J. Ausma et al., DEDIFFERENTIATED CARDIOMYOCYTES FROM CHRONIC HIBERNATING MYOCARDIUM ARE ISCHEMIA-TOLERANT, Molecular and cellular biochemistry, 186(1-2), 1998, pp. 159-168
Left ventricular biopsies from 21 patients with clinically diagnosed c
hronic hibernating myocardium (CHM) were examined by light- and electr
on microscopy. A mean of 27% of cardiomyocytes were structurally alter
ed and were characterized as hibernating, because of reduced amount of
myofibrils and increased glycogen content. Electron microscopy of the
se cells showed reduction of T-tubules and numerous small mitochondria
, but few changes associated with degeneration, acute ischemia or apop
tosis. The structural changes found in CHM are reminiscent of dediffer
entiation rather than degeneration. The expression patterns of some st
ructural proteins show resemblance with those in embryonic cardiomyocy
tes. Histochemically, mitochondrial NADH-oxidase and proton translocat
ing ATPase activities were absent, whereas cytochrome c activity was p
resent. Intracellular calcium distribution indicated normally bound sa
rcolemmal calcium and absence of excess mitochondrial calcium accumula
tion. Nuclear chromatin ranged from normal to dispersed with only a fe
w nuclei that were clumped. These results suggest that cardiomyocytes
from human CHM hearts are structurally altered, but viable, and lack m
orphologic and cytochemical characteristics suggestive of apoptosis or
acute ischemia.