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:Enhancing Natural Killer Cell-Mediated Cancer Immunotherapy by the Biological Macromolecule Nocardia rubra Cell-Wall Skeleton.
Enhancing Natural Killer Cell-Mediated Cancer Immunotherapy by the Biological Macromolecule Nocardia rubra Cell-Wall Skeleton.
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生物大分子红色诺卡氏菌细胞壁骨架(Nr-CWS)具有明确的免疫刺激和抗肿瘤活性。然而,Nr-CWS对自然杀伤(NK)细胞的作用仍不清楚。
在此,我们探讨Nr-CWS对NK细胞的功能及相关机制。利用荷瘤模型,我们发现Nr-CWS对实体瘤作用轻微。此外,利用肿瘤转移模型,我们发现Nr-CWS抑制B16F10黑色素瘤细胞诱导的小鼠肺转移,这表明Nr-CWS可能上调NK细胞的功能。
进一步研究表明,Nr-CWS可增加Nr-CWS处理的B16F10肿瘤转移小鼠脾NK细胞上TRAIL和FasL的表达。Nr-CWS处理的B16F10肿瘤转移小鼠的脾指数及血清TNF-、IFN-和IL-2水平显著升高。在体外,使用纯化或分选的NK细胞进行的研究显示,Nr-CWS增加CD69、TRAIL和FasL的表达,降低CD27的表达,并增强NK细胞细胞毒性。经Nr-CWS处理后,培养NK细胞的胞内IFN-、TNF-、穿孔素(prf)、颗粒酶-B(GrzB)表达以及分泌的TNF-、IFN-、IL-6均显著增加。
总体而言,这些发现表明Nr-CWS可抑制B16F10黑色素瘤细胞诱导的肺转移,其作用可能通过影响NK细胞实现,即促进NK细胞终末分化(CD27低CD11b高),并上调细胞因子和细胞毒性分子的产生。
The biological macromolecule Nocardia rubra cell-wall skeleton (Nr-CWS) has well-established immune-stimulating and anti-tumor activities.
However, the role of Nr-CWS on natural killer (NK) cells remains unclear.
Here, we explore the function and related mechanisms of Nr-CWS on NK cells. Using a tumor-bearing model, we show that Nr-CWS has slightly effect on solid tumor.
In addition, using a tumor metastasis model, we show that Nr-CWS suppresses the lung metastasis induced by B16F10 melanoma cells in mice, which indicates that Nr-CWS may up-regulate the function of NK cells.
Further investigation demonstrated that Nr-CWS can increase the expression of TRAIL and FasL on spleen NK cells from Nr-CWS treated B16F10 tumor metastasis mice. The spleen index and serum levels of TNF- , IFN- , and IL-2 in B16F10 tumor metastasis mice treated with Nr-CWS were significantly increased.
In vitro , the studies using purified or sorted NK cells revealed that Nr-CWS increases the expression of CD69, TRAIL, and FasL, decreases the expression of CD27, and enhances NK cell cytotoxicity. The intracellular expression of IFN- , TNF- , perforin (prf), granzyme-B (GrzB), and secreted TNF- , IFN- , IL-6 of the cultured NK cells were significantly increased after treatment with Nr-CWS.
Overall, the findings indicate that Nr-CWS could suppress the lung metastasis induced by B16F10 melanoma cells, which may be exerted through its effect on NK cells by promoting NK cell terminal differentiation (CD27 low CD11b high ), and up-regulating the production of cytokines and cytotoxic molecules.
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