Human peripheral long-term T-lymphocyte cell cultures show some characteris
tics similar to those of fibroblast cell lines, the latter of which have be
en used as in vitro systems for cellular aging studies for many years. Both
show a limited in vitro life span, as well as a progressive prolongation o
f their cell cycle with increasing age. However, whereas T-cell cultures di
e from apoptosis at the end of their proliferative capacity, fibroblasts ca
n be maintained for long periods of time in stationary cultures as postmito
tic senescent cells. Previous studies analyzing the histone variant pattern
of a human lung embryonic fibroblast cell line have shown that this patter
n changes as a function of cumulative population doublings in a manner not
unlike that found in terminally differentiating systems. In the present stu
dy the histone variant composition of long-term T-cell cultures was analyze
d as a function of population doublings and compared to a human diploid fib
roblast system. The results from this study provide a distinction at the mo
lecular level among these two in vitro aging model systems, because it was
found that long-term T-cell cultures show a constant histone variant consti
tution throughout their in vitro life, dissimilar to previous findings usin
g the fibroblast cell system. (C) 1999 Elsevier Science Inc. All rights res
erved.