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绵羊传入淋巴树突状细胞上Fcγ受体的表达以及在体内外Fcγ受体结合后细胞表面表型的快速调节。

Fc gamma receptor expression on sheep afferent lymph dendritic cells and rapid modulation of cell surface phenotype following Fc gamma receptor engagement in vitro and in vivo.

作者信息

Coughlan S N, Harkiss G D, Dickson L, Hopkins J

机构信息

Department of Veterinary Pathology, University of Edinburgh, UK.

出版信息

Scand J Immunol. 1996 Jan;43(1):31-8. doi: 10.1046/j.1365-3083.1996.d01-11.x.

Abstract

Afferent lymph dendritic cells were analysed for the presence of Fc gamma receptors by Western blotting and for modulation of surface markers following Fc gamma receptor engagement in vitro and in vivo. The results showed that unstimulated dendritic cells expressed Fc gamma RII constitutively. When dendritic cells were incubated in vitro with antigen/antibody complexes in antibody excess, a marked reduction in surface staining was observed for MHC class II, CD1, CD44, and VLA-4 after 8 h in culture. These changes did not occur with antigen or antibody alone. DC expression of LFA-1 and LFA-3 were slightly reduced after 8 h in culture with Ova alone, but this was enhanced slightly when the cells were cultured with immune complexes. Even more marked reductions in surface staining for MHC class II, CD1, CD44 and VLA-4 were observed on dendritic cells 4-8 h following secondary antigen challenge in vivo. LFA-1 and LFA-3 expression was reduced only slightly. The level of expression of MHC class II, CD1, LFA-1 and LFA-3 was substantially increased over resting values 24 h after Fc gamma R occupancy. The intensity of staining at this time was also significantly elevated for CD44, LFA-1, LFA-3 and VLA-4. These results show that engagement of Fc gamma receptors cause a substantial modulation of the dendritic cell surface phenotype after immune complex uptake. The phenomenon may function to maximize subsequent presentation of the challenge antigen to T cells.

摘要

通过蛋白质印迹法分析传入淋巴树突状细胞中Fcγ受体的存在情况,并分析其在体外和体内Fcγ受体结合后表面标志物的调节情况。结果显示,未受刺激的树突状细胞组成性表达FcγRII。当树突状细胞在体外与抗体过量的抗原/抗体复合物孵育时,培养8小时后,MHC II类分子、CD1、CD44和VLA-4的表面染色显著减少。单独使用抗原或抗体时不会出现这些变化。单独用卵清蛋白培养8小时后,树突状细胞LFA-1和LFA-3的表达略有降低,但当细胞与免疫复合物一起培养时,这种降低略有增强。在体内二次抗原攻击后4-8小时,树突状细胞上MHC II类分子、CD1、CD44和VLA-4的表面染色减少更为明显。LFA-1和LFA-3的表达仅略有降低。FcγR占据后24小时,MHC II类分子、CD1、LFA-1和LFA-3的表达水平比静息值大幅增加。此时CD44、LFA-1、LFA-3和VLA-4的染色强度也显著升高。这些结果表明,Fcγ受体的结合在免疫复合物摄取后会导致树突状细胞表面表型的显著调节。这种现象可能有助于最大限度地将随后的攻击抗原呈递给T细胞。

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