IN THE PRESENCE OF DEXAMETHASONE, GAMMA-INTERFERON INDUCES RAT OLIGODENDROCYTES TO EXPRESS MAJOR HISTOCOMPATIBILITY COMPLEX CLASS-II MOLECULES

被引:39
作者
BERGSTEINSDOTTIR, K [1 ]
BRENNAN, A [1 ]
JESSEN, KR [1 ]
MIRSKY, R [1 ]
机构
[1] UNIV LONDON UNIV COLL, DEPT ANAT & DEV BIOL, GOWER ST, LONDON WC1E 6BT, ENGLAND
关键词
IMMUNE DEFENSE; MULTIPLE SCLEROSIS; EXPERIMENTAL ALLERGIC ENCEPHALOMYELITIS; CENTRAL NERVOUS SYSTEM; GLUCOCORTICOIDS;
D O I
10.1073/pnas.89.19.9054
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
Cells that express major histocompatibility complex (MHC) class II molecules can interact directly with CD4 T lymphocytes and either activate immune reactions or become the targets of T-cell-mediated cytotoxic attack. Using rat optic nerve cultures combined with immunocytochemistry and in situ hybridization, we have shown that oligodendrocytes, the major myelin-forming cells of the central nervous system and the main casualty of the immune attacks associated with multiple sclerosis and experimental allergic encephalomyelitis, can be readily induced to express MHC class II mRNA and surface antigens in vitro by exposure to gamma interferon, provided the glucocorticoid dexamethasone is included in the culture medium. Oligodendrocytes exposed to gamma interferon without dexamethasone fail to express MHC class II molecules, which may account for the failure of previous attempts to induce expression in these cells. In the experiments reported here MHC class II expression can be demonstrated both on galactocerebroside-positive cells and on mature oligodendrocytes that express proteolipid protein. These findings expand possibilities for understanding immune-related oligodendrocyte killing and demyelination in human and experimental demyelinating diseases.
引用
收藏
页码:9054 / 9058
页数:5
相关论文
共 61 条
  • [1] BERGSTEINSDOTTI.K, 1992, THESIS U LONDON LOND
  • [2] RAT SCHWANN-CELLS CAN BE INDUCED TO EXPRESS MAJOR HISTOCOMPATIBILITY COMPLEX CLASS-II MOLECULES INVIVO
    BERGSTEINSDOTTIR, K
    KINGSTON, A
    JESSEN, KR
    [J]. JOURNAL OF NEUROCYTOLOGY, 1992, 21 (05): : 382 - 390
  • [3] LOCALIZATION OF ALDOSTERONE AND CORTICOSTERONE IN THE CENTRAL NERVOUS-SYSTEM, ASSESSED BY QUANTITATIVE AUTORADIOGRAPHY
    BIRMINGHAM, MK
    SAR, M
    STUMPF, WE
    [J]. NEUROCHEMICAL RESEARCH, 1984, 9 (03) : 333 - 350
  • [4] BLOOM BR, 1990, HARVEY LECT, V84, P41
  • [5] BOHN MC, 1982, J NEUROSCI, V2, P1292
  • [6] BASIC PROTEIN-SPECIFIC T-CELL LINES THAT INDUCE EXPERIMENTAL AUTOIMMUNE ENCEPHALOMYELITIS IN SJL/J MICE - COMPARISON WITH LEWIS RAT LINES
    BOURDETTE, DN
    VANDENBARK, AA
    MESHUL, C
    WHITHAM, R
    OFFNER, H
    [J]. CELLULAR IMMUNOLOGY, 1988, 112 (02) : 351 - 363
  • [7] HYPOTHESIS - A ROLE FOR TUMOR NECROSIS FACTOR IN IMMUNE-MEDIATED DEMYELINATION AND ITS RELEVANCE TO MULTIPLE-SCLEROSIS
    BROSNAN, CF
    SELMAJ, K
    RAINE, CS
    [J]. JOURNAL OF NEUROIMMUNOLOGY, 1988, 18 (01) : 87 - 94
  • [8] MS - A LOCALIZED IMMUNE DISEASE OF THE CENTRAL NERVOUS-SYSTEM
    CALDER, V
    OWEN, S
    WATSON, C
    FELDMANN, M
    DAVISON, A
    [J]. IMMUNOLOGY TODAY, 1989, 10 (03): : 99 - 103
  • [9] THE DIFFERENTIATION OF O-2A PROGENITOR CELLS INTO OLIGODENDROCYTES IS ASSOCIATED WITH A LOSS OF INDUCIBILITY OF IA ANTIGENS
    CALDER, VL
    WOLSWIJK, G
    NOBLE, M
    [J]. EUROPEAN JOURNAL OF IMMUNOLOGY, 1988, 18 (08) : 1195 - 1201
  • [10] THE PATHOGENESIS OF DEMYELINATING DISEASE - INSIGHTS FROM CELL BIOLOGY
    COMPSTON, A
    SCOLDING, N
    WREN, D
    NOBLE, M
    [J]. TRENDS IN NEUROSCIENCES, 1991, 14 (05) : 175 - 182