In this study, 2 distinct populations of mature dendritic cells (DCs) were
identified in the human thymus, The major population is CD11b(-), CD11c(+),
and CD45RO(low) and does not express myeloid-related markers. It displays
all the characteristics of mature DCs with a typical dendritic morphology,
high surface levels of HLA-DR, CD40, CD83, and CD86, and expression of DC-l
ysosome-associated membrane glycoprotein messenger RNA (mRNA), In addition,
CD11b(-) thymic DCs do not express macrophage inflammatory protein-1 alpha
(MIP-1 alpha) mRNA, but express thymus-expressed chemokine (TECK) mRNA and
are able to secrete bioactive interleukin 12 (IL-12) upon stimulation. In
contrast, the minor and variable thymic DC population is CD11b(+), CD11c(hi
gh), and CD45RO(high) and comprises CD83(+)CD14(-) mature and CD83(-)CD14() immature DCs, It expresses macrophage-colony stimulating factor receptor,
MIP-1 alpha mRNA and high amounts of decysin mRNA after CD40 activation, b
ut does not express TECK and is a weak bioactive IL-12 producer. Also ident
ified were the IL-3R alpha (high) plasmacytoid cells, which are present in
the thymic cortex and medulla, Upon culture with IL-3, granulocyte/macropha
ge-colony stimulating factor, and CD40 ligand, the plasmacytoid cells can a
dopt a phenotype resembling that of freshly isolated CD11b(-) thymic DCs, H
owever, these plasmacytoid-derived DCs fail to secrete bioactive IL-12; the
refore, conclusions cannot be made about a direct relation between thymic p
lasmacytoid cells and CD11b(-) DCs, Whereas CD11b(+) thymic DCs appear to b
e related to tonsillar germinal-center DCs, the major CD11b(-)IL-15-secreti
ng human thymus DC population has similarities to mouse CD11b(-)CD8(+) DCs,
(Blood, 2001;97:1733-1741) (C) 2001 by The American Society of Hematology.