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Heme protects intestinal mucosal barrier in DSS‐induced colitis through regulating macrophage polarization in both HO‐1‐dependent and HO‐1‐independent way

血红素 巨噬细胞极化 血红素 炎症 结肠炎 血红素加氧酶 巨噬细胞 免疫学 化学 基因敲除 体外 细胞生物学 生物 生物化学 细胞凋亡
作者
Yan‐Chao Wu,Bing Wu,Zongwang Zhang,Huimin Lu,Fan Chen,Qing Qi,Yuanzhuo Gao,Heng Li,Chen‐Guo Feng,Jianping Zuo,Wei Tang
出处
期刊:The FASEB Journal [Wiley]
卷期号:34 (6): 8028-8043 被引量:35
标识
DOI:10.1096/fj.202000313rr
摘要

Hemoglobin-derived heme was reported to play protective roles in hemorrhagic diseases by modulating the macrophages toward recovery. Mucosal bleeding is one of the pathological features of inflammatory bowel diseases (IBD). However, whether heme provides anti-inflammatory profiles in macrophages, thus contributing to the intestinal mucosal barrier protection, is unclear. In the current study, we investigated the beneficial effects of heme on DSS-induced colitis mice and explored the underlying mechanisms. In vivo, systemic heme supplementation by hemin injection relieved intestinal inflammation and remedied intestinal mucosal barrier damage by correcting abnormal intestinal macrophage polarization. In vitro, we confirmed the reciprocally regulating effects of hemin on M1/M2 macrophage polarization in BMDM. Intriguingly, with knockdown of HO-1, the inhibiting effects of hemin on M1 polarization were maintained, while the promoting effects on M2 polarization were reversed. Further research proved that hemin repressed the inflammatory profiles in macrophages through inhibiting the translocation of NF-κB p65 by disrupting IRF5-NF-κB p65 complex formation in Spi-C-dependent way. In conclusion, these results showed that the modification of colon tissue microenvironment with heme supplementation plays a protective role in DSS-induced colitis mice through regulating the macrophage polarization in both HO-1-dependent and HO-1-independent way, indicating a new choice to therapeutically modulate the macrophage function and prevent IBD.
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