Mc. Re et al., Human T cell leukemia virus type II increases telomerase activity in uninfected CD34(+) hematopoietic progenitor cells, J HEMATH ST, 9(4), 2000, pp. 481-487
Citations number
21
Categorie Soggetti
Hematology,"Medical Research Diagnosis & Treatment
The aging process of long-term self-renewing hematopoietic stem/progenitor
cells is not yet completely understood and recent studies on antiapoptotic
cell pathways have demonstrated a close linkage between telomerase activati
on and Bcl-2 deregulation in human cancer cells. The present work shows tha
t human T cell leukemia virus type II (HTLV-II) Mo virions that have origin
ated from the T cell line (C344), but not from the B cell line (BJAB), are
critically involved in mediating survival and growth effects on hematopoiet
ic precursors (represented by both the TF-1 CD34(+) cell line and by periph
eral blood-derived CD34+ cells) through the maintenance or enhancement of t
elomerase activity and the induction of bcl-2 expression. In addition, usin
g an interleukin-3-dependent TF-1 cell line, it was demonstrated that IL-3
deprivation was sufficient to influence the levels of telomerase activity a
nd Bcl-2 expression in CD34+ cells. Taken together, these findings suggest
that, in appropriate conditions, extended hematopoietic progenitor cell sur
vival and proliferation following HTLV-II exposure depends on a synergistic
interaction between up-regulation of Bcl-2 and activation of telomerase ac
tivity.