Topical cathelicidin (LL‐37) an innate immune peptide induces acute olfactory epithelium inflammation in a mouse model. Issue 12 (8th September 2015)

• Record Type: Journal Article
• Authors: Alt, Jeremiah A.; Qin, Xuan; Pulsipher, Abigail; Orb, Quinn; Orlandi, Richard R.; Zhang, Jianxing; Schults, Austin; Jia, Wanjian; Presson, Angela P.; Prestwich, Glenn D.; Oottamasathien, Siam
• Is Part Of: International forum of allergy & rhinology. Volume 5:Issue 12(2015:Dec.)
• Page Start: 1141
• Page End: 1150
• Publication Date: 2015-09-08
• Subjects: sinusitis -- rhinosinusitis -- chronic disease -- innate immunity -- cathelicidin; 617.51005
• DOI: 10.1002/alr.21634
• Languages: English
• ISSNs: 2042-6976

Abstract

Abstract : Background: Cathelicidin (LL‐37) is an endogenous innate immune peptide that is elevated in patients with chronic rhinosinusitis (CRS). The role of LL‐37 in olfactory epithelium (OE) inflammation remains unknown. We hypothesized that: (1) LL‐37 topically delivered would elicit profound OE inflammation; and (2) LL‐37 induced inflammation is associated with increased infiltration of neutrophils and mast cells. Methods: To test our hypothesis we challenged C57BL/6 mice intranasally with increasing concentrations of LL‐37. At 24 hours tissues were examined histologically and scored for inflammatory cell infiltrate, edema, and secretory hyperplasia. In separate experiments, fluorescently conjugated LL‐37 was instilled and tissues were examined at 0.5 and 24 hours. To test our last hypothesis, we performed tissue myeloperoxidase (MPO) assays for neutrophil activity and immunohistochemistry for tryptase to determine the mean number of mast cells per mm 2 . Results: LL‐37 caused increased inflammatory cell infiltrate, edema, and secretory cell hyperplasia of the sinonasal mucosa, with higher LL‐37 concentrations yielding significantly more inflammatory changes ( p < 0.01). Fluorescent LL‐37 demonstrated global sinonasal epithelial binding and tissue distribution. Further, higher concentrations of LL‐37 led to significantly greater MPO levels with dose‐dependent increases in mast cell infiltration ( p < 0.01). Conclusion: LL‐37 has dramatic inflammatory effects in the OE mucosa that is dose‐dependent. The observed inflammatory changes in the olfactory mucosa were associated with the infiltration of both neutrophils and mast cells. Our biologic model represents a new model to further investigate the role of LL‐37 in OE inflammation.