Proteomic identification of protein markers of stages of heart formation in humans

• Published in: Russian journal of developmental biology Vol. 48; no. 5; pp. 301 - 306
• Main Authors: Kovaleva, M. A., Kovalev, L. I., Ivanov, A. V., Serebryakova, M. V., Shishkin, S. S.
• Format: Journal Article
• Language: English
• Published: Moscow Pleiades Publishing 01-09-2017; Springer Nature B.V
• Subjects: Animal Anatomy; ATP synthase; Biomedical and Life Sciences; Contractility; Creatine; Creatine kinase; Desmin; Developmental Biology; Developmental stages; Fetuses; Heat shock proteins; Histology; Isoforms; Life Sciences; Mechanisms of Normal and Abnormal Tissue Development; Mitochondria; Morphology; Muscle contraction; Myocardium; Myosin; Protein composition; Tropomyosin; Ventricle; cardiogenesis; mass spectrometric identification; human; proteins
• ISSN: 1062-3604; 1608-3326
• DOI: 10.1134/S1062360417050046

On the basis of the results of proteomic analysis and mass spectrometric identification of human myocardium proteins exhibiting pronounced quantitative changes in the dynamics of prenatal cardiogenesis, changes in the expression level of proteins of three families (mitochondrial, contractile, and heat shock) have been identified. The complex of human myocardium mitochondrial proteins (for example, α and β isoforms of ATP synthase, aconitase 2, creatine phosphokinase M-subunit, and 60-kDa heat shock protein) largely finishes its development according to the adult type by developmental week 24. The formation of the protein composition of human myocardium contractile structures (for example, desmin, myosin regulatory light chain 2, fetal ventricular essential isoform 1, canonical α-tropomyosin, and fetal isoform 6) reflects the initial stage of myofibril development until developmental week 8 (replacement of fetal isoforms of contractile proteins with adult ones with the involvement of the phosphorylated isoform of 27-kDa heat shock protein), the stage of their qualitative and quantitative structuring by developmental weeks 20–24, and the final formation of the adult phenotype of contractile structures by 2 years of life.