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Updated: Aug 12, 2026

Generation of Human CD40-activated B cells
Published on: October 17, 2009
CD40 is functionally expressed on human thymic epithelial cells
1DNAX Research Institute, Department of Human Immunology, Palo Alto, CA 94304-1104.
Insights
CD40 is expressed on human thymic epithelial cells (TEC) and can be upregulated by inflammatory cytokines. Triggering CD40 on TEC promotes granulocyte-macrophage colony-stimulating factor secretion, indicating its functional role in the thymus.
Area of Science:
- Immunology
- Cell Biology
- Thymic Epithelial Cell Biology
Background:
- CD40 is a B cell antigen also found on some epithelial cells and carcinomas.
- Its distribution within the human thymus was previously uncharacterized.
Purpose of the Study:
- To investigate the expression and function of CD40 on human thymic epithelial cells (TEC).
Main Methods:
- Immunohistology to determine CD40 distribution in the thymus.
- Culture of TEC and thymic fibroblasts to assess CD40 expression and regulation.
- Northern blot analysis for CD40 mRNA.
- Stimulation assays using anti-CD40 monoclonal antibodies (mAbs) and cytokines to evaluate functional responses.
Main Results:
- CD40 was expressed on cortical and medullary TEC, but not on thymocytes or fibroblasts.
- IL-1 alpha, TNF-alpha, and IFN-gamma upregulated membrane CD40 expression on cultured TEC.
- CD40 mRNA in TEC was upregulated by IL-1 and IFN-gamma.
- Triggering CD40 on TEC with anti-CD40 mAb, along with IFN-gamma and IL-1, induced dose-dependent granulocyte-macrophage colony-stimulating factor secretion.
Conclusions:
- CD40 is expressed on human TEC and is a functional molecule.
- CD40 signaling in TEC can modulate cytokine secretion, suggesting a role in thymic immune regulation.
Abstract:
CD40 is a prominent B cell Ag also found on certain epithelial cells and on carcinomas. In this report, we analyzed CD40 distribution in the human thymus. CD40 was not found on the majority of CD45-positive thymocytes, but was present in a CD45-negative stromal cell population. Immunohistology showed CD40 expression on cortical thymic epithelial cells (TEC), medullary TEC, thymic interdigitating cells, and thymic B cells. CD40 was not found on thymocytes, endothelial cells, or on the fibroblasts of the septae. Expression of CD40 was specifically maintained on cultured TEC and not found on cultured thymic fibroblasts. IL-1 alpha, TNF-alpha, IFN-gamma, but not IL-4, significantly up-regulated the membrane expression of CD40 on cultured TEC. The regulation of CD40 was similar to that of ICAM-1, and contrasted with that of MHC class II Ag, which could only be induced by IFN-gamma but not by IL-1, TNF, or IL-4. Northern blot analysis showed the presence of a 1.4-kb mRNA transcript for CD40 in TEC, which was up-regulated by IL-1 and IFN-gamma. Cross-linking of CD40 at the surface of human TEC in the absence of IL-1 stimulation failed to induce cytokine secretion. Triggering of TEC with anti-CD40 mAb in conjunction with IFN-gamma and IL-1 stimulation increased granulocyte-macrophage CSF secretion in a dose-dependent manner. The effect was visible as early as 24 h after triggering, occurred in the absence of cellular proliferation, and was specific for CD40 since triggering of other TEC membrane Ag such as ICAM-1 or MHC class I molecules had no effect to increase cytokine production in TEC. These data demonstrate that CD40 is expressed and is a functional molecule at the surface of the epithelial cells of the thymus.
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