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IL-17 Receptor Signaling in Oral Epithelial Cells Is Critical for Protection against Oropharyngeal Candidiasis.
Conti, Heather R; Bruno, Vincent M; Childs, Erin E; Daugherty, Sean; Hunter, Joseph P; Mengesha, Bemnet G; Saevig, Danielle L; Hendricks, Matthew R; Coleman, Bianca M; Brane, Lucas; Solis, Norma; Cruz, J Agustin; Verma, Akash H; Garg, Abhishek V; Hise, Amy G; Richardson, Jonathan P; Naglik, Julian R; Filler, Scott G; Kolls, Jay K; Sinha, Satrajit; Gaffen, Sarah L.
Afiliação
  • Conti HR; Division of Rheumatology and Clinical Immunology, University of Pittsburgh, Pittsburgh, PA 15261, USA; Department of Biological Sciences, University of Toledo, Toledo, OH 43606, USA. Electronic address: heather.conti@utoledo.edu.
  • Bruno VM; Institute for Genome Sciences, University of Maryland School of Medicine, Baltimore, MD 21201, USA.
  • Childs EE; Division of Rheumatology and Clinical Immunology, University of Pittsburgh, Pittsburgh, PA 15261, USA.
  • Daugherty S; Institute for Genome Sciences, University of Maryland School of Medicine, Baltimore, MD 21201, USA.
  • Hunter JP; Department of Biological Sciences, University of Toledo, Toledo, OH 43606, USA.
  • Mengesha BG; Department of Biological Sciences, University of Toledo, Toledo, OH 43606, USA.
  • Saevig DL; Department of Biological Sciences, University of Toledo, Toledo, OH 43606, USA.
  • Hendricks MR; Division of Rheumatology and Clinical Immunology, University of Pittsburgh, Pittsburgh, PA 15261, USA.
  • Coleman BM; Division of Rheumatology and Clinical Immunology, University of Pittsburgh, Pittsburgh, PA 15261, USA.
  • Brane L; Division of Rheumatology and Clinical Immunology, University of Pittsburgh, Pittsburgh, PA 15261, USA.
  • Solis N; Division of Infectious Diseases, Los Angeles Biomedical Research Institute, Harbor-UCLA Medical Center, Torrance, CA 90502, USA.
  • Cruz JA; Division of Rheumatology and Clinical Immunology, University of Pittsburgh, Pittsburgh, PA 15261, USA.
  • Verma AH; Division of Rheumatology and Clinical Immunology, University of Pittsburgh, Pittsburgh, PA 15261, USA.
  • Garg AV; Division of Rheumatology and Clinical Immunology, University of Pittsburgh, Pittsburgh, PA 15261, USA.
  • Hise AG; Department of Pathology, Case Western Reserve University, Cleveland, OH 44106, USA; Louis Stokes Cleveland Veterans Affairs Medical Center, Cleveland, OH 44106, USA.
  • Richardson JP; Department of Mucosal and Salivary Biology, King's College London, London SE1 1UL, UK.
  • Naglik JR; Department of Mucosal and Salivary Biology, King's College London, London SE1 1UL, UK.
  • Filler SG; Division of Infectious Diseases, Los Angeles Biomedical Research Institute, Harbor-UCLA Medical Center, Torrance, CA 90502, USA.
  • Kolls JK; Richard King Mellon Foundation for Pediatric Research, Children's Hospital of UPMC, Pittsburgh, PA 15224, USA.
  • Sinha S; Department of Biochemistry, University at Buffalo, State University of New York, Buffalo, NY 14203, USA.
  • Gaffen SL; Division of Rheumatology and Clinical Immunology, University of Pittsburgh, Pittsburgh, PA 15261, USA; Department of Mucosal and Salivary Biology, King's College London, London SE1 1UL, UK. Electronic address: sarah.gaffen@pitt.edu.
Cell Host Microbe ; 20(5): 606-617, 2016 Nov 09.
Article em En | MEDLINE | ID: mdl-27923704
ABSTRACT
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 (Il17raΔK13). Following oral Candida infection, Il17raΔK13 mice exhibited fungal loads and weight loss indistinguishable from Il17ra-/- mice. Susceptibility in Il17raΔK13 mice correlated with expression of the antimicrobial peptide ß-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.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Candida / Candidíase Bucal / Transdução de Sinais / Beta-Defensinas / Células Epiteliais / Receptores de Interleucina-17 / Mucosa Bucal Limite: Animals / Humans Idioma: En Ano de publicação: 2016 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Candida / Candidíase Bucal / Transdução de Sinais / Beta-Defensinas / Células Epiteliais / Receptores de Interleucina-17 / Mucosa Bucal Limite: Animals / Humans Idioma: En Ano de publicação: 2016 Tipo de documento: Article