RNF43 p.G659fs 通过 PI3K/AKT/mTOR 信号通路和 HLA-E 上调导致 MSI-high 结直肠癌中 NK 细胞功能障碍
RNF43 p.G659fs leads to natural killer cell dysfunction in MSI-high colorectal cancer through PI3K/AKT/mTOR signaling and HLA-E up-regulation.
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:THEMIS2 Impairs Antitumor Activity of NK Cells by Suppressing Activating NK Receptor Signaling.
THEMIS2 Impairs Antitumor Activity of NK Cells by Suppressing Activating NK Receptor Signaling.
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NK 细胞是细胞毒性先天淋巴细胞,在抗肿瘤免疫中发挥关键作用。NK 细胞通过一组激活性 NK 受体识别靶细胞并发挥效应功能。尽管通过激活性 NK 受体的激活信号强度控制着 NK 细胞功能,但这些激活信号在 NK 细胞中如何被调控尚未被完全理解。
在本研究中,我们发现支架蛋白 THEMIS2 抑制激活性 NK 受体信号。THEMIS2 过表达减弱了人 NK 细胞的效应功能,而 THEMIS2 敲低则增强了其效应功能。在机制上,THEMIS2 在激活性 NK 受体 DNAM-1 和 NKG2D 附近与 GRB2 以及磷酸化的 SHP-1 和 SHP-2 结合。在原代人 NK 细胞中敲低 THEMIS2 促进了效应功能。
此外,Themis2 缺陷小鼠以 NK 细胞依赖的方式表现出较低的转移负荷。这些发现表明,THEMIS2 对 NK 细胞的抗肿瘤活性具有抑制作用,提示 THEMIS2 可能是 NK 细胞介导的癌症免疫治疗的潜在治疗靶点。
NK cells are cytotoxic innate lymphocytes that play a critical role in antitumor immunity. NK cells recognize target cells by using a repertoire of activating NK receptors and exert the effector functions. Although the magnitude of activation signals through activating NK receptors controls NK cell function, it has not been fully understood how these activating signals are modulated in NK cells.
In this study, we found that a scaffold protein, THEMIS2, inhibits activating NK receptor signaling. Overexpression of THEMIS2 attenuated the effector function of human NK cells, whereas knockdown of THEMIS2 enhanced it.
Mechanistically, THEMIS2 binds to GRB2 and phosphorylated SHP-1 and SHP-2 at the proximity of activating NK receptors DNAM-1 and NKG2D. Knockdown of THEMIS2 in primary human NK cells promoted the effector functions.
Furthermore, Themis2-deficient mice showed low metastatic burden in an NK cell-dependent manner.
These findings demonstrate that THEMIS2 has an inhibitory role in the antitumor activity of NK cells, suggesting that THEMIS2 might be a potential therapeutic target for NK cell-mediated cancer immunotherapy.
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