Dráberová L
Department of Immunology, Czechoslovak Academy of Sciences, Prague.
Eur J Immunol. 1989 Sep;19(9):1715-20. doi: 10.1002/eji.1830190928.
The Thy-1 antigen expressed on the surface of mouse T lymphocytes has been previously found to be involved in T cell activation. In the present study we have employed the anti-Thy-1.1 monoclonal antibody MRC OX7 and analyzed the expression and properties of Thy-1 antigen on the surface of peritoneal and pleural rat mast cells. Direct radioantibody binding assays, indirect immunofluorescence studies and flow cytometry analysis revealed that isolated rat mast cells express on their surface large amounts of the Thy-1 antigen. Scatchard analysis of the binding data indicated that at least one million Thy-1 molecules are expressed per cell. Immunoprecipitation studies carried out on mast cells demonstrated that MRC OX7 antibody recognizes a surface molecule of approximately 25 kDa that appears to correspond to Thy-1 antigen, and an additional molecule of 50 kDa. Incubation of the isolated mast cells with various concentrations of anti-Thy-1.1 antibody induced a rapid and concentration-dependent increase in the intracellular free calcium concentration ([Ca2+]i). The early increase in [Ca2+]i was observed in both Ca2+-supplemented and Ca2+-free media. This indicated that the initial increase in [Ca2+]i is due to a release of Ca2+ from internal stores. The [Ca2+]i increase was followed by an increase in the histamine release which was also dependent on antibody concentration. These data suggest that Thy-1 may act as an activation receptor on mast cells, analogously to its receptor function on T cells.
先前已发现小鼠T淋巴细胞表面表达的Thy-1抗原参与T细胞活化。在本研究中,我们使用了抗Thy-1.1单克隆抗体MRC OX7,并分析了大鼠腹膜和胸膜肥大细胞表面Thy-1抗原的表达和特性。直接放射抗体结合试验、间接免疫荧光研究和流式细胞术分析显示,分离的大鼠肥大细胞在其表面表达大量的Thy-1抗原。对结合数据的Scatchard分析表明,每个细胞至少表达100万个Thy-1分子。对肥大细胞进行的免疫沉淀研究表明,MRC OX7抗体识别一个约25 kDa的表面分子,该分子似乎对应于Thy-1抗原,以及另一个50 kDa的分子。用不同浓度的抗Thy-1.1抗体孵育分离的肥大细胞,可诱导细胞内游离钙浓度([Ca2+]i)迅速且呈浓度依赖性增加。在补充Ca2+和无Ca2+的培养基中均观察到[Ca2+]i的早期增加。这表明[Ca2+]i的初始增加是由于内部储存的Ca2+释放所致。[Ca2+]i增加之后是组胺释放增加,组胺释放也依赖于抗体浓度。这些数据表明,Thy-1可能作为肥大细胞上的活化受体,类似于其在T细胞上的受体功能。