Flynn Ciara L, Markey Gary E, Neudecker Viola, Farrelly Charlotte, Furuta Glenn T, Eltzschig Holger K, Masterson Joanne C, McNamee Eóin N
Mucosal Immunology Research Laboratory, Kathleen Lonsdale Institute for Human Health Research, Department of Biology, Maynooth University, Maynooth, Ireland.
Allergy, Inflammation & Remodelling Research Laboratory, Kathleen Lonsdale Institute for Human Health Research, Department of Biology, Maynooth University, Maynooth, Ireland.
J Immunol. 2024 Dec 15;213(12):1869-1883. doi: 10.4049/jimmunol.2400129.
Aberrant intestinal inflammation plays a critical role in the development of colitis-associated colorectal cancer (CAC), yet the mechanisms controlling tumor development by the myeloid immune compartment are not fully understood. Although altered microRNA expression is observed in CAC, it is also unclear how myeloid-specific microRNAs impact the inflammatory process that underpins the continuum from ulcerative colitis to tumorigenesis. In this study, we report that miR-223 acts to limit myeloid-driven inflammation in the azoxymethane (AOM)-dextran sodium sulfate (DSS) model of CAC in mice. In this model, miR-223-/y mice present with significantly larger tumors with an enhanced proliferative signature. Immunoprofiling showed that miR-223-/y mice have significantly increased colonic myeloid immune infiltrate (neutrophils, monocytes, and macrophages) following AOM-DSS. This was accompanied by an increased inflammatory chemokine and cytokine signature for monocytes and neutrophils. Bone marrow chimera studies demonstrate that myeloid-expressed miR-223 is responsible for the enhanced tumor proliferation and inflammatory response. RNA sequencing identified several pathways that could be contributing to the development of CAC in miR-223-/y mice, including the IL-6/IL-17a cytokine family and STAT3 signaling. Lastly, neutrophil depletion with an anti-GR1 Ab (Ly6G/Ly6C) during the initial phase of the AOM-DSS model reduced the tumor burden in miR-223-/y mice. Collectively, our data indicate that miR-223 is an important regulator of mucosal inflammation and acts to constrain the progression from ulcerative colitis to CAC by limiting myeloid-associated inflammation.
异常的肠道炎症在结肠炎相关结直肠癌(CAC)的发生发展中起关键作用,然而,髓系免疫细胞亚群控制肿瘤发生发展的机制尚未完全明确。尽管在CAC中观察到了微小RNA表达的改变,但髓系特异性微小RNA如何影响从溃疡性结肠炎到肿瘤发生这一连续过程的炎症过程也尚不清楚。在本研究中,我们报道了miR-223在小鼠CAC的氧化偶氮甲烷(AOM)-葡聚糖硫酸钠(DSS)模型中发挥限制髓系驱动的炎症作用。在该模型中,miR-223基因敲除(miR-223-/-)小鼠出现明显更大的肿瘤,且增殖特征增强。免疫分析显示,AOM-DSS处理后,miR-223-/-小鼠的结肠髓系免疫细胞浸润(中性粒细胞、单核细胞和巨噬细胞)显著增加。这伴随着单核细胞和中性粒细胞的炎症趋化因子和细胞因子特征增加。骨髓嵌合体研究表明,髓系表达的miR-223导致肿瘤增殖增强和炎症反应加剧。RNA测序确定了几个可能导致miR-223-/-小鼠CAC发生发展的途径,包括IL-6/IL-17a细胞因子家族和STAT3信号通路。最后,在AOM-DSS模型的初始阶段用抗GR1抗体(Ly6G/Ly6C)清除中性粒细胞可减轻miR-223-/-小鼠的肿瘤负担。总体而言,我们的数据表明,miR-223是黏膜炎症的重要调节因子,通过限制髓系相关炎症来抑制从溃疡性结肠炎到CAC的进展。