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α1-肾上腺素能受体(Alpha1-AR)介导的大鼠心肌细胞中钠-钾-2氯同向转运体(NKCC)的激活涉及该共转运体的细胞外信号调节激酶(ERK)依赖性磷酸化。

Alpha1-AR-mediated activation of NKCC in rat cardiomyocytes involves ERK-dependent phosphorylation of the cotransporter.

作者信息

Andersen Geir Øystein, Skomedal Tor, Enger Mette, Fidjeland Astrid, Brattelid Trond, Levy Finn Olav, Osnes Jan-Bjørn

机构信息

Department of Pharmacology, University of Oslo, Oslo, Norway.

出版信息

Am J Physiol Heart Circ Physiol. 2004 Apr;286(4):H1354-60. doi: 10.1152/ajpheart.00549.2003. Epub 2003 Nov 20.

Abstract

We studied molecular and functional characteristics as well as hormonal regulation of the Na-K-2Cl cotransporter (NKCC) in the isolated rat heart and cardiomyocytes. NKCC activity was measured as bumetanide-sensitive (86)Rb(+) influx in isolated perfused rat hearts and isolated cardiomyocytes. Stimulation of alpha(1)-adrenoceptors (AR) by phenylephrine (30 microM) increased (86)Rb(+) influx. The NKCC inhibitor bumetanide (50 microM) reduced the response to phenylephrine by 45 +/- 13% (n = 12, P < 0.01). PD-98059 (10 microM), an inhibitor of the activation of the mitogen-activated protein kinases extracellular signal-regulated protein kinase 1 and 2 (ERK1/2), reduced the total response to phenylephrine by 51 +/- 13% (n = 10, P < 0.01) and eliminated the bumetanide-sensitive component, indicating that alpha(1)-AR mediated stimulation of NKCC is dependent on activation of ERK1/2. Inhibitors of protein kinase C or phosphatidylinositol 3-kinase had no effect. The presence of NKCC mRNA and protein was demonstrated in isolated rat cardiomyocytes. Phosphorylation of NKCC after alpha(1)-AR stimulation was shown by immunoprecipitation of the phosphoprotein from (32)P(i) prelabeled cardiomyocytes. Increased phosphorylation of the NKCC protein was also abolished by PD-98059. We conclude that the NKCC is present in rat cardiomyocytes and that ion transport by the cotransporter is regulated by alpha(1)-AR stimulation through phosphorylation of this protein involving the ERK pathway.

摘要

我们研究了分离的大鼠心脏和心肌细胞中钠-钾-2氯协同转运蛋白(NKCC)的分子和功能特性以及激素调节。在分离的灌注大鼠心脏和分离的心肌细胞中,NKCC活性通过布美他尼敏感的(86)Rb(+)内流来测量。去氧肾上腺素(30 microM)刺激α(1)-肾上腺素能受体(AR)可增加(86)Rb(+)内流。NKCC抑制剂布美他尼(50 microM)使对去氧肾上腺素的反应降低了45±13%(n = 12,P < 0.01)。PD-98059(10 microM),一种丝裂原活化蛋白激酶细胞外信号调节蛋白激酶1和2(ERK1/2)激活的抑制剂,使对去氧肾上腺素的总反应降低了51±13%(n = 10,P < 0.01),并消除了布美他尼敏感成分,表明α(1)-AR介导的NKCC刺激依赖于ERK1/2的激活。蛋白激酶C或磷脂酰肌醇3激酶的抑制剂没有作用。在分离的大鼠心肌细胞中证实了NKCC mRNA和蛋白的存在。通过对(32)P(i)预标记的心肌细胞中磷蛋白的免疫沉淀显示,α(1)-AR刺激后NKCC发生了磷酸化。PD-98059也消除了NKCC蛋白磷酸化的增加。我们得出结论,NKCC存在于大鼠心肌细胞中,并且该协同转运蛋白的离子转运通过涉及ERK途径的该蛋白磷酸化受α(1)-AR刺激调节。

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