Orange R P, Moore E G, Gelfand E W
J Immunol. 1980 May;124(5):2264-7.
The capacity of the calcium ionophore A 23187 to induce the formation of SRS-A was used in an attempt to identify the nature of the cells that are responsible for the formation of this material. In agreement with previous observations, rat and mouse peritoneal mast cells were found to contribute very little to the total amount of SRS-A that was made, and in fact their removal from the cell suspensions resulted in an augmentation of the amount of SRS-A that was found. Discontinuous Ficoll and bovine serum albumin gradients were employed to further characterize these SRS-A-releasing cells from induced peritoneal cells. SRS-A was produced by nonspecific esterase-positive and latex-phagocytizing mononuclear cells. By electron microscopy, these cells had macrophage-like characteristics. In contrast, rat alveolar macrophages and a macrophage-like cell line of mouse origin both failed to produce large amounts of SRS-A. The results suggest that SRS-A formation may be the property of an as yet imperfectly characterized subclass of macrophages.
钙离子载体A 23187诱导慢反应物质A(SRS - A)形成的能力被用于尝试确定负责这种物质形成的细胞的性质。与先前的观察结果一致,发现大鼠和小鼠腹腔肥大细胞对所产生的SRS - A总量贡献很小,实际上从细胞悬液中去除它们会导致所发现的SRS - A量增加。采用不连续的菲可(Ficoll)和牛血清白蛋白梯度进一步表征来自诱导腹腔细胞的这些释放SRS - A的细胞。SRS - A由非特异性酯酶阳性且吞噬乳胶的单核细胞产生。通过电子显微镜观察,这些细胞具有巨噬细胞样特征。相比之下,大鼠肺泡巨噬细胞和小鼠来源的巨噬细胞样细胞系均未能产生大量的SRS - A。结果表明,SRS - A的形成可能是一类尚未完全表征的巨噬细胞亚类的特性。