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pH值与种群密度对动物细胞增殖的调节作用

pH and population density in the regulation of animal cell multiplication.

作者信息

Rubin H

出版信息

J Cell Biol. 1971 Dec;51(3):686-702. doi: 10.1083/jcb.51.3.686.

Abstract

Sparse and dense cultures of chick embryo cells were affected differently by pH. The rates of cell multiplication and of thymidine-(3)H incorporation into DNA of dense cultures were increased as the pH was increased from 6.6 to 7.6. At pH higher than 7.6 the rate of multiplication decreased slightly in the dense cultures, but the rate of thymidine-(3)H incorporation continued to increase. The discrepancy was due in part to cell death and detachment at very high pH, and in part to a more rapid uptake of thymidine-(3)H at very high pH. Sparse cultures were much less sensitive to pH reduction and, when a suitably conditioned medium was used to minimize cell damage, very sparse cultures grew almost as well at pH 6.7 as at higher pH. The rates of cell multiplication and thymidine-(3)H incorporation at low pH decreased in the initially sparse cultures before they reached confluent cell densities. There was no microscope evidence of direct contact between plasma membranes of cells at these densities although the parallel orientation indicated that the cells were influencing locally each other's behavior. Even at much higher cell densities, electron microscopy revealed large intercellular gaps partly filled with a fragmentary electron-opaque material suspected to be glycoprotein. Wounding experiments showed that pH affected cell migration in a manner similar to its effects on cell multiplication. Low pH inhibited cell migration, but those cells which migrated into the denuded region multiplied as rapidly at low pH as at high pH. The effects of pH on growth were correlated with effects on the uptake of 2-deoxyglucose-(3)H. Dense populations of cells inhibited by low pH were stimulated to incorporate thymidine-(3)H by the addition of small amounts of diethylaminoethyl-dextran. Rous sarcoma cells at high cell density were less sensitive to pH than were normal cells at the same density, but were more sensitive than sparse normal cultures. The results suggest that cell growth is inhibited through the combined effects of both lowered pH and high cell density on cell surface permeability.

摘要

鸡胚细胞的稀疏培养物和致密培养物受pH值的影响不同。随着pH值从6.6升高到7.6,致密培养物中的细胞增殖速率以及胸苷 -(3)H掺入DNA的速率都增加了。在pH高于7.6时,致密培养物中的增殖速率略有下降,但胸苷 -(3)H掺入速率继续增加。这种差异部分是由于在非常高的pH值下细胞死亡和脱落,部分是由于在非常高的pH值下胸苷 -(3)H的摄取更快。稀疏培养物对pH降低的敏感性要低得多,并且当使用适当条件的培养基来最小化细胞损伤时,非常稀疏的培养物在pH 6.7时的生长几乎与在较高pH值时一样好。在最初稀疏的培养物达到汇合细胞密度之前,低pH值下的细胞增殖速率和胸苷 -(3)H掺入速率会下降。尽管平行排列表明细胞在局部相互影响彼此的行为,但在这些密度下没有显微镜证据表明细胞膜之间有直接接触。即使在更高的细胞密度下,电子显微镜也显示出大的细胞间隙,部分填充有疑似糖蛋白的碎片状电子不透明物质。创伤实验表明,pH值对细胞迁移的影响与其对细胞增殖的影响方式相似。低pH值抑制细胞迁移,但那些迁移到裸露区域的细胞在低pH值下的增殖速度与在高pH值下一样快。pH值对生长的影响与对2-脱氧葡萄糖 -(3)H摄取的影响相关。通过添加少量二乙氨基乙基葡聚糖,受低pH值抑制的致密细胞群体被刺激掺入胸苷 -(3)H。高细胞密度的劳斯肉瘤细胞比相同密度的正常细胞对pH值的敏感性低,但比稀疏的正常培养物更敏感。结果表明,细胞生长通过降低的pH值和高细胞密度对细胞表面通透性的综合作用而受到抑制。

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