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3,3',5-三碘-L-甲状腺原氨酸上调肺泡上皮细胞中钠钾-ATP酶活性及细胞表面表达是依赖于Src激酶和磷脂酰肌醇3-激酶的。

3,3',5-Triiodo-L-thyronine up-regulation of Na,K-ATPase activity and cell surface expression in alveolar epithelial cells is Src kinase- and phosphoinositide 3-kinase-dependent.

作者信息

Lei Jianxun, Mariash Cary N, Ingbar David H

机构信息

Department of Medicine, University of Minnesota, Minneapolis, Minnesota 55455, USA.

出版信息

J Biol Chem. 2004 Nov 12;279(46):47589-600. doi: 10.1074/jbc.M405497200. Epub 2004 Aug 31.

Abstract

We previously reported that thyroid hormone, 3,3',5-triiodo-l-thyronine (T3), increased Na,K-ATPase activity of adult rat alveolar epithelial cells in a transcription-independent manner via increased cell surface expression of the alpha(1) and beta(1) subunits of Na,K-ATPase. Now we sought to identify signaling molecules necessary for T3 stimulation of Na,K-ATPase activity in alveolar epithelial cells. Whereas protein kinase A inhibitor H-8 and protein kinase C inhibitor bisindolymaleimide did not block the T3-induced increase in Na,K-ATPase activity, two inhibitors of phosphoinositide 3-kinase (PI3K), wortmannin and Ly294002, and two Src kinase inhibitors, PP1 and PP2, blocked the T3-induced Na,K-ATPase activity. T3 stimulated the activity of PI3K as measured by phosphatidylinositol 3-phosphate. T3 also stimulated the serine 473 phosphorylation of the PI3K downstream molecule PKB/Akt in a dose-dependent manner. Transient expression of a constitutively active mutant of the PI3K catalytic subunit p110 augmented Na,K-ATPase activity and increased the amount of cell surface Na,K-ATPase alpha(1) subunit protein. T3 also stimulated Src family kinase activity. Transient expression of a constitutively active Src kinase increased Na,K-ATPase activity, PI3K activity, and phosphorylation of PKB/Akt at serine 473. PP1 or PP2 blocked T3-stimulated PKB/Akt phosphorylation at serine 473 and PI3K activity that was activated by an active mutant of Src; however, wortmannin did not inhibit the T3-stimulated Src kinase activity. Although PP1 and wortmannin abolished the increase in Na,K-ATPase activity induced by the active mutant of Src, PP1 did not inhibit the active mutant of PI3K-up-regulated Na,K-ATPase activity. In summary, T3 stimulates the PI3K/PKB pathway via the Src family of tyrosine kinases, and activation of both the Src family kinases and PI3K is required for the T3-induced stimulation of Na,K-ATPase activity and its cell surface expression in adult rat alveolar epithelial cells.

摘要

我们之前报道过,甲状腺激素3,3',5-三碘-L-甲状腺原氨酸(T3)通过增加钠钾-ATP酶α(1)和β(1)亚基的细胞表面表达,以一种不依赖转录的方式提高成年大鼠肺泡上皮细胞的钠钾-ATP酶活性。现在我们试图确定T3刺激肺泡上皮细胞钠钾-ATP酶活性所需的信号分子。蛋白激酶A抑制剂H-8和蛋白激酶C抑制剂双吲哚马来酰亚胺并未阻断T3诱导的钠钾-ATP酶活性增加,而两种磷酸肌醇3-激酶(PI3K)抑制剂渥曼青霉素和Ly294002,以及两种Src激酶抑制剂PP1和PP2,则阻断了T3诱导的钠钾-ATP酶活性。通过磷脂酰肌醇3-磷酸测定发现,T3刺激了PI3K的活性。T3还以剂量依赖的方式刺激了PI3K下游分子蛋白激酶B/蛋白激酶B(PKB/Akt)的丝氨酸473磷酸化。PI3K催化亚基p110组成型活性突变体的瞬时表达增强了钠钾-ATP酶活性,并增加了细胞表面钠钾-ATP酶α(1)亚基蛋白的量。T3还刺激了Src家族激酶活性。组成型活性Src激酶的瞬时表达增加了钠钾-ATP酶活性、PI3K活性以及PKB/Akt在丝氨酸473处的磷酸化。PP1或PP2阻断了T3刺激的PKB/Akt在丝氨酸473处的磷酸化以及由Src活性突变体激活的PI3K活性;然而,渥曼青霉素并未抑制T3刺激的Src激酶活性。尽管PP1和渥曼青霉素消除了由Src活性突变体诱导的钠钾-ATP酶活性增加,但PP1并未抑制PI3K活性突变体上调的钠钾-ATP酶活性。总之,T3通过酪氨酸激酶Src家族刺激PI3K/PKB途径,并且Src家族激酶和PI3K的激活是T3诱导成年大鼠肺泡上皮细胞钠钾-ATP酶活性及其细胞表面表达所必需的。

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