Oliani S M, Freymüller E, Takahashi H K, Straus A H
Department of Biology IBILCE-UNESP, São José do Rio Preto, Brazil.
J Histochem Cytochem. 1997 Feb;45(2):231-5. doi: 10.1177/002215549704500208.
We performed immunogold labeling with an ST-1 monoclonal antibody (IgM), specific for intact heparin, to define the subcellular localization of heparin in mast cells. Rat peritoneal mast cells were fixed by a modified Karnovsky method and embedded in Araldite. Ultrathin sections were first treated with sodium periodate and then sequentially incubated with MAb ST-1, rabbit anti-mouse IgM, and protein A-gold. By transmission electron microscopy, gold particles were localized inside cytoplasmic granules of peritoneal mast cells. In contrast, with the same procedure, no labeling was observed in mast cells from rat intestinal mucosa. Control sections of rat peritoneal or intestinal mucosa mast cells treated with an irrelevant MAb (IgM) did not show any labeling. Treatment with nitrous acid abolished the reactivity of MAb ST-1 with peritoneal mast cells. These results show that different mast cells can be identified regarding their heparin content by immunochemical procedures using MAb ST-1.
我们使用针对完整肝素的ST-1单克隆抗体(IgM)进行免疫金标记,以确定肝素在肥大细胞中的亚细胞定位。大鼠腹膜肥大细胞采用改良的卡诺夫斯基方法固定,并用环氧树脂包埋。超薄切片先用高碘酸钠处理,然后依次与单克隆抗体ST-1、兔抗小鼠IgM和蛋白A-金孵育。通过透射电子显微镜观察,金颗粒定位于腹膜肥大细胞的细胞质颗粒内。相比之下,采用相同程序,在大鼠肠黏膜肥大细胞中未观察到标记。用无关单克隆抗体(IgM)处理的大鼠腹膜或肠黏膜肥大细胞的对照切片未显示任何标记。亚硝酸处理消除了单克隆抗体ST-1与腹膜肥大细胞的反应性。这些结果表明,使用单克隆抗体ST-1的免疫化学程序可根据肝素含量识别不同的肥大细胞。