Department of Medicine, University of Virginia School of Medicine, Charlottesville, Virginia.
Department of Medicine, Yale University, New Haven, Connecticut.
Cell Mol Gastroenterol Hepatol. 2020;10(1):101-112. doi: 10.1016/j.jcmgh.2020.01.009. Epub 2020 Jan 28.
BACKGROUND & AIMS: The inflammatory response to intestinal damage promotes healing through mechanisms that are incompletely understood. Gene expression of cluster of differentiation 74 (CD74), the receptor for cytokine macrophage migration inhibitory factor, is increased in patients with inflammatory bowel disease (IBD), however, the role of CD74 signaling in intestinal inflammation remains poorly understood. The aim of this study was to determine the functional role of CD74 signaling in intestinal inflammation.
We studied the characteristics of CD74 protein expression in human IBD and experimental colitis. The functional role of CD74 signaling in the intestine was investigated using cellular models; wild-type, CD74, and bone marrow chimera mice; neutralizing anti-CD74 antibodies; flow cytometry; immunohistochemistry; immunofluorescence; immunoblotting; and clustered regularly interspaced short palindromic repeats and associated protein 9 technology.
In IBD patients and experimental colitis, CD74-receptor protein expression was increased in inflamed intestinal tissue, prominently in the crypt epithelial cells. By using distinct but complementary chemical and non-chemically induced mouse models of colitis with genetic and antibody neutralization approaches, we found that CD74 signaling was necessary for gut repair. Mechanistically, we found that the macrophage migration inhibitory factor cytokine, which also is increased in colitis, stimulated the CD74 receptor, enhancing intestinal epithelial cell proliferation through activation of the protein kinase B and the extracellular signal-regulated kinase pathways. Our data also suggest that CD74 signaling in immune cells was not essential for mucosal healing.
CD74 signaling is strongly activated during intestinal inflammation and protects the host by promoting epithelial cell regeneration, healing, and maintaining mucosal barrier integrity. Enhancing the CD74 pathway may represent a unique therapeutic strategy for promoting healing in IBD.
肠道损伤引起的炎症反应通过尚未完全阐明的机制促进愈合。细胞分化簇 74(CD74)的基因表达,细胞因子巨噬细胞移动抑制因子的受体,在炎症性肠病(IBD)患者中增加,然而,CD74 信号在肠道炎症中的作用仍知之甚少。本研究旨在确定 CD74 信号在肠道炎症中的功能作用。
我们研究了人 IBD 和实验性结肠炎中 CD74 蛋白表达的特征。使用细胞模型;野生型、CD74 和骨髓嵌合体小鼠;中和抗 CD74 抗体;流式细胞术;免疫组织化学;免疫荧光;免疫印迹;以及成簇规律间隔短回文重复序列和相关蛋白 9 技术研究 CD74 信号在肠道中的功能作用。
在 IBD 患者和实验性结肠炎中,CD74-受体蛋白表达在炎症性肠道组织中增加,在隐窝上皮细胞中尤为明显。通过使用具有遗传和抗体中和的独特但互补的化学和非化学诱导的小鼠结肠炎模型,我们发现 CD74 信号对于肠道修复是必要的。从机制上讲,我们发现巨噬细胞移动抑制因子细胞因子,其在结肠炎中也增加,通过激活蛋白激酶 B 和细胞外信号调节激酶途径刺激 CD74 受体,增强肠道上皮细胞增殖。我们的数据还表明,免疫细胞中的 CD74 信号对于粘膜愈合不是必需的。
CD74 信号在肠道炎症期间被强烈激活,并通过促进上皮细胞再生、愈合和维持粘膜屏障完整性来保护宿主。增强 CD74 途径可能代表促进 IBD 愈合的独特治疗策略。