The antimicrobial peptide cathelicidin protects the urinary tract against invasive bacterial infection

被引:484
作者
Chromek, Milan
Slamova, Zuzana
Bergman, Peter
Kovacs, Laszlo
Podracka, L'udmila
Ehren, Ingrid
Hokfelt, Tomas
Gudmundsson, Gudmundur H.
Gallo, Richard L.
Agerberth, Birgitta
Brauner, Annelie [1 ]
机构
[1] Karolinska Univ Hosp, Dept Clin Microbiol, Microbiol & Tumorbiol Ctr, SE-17176 Stockholm, Sweden
[2] Karolinska Inst, SE-17176 Stockholm, Sweden
[3] Karolinska Inst, Dept Med Biochem & Biophys, SE-17177 Stockholm, Sweden
[4] Karolinska Inst, Dept Neurosci, SE-17177 Stockholm, Sweden
[5] Karolinska Univ Hosp, Dept Urol, SE-17176 Stockholm, Sweden
[6] Comenius Univ, Sch Med, Dept Pediat, Bratislava, Slovakia
[7] Safarik Univ, Sch Med, Dept Pediat, Kosice 04066, Slovakia
[8] Univ Iceland, Inst Biol, IS-101 Reykjavik, Iceland
[9] Univ Calif San Diego, Div Dermatol, San Diego, CA 92161 USA
关键词
D O I
10.1038/nm1407
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The urinary tract functions in close proximity to the outside environment, yet must remain free of microbial colonization to avoid disease. The mechanisms for establishing an antimicrobial barrier in this area are not completely understood. Here, we describe the production and function of the cathelicidin antimicrobial peptides LL-37, its precursor hCAP-18 and its ortholog CRAMP in epithelial cells of human and mouse urinary tract, respectively. Bacterial contact with epithelial cells resulted in rapid production and secretion of the respective peptides, and in humans LL-37/hCAP-18 was released into urine. Epithelium-derived cathelicidin substantially contributed to the protection of the urinary tract against infection, as shown using CRAMP-deficient and neutrophil-depleted mice. In addition, clinical E. coli strains that were more resistant to LL-37 caused more severe urinary tract infections than did susceptible strains. Thus, cathelicidin seems to be a key factor in mucosal immunity of the urinary tract.
引用
收藏
页码:636 / 641
页数:6
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