Department of Molecular Medicine and Surgery, Integrative Physiology, Karolinska Institutet, Stockholm, Sweden.
Am J Physiol Cell Physiol. 2011 Aug;301(2):C272-9. doi: 10.1152/ajpcell.00091.2011. Epub 2011 May 25.
Serum starvation is one of the most frequently performed procedures in molecular biology and there are literally thousands of research papers reporting its use. In fact, this method has become so ingrained in certain areas of research that reports often simply state that cells were serum starved without providing any factual details as to how the procedure was carried out. Even so, we quite obviously lack unequivocal terminology, standard protocols, and perhaps most surprisingly, a common conceptual basis when performing serum starvation. Such inconsistencies not only hinder interstudy comparability but can lead to opposing and inconsistent experimental results. Although it is frequently assumed that serum starvation reduces basal activity of cells, available experimental data do not entirely support this notion. To address this important issue, we studied primary human myotubes, rat L6 myotubes and human embryonic kidney (HEK)293 cells under different serum starvation conditions and followed time-dependent changes in important signaling pathways such as the extracellular signal-regulated kinase 1/2, the AMP-activated protein kinase, and the mammalian target of rapamycin. Serum starvation induced a swift and dynamic response, which displayed obvious qualitative and quantitative differences across different cell types and experimental conditions despite certain unifying features. There was no uniform reduction in basal signaling activity. Serum starvation clearly represents a major event that triggers a plethora of divergent responses and has therefore great potential to interfere with the experimental results and affect subsequent conclusions.
血清饥饿是分子生物学中最常进行的程序之一,实际上有数以千计的研究论文报告了它的使用。事实上,这种方法在某些研究领域已经如此根深蒂固,以至于报告中常常只是简单地说明细胞进行了血清饥饿,而没有提供关于该程序如何进行的任何实际细节。即便如此,我们显然缺乏明确的术语、标准的方案,也许最令人惊讶的是,在进行血清饥饿时缺乏共同的概念基础。这种不一致性不仅阻碍了研究之间的可比性,还可能导致相反和不一致的实验结果。尽管人们常常假设血清饥饿会降低细胞的基础活性,但现有的实验数据并不完全支持这一观点。为了解决这个重要问题,我们在不同的血清饥饿条件下研究了原代人肌管、大鼠 L6 肌管和人胚肾(HEK)293 细胞,并跟踪了细胞外信号调节激酶 1/2、AMP 激活的蛋白激酶和雷帕霉素哺乳动物靶蛋白等重要信号通路的时间依赖性变化。血清饥饿诱导了迅速而动态的反应,尽管存在某些统一特征,但在不同的细胞类型和实验条件下表现出明显的定性和定量差异。基础信号活性没有统一的降低。血清饥饿显然代表了一个主要事件,引发了大量不同的反应,因此很有可能干扰实验结果并影响后续结论。