One important question in lymphopoiesis is where stem cells commit to
T-, B- and natural killer (NK)-cell lineages. Recent findings in human
and mouse systems suggest that the thymus is seeded by a yet uncommit
ted progenitor cell. The earliest murine thymic progenitor cells have
the capacity to develop into B, T and NK cells when introduced into th
e appropriate microenvironment. The mechanisms underlying T-cell commi
tment are unknown, but cytokines might be involved. The gamma-chain of
the interleukin (IL)-2 receptor seems to play a role in development o
f T and NK cells, but the current data argue against a critical role f
or IL-2 in T- and NK-cell development. This suggests that the IL-2 rec
eptor gamma-chain is part of a receptor for another cytokine, importan
t for T- and NK-cell development. IL-7 might be involved in regulating
T-cell receptor rearrangements and in proliferation of cells within t
he thymus.