Gorlina Iu K, Golovistikov I N, Petrunin D D, Tsagaraeva T M, Tamarinov Iu S
Biull Eksp Biol Med. 1981 Mar;91(3):345-7.
A study was made of the action of trophoblastic beta 1-glycoprotein (TBG) and chorionic alpha 1-microglobulin (CAG1) on proliferation of malignant fibroblasts (transplanted L line) and on phytohemagglutinin-stimulated lymphocytes. TBG depressed proliferation of the stimulated lymphocytes and transformed fibroblasts (according to 3H-thymidine incorporation). A dose-response dependence was ascertained. CAG1 did not affect cell division. The inhibitory effect of TBG was seen to be reversed or decreased provided the lymphocyte culture was supplemented with CAG1. The decreased inhibitory effect of TBG in the presence of CAG1 was also noted in the L cell culture. It is likely that in vivo protection of intensely proliferating fetal tissues or tumor from the inhibitors is effected just in this way since placental proteins are synthesized both by embryonic and tumorous cells.
研究了滋养层β1-糖蛋白(TBG)和绒毛膜α1-微球蛋白(CAG1)对恶性成纤维细胞(移植的L系)增殖以及对植物血凝素刺激的淋巴细胞增殖的作用。TBG抑制刺激的淋巴细胞和转化的成纤维细胞的增殖(根据3H-胸腺嘧啶掺入法)。确定了剂量反应依赖性。CAG1不影响细胞分裂。如果淋巴细胞培养物中补充CAG1,可观察到TBG的抑制作用被逆转或减弱。在L细胞培养物中也注意到在CAG1存在下TBG的抑制作用减弱。很可能在体内,正是以这种方式对强烈增殖的胎儿组织或肿瘤起到了免受抑制剂影响的保护作用,因为胚胎细胞和肿瘤细胞都会合成胎盘蛋白。