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Department of Cell Biology, Faculties of
* Biology and
Medicine, Complutense University, Madrid, Spain
CD4+CD8+ double-positive (DP) T cells
represent a minor subpopulation of T lymphocytes found in the periphery
of adult rats. In this study, we show that peripheral DP T cells appear
among the first T cells that colonize the peripheral lymphoid organs
during fetal life, and represent
40% of peripheral T cells during
the perinatal period. Later their proportion decreases to reach the low
values seen in adulthood. Most DP T cells are small size lymphocytes
that do not exhibit an activated phenotype, and their proliferative
rate is similar to that of the other peripheral T cell subpopulations.
Only 3040% of DP T cells expresses CD8
chain, the remaining cells
expressing CD8
homodimers. However, both DP T cell subsets have
an intrathymic origin since they appear in the recent thymic emigrant
population after injection of FITC intrathymically. Functionally,
although DP T cells are resistant to undergo apoptosis in response to
glucocorticoids, they show poor proliferative responses upon CD3/TCR
stimulation due to their inability to produce IL-2. A fraction of DP T
cells are not actively synthesizing the CD8 coreceptor, and they
gradually differentiate to the CD4 cell lineage in reaggregation
cultures. Transfer of DP T lymphocytes into thymectomized SCID mice
demonstrates that these cells undergo post-thymic maturation in the
peripheral lymphoid organs and that their CD4 cell progeny is fully
immunocompetent, as judged by its ability to survive and expand in
peripheral lymphoid organs, to proliferate in response to CD3 ligation,
and to produce IL-2 upon stimulation.
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