Fenretinide favorably affects mucins (MUC5AC/MUC5B) and fatty acid imbalance in a manner mimicking CFTR-induced correction

. 2020 Feb ; 1865 (2) : 158538. [epub] 20191031

Jazyk angličtina Země Nizozemsko Médium print-electronic

Typ dokumentu časopisecké články, práce podpořená grantem

Perzistentní odkaz   https://www.medvik.cz/link/pmid31678518

Grantová podpora
POP90155 CIHR - Canada

Odkazy

PubMed 31678518
DOI 10.1016/j.bbalip.2019.158538
PII: S1388-1981(19)30189-1
Knihovny.cz E-zdroje

Cystic fibrosis (CF) is the most common genetic disease in Caucasians. CF is manifested by abnormal accumulation of mucus in the lungs, which serves as fertile ground for the growth of microorganisms leading to recurrent infections and ultimately, lung failure. Mucus in CF patients consists of DNA from dead neutrophils as well as mucins produced by goblet cells. MUC5AC mucin leads to pathological plugging of the airways whereas MUC5B has a protective role against bacterial infection. Therefore, decreasing the level of MUC5AC while maintaining MUC5B intact would in principle be a desirable mucoregulatory treatment outcome. Fenretinide prevented the lipopolysaccharide-induced increase of MUC5AC gene expression, without affecting the level of MUC5B, in a lung goblet cell line. Additionally, fenretinide treatment reversed the pro-inflammatory imbalance of fatty acids by increasing docosahexaenoic acid and decreasing the levels of arachidonic acid in a lung epithelial cell line and primary leukocytes derived from CF patients. Furthermore, for the first time we also demonstrate the effect of fenretinide on multiple unsaturated fatty acids, as well as differential effects on the levels of long- compared to very-long-chain saturated fatty acids which are important substrates of complex phospholipids. Finally, we demonstrate that pre-treating mice with fenretinide in a chronic model of P. aeruginosa lung infection efficiently decreases the accumulation of mucus. These findings suggest that fenretinide may offer a new approach to therapeutic modulation of pathological mucus production in CF.

Department of Biochemistry McGill University Montreal Quebec Canada

Department of Human Genetics McGill University Montreal Quebec Canada; Institute of Molecular and Translational Medicine Faculty of Medicine and Dentistry Palacky University Olomouc Czech Republic; Department of Medicine Division of Experimental Medicine McGill University Montreal Quebec Canada; Program in Infectious Diseases and Immunity in Global Health McGill University Health Center Montreal Quebec Canada

Department of Human Genetics McGill University Montreal Quebec Canada; Program in Infectious Diseases and Immunity in Global Health McGill University Health Center Montreal Quebec Canada

Department of Medicine Division of Experimental Medicine McGill University Montreal Quebec Canada; Program in Infectious Diseases and Immunity in Global Health McGill University Health Center Montreal Quebec Canada

Department of Pharmacology and Therapeutics McGill University Montreal Quebec Canada; Program in Infectious Diseases and Immunity in Global Health McGill University Health Center Montreal Quebec Canada

Institute of Immunology Faculty of Medicine Universidad Central de Venezuela Bolivarian Republic of Venezuela

Institute of Molecular and Translational Medicine Faculty of Medicine and Dentistry Palacky University Olomouc Czech Republic

Institute of Molecular and Translational Medicine Faculty of Medicine and Dentistry Palacky University Olomouc Czech Republic; Institute of Immunology Faculty of Medicine Universidad Central de Venezuela Bolivarian Republic of Venezuela

Meakins Christie Laboratories Translational Research in Respiratory Diseases Program Department of Medicine McGill University Health Centre Montreal Quebec Canada

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