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哇巴因培养的细胞中(3H)哇巴因的摄取及钠泵周转率

Uptake of ( 3 H)ouabain and Na pump turnover rates in cells cultured in ouabain.

作者信息

Boardman L J, Lamb J F, McCall D

出版信息

J Physiol. 1972 Sep;225(3):619-35. doi: 10.1113/jphysiol.1972.sp009960.

Abstract
  1. The binding of [(3)H]ouabain to fresh Girardi and Hela cells and to those cultured in low concentrations of ouabain for 24 hr has been measured.2. Fresh cells bind 1.6-2.2 x 10(6) molecules of ouabain() per cell from K-free Krebs, but less than 0.3 x 10(6) molecules from 15 mM-K Krebs. The ouabain() binds with a t((1/2)) of about 8 min from K-free 2 x 10(-7)M ouabain() and is released with a t((1/2)) of about 20 hr. Cells in a poor condition probably exchange ouabain more quickly.3. Cells incubated in ouabain() for 24 hr bind ouabain in amounts dependent on the [ouabain] and the external [K]. At the highest [ouabain] used the total amount bound exceeds that bound by fresh cells. Lowering K in the medium increases the maximum ouabain which is bound.4. Cells incubated in ouabain() for 24 hr bind an additional amount of ouabain when exposed to 2 x 10(-7)M ouabain() in K-free Krebs.5. There is a close relationship between the% of the total ouabain bound in 24 hr and the% inhibition of the Na efflux suggesting that this ouabain is bound to the Na pumps.6. Radiochromatography of the counts recovered from the cells showed that it migrated to the same place as the applied [(3)H]ouabain. The wash-off rate of ouabain bound to cells during incubation is similar to that from fresh cells, both tests suggesting that the ouabain exists in the same state in the cells.7. The number of Na ions extruded per pump is constant at about 60 sec(-1) in fresh cells and those pre-incubated in ouabain.8. The total ouabain bound by the cells is closely related to the Na in cells pre-incubated in ouabain but is unaffected by it in fresh cells where Na is raised acutely.9. These results are compatible with the hypothesis that partial blocking of Na pumps leads to the production of more pumping sites by the cell.
摘要
  1. 已测定了[(3)H]哇巴因与新鲜的吉拉尔迪细胞和海拉细胞以及在低浓度哇巴因中培养24小时的细胞的结合情况。

  2. 新鲜细胞从无钾的克氏液中每细胞结合1.6 - 2.2×10(6)个哇巴因()分子,但从含15 mMK的克氏液中结合少于0.3×10(6)个分子。哇巴因()从无钾的2×10(-7)M哇巴因(*)中结合的t((1/2))约为8分钟,释放的t((1/2))约为20小时。状态不佳的细胞可能更快地交换哇巴因。

  3. 在哇巴因(*)中孵育24小时的细胞结合哇巴因的量取决于[哇巴因]和细胞外[K]。在所用的最高[哇巴因]浓度下,结合的总量超过新鲜细胞结合的量。降低培养基中的K会增加结合的最大哇巴因量。

  4. 在哇巴因()中孵育24小时的细胞,当暴露于无钾克氏液中的2×10(-7)M哇巴因()时,会额外结合一定量的哇巴因。

  5. 24小时内结合的总哇巴因的百分比与钠外流的抑制百分比之间存在密切关系,这表明这种哇巴因与钠泵结合。

  6. 对从细胞中回收的计数进行放射性色谱分析表明,它迁移到与所加[(3)H]哇巴因相同的位置。孵育期间与细胞结合的哇巴因的洗脱速率与新鲜细胞的相似,这两个测试都表明哇巴因在细胞中以相同状态存在。

  7. 新鲜细胞和在哇巴因中预孵育的细胞中,每个泵每秒挤出的钠离子数量恒定在约60个。

  8. 在哇巴因中预孵育的细胞中,细胞结合的总哇巴因与细胞内Na密切相关,但在急性升高Na的新鲜细胞中不受其影响。

  9. 这些结果与以下假设相符,即钠泵的部分阻断会导致细胞产生更多的泵位点。

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Effect of prolonged ouabain treatment of Na, K, Cl and Ca concentration and fluxes in cultured human cells.
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Binding of the cardiac glycoside ouabain to intact cells.
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