This Article Full Text Full Text (PDF) Online Supplement All Versions of this Article: 2007-0284OCv1 39/1/19    most recent Alert me when this article is cited Alert me if a correction is posted Services Similar articles in this journal Similar articles in PubMed Alert me to new issues of the journal Download to citation manager Citing Articles Citing Articles via Google Scholar Google Scholar Articles by Hilliard, T. N. Articles by Alton, E. W. F. W. Search for Related Content PubMed PubMed Citation Articles by Hilliard, T. N. Articles by Alton, E. W. F. W.

Nasal Abnormalities in Cystic Fibrosis Mice Independent of Infection and Inflammation

¹ Department of Paediatric Respiratory Medicine, Royal Brompton Hospital, London, United Kingdom; ² Department of Gene Therapy, and ³ Department of Lung Pathology, National Heart and Lung Institute, Imperial College, London, United Kingdom; and ⁴ Institute for Molecular Bioscience, University of Queensland, St. Lucia, Queensland, Australia

Correspondence and requests for reprints should be addressed to Jane C. Davies, Department of Gene Therapy, Emmanuel Kaye Building, 1b Manresa Road, London SW3 6LR, UK. E-mail: j.c.davies{at}imperial.ac.uk

It is not known whether the progressive airway changes in cystic fibrosis (CF) are all secondary to infection and inflammation. The CF mouse nose shares electrophysiologic and cellular properties with human CF airway epithelium. In the present work, we tested the hypothesis that structural abnormalities in the nasal mucosa of CF mice develop independent of infection and inflammation. We performed nasal lavage and subsequent serial coronal section through the nasal tissue of adult CF (mutations Cftr^TgHm1G551D and Cftr^tm1Unc-TgN^(FABPCFTR)) and wild-type mice raised under normal housing conditions. Nasal tissue was also obtained from Day 17 embryos and newborn pups. Detailed histologic examination of the respiratory and olfactory epithelium within the nasal cavity was performed. Bacterial culture, cell count, and macrophage inflammatory protein-2 (MIP-2) concentration were assessed in nasal lavage fluid. Significantly thickened respiratory epithelium and increased mucous cell density was found in adult CF mice of both mutations compared with wild-type animals. In contrast, the olfactory epithelium was thinner, with a decreased cell density. Areas of lymphoid aggregates were found in CF mice but not in non-CF mice. There were no differences in bacterial growth, cell count, or MIP-2 concentrations. No genotype differences were observed in the embryonic or newborn periods. There are significant histologic changes in the nasal mucosa of adult CF mice, not associated with increased lumenal inflammation or bacterial content, and which are not present perinatally. These may be novel therapeutic targets.

Key Words: mice • cystic fibrosis • pathology • inflammation • cystic fibrosis transmembrane conductance regulator

CLINICAL RELEVANCE This study shows significant histologic changes in the nasal mucosa of cystic fibrosis mice, not associated with increased lumenal inflammation or bacterial content, and not present perinatally. They may represent novel and potentially important therapeutic targets.