SELECTIVE MODULATION OF IFN-GAMMA MESSENGER-RNA STABILITY BY IL-12 NKSF

被引:19
|
作者
NAGY, E
BUHLMANN, JE
HENICS, T
WAUGH, M
RIGBY, WFC
机构
[1] DARTMOUTH COLL, SCH MED, DEPT MED, LEBANON, NH 03756 USA
[2] DARTMOUTH COLL, SCH MED, DEPT MICROBIOL, LEBANON, NH 03756 USA
[3] WHITE RIVER JUNCT VET ADM MED CTR, WHITE RIVER JCT, VT 05001 USA
关键词
D O I
10.1006/cimm.1994.1303
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
We investigated the role of IL-12 in regulating IL-2 and IFN-gamma production in primary culture of human T cells. Addition of neutralizing antiserum against the 40-kDa subunit of IL-12 to PHA-stimulated PBMC markedly reduced both IFN-gamma protein production and mRNA accumulation and stability. Moreover, concurrent treatment of partially purified T cells (>90% CD3(+)) with PHA and rIL-12 selectively enhanced IFN-gamma mRNA stability and protein production, while IL-2 protein and mRNA levels were unaffected. These studies also show that IFN-gamma and IL-2 mRNA stability are temporally dissociated during the course of T cell activation, and we propose that this dissociation may be mediated through the production of IL-12. The effect of IL-12 on modulation of IFN-gamma mRNA turnover is not associated with detectable changes in either the levels or affinity of cytoplasmic RNA-binding proteins capable of recognizing AU-rich sequences in the 3' UTR of IFN-gamma mRNA. (C) 1994 Academic Press, Inc.
引用
收藏
页码:140 / 151
页数:12
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