Tai X G, Kita Y, Toyooka K, Hamaoka T, Fujiwara H
Biomedical Research Center, Osaka University Medical School, Japan.
Thymus. 1993 Jun;21(4):247-58.
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.
从MRL104.8a胸腺基质细胞克隆的单层培养物中获得培养上清液(SN)。单独的这种SN可诱导辅助性T细胞(Th)克隆增殖,因为它含有白细胞介素-7(IL-7)。然而,将SN添加到用抗原加抗原呈递细胞(APC)刺激的Th培养物中会导致其增殖受到强烈抑制。这种抑制作用归因于MRL104.8a SN中含有的一种因子(称为胸腺基质衍生的T细胞抑制因子,TSTIF),它与IL-7不同。TSTIF影响1型辅助性(Th1)和2型辅助性(Th2)T细胞克隆的抗原刺激增殖。在整个抗原刺激过程(48 - 72小时)中,仅在最初的24小时预培养中存在MRL104.8a SN时也观察到了TSTIF效应。在没有抗原/APC的情况下,Th细胞预先暴露于SN会使其在接下来48小时培养中受到抗原/APC刺激时发生增殖。然而,Th细胞仅在有APC(无抗原)存在的情况下与SN进行预培养会导致随后抗原/APC刺激的增殖受到强烈抑制。在以下实验中进一步证明了TSTIF与APC而非与反应性Th细胞相互作用:仅将APC暴露于MRL104.8a SN,并用于刺激未暴露于SN的Th。与新鲜制备的APC或在没有MRL104.8a SN的情况下培养的APC相比,这样的APC群体诱导抗原刺激的Th增殖的能力显著降低。这些结果表明,TSTIF通过作用于APC对抗原刺激的T细胞增殖发挥抑制作用。