REDUCED-ACTIVATION OF TRANSCRIPTIONAL FACTOR-AP-1 AMONG PERIPHERAL-BLOOD T-CELLS FROM ELDERLY HUMANS AFTER PHA STIMULATION - RESTORATIVE EFFECT OF PHORBOL DIESTERS

被引:42
作者
WHISLER, RL [1 ]
LIU, BQ [1 ]
WU, LC [1 ]
CHEN, M [1 ]
机构
[1] OHIO STATE UNIV,WILLIAM H DAVIS MED CTR,DEPT INTERNAL MED,COLUMBUS,OH 43210
关键词
D O I
10.1006/cimm.1993.1270
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
In the present study, we evaluated if aging influences the activation and characteristics of transcriptional factor AP-1 in human T cells. Using gel mobility shift assays, the activation of AP-1 was quantified in peripheral blood T cells from 11 elderly (mean 74 year) and young (mean 33 year) subjects following stimulation with PHA, PMA, or PHA plus PMA. The results showed that the activation of AP-1 was significantly reduced in PHA-stimulated T cells from the group of elderly subjects when compared to T cells from young subjects (P < 0.05). Even though PHA-stimulated T cells from 8 of the elderly subjects had pronounced impairments in the activation of AP-1, additional signals provided by costimulation with PMA frequently restored AP-1 activation to more normal levels. Other experiments demonstrated that the AP-1 complexes expressed by stimulated T cells of elderly and young subjects exhibited similar properties in gel shift assays with competing unlabeled AP-1 oligonucleotides and with blocking antibodies specific for Fos and Jun. Thus, these data suggest that the activation of AP-1 can be reduced in human T cells during aging and that these reductions may often be related to impairments in signal transduction rather than represent an absolute loss in the ability to express AP-1. © 1993 Academic Press. All rights reserved.
引用
收藏
页码:96 / 109
页数:14
相关论文
共 85 条
[1]  
ADLER V, 1992, J BIOL CHEM, V267, P17001
[2]   THE JUN PROTO-ONCOGENE IS POSITIVELY AUTOREGULATED BY ITS PRODUCT, JUN/AP-1 [J].
ANGEL, P ;
HATTORI, K ;
SMEAL, T ;
KARIN, M .
CELL, 1988, 55 (05) :875-885
[3]   PHORBOL ESTER INDUCIBLE GENES CONTAIN A COMMON CIS ELEMENT RECOGNIZED BY A TPA-MODULATED TRANS-ACTING FACTOR [J].
ANGEL, P ;
IMAGAWA, M ;
CHIU, R ;
STEIN, B ;
IMBRA, RJ ;
RAHMSDORF, HJ ;
JONAT, C ;
HERRLICH, P ;
KARIN, M .
CELL, 1987, 49 (06) :729-739
[4]   HETEROGENEITY OF IMMUNE RESPONSIVENESS IN HEALTHY ELDERLY SUBJECTS [J].
BARCELLINI, W ;
BORGHI, MO ;
SGUOTTI, C ;
PALMIERI, R ;
FRASCA, D ;
MERONI, PL ;
DORIA, G ;
ZANUSSI, C .
CLINICAL IMMUNOLOGY AND IMMUNOPATHOLOGY, 1988, 47 (02) :142-151
[5]   ACTIVATION OF RESTING HUMAN T-CELLS REQUIRES PROLONGED STIMULATION OF PROTEIN KINASE-C [J].
BERRY, N ;
ASE, K ;
KISHIMOTO, A ;
NISHIZUKA, Y .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1990, 87 (06) :2294-2298
[6]  
BIJVELD C, 1988, BIOCHEM BIOPH RES CO, V151, P193
[7]   HA-RAS AUGMENTS C-JUN ACTIVITY AND STIMULATES PHOSPHORYLATION OF ITS ACTIVATION DOMAIN [J].
BINETRUY, B ;
SMEAL, T ;
KARIN, M .
NATURE, 1991, 351 (6322) :122-127
[8]   AGE-DEPENDENT CHANGES IN MURINE PROTEIN-KINASE AND PROTEASE ENZYMES [J].
BLUMENTHAL, EJ ;
MALKINSON, AM .
MECHANISMS OF AGEING AND DEVELOPMENT, 1988, 46 (1-3) :201-217
[9]  
BOKAR JA, 1988, J BIOL CHEM, V263, P19740
[10]   DEXAMETHASONE INHIBITS HUMAN INTERLEUKIN-2 BUT NOT INTERLEUKIN-2 RECEPTOR GENE-EXPRESSION INVITRO AT THE LEVEL OF NUCLEAR TRANSCRIPTION [J].
BOUMPAS, DT ;
ANASTASSIOU, ED ;
OLDER, SA ;
TSOKOS, GC ;
NELSON, DL ;
BALOW, JE .
JOURNAL OF CLINICAL INVESTIGATION, 1991, 87 (05) :1739-1747