Sidorov N M, Krivonosov S K, Golovistikov I N, Mironov A A, Pogorelova T Iu
Ontogenez. 1988 Mar-Apr;19(2):213-7.
The influence of trophoblast-specific beta 1-glycoprotein (TSG) on the degranulation of mast cells and their saturation with heparin was studied. Introduction of the TSG into the population of mast cells of the rat peritoneal fluid practically does not change their degranulation, but lowers the degree of their saturation with heparin. An antibiotic alone increases the saturation of the cells with heparin. The serum of an allergic animal markedly stimulates the degranulation and lowers the degree of saturation of the mast cells with heparin. In an experimental model (antibiotic--the serum of the allergic mast cells) the mast cells transform into very clear (heparin-free) cells and the degree of saturation is at minimum. The TSG introduction into this system stabilizes the population of mast cells and markedly increases the degree of their saturation with heparin. Although the degranulation is rather intensive, it is less expressed, than in the experimental model. This suggests the presence of TSG receptors on the mast cells (targets of allergic reactions). The possibility to use TSG preparations in the therapy of allergic diseases is discussed.
研究了滋养层特异性β1-糖蛋白(TSG)对肥大细胞脱颗粒及其肝素饱和度的影响。将TSG引入大鼠腹腔液肥大细胞群体中,实际上不会改变其脱颗粒情况,但会降低其肝素饱和度。单独使用抗生素会增加细胞的肝素饱和度。过敏动物的血清显著刺激脱颗粒,并降低肥大细胞的肝素饱和度。在实验模型(抗生素 - 过敏肥大细胞的血清)中,肥大细胞转变为非常清亮(无肝素)的细胞,饱和度处于最低水平。将TSG引入该系统可稳定肥大细胞群体,并显著提高其肝素饱和度。尽管脱颗粒相当强烈,但比实验模型中的表现要轻。这表明肥大细胞(过敏反应的靶细胞)上存在TSG受体。讨论了使用TSG制剂治疗过敏性疾病的可能性。