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IL-17 Receptor Signaling in Oral Epithelial Cells Is Critical for Protection against Oropharyngeal Candidiasis

Authors :
Lucas Brane
Jay K. Kolls
Jonathan P. Richardson
Matthew R. Hendricks
Amy G. Hise
J. Agustin Cruz
Erin E. Childs
Sean C. Daugherty
Scott G. Filler
Norma V. Solis
Bianca M. Coleman
Joseph P. Hunter
Bemnet G. Mengesha
Abhishek V. Garg
Danielle La Saevig
Akash H. Verma
Heather R. Conti
Vincent M. Bruno
Satrajit Sinha
Sarah L. Gaffen
Julian R. Naglik
Source :
Conti, HR, Bruno, VM, Childs, EE, Daugherty, S, Hunter, JP, Mengesha, BG, Saevig, DL, Hendricks, MR, Coleman, BM, Brane, L, Solis, N, Cruz, J A, Verma, AH, Garg, AV, Hise, AG, Richardson, J P, Naglik, J R, Filler, SG, Kolls, JK, Sinha, S & Gaffen, SL 2016, ' IL-17 Receptor Signaling in Oral Epithelial Cells Is Critical for Protection against Oropharyngeal Candidiasis ', Cell Host & Microbe, vol. 20, no. 5, pp. 606–617 . https://doi.org/10.1016/j.chom.2016.10.001
Publication Year :
2016
Publisher :
Elsevier BV, 2016.

Abstract

Summary Signaling through the IL-17 receptor (IL-17R) is required to prevent oropharyngeal candidiasis (OPC) in mice and humans. However, the IL-17-responsive cell type(s) that mediate protection are unknown. Using radiation chimeras, we were able to rule out a requirement for IL-17RA in the hematopoietic compartment. We saw remarkable concordance of IL-17-controlled gene expression in C. albicans -infected human oral epithelial cells (OECs) and in tongue tissue from mice with OPC. To interrogate the role of the IL-17R in OECs, we generated mice with conditional deletion of IL-17RA in superficial oral and esophageal epithelial cells ( Il17ra ΔK13 ). Following oral Candida infection, Il17ra ΔK13 mice exhibited fungal loads and weight loss indistinguishable from Il17ra −/− mice. Susceptibility in Il17ra ΔK13 mice correlated with expression of the antimicrobial peptide β-defensin 3 (BD3, Defb3 ). Consistently, Defb3 −/− mice were susceptible to OPC. Thus, OECs dominantly control IL-17R-dependent responses to OPC through regulation of BD3 expression.

Details

ISSN :
19313128
Volume :
20
Database :
OpenAIRE
Journal :
Cell Host & Microbe
Accession number :
edsair.doi.dedup.....d064c0125699bd2170ad5994987d5847