Activation of the Na+‐K+ pump by hyposmolality through tyrosine kinase‐dependent Cl− conductance in Xenopus renal epithelial A6 cells

Activation of the Na+‐K+ pump by hyposmolality through tyrosine kinase‐dependent Cl− conductance in Xenopus renal epithelial A6 cells
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非洲爪蟾肾上皮 A6 细胞中酪氨酸激酶依赖性 Cl− 电导通过低渗透压激活 Na+-K+ 泵

DOI:
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发表时间:
1999
期刊:
Journal of Physiology
影响因子:
--
通讯作者:
Y. Marunaka
Y. Marunaka
中科院分区:
--
文献类型:
--
作者:
N. Niisato;Y. Marunaka

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1研究了低渗对肾上皮细胞A6细胞Na+转运的调节机制。2低渗透压增加(1)Na+吸收,表现为阿米洛利敏感的短路电流(INA),(2)Na+-K+泵活性,(3)基底侧Cl-−电导(GB,Cl),(4)酪氨酸磷酸化,提示蛋白酪氨酸激酶(PTK)活性增加。3氯离子−通道阻断剂5-硝基-2-(3-苯丙氨基)-苯甲酸酯(NPPB)能阻断钠钾泵,但对阿米洛利敏感的钠通道无直接作用。用通透性较差的阴离子葡萄糖酸盐取代Cl-−,减少Gb、Cl,也降低了低渗透压,从而增加了Na+-K+泵的活性。4酪氨酸氨基转移酶抑制剂Tyrphostin A23和金雀异黄素可降低低渗性刺激的Gb,Cl,这与减弱低渗性增加的Na+-K+泵活性有关。综上所述,这些观察结果表明:(1)低渗透压激活PTK;(2)激活的PTK增加GB,Cl;(3)PTK增加的GB,Cl刺激Na+-K+泵。6这种PTK激活的GB,Cl介导的低渗透压信号是一种刺激Na+-K+泵的新途径。
1 We studied the regulatory mechanism of Na+ transport by hyposmolality in renal epithelial A6 cells. 2 Hyposmolality increased (1) Na+ absorption, which was detected as an amiloride‐sensitive short‐circuit current (INa), (2) Na+‐K+ pump activity, (3) basolateral Cl− conductance (Gb,Cl), and (4) phosphorylation of tyrosine, suggesting an increase in activity of protein tyrosine kinase (PTK). 3 A Cl− channel blocker, 5‐nitro‐2‐(3‐phenylpropylamino)‐benzoate (NPPB), which abolished Gb,Cl, blocked the INa by inhibiting the Na+‐K+ pump without any direct effect on amiloride‐sensitive Na+ channels. Diminution of Gb,Cl by Cl− replacement with a less permeable anion, gluconate, also decreased the hyposmolality‐increased Na+‐K+ pump activity. 4 The PTK inhibitors tyrphostin A23 and genistein induced diminution of the hyposmolality‐stimulated Gb,Cl, which was associated with attenuation of the hyposmolality‐increased Na+‐K+ pump activity. 5 Taken together, these observations suggest that: (1) hyposmolality activates PTK; (2) the activated PTK increases Gb,Cl; and (3) the PTK‐increased Gb,Cl stimulates the Na+‐K+ pump. 6 This PTK‐activated Gb,Cl‐mediated signalling of hyposmolality is a novel pathway for stimulation of the Na+‐K+ pump.
胰岛素刺激人成纤维细胞的 Na ,K( )-ATP 酶和 Na /K /Cl- 协同转运蛋白。
DOI: 10.1016/0005-2736(96)00004-1
发表时间: 1996
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影响因子: --
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DOI: 10.1016/0076-6879(90)91045-8
发表时间: 1990
影响因子: --
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DOI: 10.1152/ajpcell.1991.260.5.c1071
发表时间: 1991-05-01
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DOI: 10.1152/ajpcell.1990.258.2.c352
发表时间: 1990
期刊: The American journal of physiology
影响因子: --
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通讯作者: Eaton,DC