Department of Biochemistry and Molecular Biology; Tongji Medical College; Huazhong University of Science and Technology; Wuhan, China ; Department of Breast and Thyroid Surgery; Union Hospital; Tongji Medical College; Huazhong University of Science and Technology; Wuhan, China.
Oncoimmunology. 2012 Aug 1;1(5):687-693. doi: 10.4161/onci.19854.
Tumor cells expressing TLRs is generally recognized to mediate tumor inflammation. However, whether and how tumor TLR signaling pathways negatively regulate tumor inflammation remains unclear. In this report, we find that TLR4 signaling of H22 hepatocarcinoma tumor cells is transduced through MyD88 pathway to actin cytoskeletons, leading to the release of microparticles (MPs), the cellular membrane-derived vesicles. As a result, tumor macrophages take up MPs and acquire MP-contained microRNA let-7b, which attenuates tumor inflammation by targeting proinflammatory cytokine IL-6. Thus, tumor TLR signaling, contrary to the original promoting effect, may play an opposite role in downregulating tumor inflammation through MP pathways.
肿瘤细胞表达 TLRs 通常被认为介导肿瘤炎症。然而,肿瘤 TLR 信号通路是否以及如何负调控肿瘤炎症尚不清楚。在本报告中,我们发现 H22 肝癌肿瘤细胞的 TLR4 信号通过 MyD88 途径转导到肌动蛋白细胞骨架,导致微颗粒(MPs)的释放,即细胞膜衍生的囊泡。结果,肿瘤巨噬细胞摄取 MPs 并获得含 MPs 的 microRNA let-7b,通过靶向促炎细胞因子 IL-6 来减弱肿瘤炎症。因此,肿瘤 TLR 信号通路与最初的促进作用相反,可能通过 MPs 途径在下调肿瘤炎症中发挥相反的作用。