INSERM, UMR-S 1180, Signalisation et Physiopathologie Cardiovasculaire, Université Paris-Saclay Châtenay-Malabry France.
J Am Heart Assoc. 2022 Sep 20;11(18):e026292. doi: 10.1161/JAHA.122.026292. Epub 2022 Sep 8.
Background Human cardiac biopsies are widely used in clinical and fundamental research to decipher molecular events that characterize cardiac physiological and pathophysiological states. One of the main approaches relies on the analysis of semiquantitative immunoblots that reveals alterations in protein expression levels occurring in diseased hearts. To maintain semiquantitative results, expression level of target proteins must be standardized. The expression of HKP (housekeeping proteins) is commonly used to this purpose. Methods and Results We evaluated the stability of HKP expression (actin, β-tubulin, GAPDH, vinculin, and calsequestrin) and total protein staining within control (coefficient of variation) and comparatively with ischemic human heart biopsies ( value). All HKP exhibited a high level of intragroup (ie, actin, β-tubulin, and GAPDH) and/or intergroup variability (ie, GAPDH, vinculin, and calsequestrin). Among all, we found total protein staining to exhibit the highest degree of stability within and between groups, which makes this reference the best to study protein expression level in human biopsies from ischemic hearts and age-matched controls. In addition, we illustrated that using an inappropriate reference protein marker misleads interpretation on SERCA2 (sarco/endoplasmic reticulum Ca ATPase) and cMyBPC (cardiac myosin binding protein-C) expression level after myocardial infarction. Conclusions These reemphasize the need to standardize the level of protein expression with total protein staining in comparative immunoblot studies on human samples from control and diseased hearts.
背景
人类心脏活检在临床和基础研究中被广泛用于解析心脏生理和病理状态特征的分子事件。其中一种主要方法依赖于半定量免疫印迹分析,该方法揭示了病变心脏中蛋白表达水平的变化。为了保持半定量结果,必须对靶蛋白的表达水平进行标准化。通常使用 HKP(管家蛋白)的表达来达到此目的。
方法和结果
我们评估了 HKP(肌动蛋白、β-微管蛋白、GAPDH、波形蛋白和钙网蛋白)表达和总蛋白染色的稳定性,包括对照组(变异系数)和缺血性人类心脏活检组( 值)。所有 HKP 都表现出高组内(即肌动蛋白、β-微管蛋白和 GAPDH)和/或组间变异性(即 GAPDH、波形蛋白和钙网蛋白)。在所有 HKP 中,我们发现总蛋白染色在组内和组间具有最高的稳定性,这使其成为研究缺血性心脏和年龄匹配对照的人类活检中蛋白表达水平的最佳参考。此外,我们还表明,使用不合适的参考蛋白标志物可能会导致肌浆网 Ca2+-ATP 酶(SERCA2)和心肌肌球蛋白结合蛋白-C(cMyBPC)表达水平在心肌梗死后的解释出现错误。
结论
这些结果再次强调了在比较免疫印迹研究中,需要用人心脏样本的总蛋白染色来标准化蛋白表达水平。