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Fas ligand- mediated killing by intestinal intraepithelial lymphocytes. Participation in intestinal graft-versus-host disease.

机译:Fas配体介导的肠上皮内淋巴细胞杀伤。参与肠道移植物抗宿主病。

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摘要

In vitro studies have demonstrated that intestinal intraepithelial lymphocytes (IEL) are constitutively cytotoxic; however, the mechanism and target of their cytotoxicity are unknown. Apoptosis of intestinal epithelial cells (IEC) and an increase in IEL numbers are classical signs of intestinal graft-versus-host disease (GVHD), although whether IEL can mediate IEC apoptosis directly in GVHD is unclear. Recent evidence suggests that target epithelial organ injury observed in GVHD is predominantly Fas-mediated; therefore, we investigated the possibility that IEL induce apoptosis of IEC through a Fas-mediated mechanism. Here, we demonstrate that the IEL isolated from normal mice readily display potent Fas ligand (FasL)-mediated killing activity after CD3 stimulation, and that IEC express Fas, suggesting that IEC are potential targets for FasL-mediated killing by IEL. In vitro, IEL isolated from GVHD mice have markedly increased FasL-mediated killing potential and are spontaneously cytolytic toward host-derived tumor cells predominantly through a Fas-mediated pathway. In vivo transfer of IEL isolated from GVHD mice induced significantly more IEC apoptosis in F1 wild-type mice than in Fas-defective F1lpr mice. Thus, these results demonstrate that FasL-mediated death of IEC by IEL is a major mechanism of IEC apoptosis seen in GVHD.
机译:体外研究表明,肠上皮内淋巴细胞(IEL)具有组成性的细胞毒性。然而,其细胞毒性的机制和靶标尚不清楚。肠上皮细胞凋亡(IEC)和IEL数量增加是肠道移植物抗宿主病(GVHD)的经典征兆,尽管IEL是否可以直接介导GVHD中的IEC凋亡尚不清楚。最近的证据表明,在GVHD中观察到的靶标上皮器官损伤主要是Fas介导的。因此,我们研究了IEL通过Fas介导的机制诱导IEC凋亡的可能性。在这里,我们证明从CD3刺激后,从正常小鼠中分离的IEL容易显示出强力的Fas配体(FasL)介导的杀伤活性,并且IEC表达Fas,这表明IEC是IEL介导FasL介导的杀伤的潜在目标。在体外,从GVHD小鼠中分离的IEL具有明显增加的FasL介导的杀伤力,并且主要通过Fas介导的途径自发地对宿主衍生的肿瘤细胞进行细胞溶解。与Fas缺陷型F1lpr小鼠相比,从GVHD小鼠中分离的IEL的体内转移在F1野生型小鼠中诱导的IEC凋亡明显更多。因此,这些结果表明IEL的FasL介导的IEC死亡是在GVHD中看到的IEC凋亡的主要机制。

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