Heywood Wendy E, Searle Jon, Collis Richard, Doykov Ivan, Ashworth Michael, Sebire Neil, Bamber Andrew, Gautel Mathias, Eaton Simon, Coats Caroline J, Elliott Perry M, Mills Kevin
UCL Great Ormond Street Institute of Child Health, 30 Guilford Street, London WC1N 1EH, UK.
Institute of Cardiovascular Science, University College London, Gower Street, London WC1E 6BT, UK.
Life (Basel). 2024 Aug 1;14(8):970. doi: 10.3390/life14080970.
Proteomics studies often explore phenotypic differences between whole organs and systems. Within the heart, more subtle variation exists. To date, differences in the underlying proteome are only described between whole cardiac chambers. This study, using the bovine heart as a model, investigates inter-regional differences and assesses the feasibility of measuring detailed, cross-tissue variance in the cardiac proteome. Using a bovine heart, we created a two-dimensional section through a plane going through two chambers. This plane was further sectioned into 4 × 4 mm cubes and analysed using label-free proteomics. We identified three distinct proteomes. When mapped to the extracted sections, the proteomes corresponded largely to the outer wall of the right ventricle and secondly to the outer wall of the left ventricle, right atrial appendage, tricuspid and mitral valves, modulator band, and parts of the left atrium. The third separate proteome corresponded to the inner walls of the left and right ventricles, septum, and left atrial appendage. Differential protein abundancies indicated differences in energy metabolism between regions. Data analyses of the mitochondrial proteins revealed a variable pattern of abundances of complexes I-V between the proteomes, indicating differences in the bioenergetics of the different cardiac sub-proteomes. Mapping of disease-associated proteins interestingly showed desmoglein-2, for which defects in this protein are known to cause Arrhythmogenic Right Ventricular Dysplasia/Cardiomyopathy, which was present predominantly in the outer wall of the left ventricle. This study highlights that organs can have variable proteomes that do not necessarily correspond to anatomical features.
蛋白质组学研究常常探索整个器官和系统之间的表型差异。在心脏内部,存在更细微的差异。迄今为止,仅描述了整个心脏腔室之间潜在蛋白质组的差异。本研究以牛心脏为模型,调查区域间差异,并评估测量心脏蛋白质组中详细的跨组织差异的可行性。我们使用牛心脏,通过穿过两个腔室的平面创建了一个二维切片。将该平面进一步切成4×4毫米的立方体,并使用无标记蛋白质组学进行分析。我们鉴定出三种不同的蛋白质组。当映射到提取的切片上时,这些蛋白质组在很大程度上对应于右心室的外壁,其次对应于左心室的外壁、右心耳、三尖瓣和二尖瓣、调节束以及左心房的部分区域。第三个独立的蛋白质组对应于左、右心室的内壁、室间隔和左心耳。蛋白质丰度差异表明各区域之间能量代谢存在差异。对线粒体蛋白质的数据分析揭示了各蛋白质组之间复合体I-V丰度的可变模式,表明不同心脏亚蛋白质组的生物能量学存在差异。有趣的是,疾病相关蛋白质的映射显示了桥粒芯糖蛋白-2,已知该蛋白缺陷会导致致心律失常性右室心肌病,其主要存在于左心室的外壁。这项研究强调,器官可能具有不一定与解剖特征相对应的可变蛋白质组。