含溴结构域 4 是肠道炎症细胞因子反应的积极调节因子。

Eleonora Franzè, Federica Laudisi, Claudia Maresca, Antonio Di Grazia, Andrea Iannucci, Teresa Pacifico, Angela Ortenzi, Giuseppe Sica, Elisabetta Lolli, Carmine Stolfi, Ivan Monteleone, Giovanni Monteleone
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摘要

背景和目的:含溴结构域蛋白4(Bromodomain-containing protein 4,BRD4)是含溴结构域和外基质结构域(BET)家族的成员之一,是细胞增殖和细胞因子产生的转录和表观遗传调节因子。在这项研究中,我们评估了 BRD4 是否调节炎症性肠病(IBD)的细胞因子反应:通过实时 PCR、Western 印迹和共聚焦显微镜分析了溃疡性结肠炎(UC)患者、克罗恩病(CD)患者、正常对照组(CTRs)和化学诱导结肠炎小鼠肠粘膜样本中 BRD4 的表达。我们还评估了 IBD 患者固有膜单核细胞(LPMCs)和接受 BRD4 抑制剂治疗的结肠炎小鼠粘膜组织中细胞因子的产生情况。最后,我们评估了 BRD4 信号通路抑制剂 JQ1 对小鼠结肠炎病程的影响:结果:在 UC 患者和 CD 患者的炎症粘膜中,BRD4 的 RNA 和蛋白表达上调,而在结肠炎小鼠的炎症结肠中,BRD4 的 RNA 和蛋白表达上调。用特异性反义寡核苷酸敲除 IBD LPMC 中的 BRD4 可降低 TNF-α、IL-6、IFN-γ 和 IL-17A 的表达。给结肠炎小鼠注射 JQ1 可抑制炎症细胞因子反应,减轻持续的结肠炎:这是第一项显示 BRD4 在 IBD 中上调的研究,表明这种蛋白质在积极控制肠道炎症细胞因子反应中的作用。
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Bromodomain-containing 4 is a positive regulator of the inflammatory cytokine response in the gut.

Background and aim: Bromodomain-containing protein 4 (BRD4), one of the components of the bromodomain and extraterminal domain (BET) family, is a transcriptional and epigenetic regulator of cellular proliferation and cytokine production. In this study, we assessed whether BRD4 regulates the cytokine response in inflammatory bowel diseases (IBD).

Materials and methods: BRD4 expression was analyzed in intestinal mucosal samples of patients with ulcerative colitis (UC), patients with Crohn's disease (CD), normal controls (CTRs), and mice with chemically-induced colitis by real-time PCR, Western blotting, and confocal microscopy. Cytokine production was evaluated in lamina propria mononuclear cells (LPMCs) of IBD patients and mucosal tissues of colitic mice treated with BRD4 inhibitors. Finally, we evaluated the effect of JQ1, an inhibitor of the BRD4 signaling pathway, on the course of murine colitis.

Results: BRD4 RNA and protein expression was up-regulated in the inflamed mucosa of patients with UC and patients with CD as compared to the uninvolved areas of the same patients and CTRs, and in the inflamed colon of colitic mice. Knockdown of BRD4 with a specific antisense oligonucleotide in IBD LPMCs led to reduced expression of TNF-α, IL-6, IFN-γ, and IL-17A. Administration of JQ1 to colitic mice inhibited the inflammatory cytokine response and attenuated the ongoing colitis.

Conclusions: This is the first study showing the up-regulation of BRD4 in IBD and suggesting the role of such a protein in the positive control of the inflammatory cytokine response in the gut.

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