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成年心脏细胞培养中肥大与萎缩的调控

Regulation of hypertrophy and atrophy in cultured adult heart cells.

作者信息

Clark W A, Rudnick S J, LaPres J J, Andersen L C, LaPointe M C

机构信息

Department of Medicine, Northwestern University Medical School, Chicago, Ill. 60611.

出版信息

Circ Res. 1993 Dec;73(6):1163-76. doi: 10.1161/01.res.73.6.1163.

Abstract

Mechanical loading and alpha-adrenergic receptor stimulation have both been shown to induce hypertrophy in isolated neonatal heart cells. The present study examined the effects of adrenergic hormones and contractile activity on the hypertrophic response in isolated adult feline cardiomyocytes maintained for more than 14 days in insulin- and serum-supplemented medium. Measurements of the hypertrophic response included cell size, total protein content, myosin heavy chain content, and the time course of activation of increased protein synthesis. Reactivation of the "fetal" gene program was evaluated by secretion of atrial natriuretic factor (ANF) into the medium. Significant myocyte hypertrophy was induced in both quiescent myocytes treated with alpha 1-adrenergic agonists and in beating myocytes treated with beta-adrenergic agonists. However, there were both quantitative and qualitative differences in the response to each type of stimulation. alpha-Adrenergic agonists promoted an increase in cell size, protein content, and ANF secretion but not myofibrillar reorganization, which was observed only in beating myocytes. In contrast to results reported for neonatal heart cells, determinants of hypertrophy in beating myocytes exceeded those in nonbeating alpha 1-adrenergic agonist-treated heart cells in every parameter examined. In addition, in the case of both beating and alpha-adrenergic stimulation, there were marked time-dependent variations in rates of protein synthesis over the interval of 4 hours to 7 days of treatment with each type of stimulus. Differences were also encountered in correlations between rates of protein synthesis and protein accumulation over this interval. The effect of beating was particularly important both to the reorganization of myofibrillar structure and the metabolism of myosin heavy chain. In cultures in which beating was inhibited with the calcium channel antagonist nifedipine, the loss of myosin heavy chain was significantly greater than that of total protein.

摘要

机械负荷和α-肾上腺素能受体刺激均已被证明可诱导离体新生心脏细胞肥大。本研究检测了肾上腺素能激素和收缩活动对在补充胰岛素和血清的培养基中维持超过14天的离体成年猫心肌细胞肥大反应的影响。肥大反应的测量指标包括细胞大小、总蛋白含量、肌球蛋白重链含量以及蛋白质合成增加的激活时间进程。通过心房利钠因子(ANF)分泌到培养基中来评估“胎儿”基因程序的重新激活。用α1-肾上腺素能激动剂处理的静止心肌细胞和用β-肾上腺素能激动剂处理的跳动心肌细胞均诱导出显著的心肌细胞肥大。然而,对每种刺激类型的反应在数量和质量上均存在差异。α-肾上腺素能激动剂促进细胞大小、蛋白质含量和ANF分泌增加,但不促进肌原纤维重组,而肌原纤维重组仅在跳动心肌细胞中观察到。与新生心脏细胞的报道结果相反,在每个检测参数中,跳动心肌细胞肥大的决定因素均超过未跳动的α1-肾上腺素能激动剂处理的心脏细胞。此外,在跳动和α-肾上腺素能刺激的情况下,在每种刺激处理4小时至7天的时间段内,蛋白质合成速率均有明显的时间依赖性变化。在该时间段内,蛋白质合成速率与蛋白质积累之间的相关性也存在差异。跳动对肌原纤维结构的重组和肌球蛋白重链的代谢尤为重要。在用钙通道拮抗剂硝苯地平抑制跳动的培养物中,肌球蛋白重链的损失明显大于总蛋白的损失。

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