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首页> 外文期刊>Science Immunology >Gab3 is required for IL-2-and IL-15-induced NK cell expansion and limits trophoblast invasion during pregnancy
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Gab3 is required for IL-2-and IL-15-induced NK cell expansion and limits trophoblast invasion during pregnancy

机译:IL-2和IL-15诱导的NK细胞扩展需要GAB3,并限制了妊娠滋养细胞的侵袭

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The scaffolding protein Grb2-associated binding protein 3 (Gab3) is a member of the Gab family, whose functions have remained elusive. Here, we identify Gab3 as a key determinant of peripheral NK cell expansion. Loss of Gab3 resulted in impaired IL-2 and IL-15-induced NK cell priming and expansion due to a selective impairment in MAPK signaling but not STAT5 signaling. In vivo, we found that Gab3 is required for recognition and elimination of "missing-self" and tumor targets. Unexpectedly, our studies also revealed that Gab3 plays an important role during pregnancy. Gab3-deficient mice exhibited impaired uterine NK cell expansion associated with abnormal spiral artery remodeling and increased trophoblast invasion in the decidua basalis. This coincided with stillbirth, retained placenta, maternal hemorrhage, and undelivered fetoplacental units at term. Thus, Gab3 is a key component required for cytokine-mediated NK cell priming and expansion that is essential for antitumor responses and limits trophoblast cell invasion during pregnancy.
机译:脚手架蛋白GRB2相关的结合蛋白3(GAB3)是GAB家族的成员,其功能仍然难以捉摸。在这里,我们将GAB3识别为外围NK细胞扩展的关键决定因素。 GAB3的丢失导致IL-2和IL-15诱导的NK细胞启动和扩张受损,这是由于MAPK信号传导中的选择性损伤而不是STAT5信号传导。在体内,我们发现GAB3是识别和消除“缺失自身”和肿瘤靶标的所必需的。出乎意料的是,我们的研究还表明,GAB3在怀孕期间起着重要作用。缺乏GAB3的小鼠表现出与异常螺旋动脉重塑相关的子宫NK细胞扩张受损,并增加了Decidua basalis的滋养细胞侵袭。这与死产,保留的胎盘,母体出血和未交付的胎儿单位相吻合。因此,GAB3是细胞因子介导的NK细胞启动和膨胀所需的关键成分,这对于抗肿瘤反应至关重要,并且限制了妊娠期间滋养细胞的侵袭。

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