Three distinct subtypes of dendritic cells (DC) are present in mouse spleen
, separable as CD4(-)8 alpha (-), CD4(+)8 alpha (-), and CD4(-)8 alpha (+)
DC. We have tested whether these represent stages of development or activat
ion within one DC lineage, or whether they represent separate DC lineages.
All three DC subtypes appear relatively mature by many criteria, but all re
tain a capacity to phagocytose particulate material in vivo. Although furth
er 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 effec
t on the levels of the other DC subtypes, Bromodeoxyuridine labeling experi
ments indicated that all three DC subtypes have a rapid turnover (half-life
, 1.5-2.9 days) in the spleen, with none being the precursor of another, Th
e three DC subtypes showed different kinetics of development from bone marr
ow precursors. The CD8 alpha (+) spleen DC, apparently the most mature, dis
played an extremely rapid turnover based on bromodeoxyuridine uptake and th
e fastest generation from hone marrow precursors. In conclusion, the three
splenic DC subtypes behave as rapidly turning over products of three indepe
ndent developmental streams.