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We have identified three distinct populations of mouse lymph node dendritic cells (DC) that differ in their capacity to uptake Ag delivered by different routes, and in their dynamics. The “l-DCs” are large cells that resemble the interdigitating cells and have a mature phenotype and a slow turnover. They derive from the regional tissues. The “sm-DCs” and “sl-DCs” are smaller (hence s-DC), have a more immature phenotype and a rapid turnover. The sl-DC phenotype, including CD8α expression, suggests a lymphoid-related origin. The sl-DC population is expanded 100-fold after an in vivo flt3 ligand treatment. The sm-DC phenotype suggests a myeloid-related origin. Interestingly, sm-DCs can acquire i.v. injected macromolecules in less than 30 min after injection. They may, therefore, play an important role in the immune response against blood Ags.
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Salomon et al. (1998) studied this question.
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