Antimicrobial Human beta-Defensins in the Colon and Their Role in Infectious and Non-Infectious Diseases

被引:59
作者
Cobo, Eduardo R. [1 ]
Chadee, Kris [1 ]
机构
[1] Univ Calgary, Fac Med, Snyder Inst Chron Dis, Dept Microbiol Immunol & Infect Dis,Gastrointesti, 3330 Hosp Dr NW, Calgary, AB T2N 4N1, Canada
关键词
innate immunity; antimicrobial peptides; beta-defensin; colon; intestinal mucosa; parasites; infection;
D O I
10.3390/pathogens2010177
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
beta-defensins are small cationic antimicrobial peptides secreted by diverse cell types including colonic epithelial cells. Human beta-defensins form an essential component of the intestinal lumen in innate immunity. The defensive mechanisms of beta-defensins include binding to negatively charged microbial membranes that cause cell death and chemoattraction of immune cells. The antimicrobial activity of beta-defensin is well reported in vitro against several enteric pathogens and in non-infectious processes such as inflammatory bowel diseases, which alters beta-defensin production. However, the role of beta-defensin in vivo in its interaction with other immune components in host defense against bacteria, viruses and parasites with more complex membranes is still not well known. This review focuses on the latest findings regarding the role of beta-defensin in relevant human infectious and non-infectious diseases of the colonic mucosa. In addition, we summarize the most significant aspects of beta-defensin and its antimicrobial role in a variety of disease processes.
引用
收藏
页码:177 / 192
页数:16
相关论文
共 71 条
[1]   KILLING OF GIARDIA-LAMBLIA BY CRYPTDINS AND CATIONIC NEUTROPHIL PEPTIDES [J].
ALEY, SB ;
ZIMMERMAN, M ;
HETSKO, M ;
SELSTED, ME ;
GILLIN, FD .
INFECTION AND IMMUNITY, 1994, 62 (12) :5397-5403
[2]   Human β-defensin 2 is a salt-sensitive peptide antibiotic expressed in human lung [J].
Bals, R ;
Wang, XR ;
Wu, ZR ;
Freeman, T ;
Bafna, V ;
Zasloff, M ;
Wilson, JM .
JOURNAL OF CLINICAL INVESTIGATION, 1998, 102 (05) :874-880
[3]   HBD-1 - A NOVEL BETA-DEFENSIN FROM HUMAN PLASMA [J].
BENSCH, KW ;
RAIDA, M ;
MAGERT, HJ ;
SCHULZKNAPPE, P ;
FORSSMANN, WG .
FEBS LETTERS, 1995, 368 (02) :331-335
[4]   PHOSPHOLIPASES AND CATIONIC PEPTIDES INHIBIT CRYPTOSPORIDIUM PARVUM SPOROZOITE INFECTIVITY BY PARASITICIDAL AND NON-PARASITICIDAL MECHANISMS [J].
Carryn, Stephane ;
Schaefer, Deborah A. ;
Imboden, Michael ;
Homan, E. Jane ;
Bremel, Robert D. ;
Riggs, Michael W. .
JOURNAL OF PARASITOLOGY, 2012, 98 (01) :199-204
[5]   Multiple TLRs are expressed in human cholangiocytes and mediate host epithelial defense responses to Cryptosporidium parvum via activation of NF-κB [J].
Chen, XM ;
O'Hara, SP ;
Nelson, JB ;
Splinter, PL ;
Small, AJ ;
Tietz, PS ;
Limper, AH ;
LaRusso, NF .
JOURNAL OF IMMUNOLOGY, 2005, 175 (11) :7447-7456
[6]   Immunobiology of Human Cytomegalovirus: from Bench to Bedside [J].
Crough, Tania ;
Khanna, Rajiv .
CLINICAL MICROBIOLOGY REVIEWS, 2009, 22 (01) :76-+
[7]   Optimization of the antimicrobial activity of magainin peptides by modification of charge [J].
Dathe, M ;
Nikolenko, H ;
Meyer, J ;
Beyermann, M ;
Bienert, M .
FEBS LETTERS, 2001, 501 (2-3) :146-150
[8]   Microsporidiosis: current status [J].
Didier, Elizabeth S. ;
Weiss, Louis M. .
CURRENT OPINION IN INFECTIOUS DISEASES, 2006, 19 (05) :485-492
[9]  
DIETERICH DT, 1991, J ACQ IMMUN DEF SYND, V4, pS29
[10]   β-Defensin-3 and -4 in intestinal epithelial cells display increased mRNA expression in ulcerative colitis [J].
Fahlgren, A ;
Hammarström, S ;
Danielsson, Å ;
Hammarström, ML .
CLINICAL AND EXPERIMENTAL IMMUNOLOGY, 2004, 137 (02) :379-385