THE NOD MOUSE - RECESSIVE DIABETOGENIC GENE IN THE MAJOR HISTOCOMPATIBILITY COMPLEX

被引:408
作者
HATTORI, M
BUSE, JB
JACKSON, RA
GLIMCHER, L
DORF, ME
MINAMI, M
MAKINO, S
MORIWAKI, K
KUZUYA, H
IMURA, H
STRAUSS, WM
SEIDMAN, JG
EISENBARTH, GS
机构
[1] HARVARD UNIV, BRIGHAM & WOMENS HOSP, SCH MED, JOSLIN DIABET CTR, BOSTON, MA 02215 USA
[2] SHIONOGI ABURAHI LABS, SHIGA, JAPAN
[3] NATL INST GENET, SHIZUOKA, JAPAN
[4] KYOTO UNIV, SCH MED, KYOTO 606, JAPAN
关键词
D O I
10.1126/science.3003909
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Examination of the histocompatibility region of the nonobese diabetic (NOD) mouse with antibodies against class II glycoproteins (products of immune response genes of the major histocompatibility complex I-A and I-E), hybrid T-cell clones, and mixed-lymphocyte cultures and analysis of restriction fragment length polymorphisms indicate that the NOD mouse has a unique class II major histocompatibility complex with no expression of surface I-E, no messenger RNA for I-E.alpha., and an I-A not recognized by any monoclonal antibodies or hybrid T-cell clones studied. In crosses of NOD mice with control C3H mice, the development of diabetes was dependent on homozygosity for the NOD mouse''s unique major histocompatibility region.
引用
收藏
页码:733 / 735
页数:3
相关论文
共 25 条
  • [1] HISTOCOMPATIBILITY-LINKED IMMUNE-RESPONSE GENES
    BENACERR.B
    MCDEVITT, HO
    [J]. SCIENCE, 1972, 175 (4019) : 273 - &
  • [2] BHATTACHARYA A, 1981, J IMMUNOL, V127, P2488
  • [3] MAJOR HISTOCOMPATIBILITY COMPLEX RESTRICTION FRAGMENT LENGTH POLYMORPHISMS DEFINE 3 DIABETOGENIC HAPLOTYPES IN BB AND BBN RATS
    BUSE, JB
    RIFAIHADDAD, R
    LEES, S
    TANIGUCHI, H
    CHAPLIN, D
    MILFORD, EM
    SEIDMAN, JG
    EISENBARTH, GS
    JACKSON, RA
    [J]. JOURNAL OF EXPERIMENTAL MEDICINE, 1985, 162 (02) : 444 - 458
  • [4] SPECIFIC CLASS II HISTOCOMPATIBILITY GENE POLYMORPHISM IN BB RATS
    BUSE, JB
    BENNUN, A
    KLEIN, KA
    EISENBARTH, GS
    SEIDMAN, JG
    JACKSON, RA
    [J]. DIABETES, 1984, 33 (07) : 700 - 703
  • [5] MURINE I-A-BETA CHAIN POLYMORPHISM - NUCLEOTIDE-SEQUENCES OF 3 ALLELIC I-A-BETA GENES
    CHOI, E
    MCINTYRE, K
    GERMAIN, RN
    SEIDMAN, JG
    [J]. SCIENCE, 1983, 221 (4607) : 283 - 286
  • [6] NEW LYMPHOCYTE ANTIGEN SYSTEM (LNA) CONTROLLED BY IR-REGION OF MOUSE H-2 COMPLEX
    DAVID, CS
    SHREFFLER, DC
    FRELINGER, JA
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1973, 70 (09) : 2509 - 2514
  • [7] GENETIC-CONTROL OF SPECIFIC IMMUNE SUPPRESSION .3. MAPPING OF H-2 COMPLEX COMPLEMENTING GENES CONTROLLING IMMUNE SUPPRESSION BY RANDOM COPOLYMER L-GLUTAMIC ACID 50 L-TYROSINE 50 (GT)
    DEBRE, P
    WALTENBAUGH, C
    DORF, M
    BENACERRAF, B
    [J]. JOURNAL OF EXPERIMENTAL MEDICINE, 1976, 144 (01) : 272 - 276
  • [8] PRODUCTION OF AUTOREACTIVE I-REGION-RESTRICTED T-CELL HYBRIDOMAS
    GLIMCHER, LH
    SHEVACH, EM
    [J]. JOURNAL OF EXPERIMENTAL MEDICINE, 1982, 156 (02) : 640 - 645
  • [9] CAN FUTURE TYPE-1 DIABETES BE PREDICTED QUESTIONABLE - A STUDY IN FAMILIES OF AFFECTED CHILDREN
    GORSUCH, AN
    SPENCER, KM
    LISTER, J
    WOLF, E
    BOTTAZZO, GF
    CUDWORTH, AG
    [J]. DIABETES, 1982, 31 (10) : 862 - 866
  • [10] ISOLATION OF 12 MONOCLONAL ANTIBODIES AGAINST IA AND H-2-ANTIGENS - SEROLOGICAL CHARACTERIZATION AND REACTIVITY WITH LYMPHOCYTE-B AND LYMPHOCYTE-T
    HAMMERLING, GJ
    HAMMERLING, U
    LEMKE, H
    [J]. IMMUNOGENETICS, 1979, 8 (5-6) : 433 - 445