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首页> 外文期刊>The Journal of Immunology: Official Journal of the American Association of Immunologists >Enhanced expression of Fas-associated death domain-like IL-1-converting enzyme (FLICE)-inhibitory protein induces resistance to Fas-mediated apoptosis in activated mast cells.
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Enhanced expression of Fas-associated death domain-like IL-1-converting enzyme (FLICE)-inhibitory protein induces resistance to Fas-mediated apoptosis in activated mast cells.

机译:Fas相关的死亡域样IL-1转换酶(FLICE)抑制蛋白的增强表达诱导对激活的肥大细胞中Fas介导的凋亡的抵抗。

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摘要

Mast cells play a critical role in host immune responses and are implicated in the pathogenesis of allergic inflammation. Though mouse mast cell line MC/9 expresses cell surface Fas Ag and is sensitive to Fas-induced apoptosis, activated MC/9 cells are resistant to Fas-induced cell death by cross-linking of FcepsilonRI or FcgammaR. Fas-associated death domain-like IL-1-converting enzyme (FLICE)-inhibitory protein (FLIP), a caspase-8 inhibitor that lacks the cysteine domain, is one of the negative regulators of receptor-mediated apoptosis. In this report, we show that activation of mast cells by cross-linking of FcepsilonRI or FcgammaR can induce enhanced expression of FLIP and consequently a resistance to Fas-induced apoptosis, although the expression level of Fas Ag is not changed. Addition of antisense oligonucleotide for FLIP prevents resistance to Fas-induced apoptosis of activated mast cells, suggesting that endogenous FLIP inhibits Fas-mediated apoptosis in activated mast cells. Thus, the enhanced expression of FLIP in activated mast cells contributes to the resistance to Fas-induced apoptosis, which may result in the development and prolongation of allergic inflammation.
机译:肥大细胞在宿主免疫反应中起关键作用,并与过敏性炎症的发病机制有关。尽管小鼠肥大细胞系MC / 9表达细胞表面Fas Ag,并且对Fas诱导的凋亡敏感,但活化的MC / 9细胞通过FcepsilonRI或FcgammaR的交联抵抗Fas诱导的细胞死亡。 Fas相关的死亡域样IL-1转换酶(FLICE)抑制蛋白(FLIP)是一种缺乏半胱氨酸域的caspase-8抑制剂,是受体介导的细胞凋亡的负调节剂之一。在此报告中,我们显示通过FcepsilonRI或FcgammaR交联激活肥大细胞可以诱导FLIP表达增强,因此对Fas诱导的细胞凋亡具有抗性,尽管Fas Ag的表达水平没有改变。为FLIP添加反义寡核苷酸可防止对Fas诱导的活化肥大细胞凋亡的抵抗,这表明内源性FLIP抑制Fas介导的活化肥大细胞凋亡。因此,活化的肥大细胞中FLIP表达的增强有助于抵抗Fas诱导的凋亡,这可能导致过敏性炎症的发展和延长。

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