Flagellin‐induced expression of CXCL10 mediates direct fungal killing and recruitment of NK cells to the cornea in response to Candida albicans infection

• Published in: European journal of immunology 2014-09, Vol.44 (9), p.2667-2679
• Main Authors: Liu, Xiaowei, Gao, Nan, Dong, Chen, Zhou, Li, Mi, Qing‐Sheng, Standiford, Theodore J., Yu, Fu‐Shin X.
• Format: Article
• Language: English
• Subjects: Animals; Antimicrobial peptides; Candida albicans; Candida albicans - immunology; Candidiasis - genetics; Candidiasis - immunology; Candidiasis - therapy; Chemokine CXCL10 - genetics; Chemokine CXCL10 - immunology; Cornea - immunology; Cornea - microbiology; Cornea - pathology; CXCL10; Flagellin - chemistry; Flagellin - immunology; Flagellin - isolation & purification; Flagellin - pharmacology; Fungal keratitis; Gene Expression Regulation - drug effects; Gene Expression Regulation - genetics; Gene Expression Regulation - immunology; Homeodomain Proteins - genetics; Homeodomain Proteins - immunology; Immunity, Cellular; Immunity, Mucosal - drug effects; Immunity, Mucosal - genetics; Immunity, Mucosal - immunology; Infections; Innate immunity; Keratitis - genetics; Keratitis - immunology; Keratitis - microbiology; Keratitis - pathology; Keratitis - therapy; Killer Cells, Natural - immunology; Killer Cells, Natural - pathology; Medical research; Mice; Mice, Knockout; Natural killer cells; Pseudomonas aeruginosa - chemistry; Receptors, CXCR3 - genetics; Receptors, CXCR3 - immunology
• ISSN: 0014-2980; 1521-4141
• DOI: 10.1002/eji.201444490

We previously showed that topical flagellin induces profound mucosal innate protection in the cornea against microbial infection, a response involving multiple genes and cell types. In this study, we used a Candida albicans (CA)‐C57BL/6 mouse keratitis model to delineate the contribution of CXCL10‐ and CXCR3‐expressing cells in flagellin‐induced protection. Flagellin pretreatment markedly enhanced CXCL10 expression at 6 h post CA infection (hpi), but significantly dampened CXCL10 expression at 24 hpi. At the cellular level, CXCL10 was expressed in the epithelia at 6 hpi in flagellin‐pretreated corneas, and concentrated at lesion sites 24 hpi. CXCR3‐expressing cells were detected in great numbers at 24 hpi, organized within clusters at the lesion sites in CA‐infected corneas. CXCL10 or CXCR3 neutralization increased keratitis severity and dampened flagellin‐induced protection. CXCR3‐positive cells were identified as NK cells, the depletion of which resulted in severe CA keratitis. Contributions from NK T‐cells were excluded by finding no change in flagellin‐induced protection in Rag1 KO mice. Recombinant CXCL10 inhibited CA growth in vitro and accelerated fungal clearance and inflammation resolution in vivo. Taken together, our data indicate that epithelium‐expressed CXCL10 plays a critical role in fungal clearance and that CXCR3‐expressing NK cells contribute to CA eradication in mouse corneas.