Transgenic mice expressing a truncated Peromyscus leucopus TNF-α gene manifest an arthritis resembling ankylosing spondylitis

被引:41
作者
Crew, MD
Effros, RB
Walford, RL
Zeller, E
Cheroutre, H
Brahn, E
机构
[1] John L McClellan Mem Vet Hosp, Gerontol Res Educ & Clin Ctr, Little Rock, AR 72205 USA
[2] Univ Arkansas Med Sci, Dept Geriatr, Little Rock, AR 72205 USA
[3] Univ Arkansas Med Sci, Dept Biochem & Mol Biol, Little Rock, AR 72205 USA
[4] Univ Calif Los Angeles, Sch Med, Dept Pathol & Lab Med, Los Angeles, CA 90024 USA
[5] Univ Calif Los Angeles, Sch Med, Dept Microbiol & Immunol, Los Angeles, CA 90024 USA
[6] Univ Calif Los Angeles, Sch Med, Dept Med, Div Rheumatol, Los Angeles, CA 90024 USA
关键词
D O I
10.1089/jir.1998.18.219
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Several studies have implicated tumor necrosis factor-alpha (TNF-alpha) in autoimmune diseases, such as rheumatoid arthritis (RA), To elucidate further the role of TNF-alpha in inflammatory arthritis, we generated transgenic mice harboring a truncated Peromyscus leucopus TNF-alpha (Pe-TNF) gene. An arthritic phenotype closely resembling human ankylosing spondylitis was observed only in transgenic lines expressing the Pe-TNF transgene at the mRNA level. We characterized the arthritic phenotype in detail by radiographic and histologic techniques. It consisted of severe axial skeletal kyphosis and ankylosis, accompanied by an inflammatory and fibrotic process at the end plates and enthesis, Peripheral joint lesions were absent in mice expressing the P, leucopus TNF-alpha gene, in contrast to the RA-like phenotype described in transgenic mice expressing a truncated human TNF-alpha gene. The Pe-TNF transgenic mouse model provides a unique opportunity to explore potential mechanisms whereby TNF-alpha may initiate an autoimmune arthritis resembling ankylosing spondylitis.
引用
收藏
页码:219 / 225
页数:7
相关论文
共 33 条
  • [11] ELLIOTT MJ, 1993, ARTHRITIS RHEUM, V36, P1681, DOI 10.1002/art.23362
  • [12] SPONTANEOUS INFLAMMATORY DISEASE IN TRANSGENIC RATS EXPRESSING HLA-B27 AND HUMAN BETA-2M - AN ANIMAL-MODEL OF HLA-B27-ASSOCIATED HUMAN DISORDERS
    HAMMER, RE
    MAIKA, SD
    RICHARDSON, JA
    TANG, JP
    TAUROG, JD
    [J]. CELL, 1990, 63 (05) : 1099 - 1112
  • [14] Hogan B., 1986, MANIPULATING MOUSE E
  • [15] STRUCTURE OF TUMOR NECROSIS FACTOR
    JONES, EY
    STUART, DI
    WALKER, NPC
    [J]. NATURE, 1989, 338 (6212) : 225 - 228
  • [16] TRANSGENIC MICE EXPRESSING HUMAN TUMOR-NECROSIS-FACTOR - A PREDICTIVE GENETIC MODEL OF ARTHRITIS
    KEFFER, J
    PROBERT, L
    CAZLARIS, H
    GEORGOPOULOS, S
    KASLARIS, E
    KIOUSSIS, D
    KOLLIAS, G
    [J]. EMBO JOURNAL, 1991, 10 (13) : 4025 - 4031
  • [17] MACNAUL KL, 1990, J BIOL CHEM, V265, P17238
  • [18] LEVELS OF CIRCULATING TUMOR-NECROSIS-FACTOR-ALPHA AND INTERLEUKIN-6 IN PATIENTS WITH RHEUMATOID-ARTHRITIS - RELATIONSHIP TO SERUM LEVELS OF HYALURONAN AND ANTIGENIC KERATAN SULFATE
    MANICOURT, DH
    TRIKI, R
    FUKUDA, K
    DEVOGELAER, JP
    DEDEUXCHAISNES, CN
    THONAR, EJMA
    [J]. ARTHRITIS AND RHEUMATISM, 1993, 36 (04): : 490 - 499
  • [19] NEDOSPASOV SA, 1991, J IMMUNOL, V147, P1053
  • [20] THE ROLE OF THE MAJOR HISTOCOMPATIBILITY COMPLEX IN AUTOIMMUNITY
    NEPOM, BS
    [J]. CLINICAL IMMUNOLOGY AND IMMUNOPATHOLOGY, 1993, 67 (03): : S50 - S55