Stinnett J D, Kaplan A M, Morahan P S
J Immunol. 1976 Feb;116(2):273-8.
A mouse-specific macrophage antigen (MSMA) was identified in NP-40 extracts of 125I-radiolabeled mouse preitoneal macrophages by using a rabbit anti-mouse macrophage serum (AMS) and SDS-polyacrylamide gel electrophoresis. The antigen was shown to have a m.w. of 83,000 daltons and was present on both normal and "activated" peritoneal macrophages. MSMA was also present on syngeneic adherent spleen cells, allogeneic peritoneal macrophages, a mouse macrophage cell line (P388D1), and exhibited some cross-reactivity with peritoneal macrophages from closely related species (rats and hamsters). MSMA was not present on nonadherent peritoneal exudate cells, spleen cells, erythrocytes, thymocytes, or bone marrow cells. Extensive absorptions of AMS with thymocytes and erytrocytes from mice were necessary to remove other antibodies that reacted with other mouse membrane antigens. An antiserum directed against a specific membrane antigen has great potential in elucidating structure-function relationships with regard to a number of macrophage activities.
通过使用兔抗小鼠巨噬细胞血清(AMS)和SDS-聚丙烯酰胺凝胶电泳,在125I放射性标记的小鼠腹腔巨噬细胞的NP-40提取物中鉴定出一种小鼠特异性巨噬细胞抗原(MSMA)。该抗原的分子量为83,000道尔顿,存在于正常和“活化”的腹腔巨噬细胞上。MSMA也存在于同基因贴壁脾细胞、异基因腹腔巨噬细胞、一种小鼠巨噬细胞系(P388D1)上,并且与来自密切相关物种(大鼠和仓鼠)的腹腔巨噬细胞表现出一些交叉反应性。MSMA不存在于非贴壁腹腔渗出细胞、脾细胞、红细胞、胸腺细胞或骨髓细胞上。用小鼠的胸腺细胞和红细胞对AMS进行广泛吸收,对于去除与其他小鼠膜抗原反应的其他抗体是必要的。针对特定膜抗原的抗血清在阐明与多种巨噬细胞活性相关的结构-功能关系方面具有巨大潜力。