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蛋白激酶B/Akt在胃酸分泌中的功能作用。

Functional role of protein kinase B/Akt in gastric acid secretion.

作者信息

Todisco A, Pausawasdi N, Ramamoorthy S, Del Valle J, Van Dyke R W, Askari F K

机构信息

Department of Internal Medicine, University of Michigan Medical Center, Ann Arbor, Michigan 48109, USA.

出版信息

J Biol Chem. 2001 Dec 7;276(49):46436-44. doi: 10.1074/jbc.M009645200. Epub 2001 Sep 19.

Abstract

Epidermal growth factor (EGF) stimulates gastric acid secretion and H(+)/K(+)-ATPase alpha-subunit gene expression. Because EGF activates the serine-threonine protein kinase Akt, we explored the role of Akt in gastric acid secretion. Akt phosphorylation and activation were measured by kinase assays and by Western blots with an anti-phospho-Akt antibody, using lysates of purified (>95%) canine gastric parietal cells in primary culture. EGF induced Akt phosphorylation and activation, whereas carbachol had no effect. LY294002, an inhibitor of phosphoinositide 3-kinase, completely blocked EGF induction of Akt phosphorylation, whereas the MEK1 inhibitor PD98059 and the protein kinase C inhibitor GF109203X had no effect. We examined the role of Akt in H(+)/K(+)-ATPase gene expression by Northern blotting using a canine H(+)/K(+)-ATPase alpha-subunit cDNA probe. The parietal cells were transduced with a multiplicity of infection of 100 of the adenoviral vector Ad.Myr-Akt, which overexpresses a constitutively active Akt gene, or with the control vector Ad.CMV-beta-gal, which expresses beta-galactosidase. Ad.Myr-Akt induced H(+)/K(+)-ATPase alpha-subunit gene expression 3-fold, whereas it failed to stimulate the gene cyclooxygenase-2, which was potently induced by carbachol in the same parietal cells. Ad.Myr-Akt induced aminopyrine uptake 4-fold, and it potentiated the stimulatory action of carbachol 3-fold. In contrast, Ad.Myr-Akt failed to induce changes in either parietal cell actin content, measured by Western blots with an anti-actin antibody or in the organization of the actin cellular cytoskeleton, visualized by fluorescein phalloidin staining and confocal microscopy. Transduction of the parietal cells with a multiplicity of infection of 100 of the adenoviral vector Ad.dom.neg.Akt, which overexpresses an inhibitor of Akt, blocked the stimulatory effect of EGF on both aminopyrine uptake and H(+)/K(+)-ATPase production, measured by Western blots with an anti-H(+)/K(+)-ATPase alpha-subunit antibody. Thus, EGF induces a cascade of events in the parietal cells that results in the activation of Akt. The functional role of Akt appears to be stimulation of gastric acid secretion through induction of H(+)/K(+)-ATPase expression.

摘要

表皮生长因子(EGF)可刺激胃酸分泌及H(+)/K(+)-ATP酶α亚基基因表达。由于EGF可激活丝氨酸-苏氨酸蛋白激酶Akt,我们探讨了Akt在胃酸分泌中的作用。采用激酶分析及抗磷酸化Akt抗体进行蛋白质印迹法,利用原代培养的纯化(>95%)犬胃壁细胞裂解物检测Akt的磷酸化及激活情况。EGF可诱导Akt磷酸化及激活,而卡巴胆碱无此作用。磷酸肌醇3激酶抑制剂LY294002可完全阻断EGF诱导的Akt磷酸化,而MEK1抑制剂PD98059及蛋白激酶C抑制剂GF109203X则无此作用。我们使用犬H(+)/K(+)-ATP酶α亚基cDNA探针,通过Northern印迹法检测Akt在H(+)/K(+)-ATP酶基因表达中的作用。以感染复数100用腺病毒载体Ad.Myr-Akt转导壁细胞,该载体可过表达组成型活性Akt基因,或以表达β-半乳糖苷酶的对照载体Ad.CMV-β-gal进行转导。Ad.Myr-Akt可使H(+)/K(+)-ATP酶α亚基基因表达增加3倍,而它未能刺激环氧合酶-2基因,在相同壁细胞中该基因可被卡巴胆碱有效诱导。Ad.Myr-Akt可使氨基比林摄取增加4倍,并使卡巴胆碱的刺激作用增强3倍。相反,Ad.Myr-Akt未能诱导壁细胞肌动蛋白含量的变化(采用抗肌动蛋白抗体进行蛋白质印迹法检测),也未引起肌动蛋白细胞骨架组织的改变(通过荧光素鬼笔环肽染色及共聚焦显微镜观察)。以感染复数100用腺病毒载体Ad.dom.neg.Akt转导壁细胞,该载体可过表达Akt抑制剂,可阻断EGF对氨基比林摄取及H(+)/K(+)-ATP酶产生的刺激作用(采用抗H(+)/K(+)-ATP酶α亚基抗体进行蛋白质印迹法检测)。因此,EGF可在壁细胞中诱导一系列事件,导致Akt激活。Akt的功能作用似乎是通过诱导H(+)/K(+)-ATP酶表达来刺激胃酸分泌。

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