Induction of a rat enteric defensin gene by hemorrhagic shock

被引:24
作者
Condon, MR
Viera, A
D'Alessio, M
Diamond, G
机构
[1] Univ Med & Dent New Jersey, Dept Surg, Newark, NJ 07103 USA
[2] Univ Med & Dent New Jersey, Dept Anat Cell Biol & Injury Sci, Newark, NJ 07103 USA
[3] Dept Vet Affairs Med Ctr, E Orange, NJ USA
[4] Univ Med & Dent New Jersey, Grad Sch Biomed Sci, Newark, NJ 07103 USA
关键词
D O I
10.1128/IAI.67.9.4787-4793.1999
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Multicellular organisms utilize a battery of extracellular and cellular mechanisms to defend against microbial infiltration. Among the armamentarium used by the small intestine to defend against microbial invasion are antimicrobial peptides called defensins, We previously have shown that gut barrier function is impaired following hemorrhagic shock, resulting in translocation of bacteria or endotoxin, Using a rat model, we examined the effect of hemorrhagic shock on alpha-defensin expression, We utilized the anchored reverse transcriptase PCR strategy to isolate a rat enteric defensin cDNA, The cDNA is 406 bases in length and encodes a putative prepro-enteric defensin that we have named rat defensin 5 (RD-5). RD-5 expression is restricted to the small intestine and is specifically localized by in situ hybridization to the Paneth cells. A 10-fold increase in its steady state levels was observed in the distal intestine immediately after the termination of shock This is the first study to show that enteric defensins are inducible following injury. We suggest that enteric defensins may contribute to the complex and integrated barrier function of the intestinal mucosal surface.
引用
收藏
页码:4787 / 4793
页数:7
相关论文
共 57 条
[1]   TRANSLOCATION OF CERTAIN INDIGENOUS BACTERIA FROM THE GASTRO-INTESTINAL TRACT TO THE MESENTERIC LYMPH-NODES AND OTHER ORGANS IN A GNOTOBIOTIC MOUSE MODEL [J].
BERG, RD ;
GARLINGTON, AW .
INFECTION AND IMMUNITY, 1979, 23 (02) :403-411
[2]  
Bevins Charles L., 1997, V78, P151
[3]  
CHOMCZYNSKI P, 1987, ANAL BIOCHEM, V162, P156, DOI 10.1016/0003-2697(87)90021-2
[4]   LOCALIZATION OF LYSOZYME ACTIVITY IN A PANETH CELL GRANULE FRACTION [J].
DECKX, RJ ;
VANTRAPPEN, GR ;
PAREIN, MM .
BIOCHIMICA ET BIOPHYSICA ACTA, 1967, 139 (01) :204-+
[5]  
DEITCH EA, 1990, J TRAUMA, V30, pS184
[6]   EFFECT OF ORAL ANTIBIOTICS AND BACTERIAL OVERGROWTH ON THE TRANSLOCATION OF THE GI TRACT MICROFLORA IN BURNED RATS [J].
DEITCH, EA ;
MAEJIMA, K ;
BERG, R .
JOURNAL OF TRAUMA-INJURY INFECTION AND CRITICAL CARE, 1985, 25 (05) :385-392
[7]   EVIDENCE FAVORING THE ROLE OF THE GUT AS A CYTOKINE-GENERATING ORGAN IN RATS SUBJECTED TO HEMORRHAGIC-SHOCK [J].
DEITCH, EA ;
XU, DZ ;
FRANKO, L ;
AYALA, A ;
CHAUDRY, IH .
SHOCK, 1994, 1 (02) :141-146
[8]   β-defensins:: Endogenous antibiotics of the innate host defense response [J].
Diamond, G ;
Bevins, CL .
CLINICAL IMMUNOLOGY AND IMMUNOPATHOLOGY, 1998, 88 (03) :221-225
[9]   HOST-MICROBE INTERACTION IN THE GASTROINTESTINAL-TRACT [J].
DUNCAN, HE ;
EDBERG, SC .
CRITICAL REVIEWS IN MICROBIOLOGY, 1995, 21 (02) :85-100
[10]  
EISNHAUER PB, 1992, INFECT IMMUN, V60, P3556