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钠钾ATP酶参与胰岛素样生长因子-I对培养的大鼠星形胶质细胞的促有丝分裂作用。

Involvement of Na+,K(+)ATPase in the mitogenic effect of insulin-like growth factor-I on cultured rat astrocytes.

作者信息

Matsuda T, Murata Y, Tanaka K, Hosoi R, Hayashi M, Tamada K, Takuma K, Baba A

机构信息

Department of Pharmacology, Faculty of Pharmaceutical Sciences, Osaka University, Japan.

出版信息

J Neurochem. 1996 Feb;66(2):511-6. doi: 10.1046/j.1471-4159.1996.66020511.x.

Abstract

We have previously reported that insulin/insulin-like growth factor (IGF)-I induced the alpha 1 isoform of Na+,K(+)-ATPase in cultured astrocytes. In this study the effects of insulin/IGF-I on Na+,K(+)-ATPase activity and cell proliferation were examined in astrocytes cultured under the various conditions, to test the possible involvement of the enzyme activity in the mitogenic action of IGF-I on astrocytes. Insulin increased Na+,K(+)-ATPase activity and stimulated cell proliferation in subconfluent astrocytes (cultured for 7-14 days in vitro). In contrast, these effects were not observed in confluent cells (cultured for 28 days). Furthermore, insulin stimulated neither the enzyme activity nor [3H]thymidine incorporation in astrocytes preincubated in fetal calf serum-free medium for 2 days (quiescent cells) and treated with dibutyryl cyclic AMP (differentiated cells). The increases in Na+,K(+)-ATPase activity and expression of the alpha 1 mRNA preceded the mitogenic effect. 125I-IGF-I binding experiment showed that all the cells used here had similar binding characteristics. The insulin-induced increase in enzyme activity was not affected by 1-(5-isoquinolinesulfonyl)-2-methylpiperazine (H-7), and it was observed even in Ca(2+)-free medium. The stimulation by IGF-I of [3H]thymidine incorporation was attenuated by ouabain and a low external K+ level. These findings suggest that stimulation of Na+,K(+)-ATPase activity is involved in the mitogenic action of IGF-I on cultured astrocytes.

摘要

我们之前曾报道,胰岛素/胰岛素样生长因子(IGF)-I可诱导培养的星形胶质细胞中Na⁺,K⁺-ATP酶的α1亚型。在本研究中,我们检测了胰岛素/IGF-I在不同条件下培养的星形胶质细胞中对Na⁺,K⁺-ATP酶活性和细胞增殖的影响,以测试该酶活性在IGF-I对星形胶质细胞的促有丝分裂作用中可能的参与情况。胰岛素增加了亚汇合星形胶质细胞(体外培养7 - 14天)的Na⁺,K⁺-ATP酶活性并刺激了细胞增殖。相比之下,在汇合细胞(培养28天)中未观察到这些效应。此外,胰岛素对在无胎牛血清培养基中预孵育2天的星形胶质细胞(静止细胞)和用二丁酰环磷腺苷处理的细胞(分化细胞)的酶活性和[³H]胸腺嘧啶核苷掺入均无刺激作用。Na⁺,K⁺-ATP酶活性的增加和α1 mRNA的表达先于促有丝分裂效应。¹²⁵I-IGF-I结合实验表明,这里使用的所有细胞具有相似的结合特性。胰岛素诱导的酶活性增加不受1-(5-异喹啉磺酰基)-2-甲基哌嗪(H-7)影响,甚至在无钙培养基中也可观察到。哇巴因和低细胞外钾水平减弱了IGF-I对[³H]胸腺嘧啶核苷掺入的刺激作用。这些发现表明,Na⁺,K⁺-ATP酶活性的刺激参与了IGF-I对培养的星形胶质细胞的促有丝分裂作用。

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