IFN-γ-dependent transcription of MHC class IIIA is impaired in macrophages from aged mice

被引:120
作者
Herrero, C
Marqués, L
Lloberas, J
Celada, A
机构
[1] Univ Barcelona, Fac Biol, Dept Fisiol Biol Macrofag, E-08028 Barcelona, Spain
[2] Univ Barcelona, Fundacio August Pi & Sunyer, E-08028 Barcelona, Spain
关键词
D O I
10.1172/JCI11696
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
To determine the effect of aging on IFN-gamma -induced MHC class II antigen expression, we produced bone marrow-derived macrophages in vitro. In these conditions, we analyzed the effect of aging on the genomic expression of macrophages without the influence of other cell types that may be affected by aging. Although macrophages from young and aged mice showed an identical degree of differentiation, after incubation with IFN-gamma, the expression at the cell surface of the IA complex and the levels of IA beta protein and mRNA were lower in aged macrophages. Moreover, the transcription of the IA beta gene was impaired in aged macrophages, The amount of transcription factors that bound to the W and X, but not to the Y, boxes of the IA beta promoter gene was lower in aged macrophages. Similar levels of CIITA mRNA were found after IFN-gamma treatment of both young and aged macrophages. This shows that neither the initial cascade that starts after the interaction of IFN-gamma with the receptor nor the second signals involved in the expression of CIITA are impaired in aged macrophages. These data indicate that aging is associated with low levels of MHC class II gene induction by IFN-gamma because of impaired transcription.
引用
收藏
页码:485 / 493
页数:9
相关论文
共 49 条
[1]  
AMMENDOLA R, 1992, J BIOL CHEM, V267, P17944
[2]  
[Anonymous], 1999, FUNDAMENTAL IMMUNOLO
[3]   LPS upregulates MHC class III-A expression in B lymphocytes at transcriptional and at translational levels [J].
Barrachina, M ;
Goñalons, E ;
Celada, A .
TISSUE ANTIGENS, 1999, 54 (05) :461-470
[4]   REGULATION OF MAJOR HISTOCOMPATIBILITY COMPLEX CLASS-II GENES - X, Y AND OTHER LETTERS OF THE ALPHABET [J].
BENOIST, C ;
MATHIS, D .
ANNUAL REVIEW OF IMMUNOLOGY, 1990, 8 :681-715
[5]  
BOTTAZZO GF, 1983, LANCET, V2, P1115
[6]   INTERFERON-GAMMA ACTIVATES MULTIPLE PATHWAYS TO REGULATE THE EXPRESSION OF THE GENES FOR MAJOR HISTOCOMPATIBILITY CLASS-II I-A-BETA, TUMOR NECROSIS FACTOR AND COMPLEMENT COMPONENT C-3 IN MOUSE MACROPHAGES [J].
CELADA, A ;
KLEMSZ, MJ ;
MAKI, RA .
EUROPEAN JOURNAL OF IMMUNOLOGY, 1989, 19 (06) :1103-1109
[7]   EVIDENCE FOR A GAMMA-INTERFERON RECEPTOR THAT REGULATES MACROPHAGE TUMORICIDAL ACTIVITY [J].
CELADA, A ;
GRAY, PW ;
RINDERKNECHT, E ;
SCHREIBER, RD .
JOURNAL OF EXPERIMENTAL MEDICINE, 1984, 160 (01) :55-74
[8]   REPRESSION OF MAJOR HISTOCOMPATIBILITY COMPLEX-IA EXPRESSION BY GLUCOCORTICOIDS - THE GLUCOCORTICOID RECEPTOR INHIBITS THE DNA-BINDING OF THE X-BOX DNA-BINDING PROTEIN [J].
CELADA, A ;
MCKERCHER, S ;
MAKI, RA .
JOURNAL OF EXPERIMENTAL MEDICINE, 1993, 177 (03) :691-698
[9]   Identification of the transcription factors NF-YA and NF-YB as factors A and B that bound to the promoter of the major histocompatibility complex class II gene I-A beta [J].
Celada, A ;
McKercher, SR ;
Maki, RA .
BIOCHEMICAL JOURNAL, 1996, 317 :771-777
[10]  
CELADA A, 1988, J IMMUNOL, V140, P3995