MHC class II gene silencing in trophoblast cells is caused by inhibition of CIITA expression

被引:41
作者
Morris, AC
Riley, JL
Fleming, WH
Boss, JM
机构
[1] Emory Univ, Sch Med, Dept Microbiol & Immunol, Atlanta, GA 30322 USA
[2] Oregon Hlth & Sci Univ, Dept Med, Portland, OR 97201 USA
关键词
MHC class II; maternal-fetal tolerance; IFN-gamma; gene regulation; trophoblasts;
D O I
10.1111/j.1600-0897.1998.tb00423.x
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
PROBLEM: Major histocompatibility complex (MHC) class II molecule expression is specifically suppressed on fetal trophoblasts, even in response to interferon (IFN)-gamma, a potent inducer of MHC class II genes. The suppression of class II induction has been suggested to play a role in preventing rejection of the fetal allograft. The mechanism of this suppression is unknown. METHOD OF STUDY: Human trophoblast cell lines were examined for expression of MHC class II transcription factors and for activity of the IFN-gamma signaling pathway. Additionally, trophoblast cells were transfected with a vector expressing the class II transtictivator, CIITA, and assayed for class II expression. RESULTS: The MHC class II transcription factors RFX and X2BP and the IFN-gamma signaling pathway components are expressed constitutively and are functional in trophoblasts. However, CIITA expression was absent in trophoblasts and could not be induced by IFN-gamma. Transfection of CIITA into trophoblast cells resulted in derepression of class II gene expression. CONCLUSIONS: The lack of induction of MHC class II genes in response to IFN-gamma in trophoblast cells is caused neither by the absence of factors that bind class II promoters, nor by a lesion in the IFN-gamma signaling pathway, but results from a specific inhibition of the CIITA gene.
引用
收藏
页码:385 / 394
页数:10
相关论文
共 65 条
[1]   CHRONIC VILLITIS OF UNKNOWN ETIOLOGY AND INTRAUTERINE GROWTH-RETARDED INFANTS OF NORMAL AND LOW PONDERAL INDEX [J].
ALTHABE, O ;
LABARRERE, C .
PLACENTA, 1985, 6 (04) :369-373
[2]   A TRANSFORMING GROWTH-FACTOR-BETA-2 (TGF-BETA-2)-LIKE IMMUNOSUPPRESSIVE FACTOR IN AMNIOTIC-FLUID AND LOCALIZATION OF TGF-BETA-2 MESSENGER-RNA IN THE PREGNANT UTERUS [J].
ALTMAN, DJ ;
SCHNEIDER, SL ;
THOMPSON, DA ;
CHENG, HL ;
TOMASI, TB .
JOURNAL OF EXPERIMENTAL MEDICINE, 1990, 172 (05) :1391-1401
[3]   INDUCTION OF CLASS-II MHC ANTIGEN EXPRESSION ON THE MURINE PLACENTA BY 5-AZACYTIDINE CORRELATES WITH FETAL ABORTION [J].
ATHANASSAKISVASSILIADIS, I ;
GALANOPOULOS, VK ;
GRIGORIOU, M ;
PAPAMATHEAKIS, J .
CELLULAR IMMUNOLOGY, 1990, 128 (02) :438-449
[4]  
Billington W D, 1982, Placenta Suppl, V4, P13
[5]   REGULATION OF A TRANSFECTED HUMAN CLASS-II MAJOR HISTOCOMPATIBILITY COMPLEX GENE IN HUMAN-FIBROBLASTS [J].
BOSS, JM ;
STROMINGER, JL .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1986, 83 (23) :9139-9143
[6]   A NOVEL MULTIGENE FAMILY MAY ENCODE ODORANT RECEPTORS - A MOLECULAR-BASIS FOR ODOR RECOGNITION [J].
BUCK, L ;
AXEL, R .
CELL, 1991, 65 (01) :175-187
[7]   CLASS-II TRANSACTIVATOR REGULATES THE EXPRESSION OF MULTIPLE GENES INVOLVED IN ANTIGEN PRESENTATION [J].
CHANG, CH ;
FLAVELL, RA .
JOURNAL OF EXPERIMENTAL MEDICINE, 1995, 181 (02) :765-767
[8]   CLASS-II TRANSACTIVATOR (CIITA) IS SUFFICIENT FOR THE INDUCIBLE EXPRESSION OF MAJOR HISTOCOMPATIBILITY COMPLEX CLASS-II GENES [J].
CHANG, CH ;
FONTES, JD ;
PETERLIN, M ;
FLAVELL, RA .
JOURNAL OF EXPERIMENTAL MEDICINE, 1994, 180 (04) :1367-1374
[9]   NUCLEAR-REGULATION OF HLA CLASS-I GENES IN HUMAN TROPHOBLASTS [J].
CHIANG, MH ;
MAIN, EK .
AMERICAN JOURNAL OF REPRODUCTIVE IMMUNOLOGY, 1994, 32 (03) :167-172
[10]   MOLECULAR ANALYSIS OF G1B AND G3A IFN-GAMMA MUTANTS REVEALS THAT DEFECTS IN CIITA OR RFX RESULT IN DEFECTIVE CLASS-II MHC AND II-GENE INDUCTION [J].
CHIN, KC ;
MAO, C ;
SKINNER, C ;
RILEY, JL ;
WRIGHT, KL ;
MORENO, CS ;
STARK, GR ;
BOSS, JM ;
TING, JPY .
IMMUNITY, 1994, 1 (08) :687-697