Expression of transgene encoded TGF-β in islets prevents autoimmune diabetes in NOD mice by a local mechanism

被引:54
作者
Grewal, IS
Grewal, KD
Wong, FS
Wang, H
Picarella, DE
Janeway, CA
Flavell, RA
机构
[1] Genentech Inc, Dept Immunol, San Francisco, CA 94080 USA
[2] Yale Univ, Sch Med, Howard Hughes Med Inst, New Haven, CT 06520 USA
[3] Yale Univ, Sch Med, Immunol Sect, New Haven, CT 06520 USA
关键词
autoimmunity; cytokines; immune-regulation; suppression; pancreas;
D O I
10.1006/jaut.2002.0599
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
To analyse the effects of TGF-beta in insulin dependent diabetes mellitus (IDDM), we have developed non-obese diabetic (NOD) transgenic mice expressing TGF-beta under the control of the rat insulin II promoter. Pancreata of TGF-beta transgenic mice were roughly one twentieth of the size of pancreata of wild-type NOD mice and showed small clusters of micro-islets rather than normal adult islets. However, these islets produced sufficient levels of insulin to maintain normal glucose levels and mice were protected from the diabetes, which developed in their negative littermates. A massive fibrosis was seen in the transgenic pancreata that was accompanied with infiltration of mononuclear cells that decreased with age. Interestingly, these mice showed normal anti-islet immune response in their spleens and remained susceptible to adoptive transfer of IDDM by mature cloned CD8 effector cells. TUNEL assays revealed increased apoptosis of invading cells when compared to non-transgenic NOD mice. Taken together, these results suggest that TGF-beta protects islets by a local event. (C) 2002 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:9 / 22
页数:14
相关论文
共 56 条
[1]   ALTERED METABOLIC AND ADHESIVE PROPERTIES AND INCREASED TUMORIGENESIS ASSOCIATED WITH INCREASED EXPRESSION OF TRANSFORMING GROWTH FACTOR-BETA-1 [J].
ARRICK, BA ;
LOPEZ, AR ;
ELFMAN, F ;
EBNER, R ;
DAMSKY, CH ;
DERYNCK, R .
JOURNAL OF CELL BIOLOGY, 1992, 118 (03) :715-726
[2]  
BAUER GE, 1983, HISTOLOGY CELL TISSU, P781
[3]   PREVENTION OF DIABETES IN NONOBESE DIABETIC MICE BY ANTI-I-A MONOCLONAL-ANTIBODIES - TRANSFER OF PROTECTION BY SPLENIC T-CELLS [J].
BOITARD, C ;
BENDELAC, A ;
RICHARD, MF ;
CARNAUD, C ;
BACH, JF .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1988, 85 (24) :9719-9723
[4]   T-CELL-MEDIATED INHIBITION OF THE TRANSFER OF AUTOIMMUNE DIABETES IN NOD MICE [J].
BOITARD, C ;
YASUNAMI, R ;
DARDENNE, M ;
BACH, JF .
JOURNAL OF EXPERIMENTAL MEDICINE, 1989, 169 (05) :1669-1680
[5]   TRANSFORMING GROWTH-FACTOR-BETA IN DISEASE - THE DARK SIDE OF TISSUE-REPAIR [J].
BORDER, WA ;
RUOSLAHTI, E .
JOURNAL OF CLINICAL INVESTIGATION, 1992, 90 (01) :1-7
[6]   TRANSFORMING GROWTH-FACTOR BETA-1 SUPPRESSES ACUTE AND CHRONIC ARTHRITIS IN EXPERIMENTAL-ANIMALS [J].
BRANDES, ME ;
ALLEN, JB ;
OGAWA, Y ;
WAHL, SM .
JOURNAL OF CLINICAL INVESTIGATION, 1991, 87 (03) :1108-1113
[7]  
Bright JJ, 1998, J IMMUNOL, V161, P1772
[8]  
Bright JJ, 1997, J IMMUNOL, V159, P175
[9]   TYPE-I DIABETES - A CHRONIC AUTOIMMUNE-DISEASE OF HUMAN, MOUSE, AND RAT [J].
CASTANO, L ;
EISENBARTH, GS .
ANNUAL REVIEW OF IMMUNOLOGY, 1990, 8 :647-679
[10]  
CHRIST M, 1994, J IMMUNOL, V153, P1936