Cryptosporidium parvum infection attenuates the ex vivo propagation of murine intestinal enteroids
Authors:
Open Access
- 30 December 2016
- journal article
- research article
- Published by Wiley in Physiological Reports
- Vol. 4 (24) , e13060
Abstract
Cryptosporidium, a ubiquitous coccidian protozoan parasite that infects the gastrointestinal epithelium and other mucosal surfaces, is an important opportunistic pathogen for immunocompromised individuals and a common cause of diarrhea in young children in the developing countries. One of the pathological hallmarks of intestinal cryptosporidiosis is villous atrophy, which results in a shorter height of intestinal villi. Here, we investigated the effects of Cryptosporidium infection on intestinal epithelial growth, using an ex vivo model of intestinal cryptosporidiosis employing enteroids from mice. We detected infection of enteroids isolated from immunocompetent adult and neonatal mice after ex vivo exposure to Cryptosporidium sporozoites. We observed a significant inhibition of enteroid propagation following infection. Intriguingly, we identified a decreased expression level of intestinal stem cell markers in enteroids following C. parvum infection. We further measured the expression levels of several Wnt antagonists or agonists in infected enteroids, as induction of the Wnt/β‐catenin activation is a key factor for intestinal stem cell function. We detected a markedly increased level of the Dickkopf‐related protein 1 and decreased level of the Wnt family member 5a in enteroids after infection. The low density lipoprotein receptor‐related protein 5, one of the Wnt co‐receptors, is downregulated in the infected enteroids. In addition, increased apoptotic cell death and cell senescence were observed in the infected enteroids. Our results demonstrate a significant inhibitory effect of Cryptosporidium infection on the ex vivo propagation of enteroids from mice, providing additional insights into the impact of Cryptosporidium infection on intestinal epithelial growth.Keywords
Funding Information
- National Institute of Allergy and Infectious Diseases (AI116323)
- National Center for Research Resources (G20RR024001)
This publication has 42 references indexed in Scilit:
- R-Spondin Potentiates Wnt/β-Catenin Signaling through Orphan Receptors LGR4 and LGR5PLOS ONE, 2012
- miR-27b Targets KSRP to Coordinate TLR4-Mediated Epithelial Defense against Cryptosporidium parvum InfectionPLOS Pathogens, 2012
- Functional Cftr in crypt epithelium of organotypic enteroid cultures from murine small intestineAmerican Journal of Physiology-Cell Physiology, 2012
- The intestinal stem cell markers Bmi1 and Lgr5 identify two functionally distinct populationsProceedings of the National Academy of Sciences, 2011
- The cell biology of cryptosporidium infectionMicrobes and Infection, 2011
- Cdx2 regulates endo-lysosomal function and epithelial cell polarityGenes & Development, 2010
- Global Distribution, Public Health and Clinical Impact of the Protozoan PathogenCryptosporidiumInterdisciplinary Perspectives on Infectious Diseases, 2010
- Over-expression and localization of a host protein on the membrane of Cryptosporidium parvum infected epithelial cellsMolecular and Biochemical Parasitology, 2009
- Identification of stem cells in small intestine and colon by marker gene Lgr5Nature, 2007
- A Cellular Micro-RNA, let-7i, Regulates Toll-like Receptor 4 Expression and Contributes to Cholangiocyte Immune Responses against Cryptosporidium parvum InfectionJournal of Biological Chemistry, 2007