V. Pelouch et al., DIFFERENCES BETWEEN ATRIAL AND VENTRICULAR PROTEIN PROFILING IN CHILDREN WITH CONGENITAL HEART-DISEASE, Molecular and cellular biochemistry, 147(1-2), 1995, pp. 43-49
The purpose of the present study was to compare protein profiling of a
tria and ventricles in children operated for congenital heart disease.
Tissue samples were obtained during surgery from patients with normox
emic (ventricular and atrial septal defects) and hypoxemic (tetralogy
of Fallot) diseases. Protein fractions were isolated by stepwise extra
ction from both right ventricular and atrial musculature. The concentr
ation of total atrial protein in the normoxemic patients exceeded the
ventricular value (110 +/- 2.1 vs 99.9 +/- 4.0 mg.g(-1) wet weight, re
spectively); in the hypoxemic group this atrio-ventricular difference
disappeared. The concentration of contractile proteins in all cardiac
samples was significantly higher in the ventricles as compared with at
ria, while the concentration of collagenous proteins was significantly
higher in the atria (due to a higher amount of the insoluble collagen
ous fraction). The concentration of sarcoplasmic proteins (containing
predominantly enzyme systems for aerobic and anaerobic substrate utili
zation), however did not differ between ventricles and atria. Furtherm
ore, ventricular contractile fractions obtained from both normoxemic a
nd hypoxemic patients were contaminated with the myosin light chain of
atrial origin. Soluble collagenous fractions (containing newly synthe
sized collagenous proteins, predominantly collagen I and III), derived
from all ventricular samples, were contaminated by low molecular weig
ht fragments (mol. weight 29-35 kDa). The proportion of the soluble co
llagenous fraction was significantly higher in atrial but not in ventr
icular myocardium of hypoxemic children as compared with the normoxemi
c group. It seems, therefore, that lower oxygen saturation affects the
synthesis of collagen preferentially in atrial tissue.