Chan S H, Kobayashi M, Santoli D, Perussia B, Trinchieri G
Wistar Institute, Philadelphia, PA 19104.
J Immunol. 1992 Jan 1;148(1):92-8.
We have investigated the molecular mechanisms regulating IFN-gamma production in human T lymphocytes stimulated by NK cell stimulatory factor (NKSF/IL-12). We show that NKSF synergizes with IL-2 and phorbol diesters inducing the accumulation of IFN-gamma mRNA in PHA-activated T cell blasts. NKSF regulates IFN-gamma mRNA expression in PHA blasts and the T leukemia cell line, TALL-103/2, at both the transcriptional and posttranscriptional levels. NKSF increases the transcriptional rate for IFN-gamma in both these cell types, as determined by nuclear run-on analysis. However, synergy between NKSF and IL-2 can be demonstrated only at the level of mRNA stability, and both cytokines are required to increase IFN-gamma mRNA half-life.
我们研究了自然杀伤细胞刺激因子(NKSF/IL-12)刺激人T淋巴细胞时调节γ干扰素产生的分子机制。我们发现,NKSF与白细胞介素-2(IL-2)和佛波酯协同作用,可诱导PHA激活的T细胞母细胞中γ干扰素mRNA的积累。NKSF在转录和转录后水平上调节PHA母细胞和T白血病细胞系TALL-103/2中γ干扰素mRNA的表达。通过细胞核连续分析确定,NKSF在这两种细胞类型中均提高了γ干扰素的转录速率。然而,NKSF与IL-2之间的协同作用仅在mRNA稳定性水平上得到证实,两种细胞因子都需要增加γ干扰素mRNA的半衰期。