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首页> 外文期刊>Life sciences >ENDOTHELIN-1 INDUCES AN INCREASE IN TOTAL PROTEIN SYNTHESIS AND EXPRESSION OF THE SMOOTH MUSCLE ALPHA-ACTIN GENE IN VASCULAR SMOOTH MUSCLE CELLS
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ENDOTHELIN-1 INDUCES AN INCREASE IN TOTAL PROTEIN SYNTHESIS AND EXPRESSION OF THE SMOOTH MUSCLE ALPHA-ACTIN GENE IN VASCULAR SMOOTH MUSCLE CELLS

机译:内皮素-1诱导总蛋白合成和血管平滑肌细胞中平滑肌α-肌动蛋白基因的表达

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摘要

The growth response of aortic vascular smooth muscle cells (VSMCs) to chronic hypertension includes vascular hypertrophy. We have shown previously that angiotensin II positively regulates the expression of the human vascular smooth muscle (SM) alpha-actin gene. To further expand our understanding of vasoactive peptide-induced vascular hypertrophy, we studied endothelin-1 (ET-1) regulation of total protein synthesis and cytoskeletal gene expression in VSMCs. In a concentration-dependent manner ET-1 increased [H-3] leucine incorporation by VSMCs (122.4 +/- 5.5%, mean +/- SEM, n = 5). ET-1 (0.1 mu M) induced expression of SM alpha-actin mRNA as detected by Northern blot analysis. Also, ET-1 in a concentration-dependent manner (0.1 nM-0.1 mu M) induced expression of the chloramphenicol acetyl transferase gene driven by 896 bp of the human SM alpha-actin promoter when transiently transfected into rat aortic VSMCs by the calcium phosphate method (141.2 +/- 9.8%, mean +/- SEM, n = 10). These data suggest that part of ET-1-induced increase in protein synthesis is achieved through transcriptional regulation of the SM alpha-actin gene via activation of cis-acting element(s) in the promoter. Such findings help elucidate the role of ET-1 in regulation of vascular growth. [References: 35]
机译:主动脉血管平滑肌细胞(VSMC)对慢性高血压的生长反应包括血管肥大。以前我们已经表明,血管紧张素II积极调节人血管平滑肌(SM)α-肌动蛋白基因的表达。为了进一步扩大我们对血管活性肽诱导的血管肥大的理解,我们研究了内皮素-1(ET-1)对VSMC中总蛋白合成和细胞骨架基因表达的调节。 ET-1以浓度依赖性方式增加了VSMC的[H-3]亮氨酸掺入(122.4 +/- 5.5%,平均值+/- SEM,n = 5)。通过Northern印迹分析检测到ET-1(0.1μM)诱导SMα-肌动蛋白mRNA的表达。同样,当通过磷酸钙瞬时转染到大鼠主动脉VSMC中时,ET-1以浓度依赖性方式(0.1 nM-0.1μM)诱导由人SMα-肌动蛋白启动子896 bp驱动的氯霉素乙酰转移酶基因的表达方法(141.2 +/- 9.8%,平均值+/- SEM,n = 10)。这些数据表明,通过启动子中顺式作用元件的激活,通过SMα-肌动蛋白基因的转录调控,实现了ET-1诱导的蛋白质合成的增加。这些发现有助于阐明ET-1在调节血管生长中的作用。 [参考:35]

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