H. Weirichschwaiger et al., CORRELATION BETWEEN SENESCENCE AND DNA-REPAIR IN CELLS FROM YOUNG ANDOLD INDIVIDUALS AND IN PREMATURE AGING SYNDROMES, MUTATION RESEARCH, 316(1), 1994, pp. 37-48
Cellular aging appears to be related to and perhaps caused by diminish
ed DNA repair. To elucidate direct correlations between DNA repair cap
acity and senescence various parameters of cellular aging and DNA repa
ir were studied simultaneously. Of special interest are features of DN
A repair and senescence in cultured diploid fibroblasts derived either
from healthy young or elderly probands as well as from patients suffe
ring from premature senescence syndromes (Werner syndrome, Cockayne sy
ndrome, ataxia telangiectasia and Down syndrome). Here we demonstrate
the striking parallelism between reduced maximal lifespan, elevated le
vels of spontaneous chromosomal breaks, higher incidence of formation
of micronuclei, a significant prolongation of cell cycle duration and
a diminished reactivation of in vitro injured plasmid after transfecti
on in cells from old individuals and from patients with premature sene
scence syndromes, suggesting a causal relationship between senescence
and DNA damage.