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pH对原代培养的小鼠肾皮质肾小管细胞生长的影响。

Effect of pH on growth of mouse renal cortical tubule cells in primary culture.

作者信息

Blumenthal S S, Lewand D L, Buday M A, Mandel N S, Mandel G S, Kleinman J G

机构信息

Department of Medicine, Medical College of Wisconsin, Milwaukee.

出版信息

Am J Physiol. 1989 Sep;257(3 Pt 1):C419-26. doi: 10.1152/ajpcell.1989.257.3.C419.

Abstract

We examined the effect of the medium pH on growth of primary cultures of mouse cortical tubule cells grown in defined medium. A significantly higher DNA content was observed within 24 h of lowering medium pH from 7.4 to 6.8 or 7.1 and persisted for the duration of the study. Further studies revealed that either medium acidification or insulin plus prostaglandin E1 nearly doubled uptake of [3H]thymidine in cells deprived of other growth factors for the previous 72-110 h. Moreover, the effects of insulin, prostaglandin E1, and medium acidification on [3H]thymidine uptake of quiescent cells were additive. An alkaline medium pH appeared to have a small but significant effect on cell hypertrophy, since cells exposed to pH 7.4 and 7.7 had a higher protein-to-DNA ratio than cells incubated at a lower pH. Cell pH of monolayers grown on glass slides determined from fluorescence of the carboxyfluorescein analogue 2',7'-biscarboxyethyl-5(6)-carboxyfluorescein (BCECF) was linearly correlated with medium pH, and changes in medium pH resulted in changes in steady-state cell pH of a similar magnitude. Four hours after medium acidification, relative increases in cell Na+ and water content occurred, whereas medium alkalinization led to decreases in cell Na+ and water content. The increases in cell Na+ and cell water content at pH 6.8 could be inhibited by amiloride. We conclude that decreasing the cell pH can be a mitogenic stimulus for renal tubule cells. Medium acidification is accompanied by changes in cell Na+ transport, which may be mediated in part by altered Na+-H+ antiporter activity.

摘要

我们研究了培养基pH值对在限定培养基中生长的小鼠皮质肾小管细胞原代培养物生长的影响。将培养基pH值从7.4降至6.8或7.1后24小时内,观察到DNA含量显著升高,并在研究期间持续存在。进一步的研究表明,对于之前72 - 110小时缺乏其他生长因子的细胞,培养基酸化或胰岛素加前列腺素E1可使[3H]胸苷摄取量增加近一倍。此外,胰岛素、前列腺素E1和培养基酸化对静止细胞[3H]胸苷摄取的影响具有相加性。碱性培养基pH值似乎对细胞肥大有微小但显著的影响,因为暴露于pH 7.4和7.7的细胞比在较低pH下孵育的细胞具有更高的蛋白质与DNA比率。通过羧基荧光素类似物2',7'-双羧乙基-5(6)-羧基荧光素(BCECF)荧光测定的玻片上生长的单层细胞的细胞pH值与培养基pH值呈线性相关,培养基pH值的变化导致稳态细胞pH值发生类似幅度的变化。培养基酸化4小时后,细胞Na+和水分含量相对增加,而培养基碱化导致细胞Na+和水分含量降低。pH 6.8时细胞Na+和细胞水分含量的增加可被氨氯吡咪抑制。我们得出结论,降低细胞pH值可能是肾小管细胞的一种促有丝分裂刺激。培养基酸化伴随着细胞Na+转运的变化,这可能部分由改变的Na+-H+反向转运体活性介导。

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