Related Experiment Video
Updated: Aug 14, 2026

Murine Model of CD40-activation of B cells
Published on: March 6, 2010
Marrow-derived CD40-positive cells are required for mice to clear Cryptosporidium parvum infection
A R Hayward1, M Cosyns, M Jones
1Department of Pediatrics and the Barbara Davis Childhood Diabetes Center, University of Colorado School of Medicine, Denver, Colorado, USA. anthony.hayward@uchsc.edu
Abstract:
To clear a Cryptosporidium parvum infection, mice need CD4+ T cells, major histocompatibility complex class II, and an intact CD40-CD154 signaling pathway. CD40 is constitutively expressed on marrow-derived cells such as dendritic cells and B lymphocytes and is induced by gamma interferon (IFN-gamma) on most somatic cells. To determine whether the CD40 needed to clear a C. parvum infection has to be on marrow-derived mononuclear cells or on the epithelial cells that normally harbor the parasite, we transplanted CD40-/- mice with CD40+/- bone marrow and then infected them with C. parvum. These chimeras cleared the C. parvum infection, while CD40+/- controls transplanted with CD40-/- marrow cells remained infected. CD40 expression on marrow-derived cells therefore suffices for a C. parvum infection to be cleared, while CD40 expression on intestinal epithelial cells is not sufficient. There was no difference between the acquisition of CD69 and CD154 by mesenteric lymph node T cells of C. parvum-infected animals with intact or disrupted CD40-CD154 pathways. CD4 T cells entered the intestinal laminae propriae of C. parvum-infected animals whether or not the CD40 genes of these recipients were intact. These results suggest that, for a C. parvum infection to be cleared, CD40 is not necessary for T-cell activation but may instead contribute to an effector pathway of marrow-derived cells.
Insights
Marrow-derived cells expressing CD40 are sufficient for clearing Cryptosporidium parvum infections. CD40 on intestinal epithelial cells is not sufficient, suggesting a role in effector pathways, not T-cell activation.
Area of Science:
- Immunology
- Parasitology
- Cell Biology
Background:
- Cryptosporidium parvum infections require CD4+ T cells, MHC class II, and functional CD40-CD154 signaling.
- CD40 is expressed on immune cells and can be induced on somatic cells, including intestinal epithelial cells.
Purpose of the Study:
- To investigate whether CD40 expression on marrow-derived cells or intestinal epithelial cells is critical for clearing C. parvum infections.
- To elucidate the specific role of CD40 in the immune response to C. parvum.
Main Methods:
- Bone marrow transplantation experiments were conducted using CD40 knockout mice and chimeric models.
- Mice were infected with C. parvum, and infection clearance, T-cell activation markers (CD69, CD154), and T-cell infiltration were assessed.
Main Results:
- Chimeric mice with CD40 expressed on marrow-derived cells cleared C. parvum infection.
- Mice lacking CD40 on intestinal epithelial cells but with functional marrow-derived CD40 cleared the infection.
- T-cell activation and intestinal infiltration were not dependent on CD40 expression in the recipient cells.
Conclusions:
- CD40 expression on marrow-derived cells is sufficient for C. parvum infection clearance.
- CD40 is not essential for T-cell activation or homing in this context but likely contributes to effector mechanisms mediated by immune cells.
More Related Videos
14:43Differentiating Functional Roles of Gene Expression from Immune and Non-immune Cells in Mouse Colitis by Bone Marrow Transplantation
Published on: October 1, 2012
08:37Induction of Murine Intestinal Inflammation by Adoptive Transfer of Effector CD4+CD45RBhigh T Cells into Immunodeficient Mice
Published on: April 21, 2015