Wieser R J, Heck R, Oesch F
Exp Cell Res. 1985 Jun;158(2):493-9. doi: 10.1016/0014-4827(85)90472-0.
The human embryonal lung fibroblasts used in this study showed a pronounced inhibition of growth when reaching a critical cell density. This effect has been mimicked by the addition of glutaraldehyde-fixed human fibroblasts to sparsely seeded growing cells. Inhibition of growth was not observed when glutaraldehyde-fixed cells were pretreated with galactosidase or with galactose-specific lectins, or when glutaraldehyde-fixed human or rabbit erythrocytes were added to the proliferating fibroblasts. In addition, glutaraldehyde-fixed mitotic cells were without effect on the proliferation, while cells prepared from sparse culture had lesser potency than cells prepared from confluent cultures. Plasma membranes, isolated from cells of confluent cultures, when added to growing cultures of human fibroblasts inhibited DNA synthesis in a concentration-dependent manner. On the other hand, plasma membranes isolated from sparsely seeded cells had only minor inhibitory potency. When the plasma membranes were isolated from cells treated previously with tunicamycin, an antibiotic which inhibits the synthesis of the oligosaccharide portion of asparagine-linked glycoproteins, the inhibitory effect was abolished. The same effect was observed when plasma membranes were pretreated with galactosidase. These data indicate that the growth of cells in vitro is regulated by specific cell-cell contacts. They also show that one of the molecular reactants in this process are membrane glycoproteins with asparagine-linked oligosaccharides.
本研究中使用的人胚肺成纤维细胞在达到临界细胞密度时生长受到显著抑制。向稀疏接种的生长细胞中添加戊二醛固定的人成纤维细胞可模拟这种效应。当用半乳糖苷酶或半乳糖特异性凝集素预处理戊二醛固定的细胞,或者将戊二醛固定的人或兔红细胞添加到增殖的成纤维细胞中时,未观察到生长抑制。此外,戊二醛固定的有丝分裂细胞对增殖没有影响,而从稀疏培养物中制备的细胞比从汇合培养物中制备的细胞效力更低。从汇合培养物的细胞中分离的质膜,当添加到人类成纤维细胞的生长培养物中时,以浓度依赖的方式抑制DNA合成。另一方面,从稀疏接种的细胞中分离的质膜只有轻微的抑制效力。当质膜从先前用衣霉素处理的细胞中分离时,衣霉素是一种抑制天冬酰胺连接糖蛋白寡糖部分合成的抗生素,其抑制作用被消除。当质膜用半乳糖苷酶预处理时也观察到相同的效果。这些数据表明体外细胞的生长受特定细胞间接触的调节。它们还表明该过程中的分子反应物之一是具有天冬酰胺连接寡糖的膜糖蛋白。