胸腺基质源性t细胞抑制因子。2: TSTIF作用于抗原提呈细胞,抑制抗原刺激t细胞增殖。

Thymus Pub Date : 1993-06-01
X G Tai, Y Kita, K Toyooka, T Hamaoka, H Fujiwara
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引用次数: 0

摘要

从MRL104.8a胸腺基质细胞克隆的单层中获得培养上清(SN)。这个SN单独诱导辅助性t细胞(Th)克隆的增殖,因为它含有IL-7。然而,将SN添加到抗原+抗原呈递细胞(APC)刺激的Th培养物中,可有效抑制其增殖。这种抑制归因于MRL104.8a SN中含有的一种因子(称为胸腺基质源性t细胞抑制因子,TSTIF),与IL-7不同。TSTIF影响抗原刺激的1型辅助t细胞(Th1)和2型辅助t细胞(Th2)克隆的增殖。在整个抗原刺激过程(48-72小时)中,MRL104.8a SN仅在最初的24小时预培养中存在,也观察到TSTIF效应。在没有Ag/APC的情况下,将Th细胞预先暴露于SN中,在接下来的48小时培养中,Ag/APC刺激可诱导细胞增殖。然而,在APC单独存在(无抗原)的情况下,将SN与Th细胞进行预培养,可有效抑制随后Ag/APC刺激的增殖。在接下来的实验中进一步证明了TSTIF与APC的相互作用,而不是与应答的Th细胞的相互作用:APC单独暴露于MRL104.8a SN,并用于刺激未暴露于SN的Th细胞。与新鲜制备的APC或在没有MRL104.8a SN的情况下培养的APC相比,这种APC群体诱导抗原刺激的Th增殖能力明显降低。这些结果表明,TSTIF是通过作用于APC来抑制抗原刺激t细胞增殖的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Thymic stroma-derived T-cell inhibitory factor (TSTIF). 2: TSTIF acts on the antigen-presenting cell to inhibit antigen-stimulated T-cell proliferation.

Culture supernatant (SN) was obtained from the monolayer of the MRL104.8a thymic stromal cell clone. This SN alone induced proliferation of helper T-cell (Th) clones because it contained IL-7. However, addition of the SN to cultures of Th stimulated with antigen plus antigen-presenting cells (APC) resulted in potent inhibition of their proliferation. This suppression was ascribed to a factor (designated thymic stroma-derived T-cell inhibitory factor, TSTIF) that is contained in the MRL104.8a SN and distinct from IL-7. TSTIF affected antigen-stimulated proliferation of both type 1 helper (Th1) and type 2 helper (Th2) T-cell clones. The TSTIF effect was also observed by the presence of the MRL104.8a SN only in the initial 24 hr pre-culture during the entire course (48-72 hr) of antigenic stimulation. Pre-exposure of Th cells to the SN in the absence of Ag/APC induced their proliferation upon stimulation with Ag/APC in the next 48 hr cultures. However, pre-cultures of Th cells with the SN in the presence of APC alone (without antigen) resulted in potent inhibition of the subsequent Ag/APC-stimulated proliferation. Interaction of TSTIF with APC but not with responding Th cells was further demonstrated in the following experiment: APC alone were exposed to the MRL104.8a SN and used for stimulation of Th that had not been exposed to the SN. Such an APC population exhibited a remarkably reduced capacity to induce antigen-stimulated Th proliferation when compared to that induced by freshly prepared APC or APC cultured in the absence of the MRL104.8a SN. These results indicate that TSTIF exerts its inhibitory effect on the antigen-stimulated T-cell proliferation by acting on APC.

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