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培养的肾上皮细胞生长:自分泌控制的证据。

Growth of kidney epithelial cells in culture: evidence for autocrine control.

作者信息

Mordan L J, Toback F G

出版信息

Am J Physiol. 1984 Mar;246(3 Pt 1):C351-4. doi: 10.1152/ajpcell.1984.246.3.C351.

Abstract

The factors that stimulate kidney growth in K+-deficient animals are unknown. Cultures of renal epithelial cells (BSC-1 line) were used to study this phenomenon because their growth is accelerated in medium containing a reduced K+ concentration. We tested the hypothesis that growth induced by low-K+ medium is mediated by factors produced by the cells; i.e., is subject to autocrine control. Low-K+ (3.2 mM) or control (5.4 mM) medium was conditioned by placing it on confluent cultures of BSC-1 cells for 1 h and was then collected. The K+ concentration of the low-K+ conditioned medium was then adjusted to the control value by addition of KCl. This conditioned medium stimulated growth of fresh cultures of cells to the same extent as did unconditioned low-K+ medium. The appearance of growth-promoting activity was maximal at a K+ concentration of 3.2 mM during conditioning of the medium. Low-K+ conditioned medium, corrected to a K+ concentration of 5.4 mM, required 6 h to commit cells to enhanced proliferation. Growth-stimulating activity in low-K+ conditioned medium was antagonized by a purified growth inhibitor produced by the cells. These observations are consistent with the hypothesis that autocrine products with opposite effects on growth can regulate proliferation of renal epithelial cells.

摘要

在钾缺乏的动物中刺激肾脏生长的因素尚不清楚。肾上皮细胞(BSC-1系)培养物被用于研究这一现象,因为它们在钾浓度降低的培养基中生长加速。我们检验了这样一个假设,即低钾培养基诱导的生长是由细胞产生的因子介导的;也就是说,受自分泌控制。低钾(3.2 mM)或对照(5.4 mM)培养基通过置于BSC-1细胞的汇合培养物上1小时进行条件处理,然后收集。然后通过添加氯化钾将低钾条件培养基的钾浓度调整到对照值。这种条件培养基刺激新鲜细胞培养物生长的程度与未处理的低钾培养基相同。在培养基条件处理期间,促生长活性在钾浓度为3.2 mM时最大。校正到钾浓度为5.4 mM的低钾条件培养基需要6小时才能使细胞开始增强增殖。低钾条件培养基中的生长刺激活性被细胞产生的一种纯化生长抑制剂所拮抗。这些观察结果与以下假设一致,即对生长有相反作用的自分泌产物可以调节肾上皮细胞的增殖。

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Lowering extracellular Na+ concentration releases autocrine growth factors from renal epithelial cells.
Proc Natl Acad Sci U S A. 1986 Jul;83(13):4764-8. doi: 10.1073/pnas.83.13.4764.

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