表达在表型上鉴定出的静息和活化NK细胞亚群的水平进行了评估。CD56+细胞上所有三种CReg蛋白的水平均低于T细胞(p<0.05)。新鲜分离的CD56(明亮)细胞比CD56暗淡细胞表达更高水平的CD55(p<0.05)。与CD158a(-)CD158e(-)细胞相比,CD158a+细胞分别表达显著更低水平的CD46和CD59,而CD158e+细胞表达显著更低水平的CD46(均p<0.05)。用PHA刺激并未显著改变NK细胞表面CReg蛋白水平,而在用IL-2培养后,CD56明亮和CD56暗淡亚群上的CD46和CD59均降低(p<0.05)。就CD59而言,这与T细胞无关。仅CD46在CD158b+(GL183+)和CD158e(NKB1+)亚群上显著下调(p<0.05)。然而,在IL-15中培养显著增加了所有三种CReg蛋白的水平。这些关于在用IL-2激活后某些NK细胞亚群上CReg蛋白下调的观察结果与先前关于其他白细胞亚群的发现相反。活化的NK细胞可能转而使用其他策略来防止局部炎症反应中补体介导的损伤。

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