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*
The Walter and Eliza Hall Institute of Medical Research, Melbourne, Victoria, Australia; and
The Edward Jenner Institute for Vaccine Research, Compton, Newbury, United Kingdom
Three distinct subtypes of dendritic cells (DC) are present in
mouse spleen, separable as CD4-8
-,
CD4+8
-, and
CD4-8
+ DC. We have tested whether these
represent stages of development or activation within one DC lineage, or
whether they represent separate DC lineages. All three DC subtypes
appear relatively mature by many criteria, but all retain a capacity to
phagocytose particulate material in vivo. Although further maturation
or activation could be induced by bacterially derived stimuli,
phagocytic capacity was retained, and no DC subtype was converted to
the other. Continuous elimination of CD4+8- DC
by Ab depletion had no effect on the levels of the other DC subtypes.
Bromodeoxyuridine labeling experiments indicated that all three DC
subtypes have a rapid turnover (half-life, 1.52.9 days) in the
spleen, with none being the precursor of another. The three DC subtypes
showed different kinetics of development from bone marrow precursors.
The CD8
+ spleen DC, apparently the most mature,
displayed an extremely rapid turnover based on bromodeoxyuridine uptake
and the fastest generation from bone marrow precursors. In conclusion,
the three splenic DC subtypes behave as rapidly turning over products
of three independent developmental streams.
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