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蛋白磷酸酶2A对于气管平滑肌和中国仓鼠卵巢细胞中cGMP依赖性蛋白激酶激活钙激活钾电流至关重要。

Protein phosphatase 2A is essential for the activation of Ca2+-activated K+ currents by cGMP-dependent protein kinase in tracheal smooth muscle and Chinese hamster ovary cells.

作者信息

Zhou X B, Ruth P, Schlossmann J, Hofmann F, Korth M

机构信息

Institut für Pharmakologie und Toxikologie der Technischen Universität München, Biedersteinerstrasse 29, D-80802 München, Federal Republic of Germany.

出版信息

J Biol Chem. 1996 Aug 16;271(33):19760-7. doi: 10.1074/jbc.271.33.19760.

Abstract

The regulation of Ca2+-activated K+ channels (KCa channels) by cGMP-dependent protein kinase (cGMP kinase) and its molecular mechanism were investigated in Chinese hamster ovary (CHO) and tracheal smooth muscle cells. In CHO wild-type cells (CHO-WT cells) and in CHO cells stably transfected with cGMP kinase Ialpha (CHO-cGK cells), KCa channels with intermediate conductance (approximately 50 picosiemens) were identified. Due to the basal activity of cGMP kinase, Ca2+-activated K+ currents had a higher sensitivity toward the cytosolic Ca2+ concentration in CHO-cGK cells than in CHO-WT cells. Dialysis of the active fragment of cGMP kinase (300 n) into CHO-WT cells or of cGMP into CHO-cGK cells increased the Ca2+-activated K+ current, while the catalytic subunit of cAMP-dependent protein kinase (cAMP kinase) was without effect. In cell-attached patches obtained from freshly isolated bovine tracheal smooth muscle cells, the open state probability (NPo) of maxi-KCa channels (conductance of approximately 260 picosiemens) was enhanced by 300 microM 8-(4-chlorophenylthio)-cGMP, a specific and potent activator of cGMP kinase. In contrast, 1 microM isoprenaline, 20 microM forskolin, and 3 mM 8-bromo-cAMP failed to enhance KCa channel activity. In excised inside-out patches, only the active fragment of cGMP kinase (but not that of cAMP kinase) increased NPo when applied to the cytosolic side of the patch. The enhancement of NPo by cGMP kinase was inhibited in CHO cells as well as in tracheal smooth muscle cells by the cGMP kinase inhibitor KT 5823 (1 microM) and the protein phosphatase (PP) inhibitors microcystin (5 microM) and okadaic acid (10 nM). The catalytic subunit of PP2A (but not that of PP1) mimicked the effect of cGMP kinase on NPo in excised inside-out patches. The results show that cGMP kinase regulates two different KCa channels in two unrelated cell types by the same indirect mechanism, which requires the activity of PP2A. The regulation of the KCa channel is specific for cGMP kinase and is not mimicked by cAMP kinase.

摘要

在中国仓鼠卵巢(CHO)细胞和气管平滑肌细胞中,研究了环磷酸鸟苷依赖性蛋白激酶(cGMP激酶)对钙激活钾通道(KCa通道)的调节作用及其分子机制。在CHO野生型细胞(CHO-WT细胞)和稳定转染cGMP激酶Iα的CHO细胞(CHO-cGK细胞)中,鉴定出了具有中等电导(约50皮西门子)的KCa通道。由于cGMP激酶的基础活性,钙激活钾电流在CHO-cGK细胞中对胞质钙浓度的敏感性高于CHO-WT细胞。将cGMP激酶的活性片段(300 n)注入CHO-WT细胞或将cGMP注入CHO-cGK细胞可增加钙激活钾电流,而环磷酸腺苷依赖性蛋白激酶(cAMP激酶)的催化亚基则无此作用。在从新鲜分离的牛气管平滑肌细胞获得的细胞贴附片中,cGMP激酶的特异性强效激活剂300 microM 8-(4-氯苯硫基)-cGMP可增强大电导KCa通道(电导约为260皮西门子)的开放概率(NPo)。相比之下,1 microM异丙肾上腺素、20 microM福斯可林和3 mM 8-溴环磷酸腺苷未能增强KCa通道活性。在切除的内面向外的片中,仅将cGMP激酶的活性片段(而非cAMP激酶的活性片段)应用于片的胞质侧时可增加NPo。cGMP激酶抑制剂KT 5823(1 microM)以及蛋白磷酸酶(PP)抑制剂微囊藻毒素(5 microM)和冈田酸(10 nM)可抑制CHO细胞和气管平滑肌细胞中cGMP激酶对NPo的增强作用。蛋白磷酸酶2A(PP2A)的催化亚基(而非PP1的催化亚基)在切除的内面向外的片中模拟了cGMP激酶对NPo的作用。结果表明,cGMP激酶通过相同的间接机制调节两种不相关细胞类型中的两种不同KCa通道,这需要PP2A的活性。KCa通道的调节对cGMP激酶具有特异性,cAMP激酶不能模拟其作用。

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