AI Article Synopsis

  • This study analyzes the proteomic differences within specific regions of the bovine heart, aiming to understand variations beyond just whole cardiac chambers.
  • Researchers identified three distinct proteomes based on samples taken from different heart sections, revealing relationships between proteomic variations and cardiac regions like the outer walls of ventricles and the septum.
  • Findings showed differences in protein abundances related to energy metabolism, and a specific disease-related protein was linked predominantly to the outer wall of the left ventricle, emphasizing that proteomic diversity doesn't always align with anatomical structures.

Article Abstract

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.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11355120PMC
http://dx.doi.org/10.3390/life14080970DOI Listing

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