Interleukin-7 (IL-7) has been shown to be a critical factor in B and T
lymphopoiesis, and to influence the differentiation of myeloid cell l
ineages. In the present study we extend these results demonstrating th
at IL-7 also plays an important role in the development of thymic dend
ritic cells (DC). The addition of IL-7 to rat fetal thymus organ cultu
res (FTOC) resulted in a drastic increase in the number of CD3(-)CD4(-
)CD8(-) cells, which mostly expressed typical DC markers, including ma
jor histocompatibility complex class II, OX-62, CD11b, CD68, and CD54.
These cells exhibited morphological and ultrastructural features of D
C, and were potent stimulators of the allogeneic mixed leukocyte react
ion. Although increased numbers of DC were continuously generated thro
ughout the culture period in the presence of IL-7, they were not activ
ely dividing, indicating that DC in IL-7-treated cultures did not aris
e by expansion of pre-existing cells. Reduced DC numbers obtained afte
r the addition of neutralizing anti-IL-7 antibodies to mouse FTOC conf
irmed the relevance of endogenously produced IL-7 on thymic DC develop
ment. Furthermore, the addition of IL-7 to FTOC derived from severe co
mbined immunodeficient mice also generated large numbers of DC in the
absence of thymocyte maturation. (C) 1998 by The American Society of H
ematology.