β-defensins in lung host defense

被引:195
作者
Schutte, BC [1 ]
McCray, PB [1 ]
机构
[1] Univ Iowa, Coll Med, Dept Pediat, Genet PhD Program, Iowa City, IA 52242 USA
关键词
innate defense; epithelia; antimicrobial peptides; mucosa;
D O I
10.1146/annurev.physiol.64.081501.134340
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
Host defenses at the mucosal surface of the airways evolved to present many layers of protection against inhaled microbes. Normally, the intrapulmonary airways are sterile. Airway secretions contain numerous factors with antimicrobial activity that contribute to innate defenses. Many protein and peptide components exert bacteriostatic or bacteriocidal effects against a wide variety of organisms and may act in synergistic or additive combinations. The beta-defensins are a relatively recently described family of peptide antimicrobials that are widely expressed at mucosal surfaces, including airway and submucosal gland epithelia. These small cationic peptides are products of individual genes that exhibit broad-spectrum activity against bacteria, fungi, and some enveloped viruses. Their expression in airway epithelia may be constitutive or inducible by bacterial products or pro-inflammatory cytokines. beta-defensins also act as chemokines for adaptive immune cells, including immature dendritic cells and T cells via the CCR6 receptor, and provide a link between innate and adaptive immunity. Alterations in the function of the beta-defensins may contribute to disease states. Here we review much of the biology of the beta-defensins, including gene discovery, genomic organization, molecular structure, regulation of expression, and function.
引用
收藏
页码:709 / 748
页数:44
相关论文
共 203 条
[141]  
O'Neil DA, 1999, J IMMUNOL, V163, P6718
[142]   MOLECULAR-CLONING AND CHARACTERIZATION OF A NOVEL HUMAN SPERM ANTIGEN (HE-2) SPECIFICALLY EXPRESSED IN THE PROXIMAL EPIDIDYMIS [J].
OSTERHOFF, C ;
KIRCHHOFF, C ;
KRULL, N ;
IVELL, R .
BIOLOGY OF REPRODUCTION, 1994, 50 (03) :516-525
[143]   The repertoire for pattern recognition of pathogens by the innate immune system is defined by cooperation between Toll-like receptors [J].
Ozinsky, A ;
Underhill, DM ;
Fontenot, JD ;
Hajjar, AM ;
Smith, KD ;
Wilson, CB ;
Schroeder, L ;
Aderem, A .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2000, 97 (25) :13766-13771
[144]   SOLUTION STRUCTURES OF THE RABBIT NEUTROPHIL DEFENSIN NP-5 [J].
PARDI, A ;
HARE, DR ;
SELSTED, ME ;
MORRISON, RD ;
BASSOLINO, DA ;
BACH, AC .
JOURNAL OF MOLECULAR BIOLOGY, 1988, 201 (03) :625-636
[145]   NMR-STUDIES OF DEFENSIN ANTIMICROBIAL PEPTIDES .2. 3-DIMENSIONAL STRUCTURES OF RABBIT NP-2 AND HUMAN HNP-1 [J].
PARDI, A ;
ZHANG, XL ;
SELSTED, ME ;
SKALICKY, JJ ;
YIP, PF .
BIOCHEMISTRY, 1992, 31 (46) :11357-11364
[146]   Defensins purified from human granulocytes bind Clq and activate the classical complement pathway like the transmembrane glycoprotein gp41 of HIV-1 [J].
Prohaszka, Z ;
Nemet, K ;
Csermely, P ;
Hudecz, F ;
Mezo, G ;
Füst, G .
MOLECULAR IMMUNOLOGY, 1997, 34 (11) :809-816
[147]  
REYNOLDS HY, 1997, LUNG, P2353
[148]   Coordinate induction of two antibiotic genes in tracheal epithelial cells exposed to the inflammatory mediators lipopolysaccharide and tumor necrosis factor alpha [J].
Russell, JP ;
Diamond, G ;
Tarver, AP ;
Scanlin, TF ;
Bevins, CL .
INFECTION AND IMMUNITY, 1996, 64 (05) :1565-1568
[149]   Expression of β-defensin genes in bovine alveolar macrophages [J].
Ryan, LK ;
Rhodes, J ;
Bhat, M ;
Diamond, G .
INFECTION AND IMMUNITY, 1998, 66 (02) :878-881
[150]   Isolation and characterization of a peroxidase from the airway [J].
Salathe, M ;
Holderby, M ;
Forteza, R ;
Abraham, WM ;
Wanner, A ;
Conner, GE .
AMERICAN JOURNAL OF RESPIRATORY CELL AND MOLECULAR BIOLOGY, 1997, 17 (01) :97-105