Telomeres are supposed to play a role in cellular aging and might contribut
e to the genetic background of human aging and longevity. During the past f
ew years telomere length has been measured in various human tissues. Howeve
r, very little is known about the individual telomere loss in different tis
sues from the same donor. Therefore we have measured telomere restriction f
ragment (TRF) length in three unrelated tissues (leukocytes, skin and synov
ial tissue) of nine elderly patients (age range 73-95 years old). Dependent
on the tissue specific proliferation rate we have found significantly shor
ter telomeres (6546 +/- 519 bp, mean +/- S.D.) in leukocytes compared to sk
in (7792 +/- 596 bp, P < 0.01) and synovial tissue (7910 +/- 420 bp, P < 0.
001). In general, we have observed an inverse relationship between donor ag
e and TRF length which becomes significant in leukocytes (P = 0.04, R-2 = 0
.49) and skin specimens (P = 0.006, R-2 = 0.81). Interestingly, linear corr
elations (P values between 0.017 and 0.038, R-2 values between 0.54 and 0.7
9) were also obtained on comparison of telomere length in each pair of two
different tissues from the same donor without taking donor age into account
. This suggests that genetic determination of the regulation of telomere le
ngth is tissue-independent. Furthermore, our results indicate that TRF meas
urement in easily accessible tissues such as blood could serve as a surroga
te parameter for the relative telomere length in other tissues. (C) 2000 El
sevier Science ireland Ltd. All rights reserved.