Functional imaging of interleukin 1 beta expression in inflammatory process using bioluminescence imaging in transgenic mice

被引:56
作者
Li, Limei [2 ,4 ,6 ]
Fei, Zhaoliang [1 ]
Ren, Jianke [1 ,2 ]
Sun, Ruilin [1 ,2 ]
Liu, Zhihui [2 ]
Sheng, Zhejin [3 ]
Wang, Long [1 ]
Sun, Xia [1 ]
Yu, Jun [5 ]
Wang, Zhugang [1 ]
Fei, Jian [1 ,3 ]
机构
[1] Shanghai Res Ctr Model Organisms, Shanghai, Peoples R China
[2] Chinese Acad Sci, Mol Cell Biol Lab, Inst Biochem & Cell Biol, Shanghai Inst Biol Sci, Shanghai, Peoples R China
[3] Tongji Univ, Sch Life Sci & Technol, Shanghai, Peoples R China
[4] Chinese Acad Sci, Grad Sch, Beijing 100864, Peoples R China
[5] Shanghai Genom Inc, Shanghai, Peoples R China
[6] Shanghai Nan Fang Model Organism Res Ctr, Shanghai, Peoples R China
关键词
D O I
10.1186/1471-2172-9-49
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Background: Interleukin 1 beta ( IL-1 beta) plays an important role in a number of chronic and acute inflammatory diseases. To understand the role of IL-1 beta in disease processes and develop an in vivo screening system for anti-inflammatory drugs, a transgenic mouse line was generated which incorporated the transgene firefly luciferase gene driven by a 4.5-kb fragment of the human IL-1 beta gene promoter. Luciferase gene expression was monitored in live mice under anesthesia using bioluminescence imaging in a number of inflammatory disease models. Results: In a LPS-induced sepsis model, dramatic increase in luciferase activity was observed in the mice. This transgene induction was time dependent and correlated with an increase of endogenous IL-1 beta mRNA and pro-IL-1 beta protein levels in the mice. In a zymosan-induced arthritis model and an oxazolone-induced skin hypersensitivity reaction model, luciferase expression was locally induced in the zymosan injected knee joint and in the ear with oxazolone application, respectively. Dexamethasone suppressed the expression of luciferase gene both in the acute sepsis model and in the acute arthritis model. Conclusion: Our data suggest that the transgenic mice model could be used to study transcriptional regulation of the IL-1 beta gene expression in the inflammatory process and evaluation the effect of anti-inflammatory drug in vivo.
引用
收藏
页数:9
相关论文
共 33 条
[1]   RECOMBINANT HUMAN INTERLEUKIN-1 RECEPTOR ANTAGONIST IN THE TREATMENT OF STEROID-RESISTANT GRAFT-VERSUS-HOST DISEASE [J].
ANTIN, JH ;
WEINSTEIN, HJ ;
GUINAN, EC ;
MCCARTHY, P ;
BIERER, BE ;
GILLILAND, DG ;
PARSONS, SK ;
BALLEN, KK ;
RIMM, IJ ;
FALZARANO, G ;
BLOEDOW, DC ;
ABATE, L ;
LEBSACK, M ;
BURAKOFF, SJ ;
FERRARA, JLM .
BLOOD, 1994, 84 (04) :1342-1348
[2]  
AURON PE, 1994, EUR CYTOKINE NETW, V5, P573
[3]   NF-BETA-A, A FACTOR REQUIRED FOR MAXIMAL INTERLEUKIN-1-BETA GENE-EXPRESSION IS IDENTICAL TO THE ETS FAMILY MEMBER PU.1 - EVIDENCE FOR STRUCTURAL ALTERATION FOLLOWING LPS ACTIVATION [J].
BURAS, JA ;
REENSTRA, WR ;
FENTON, MJ .
MOLECULAR IMMUNOLOGY, 1995, 32 (08) :541-&
[4]  
BURAS JA, 1994, J IMMUNOL, V152, P4444
[5]   CIRCULATING INTERLEUKIN-1-BETA AND TUMOR NECROSIS FACTOR-BETA CONCENTRATIONS AFTER BURN INJURY IN HUMANS [J].
CANNON, JG ;
FRIEDBERG, JS ;
GELFAND, JA ;
TOMPKINS, RG ;
BURKE, JF ;
DINARELLO, CA .
CRITICAL CARE MEDICINE, 1992, 20 (10) :1414-1419
[6]   In vivo imaging of NF-κB activity [J].
Carlsen, H ;
Moskaug, JO ;
Fromm, SH ;
Blomhoff, R .
JOURNAL OF IMMUNOLOGY, 2002, 168 (03) :1441-1446
[7]   PLASMA CYTOKINE AND ENDOTOXIN LEVELS CORRELATE WITH SURVIVAL IN PATIENTS WITH THE SEPSIS SYNDROME [J].
CASEY, LC ;
BALK, RA ;
BONE, RC .
ANNALS OF INTERNAL MEDICINE, 1993, 119 (08) :771-778
[8]  
COGSWELL JP, 1994, J IMMUNOL, V153, P712
[9]   Bioluminescent indicators in living mammals [J].
Contag, PR ;
Olomu, IN ;
Stevenson, DK ;
Contag, CH .
NATURE MEDICINE, 1998, 4 (02) :245-247
[10]   Acute stress effects on local Il-1β responses to pathogens in a human in vivo model [J].
Deinzer, R ;
Granrath, N ;
Stuhl, H ;
Twork, L ;
Idel, H ;
Waschul, B ;
Herforth, A .
BRAIN BEHAVIOR AND IMMUNITY, 2004, 18 (05) :458-467