Defensins - innate immunity at the epithelial frontier

被引:66
作者
Fellermann, K [1 ]
Stange, EF [1 ]
机构
[1] Med Univ Lubeck, Dept Internal Med 1, Div Gastroenterol, D-23538 Lubeck, Germany
关键词
antimicrobial peptide; defensin; epithelial cell; innate immunity;
D O I
10.1097/00042737-200107000-00003
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Physical barrier function was formerly believed to play the major role in mucosal protection against luminal bacteria. This view has now been challenged by the discovery of specialized molecules that possess antimicrobial activity, More than 100 peptides have been identified so far, and the number is still growing, These peptides are distributed widely and conserved throughout phylogeny, The epithelial expression of antimicrobial peptides is of particular interest as many pathogens adhere to epithelial surfaces and may eventually invade the host. This rapidly acting defence system of innate immunity is already engaged before adoptive immune interactions take place, These antimicrobial peptides consist of constitutive and inducible forms, potentiating this barrier function in terms of an inflammatory response, One important subgroup of antimicrobial peptides is the family of defensins, which are classified as alpha (alpha-) and beta (beta-) defensins, Eight different peptides with varying antimicrobial properties have been identified. They are distributed widely in humans, and organ-specific expression patterns have been observed. Homologous peptides have been found in other mammals, vertebrates, invertebrates, insects and plants, The identification of alpha -defensins and their murine counterparts, cryptdins, in the small intestine prompted intensive research into epithelial antimicrobial defence. (C) 2001 Lippincott Williams & Wilkins.
引用
收藏
页码:771 / 776
页数:6
相关论文
共 83 条
[71]  
SYMONDS DA, 1974, ARCH PATHOL, V97, P343
[72]   Enteric β-defensin:: Molecular cloning and characterization of a gene with inducible intestinal epithelial cell expression associated with Cryptosporidium parvum infection [J].
Tarver, AP ;
Clark, DP ;
Diamond, G ;
Russell, JP ;
Erdjument-Bromage, H ;
Tempst, P ;
Cohen, KS ;
Jones, DE ;
Sweeny, RW ;
Wines, M ;
Hwang, S ;
Bevins, CL .
INFECTION AND IMMUNITY, 1998, 66 (03) :1045-1056
[73]   β-defensin expression in human mammary gland epithelia [J].
Tunzi, CR ;
Harper, PA ;
Bar-Oz, B ;
Valore, EV ;
Semple, JL ;
Watson-MacDonell, J ;
Ganz, T ;
Ito, S .
PEDIATRIC RESEARCH, 2000, 48 (01) :30-35
[74]   Human β-defensin-1:: An antimicrobial peptide of urogenital tissues [J].
Valore, EV ;
Park, CH ;
Quayle, AJ ;
Wiles, KR ;
McCray, PB ;
Ganz, T .
JOURNAL OF CLINICAL INVESTIGATION, 1998, 101 (08) :1633-1642
[75]  
Vatta S, 2000, Hum Mutat, V15, P582
[76]   Induction of human β-defensin-2 mRNA expression by Helicobacter pylori in human gastric cell line MKN45 cells on cag Pathogenicity Island [J].
Wada, A ;
Mori, N ;
Oishi, K ;
Hojo, H ;
Nakahara, Y ;
Hamanaka, Y ;
Nagashima, M ;
Sekine, I ;
Ogushi, K ;
Niidome, T ;
Nagatake, T ;
Moss, J ;
Hirayama, T .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1999, 263 (03) :770-774
[77]   Regulation of intestinal α-defensin activation by the metalloproteinase matrilysin in innate host defense [J].
Wilson, CL ;
Ouellette, AJ ;
Satchell, DP ;
Ayabe, T ;
López-Boado, YS ;
Stratman, JL ;
Hultgren, SJ ;
Matrisian, LM ;
Parks, WC .
SCIENCE, 1999, 286 (5437) :113-117
[78]   INTERACTIONS BETWEEN HUMAN DEFENSINS AND LIPID BILAYERS - EVIDENCE FOR FORMATION OF MULTIMERIC PORES [J].
WIMLEY, WC ;
SELSTED, ME ;
WHITE, SH .
PROTEIN SCIENCE, 1994, 3 (09) :1362-1373
[79]  
Yang D, 2000, J LEUKOCYTE BIOL, V68, P9
[80]   β-defensins:: Linking innate and adaptive immunity through dendritic and T cell CCR6 [J].
Yang, D ;
Chertov, O ;
Bykovskaia, N ;
Chen, Q ;
Buffo, MJ ;
Shogan, J ;
Anderson, M ;
Schröder, JM ;
Wang, JM ;
Howard, OMZ ;
Oppenheim, JJ .
SCIENCE, 1999, 286 (5439) :525-528