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Updated: Aug 15, 2026

Isolation of Myeloid Dendritic Cells and Epithelial Cells from Human Thymus
Published on: September 20, 2013
Human thymus contains 2 distinct dendritic cell populations
S Vandenabeele1, H Hochrein, N Mavaddat
1The Walter and Eliza Hall Institute of Medical Research, P.O. Royal Melbourne Hospital, 3050 Melbourne, Victoria, Australia. vandenabeele@wehi.edu.au
Insights
Researchers identified two distinct dendritic cell (DC) populations in the human thymus. The major CD11b- DCs secrete IL-12, while the minor CD11b+ DCs do not, suggesting different roles in immune responses.
Area of Science:
- Immunology
- Cell Biology
Background:
- Dendritic cells (DCs) are crucial for initiating immune responses.
- The human thymus harbors diverse DC populations with incompletely understood functions.
Purpose of the Study:
- To characterize distinct DC subsets within the human thymus.
- To investigate the functional properties, including cytokine secretion, of these thymic DC populations.
Main Methods:
- Flow cytometry was used to identify and distinguish DC populations based on surface markers (CD11b, CD11c, CD45RO, CD83, CD14, IL-3Ralpha).
- Messenger RNA (mRNA) expression analysis was performed for key immune-related genes (MIP-1alpha, TECK, decysin).
- Interleukin 12 (IL-12) production was assessed upon stimulation.
Main Results:
- Two major DC populations were identified: CD11b- DCs (major) and CD11b+ DCs (minor).
- CD11b- DCs exhibited mature DC characteristics, expressed TECK mRNA, and secreted bioactive IL-12.
- CD11b+ DCs showed mixed maturity, expressed MIP-1alpha and decysin mRNA, and were weak IL-12 producers.
- Plasmacytoid cells could differentiate into DC-like cells but did not secrete IL-12.
Conclusions:
- The human thymus contains at least two distinct DC subsets with differing functional capacities.
- The CD11b- DC population is the primary IL-12 secreting subset in the thymus, potentially analogous to mouse CD11b- CD8+ DCs.
- The CD11b+ DCs may share similarities with tonsillar germinal-center DCs, indicating distinct origins or roles.
Abstract:
In this study, 2 distinct populations of mature dendritic cells (DCs) were identified in the human thymus. The major population is CD11b-, CD11c+, and CD45RO(low) and does not express myeloid-related markers. It displays all the characteristics of mature DCs with a typical dendritic morphology, high surface levels of HLA-DR, CD40, CD83, and CD86, and expression of DC-lysosome-associated membrane glycoprotein messenger RNA (mRNA). In addition, CD11b- thymic DCs do not express macrophage inflammatory protein-1alpha (MIP-1alpha) mRNA, but express thymus-expressed chemokine (TECK) mRNA and are able to secrete bioactive interleukin 12 (IL-12) upon stimulation. In contrast, the minor and variable thymic DC population is CD11b+, CD11c(high), and CD45RO(high) and comprises CD83+CD14- mature and CD83- CD14+ immature DCs. It expresses macrophage-colony stimulating factor receptor, MIP-1alpha mRNA and high amounts of decysin mRNA after CD40 activation, but does not express TECK and is a weak bioactive IL-12 producer. Also identified were the IL-3Ralpha(high) plasmacytoid cells, which are present in the thymic cortex and medulla. Upon culture with IL-3, granulocyte/macrophage-colony stimulating factor, and CD40 ligand, the plasmacytoid cells can adopt a phenotype resembling that of freshly isolated CD11b- thymic DCs. However, these plasmacytoid-derived DCs fail to secrete bioactive IL-12; therefore, conclusions cannot be made about a direct relation between thymic plasmacytoid cells and CD11b- DCs. Whereas CD11b+ thymic DCs appear to be related to tonsillar germinal-center DCs, the major CD11b- IL-12-secreting human thymus DC population has similarities to mouse CD11b- CD8+ DCs.
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