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控制大鼠气管上皮细胞原代培养中细胞增殖的关键变量。

Critical variables controlling cell proliferation in primary cultures of rat tracheal epithelial cells.

作者信息

Gray T, Rundhaug J, Nettesheim P

机构信息

National Institute of Environmental Health Sciences, Laboratory of Pulmonary Pathobiology, Research Triangle Park, North Carolina 27709.

出版信息

In Vitro Cell Dev Biol. 1991 Oct;27A(10):805-14. doi: 10.1007/BF02631247.

Abstract

The purpose of our experiments was to examine variables affecting early events in the establishment of rat tracheal epithelial (RTE) cultures as well as factors regulating long-term RTE cell growth. The experiments showed that when RTE cells were seeded into complete serum-free medium between 13 and 30% of the seeded cells attached. Of the seeded cells, only approximately 2% entered into DNA synthesis and underwent repeated cell divisions to form colonies containing greater than 20 cells. Coating the dishes with extracellular matrix components had little effect on cell attachment or colony forming efficiency (CFE). However, coating the dishes with fetal bovine serum markedly increased CFE. The media components bovine serum albumin and bovine pituitary extract were shown to be important in promoting cell attachment as well as CFE. Cholera toxin on the other hand had no effect on cell attachment but significantly increased CFE. These and other studies showed that cell attachment and cell proliferation are independently regulated. Studies on long-term culture growth indicated that the number of progeny produced per colony forming unit (CFU) is inversely proportional to the number of CFUs seeded. Inasmuch as the cultures did not become confluent under any of the culture conditions tested and media obtained from high density cultures were shown to be growth inhibitory, these findings suggest that a diffusible growth restraining factor is being produced by the cultures limiting clonal expansion. Experiments showing growth inhibitory effects of media conditioned by high cell density cultures support this interpretation. The putative factor reaches critical concentrations earlier in cultures seeded with high numbers of CFU than in cultures seeded with low numbers of CFU. Because the cultures are known to produce transforming growth factor-beta, this growth regulator probably plays a role in controlling RTE cell proliferation. However, it is likely than other events, such as depletion of growth factors from the media, also are significant in regulating the growth of the cultures.

摘要

我们实验的目的是研究影响大鼠气管上皮(RTE)细胞培养早期事件的变量,以及调节RTE细胞长期生长的因素。实验表明,当将RTE细胞接种到完全无血清培养基中时,13%至30%的接种细胞会附着。在接种的细胞中,只有约2%进入DNA合成并进行反复细胞分裂以形成包含超过20个细胞的集落。用细胞外基质成分包被培养皿对细胞附着或集落形成效率(CFE)影响不大。然而,用胎牛血清包被培养皿显著提高了CFE。培养基成分牛血清白蛋白和牛垂体提取物在促进细胞附着以及CFE方面显示出重要作用。另一方面,霍乱毒素对细胞附着没有影响,但显著提高了CFE。这些以及其他研究表明,细胞附着和细胞增殖是独立调节的。对长期培养生长的研究表明,每个集落形成单位(CFU)产生的子代数量与接种的CFU数量成反比。由于在所测试的任何培养条件下培养物都不会汇合,并且从高密度培养物中获得的培养基被证明具有生长抑制作用,这些发现表明培养物正在产生一种可扩散的生长抑制因子,限制克隆扩增。显示高细胞密度培养物条件培养基具有生长抑制作用的实验支持了这一解释。假定的因子在接种大量CFU的培养物中比在接种少量CFU的培养物中更早达到临界浓度。因为已知培养物会产生转化生长因子-β,这种生长调节剂可能在控制RTE细胞增殖中起作用。然而,其他事件,如培养基中生长因子的耗尽,也可能在调节培养物生长方面具有重要意义。

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