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首页> 外文期刊>The Journal of investigative dermatology. >1alpha,25-Dihydroxyvitamin D3 Stimulates Activator Protein 1 DNA-Binding Activity by a Phosphatidylinositol 3-Kinase/Ras/MEK/Extracellular Signal Regulated Kinase 1/2 and c-Jun N-Terminal Kinase 1-Dependent Increase in c-Fos, Fra1, and c-Jun Expressi
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1alpha,25-Dihydroxyvitamin D3 Stimulates Activator Protein 1 DNA-Binding Activity by a Phosphatidylinositol 3-Kinase/Ras/MEK/Extracellular Signal Regulated Kinase 1/2 and c-Jun N-Terminal Kinase 1-Dependent Increase in c-Fos, Fra1, and c-Jun Expressi

机译:1alpha,25-Dihydroxyvitamin D3刺激磷脂酰肌醇3-激酶/ Ras / MEK /细胞外信号调节激酶1/2和c-Jun N-末端激酶1依赖性增加c-Fos,Fra1活化蛋白1 DNA结合活性和c-Jun Expressi

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摘要

1alpha,25-Dihydroxyvitamin D3 added to human keratinocytes increases differentiation through an activation of the transcription factor activator protein 1. We have previously reported that the 1alpha,25-dihydroxyvitamin D3-induced increase of activator protein 1 DNA binding activity is mediated by a protein kinase C-independent mechanism. The purpose of this study was to investigate further the mechanisms by which 1alpha,25-dihydroxyvitamin D3 modulates activator protein 1 DNA binding activity in cultured normal human keratinocytes. Western blotting experiments revealed that 1alpha,25-dihydroxyvitamin D3 caused a rapid and transient activation of the mitogen-activated protein kinases, extracellular signal regulated kinase 1/2 and c-Jun N-terminal kinase 1. 1alpha,25-Dihydroxyvitamin D3 also enhanced the expression of the activator protein 1 subunits, c-Fos, Fra1, and c-Jun as determined by northern and western blotting. The 1alpha,25-dihydroxyvitamin D3-induced activator protein 1 DNA binding activity was completely blocked by the MEK inhibitor PD 98059 indicating that the MEK/extracellular signal regulated kinase pathway is involved in the activation of activator protein 1. Transfection experiments showed that 1alpha,25-dihydroxyvitamin D3 also increased the activator protein 1-dependent transactivation, which was completely blocked by expression of a dominant negative Ras, suggesting that the 1alpha,25-dihydroxyvitamin D3-induced activator protein 1 activity involves Ras-dependent signaling. Furthermore, preincubation of the keratinocytes with the specific phosphatidylinositol 3-kinase inhibitors, Wortmannin and LY294002, demonstrated that the 1alpha,25-dihydroxyvitamin D3-induced activation of extracellular signal regulated kinase 1/2 and c-Jun N-terminal kinase 1 required phosphatidylinositol 3-kinase activity. Finally, preincubation of keratinocytes with a polyclonal antibody against the membrane receptor annexin II, blocked the 1alpha,25-dihydroxyvitamin D3-induced activation of extracellular signal regulated kinase 1/2 and c-Jun N-terminal kinase 1. Taken together, our results indicate that 1alpha,25-dihydroxyvitamin D3, via binding to the membrane receptor annexin II, induces activation of the phos-phatidylinositol 3-kinase/Ras/MEK/extracellular signal regulated kinase 1/2 and c-Jun N-terminal kinase 1 signal transduction pathway resulting in increased expression of c-Fos, Fra1, and c-Jun, and subsequently increased activator protein 1 DNA binding activity and gene transcription.
机译:添加到人角质形成细胞中的1alpha,25-二羟基维生素D3通过激活转录因子激活蛋白1来增加分化。我们先前已经报道过1alpha,25-dihydroxyvitamin D3诱导的激活蛋白1 DNA结合活性的增加是由一种蛋白质介导的。激酶C独立机制。这项研究的目的是进一步研究1α,25-二羟基维生素D3调节正常人角质形成细胞中激活蛋白1 DNA结合活性的机制。蛋白质印迹实验表明,1alpha,25-dihydroxyvitamin D3引起了丝裂原激活的蛋白激酶,细胞外信号调节激酶1/2和c-Jun N-末端激酶1的快速和瞬时激活。1alpha,25-dihydroxyvitamin D3也增强了通过Northern和Western印迹确定活化蛋白1亚基c-Fos,Fra1和c-Jun的表达。 1α,25-二羟基维生素D3诱导的激活蛋白1 DNA结合活性被MEK抑制剂PD 98059完全阻断,表明MEK /细胞外信号调节激酶途径与激活蛋白1的激活有关。转染实验表明1alpha, 25-二羟基维生素D3也增加了激活蛋白1依赖性反式激活,该激活被显性负性Ras的表达完全阻断,表明1α,25-二羟基维生素D3诱导的激活蛋白1活性涉及Ras依赖性信号传导。此外,用特定的磷脂酰肌醇3-激酶抑制剂Wortmannin和LY294002对角质形成细胞进行预培养,结果表明1α,25-二羟基维生素D3诱导的细胞外信号调节激酶1/2和c-Jun N端激酶1的活化需要磷脂酰肌醇。 3-激酶活性。最后,用针对膜受体膜联蛋白II的多克隆抗体对角质形成细胞进行预培养,阻断了1alpha,25-dihydroxyvitamin D3诱导的细胞外信号调节激酶1/2和c-Jun N-末端激酶1的活化。表明1alpha,25-dihydroxyvitamin D3,通过与膜受体膜联蛋白II的结合,诱导磷酸化磷脂酰肌醇3-激酶/ Ras / MEK /细胞外信号调节激酶1/2和c-Jun N端激酶1信号的激活转导途径导致c-Fos,Fra1和c-Jun的表达增加,随后激活蛋白1 DNA结合活性和基因转录增加。

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