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人类细胞间黏附分子-1(ICAM-1)在免疫反应产生中的作用。

The function of human intercellular adhesion molecule-1 (ICAM-1) in the generation of an immune response.

作者信息

Dougherty G J, Murdoch S, Hogg N

机构信息

Macrophage Laboratory, Imperial Cancer Research Fund, London, GB.

出版信息

Eur J Immunol. 1988 Jan;18(1):35-9. doi: 10.1002/eji.1830180107.

Abstract

Monoclonal antibody RR 1/1 directed against the putative LFA-1 ligand molecule intracellular adhesion molecule-1 (ICAM-1) was found to inhibit the T cell proliferative response to the antigen PPD. Interestingly, the percentage of unstimulated monocytes which expressed ICAM-1 on their surface appeared to vary greatly from person to person although the majority of monocytes did express high levels of ICAM-1 within their cytoplasm and surface expression could be rapidly induced on most cells by adherence to fibronectin. Resting T cells showed no evidence of surface or cytoplasmic ICAM-1 although expression was induced both within the cell and on the membrane as a result of activation with phytohemagglutinin or a combination of OKT3 and phorbol 12,13-dibutyrate. The significance of these findings with respect to the function of monocyte and T cell in the generation of an immune response is discussed.

摘要

发现针对假定的淋巴细胞功能相关抗原-1(LFA-1)配体分子细胞间黏附分子-1(ICAM-1)的单克隆抗体RR 1/1可抑制T细胞对抗原结核菌素纯蛋白衍生物(PPD)的增殖反应。有趣的是,尽管大多数单核细胞在其细胞质内确实表达高水平的ICAM-1,并且通过黏附于纤连蛋白可在大多数细胞上迅速诱导表面表达,但未受刺激的单核细胞表面表达ICAM-1的百分比似乎因人而异。静息T细胞未显示表面或细胞质ICAM-1的迹象,尽管用植物血凝素或OKT3与佛波醇12,13-二丁酸酯的组合激活后,细胞内和细胞膜上均诱导了ICAM-1的表达。讨论了这些发现对于单核细胞和T细胞在免疫反应产生中的功能的意义。

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