Studies on terminal differentiation of rat renal proximal tubular cells in culture: ouabain-sensitive K and Na transport.
Studies on terminal differentiation of rat renal proximal tubular cells in culture: ouabain-sensitive K and Na transport.
复制标题
培养中大鼠肾近端肾小管细胞终末分化的研究:哇巴因敏感的 K 和 Na 转运。
DOI:
10.1111/j.1748-1716.1988.tb08309.x
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发表时间:
1988
期刊:
影响因子:
--
通讯作者:
Lechene,C
中科院分区:
文献类型:
--
作者:
Larsson,SH;Aperia,A;Lechene,C
We have studied the ontogeny of Na‐K ATPase‐mediated Na and K transport in rat renal proximal tubular cells using electron probe analysis. The cells were cultured from kidneys of 10‐day‐old, young (Y), and 40‐day‐old, adult (A) rats. Before an experiment cells were Na‐loaded and K‐dcpleted by incubation in K‐free medium. The maximum rate of ouabain‐sensitive Na and K transport was measured after reactivating the Na‐K pump by transferring the cells from K‐free medium to medium containing 5 mM K. In cells cultured for 2 days, ouabain‐sensitive Na and K net initial transport rates were significantly higher in A than in Y cells. Between 2 and 4 days in culture there was a significant decrease in ouabain‐sensitive Na and K transport rates in both Y and A cells. From 2 to 4 days of culture there was, in Y but not in A cells, a significant decrease in K/Na ratio. The decrease in K/Na ratio was due to a significant increase in Na content. After incubation in K‐free medium, net intracellular solute accumulation was observed in A and Y cells cultured for 4 days but not in A and Y cells cultured for 2 days.In conclusion, maximal Na‐ and K‐pump‐mediated transport increases during terminal differentiation. This increase can be measured in cells cultured for 2 days. With longer time in culture, Na K pump activity decreases and the difference between A and Y cells is not measurable. We had previously observed that net Na and K permeabilities decrease from 2 to 4 days in culture in A but not in Y cells. In Y cells cultured for 4 days, a decrease in pump activity without a change in Na and K permeability causes an increase in intracellular Na content.