School of Biomolecular and Biomedical Sciences, University College Dublin, Belfield, Dublin, Ireland.
Conway Institute of Biomolecular and Biomedical Research, University College Dublin, Belfield, Dublin, Ireland.
J Immunol. 2024 Jun 15;212(12):1958-1970. doi: 10.4049/jimmunol.2300762.
Fibroblasts acquire a proinflammatory phenotype in inflammatory bowel disease, but the factors driving this process and how fibroblasts contribute to mucosal immune responses are incompletely understood. TNF superfamily member 12 (TNFSF12, or TNF-like weak inducer of apoptosis [TWEAK]) has gained interest as a mediator of chronic inflammation. In this study, we explore its role as a driver of inflammatory responses in fibroblasts and its contribution to fibroblast-monocyte interaction using human primary colonic fibroblasts, THP-1 and primary monocytes. Recombinant human TWEAK induced the expression of cytokines, chemokines, and immune receptors in primary colonic fibroblasts. The TWEAK upregulated transcriptome shared 29% homology with a previously published transcriptional profile of inflammatory fibroblasts from ulcerative colitis. TWEAK elevated surface expression of activated fibroblast markers and adhesion molecules (podoplanin [PDPN], ICAM-1, and VCAM-1) and secretion of IL-6, CCL2, and CXCL10. In coculture, fibroblasts induced monocyte adhesion and secretion of CXCL1 and IL-8, and they promoted a CD14high/ICAM-1high phenotype in THP-1 cells, which was enhanced when fibroblasts were prestimulated with TWEAK. Primary monocytes in coculture with TWEAK-treated fibroblasts had altered surface expression of CD16 and triggering receptor expressed on myeloid cells-1 (TREM-1) as well as increased CXCL1 and CXCL10 secretion. Conversely, inhibition of the noncanonical NF-κB pathway on colonic fibroblasts with a NF-κB-inducing kinase small molecule inhibitor impaired their ability to induce a CD14high phenotype on monocytes. Our results indicate that TWEAK promotes an inflammatory fibroblast-monocyte crosstalk that may be amenable for therapeutic intervention.
成纤维细胞在炎症性肠病中获得促炎表型,但驱动这一过程的因素以及成纤维细胞如何促进黏膜免疫反应尚不完全清楚。肿瘤坏死因子超家族成员 12(TNFSF12,或 TNF 样弱凋亡诱导因子[TWEAK])作为慢性炎症的介质引起了人们的兴趣。在这项研究中,我们探讨了它作为成纤维细胞炎症反应的驱动因素及其对成纤维细胞-单核细胞相互作用的贡献,使用人原代结肠成纤维细胞、THP-1 和原代单核细胞。重组人 TWEAK 诱导原代结肠成纤维细胞细胞因子、趋化因子和免疫受体的表达。TWEAK 上调的转录组与先前发表的溃疡性结肠炎炎症性成纤维细胞的转录谱有 29%的同源性。TWEAK 增加了活化成纤维细胞标志物和粘附分子(Podoplanin [PDPN]、ICAM-1 和 VCAM-1)的表面表达以及 IL-6、CCL2 和 CXCL10 的分泌。在共培养中,成纤维细胞诱导单核细胞粘附和 CXCL1 和 IL-8 的分泌,并促进 THP-1 细胞中 CD14high/ICAM-1high 表型,当成纤维细胞用 TWEAK 预先刺激时,这种表型增强。与用 TWEAK 处理的成纤维细胞共培养的原代单核细胞表面表达 CD16 和髓样细胞表达的触发受体-1(TREM-1)发生改变,以及 CXCL1 和 CXCL10 分泌增加。相反,用一种非经典 NF-κB 通路诱导激酶小分子抑制剂抑制结肠成纤维细胞的 NF-κB 通路会损害其诱导单核细胞中 CD14high 表型的能力。我们的结果表明,TWEAK 促进了促炎成纤维细胞-单核细胞的串扰,这可能适合治疗干预。