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参与二倍体人成纤维细胞生长接触依赖性抑制的质膜糖蛋白的鉴定

Identification of plasma membrane glycoproteins involved in the contact-dependent inhibition of growth of diploid human fibroblasts.

作者信息

Renauer D, Oesch F, Heck R, Wieser R

机构信息

Institut für Toxikologie, Mainz, Federal Republic of Germany.

出版信息

Exp Cell Res. 1989 Feb;180(2):504-14. doi: 10.1016/0014-4827(89)90077-3.

Abstract

Growth of normal, nontransformed cells is regulated by the interplay between growth stimulating compounds and growth inhibiting cell-cell contacts. We have previously shown that the growth of normal diploid human fibroblasts is mainly regulated by a specific class of plasma membrane glycoproteins (R. J. Wieser and F. Oesch (1986) J. Cell Biol. 103, 361-367). Because it was found that immobilization of the glycoproteins involved in contact-dependent inhibition of growth is an essential step in the recovery of the biological activity of the glycoproteins, we developed a technique for a first characterization of the active compounds. After SDS-PAGE separation of plasma membrane glycoproteins, they were transferred onto nitrocellulose. The nitrocellulose was cut along the separation track into circles which fit into wells of a 96-well microtiter plate. Culturing human diploid fibroblasts on the nitrocellulose circles resulted in characteristic growth patterns, which were dependent upon the source and the treatment of the plasma membrane proteins which had been separated. Five major inhibitory fractions with apparent molecular masses of 300, 170, 90, 50, and 25 kDa have been identified in plasma membranes from confluent fibroblast cultures.

摘要

正常的、未转化细胞的生长受到生长刺激化合物与抑制生长的细胞间接触之间相互作用的调节。我们之前已经表明,正常二倍体人成纤维细胞的生长主要受一类特定的质膜糖蛋白调控(R. J. 维泽尔和F. 厄施(1986年)《细胞生物学杂志》103卷,361 - 367页)。由于发现参与接触依赖性生长抑制的糖蛋白的固定化是糖蛋白生物活性恢复的关键步骤,我们开发了一种对活性化合物进行初步表征的技术。在对质膜糖蛋白进行SDS - 聚丙烯酰胺凝胶电泳分离后,将它们转移到硝酸纤维素膜上。将硝酸纤维素膜沿分离轨道切成适合96孔微量滴定板孔的圆形。在硝酸纤维素圆片上培养人二倍体成纤维细胞会产生特征性的生长模式,这取决于已分离的质膜蛋白的来源和处理方式。在汇合的成纤维细胞培养物的质膜中已鉴定出五个主要的抑制组分,其表观分子量分别为300、170、90、50和25 kDa。

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