The development, maturation, and turnover rate of mouse spleen dendritic cell populations

Citation
At. Kamath et al., The development, maturation, and turnover rate of mouse spleen dendritic cell populations, J IMMUNOL, 165(12), 2000, pp. 6762-6770
Citations number
31
Categorie Soggetti
Immunology
Journal title
JOURNAL OF IMMUNOLOGY
ISSN journal
00221767 → ACNP
Volume
165
Issue
12
Year of publication
2000
Pages
6762 - 6770
Database
ISI
SICI code
0022-1767(200012)165:12<6762:TDMATR>2.0.ZU;2-O
Abstract
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.