Kvist S, Ostberg L, Peterson P A
Proc Natl Acad Sci U S A. 1979 Aug;76(8):4051-5. doi: 10.1073/pnas.76.8.4051.
The murine embryocarcinoma cell line F9 lacks the classical transplantation antigens. However, rabbit anti-H-2 antigen sera, recognizing "backbone structures" of H-2 K and D antigens, react with three types of molecules manufactured by F9 cells. A 49,000- and a 25,000-dalton chain are glycoproteins located on the cell surface. The third component with an apparent molecular weight of 15,000, and the 25,000-dalton chain seem to be unrelated to the 49,000-dalton glycoprotein. The 25,000- and 15,000-dalton components are not manufactured by splenocytes, thymocytes, hepatocytes, or various lymphoma, mastocytoma, and plasmacytoma cell lines. However, fibroblasts derived from both embryos and adult animals synthesize 25,000- and 15,000-dalton molecules reactive with the rabbit anti-H-2 antigen sera. The 49,000-, 25,000-, and 15,000-dalton molecules are not recognized by a syngeneic anti-F9 cell serum.
小鼠胚胎癌细胞系F9缺乏经典的移植抗原。然而,识别H-2 K和D抗原“主干结构”的兔抗H-2抗原血清,能与F9细胞产生的三种分子发生反应。一条49000道尔顿和一条25000道尔顿的链是位于细胞表面的糖蛋白。第三种成分的表观分子量为15000道尔顿,25000道尔顿的链似乎与49000道尔顿的糖蛋白无关。25000道尔顿和15000道尔顿的成分不是由脾细胞、胸腺细胞、肝细胞或各种淋巴瘤、肥大细胞瘤和浆细胞瘤细胞系产生的。然而,来自胚胎和成年动物的成纤维细胞能合成与兔抗H-2抗原血清发生反应的25000道尔顿和15000道尔顿的分子。49000道尔顿、25000道尔顿和15000道尔顿的分子不能被同基因抗F9细胞血清识别。