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肺动脉平滑肌细胞中对肥厚性和增殖性刺激作出反应的即早基因表达。

Immediate-early gene expression in response to hypertrophic and proliferative stimuli in pulmonary arterial smooth muscle cells.

作者信息

Rothman A, Wolner B, Button D, Taylor P

机构信息

Department of Pediatrics, University of California at San Diego, La Jolla 92093.

出版信息

J Biol Chem. 1994 Mar 4;269(9):6399-404.

PMID:8119989
Abstract

Remodeling of the pulmonary vascular tree in pulmonary hypertension is associated with hypertrophy and proliferation of smooth muscle cells. Since the stimuli and signaling pathways for these processes are not well understood, we used a rat pulmonary arterial smooth muscle cell line (PAC1) to examine the effects of thrombin and platelet-derived growth factor (PDGF) on cellular growth and immediate-early gene expression. Over 72 h, thrombin (1 unit/ml) caused hypertrophy as reflected by a 102 +/- 12% increase in protein synthesis and a 49 +/- 11% increase in protein content per cell, but no change in cell number. PDGF (2.5 ng/ml) stimulated proliferation as evidenced by an increase in cell number (doubling in 5 days), but no significant change in protein content per cell. Immediate-early gene expression was examined by Northern blotting: both thrombin and PDGF induced egr-1, c-fos, c-jun, junB, and fra-1 mRNAs within 15 min; the response was maximal at 30-60 min (increases ranging from 2.9- to 9.3-fold over control serum-deprived cells) and returned to base-line levels within 2-4 h. Neither agent affected junD mRNA levels. However, thrombin but not PDGF, caused an increase in fosB mRNA levels (7.7 +/- 4.0-fold higher than control, n = 12, p < 0.0005). The immediate-early gene response to both agonists was generally dependent on extracellular Ca2+, Na2+/H+ exchange, and protein kinase C activation, but not on cAMP. The exception was c-jun mRNA, the levels of which were not affected by inhibition of protein kinase C, but decreased significantly by prevention of cAMP formation. Thapsigargin-sensitive intracellular Ca2+ stores were necessary for the response to thrombin, but not to PDGF. These results demonstrate that thrombin is a hypertrophic agent and that PDGF is a proliferative agent in PAC1 cells. These two agonists stimulate increases in a variety of immediate-early gene mRNAs, but only thrombin induces fosB mRNA.

摘要

肺动脉高压时肺血管树的重塑与平滑肌细胞的肥大和增殖有关。由于这些过程的刺激因素和信号通路尚未完全明确,我们使用大鼠肺动脉平滑肌细胞系(PAC1)来研究凝血酶和血小板衍生生长因子(PDGF)对细胞生长和即刻早期基因表达的影响。在72小时内,凝血酶(1单位/毫升)导致细胞肥大,表现为蛋白质合成增加102±12%,每个细胞的蛋白质含量增加49±11%,但细胞数量无变化。PDGF(2.5纳克/毫升)刺激细胞增殖,表现为细胞数量增加(5天内翻倍),但每个细胞的蛋白质含量无显著变化。通过Northern印迹法检测即刻早期基因表达:凝血酶和PDGF在15分钟内均可诱导egr-1、c-fos、c-jun、junB和fra-1 mRNA表达;反应在30 - 60分钟时达到最大值(比血清饥饿对照细胞增加2.9至9.3倍),并在2 - 4小时内恢复到基线水平。两种因子均不影响junD mRNA水平。然而,凝血酶而非PDGF导致fosB mRNA水平升高(比对照高7.7±4.0倍,n = 12,p < 0.0005)。对两种激动剂的即刻早期基因反应通常依赖于细胞外Ca2+、Na2+/H+交换和蛋白激酶C激活,但不依赖于cAMP。例外的是c-jun mRNA,其水平不受蛋白激酶C抑制的影响,但通过阻止cAMP形成而显著降低。对凝血酶反应而言,毒胡萝卜素敏感的细胞内Ca2+储存是必需的,但对PDGF反应则不是。这些结果表明,凝血酶是PAC1细胞中的肥大因子,而PDGF是增殖因子。这两种激动剂刺激多种即刻早期基因mRNA增加,但只有凝血酶诱导fosB mRNA。

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