Measurement of protein synthesis and degradation in C2C2) myoblasts using extracts of muscle from hormone treated bovine.

J L Montgomery, W M Harper, M F Miller, K J Morrow, J R Blanton
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引用次数: 10

Abstract

A detailed methodology is described for determination of treatment effects on muscle cell protein synthesis and muscle cell protein degradation in a cell culture system. C(2)C(22) mouse myoblasts were treated with growth media containing muscle extracts from bovine treated with different pharmaceutical agents. Radiolabeled amino acids were added to the growth media to determine treatment effects on protein synthesis and protein degradation. Percent protein synthesis was calculated by measuring amino acid uptake as a percentage over internal control. Percent protein degradation was measured using a pulse chase technique. These procedures will allow researchers to determine treatment effects on overall protein synthesis and degradation in vitro in a relatively short amount of time without excessive costs. A second benefit is that animals do not have to be fed radiolabeled feedstuffs. These procedures are not intended to elucidate the mechanisms behind pharmaceutical enhancement of muscle cell protein synthesis or protein degradation.

用激素处理牛肌肉提取物测定C2C2成肌细胞蛋白质合成和降解。
详细的方法描述了在细胞培养系统中测定对肌肉细胞蛋白质合成和肌肉细胞蛋白质降解的治疗效果。用含有不同药物处理过的牛肌肉提取物的生长培养基处理C(2)C(22)小鼠成肌细胞。在生长培养基中添加放射性标记氨基酸,以确定处理对蛋白质合成和蛋白质降解的影响。蛋白质合成百分比是通过测量氨基酸摄取作为内部控制的百分比来计算的。使用脉冲追踪技术测量蛋白质降解的百分比。这些程序将使研究人员能够在相对较短的时间内确定治疗对体外整体蛋白质合成和降解的影响,而不需要过多的成本。第二个好处是动物不需要喂食放射性标签饲料。这些程序并不是为了阐明药物增强肌肉细胞蛋白质合成或蛋白质降解的机制。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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