Prieto J, Takei F, Gendelman R, Christenson B, Biberfeld P, Patarroyo M
Department of Immunology, Karolinska Institute, Stockholm, Sweden.
Eur J Immunol. 1989 Sep;19(9):1551-7. doi: 10.1002/eji.1830190906.
In humans, lymphocyte adhesion to cells is mediated by the protein heterodimer CD11a/CD18 (Leu-CAMa, LFA-1) and its ligand CD54 (ICAM-1). Although the murine CD11a/CD18 is well characterized, the mouse homologue of human ICAM-1 has not been identified. In the present study a rat monoclonal antibody to the murine lymphocyte activation antigen MALA-2 was found to inhibit in a dose-dependent manner the phorbol ester-enhanced aggregation of mouse lymphoblasts, an adhesion-specific assay, and hence to define an adhesion molecule. By immunofluorescence flow cytometry the antigen expression was low on spleen cells but it largely increased after stimulation with mitogens. The antigen was expressed by some, but not all, lymphoid cell lines, and myelomonocytic and mastocytoma cells were also positive. In frozen tissue sections MALA-2 was mainly detected on germinal center B cells, dendritic cells, macrophages and vascular endothelium, including high endothelial venules. Cell surface labeling followed by immunoprecipitation and gel electrophoresis indicated that the antigen is a sialoglycoprotein which has a relative molecular mass of 95 kDa and displays a faster electrophoretic mobility under non-reducing conditions. The function, cellular distribution and molecular properties of MALA-2 are indistinguishable from those of human ICAM-1.
在人类中,淋巴细胞与细胞的黏附由蛋白异二聚体CD11a/CD18(白细胞黏附分子α,淋巴细胞功能相关抗原-1)及其配体CD54(细胞间黏附分子-1)介导。尽管鼠类CD11a/CD18已得到充分表征,但人类ICAM-1的小鼠同源物尚未被鉴定出来。在本研究中,发现一种针对鼠淋巴细胞活化抗原MALA-2的大鼠单克隆抗体能够以剂量依赖的方式抑制佛波酯增强的小鼠淋巴母细胞聚集,这是一种黏附特异性检测方法,因此可确定一种黏附分子。通过免疫荧光流式细胞术检测发现,该抗原在脾细胞上表达较低,但在用丝裂原刺激后其表达大幅增加。该抗原在部分而非全部淋巴样细胞系中表达,骨髓单核细胞和肥大细胞瘤细胞也呈阳性。在冰冻组织切片中,MALA-2主要在生发中心B细胞、树突状细胞、巨噬细胞和血管内皮(包括高内皮微静脉)上检测到。细胞表面标记后进行免疫沉淀和凝胶电泳表明,该抗原是一种唾液糖蛋白,相对分子质量为95 kDa,在非还原条件下显示出更快的电泳迁移率。MALA-2的功能、细胞分布和分子特性与人类ICAM-1无法区分。