Bhardwaj R S, Zotz C, Zwadlo-Klarwasser G, Roth J, Goebeler M, Mahnke K, Falk M, Meinardus-Hager G, Sorg C
Institute of Experimental Dermatology, University of Münster, FRG.
Eur J Immunol. 1992 Jul;22(7):1891-7. doi: 10.1002/eji.1830220732.
Monocytes/macrophages expressing an epitope recognized by a monoclonal antibody 27E10 are present in acute but are absent in chronic inflammatory disorders. This report shows that the 27E10 antigen is formed by noncovalent association of the two Ca(2+)-binding proteins MRP8 and MRP14 which belong to the S100 protein family. Identification has been confirmed immunochemically, by matrix-assisted UV-laser desorption/ionization spectrometry and by partial amino acid sequencing. Surface expression of the MRP8/MRP14 complex on a subset of monocytes is reported for the first time and shown to be up-regulated in a Ca(2+)-dependent manner. The 27E10 surface-positive monocytes isolated by cell separation techniques release high amounts of tumor necrosis factor-alpha and interleukin-1 beta in contrast to their 27E10 surface-negative counterparts thus emphasizing their role in inflammation.
表达可被单克隆抗体27E10识别的表位的单核细胞/巨噬细胞存在于急性炎症疾病中,但不存在于慢性炎症疾病中。本报告显示,27E10抗原由属于S100蛋白家族的两种钙结合蛋白MRP8和MRP14通过非共价结合形成。通过免疫化学、基质辅助紫外激光解吸/电离光谱法和部分氨基酸测序已证实了该鉴定。首次报道了MRP8/MRP14复合物在一部分单核细胞上的表面表达,并显示其以钙依赖的方式上调。通过细胞分离技术分离出的27E10表面阳性单核细胞与其27E10表面阴性对应物相比,释放大量的肿瘤坏死因子-α和白细胞介素-1β,从而强调了它们在炎症中的作用。