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Generation of Immature, Mature and Tolerogenic Dendritic Cells with Differing Metabolic Phenotypes
Published on: June 22, 2016
Human peripheral blood contains two distinct lineages of dendritic cells
S P Robinson1, S Patterson, N English
1Antigen Presentation Research Group, Imperial College School of Medicine at St Mary's, Northwick Park Institute for Medical Research, Harrow, GB.
Insights
Human peripheral blood contains two distinct dendritic cell (DC) lineages. These distinct cell populations differ in markers, antigen uptake, and differentiation potential, suggesting separate developmental origins.
Area of Science:
- Immunology
- Cell Biology
Background:
- Human peripheral blood contains two distinct populations of dendritic cells (DCs).
- The developmental relationship between these DC populations remains unclear.
Purpose of the Study:
- To investigate the developmental relationship between CD11c- and CD11c+ dendritic cells.
- To characterize the distinct phenotypes and functions of these two DC populations.
Main Methods:
- Isolation and phenotypic characterization of CD11c- and CD11c+ DCs from human peripheral blood.
- In vitro culture of DCs under various conditions.
- Analysis of cell morphology, marker expression (including lymphoid and myeloid markers), antigen uptake, and differentiation potential.
- Assessment of macrophage colony-stimulating factor (M-CSF) receptor expression and differentiation into macrophages.
Main Results:
- CD11c- DCs exhibited lymphoid morphology and markers (CD4+, CD10+), while CD11c+ DCs showed monocytoid appearance and myeloid markers.
- Both DC populations were allostimulatory, but only CD11c+ DCs could uptake antigen.
- CD11c- cells differentiated into CD11c-, CD13-, CD33-, CD4+, CD1a-, CD83+/- DCs.
- CD11c+ cells differentiated into CD11c+, CD13+, CD33+/-, CD4-, CD1a+, CD83+, CD9+ DCs.
- Only CD11c+ DCs expressed the M-CSF receptor and differentiated into CD14+, esterase+, phagocytic macrophages.
Conclusions:
- The findings suggest that CD11c- and CD11c+ dendritic cells represent distinct lineages of antigen-presenting cells.
- These distinct lineages possess unique developmental pathways and functional capabilities.
Abstract:
Human peripheral blood contains two populations of dendritic cells (DC) but their developmental relationship has not been established. Freshly isolated CD11c- DC possessed a lymphoid morphology, lacked myeloid markers but expressed lymphoid markers (CD4+ CD10+) whilst the CD11c+ DC were monocytoid in appearance and expressed myeloid markers. Although both populations were allostimulatory, only the CD11c+ DC were able to take up antigen. Irrespective of the culture conditions the CD11c- cells developed into CD11c- CD13- CD33- CD4+ CD1a- CD83+/- DC. In contrast, cultured CD11c+ cells developed the phenotype CD11c+ CD13+ CD33+/- CD4- CD1a+ CD83+ CD9+. Only the CD11c+ DC expressed macrophage colony-stimulating factor (M-CSF) receptor and gave rise to CD14+, esterase+, phagocytic macrophages when cultured in M-CSF. These data suggest that these two populations of DC represent distinct lineages of antigen-presenting DC.
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