Nishioka Kei, Ogino Haruei, Ihara Eikichi, Chinen Takatoshi, Kimura Yusuke, Esaki Mitsuru, Bai Xiaopeng, Minoda Yosuke, Tanaka Yoshimasa, Wada Masafumi, Hata Yoshitaka, Ambrosini Yoko M, Ogawa Yoshihiro
Department of Gastroenterology, Saiseikai Futsukaichi Hospital, Chikushino, Japan.
Department of Medicine and Bioregulatory Science, Graduate School of Medical Sciences, Kyushu University, Fukuoka, Japan.
J Gastroenterol. 2025 Apr;60(4):416-429. doi: 10.1007/s00535-024-02199-4. Epub 2024 Dec 13.
Ulcerative colitis (UC) is a refractory inflammatory disease that affects the rectum and colon, with pivotal involvement of the rectal environment in relapse initiation. This study was conducted in two phases to examine the differences in gene expression between the rectum and colon and to identify relapse factors.
In ***Study 1, RNA sequencing was performed on biopsies from the colon and rectum of patients with active UC, those with remission UC, and controls. In Study 2, the mucosal impedance (MI) values reflecting mucosal barrier function and the mRNA expression of tight junction proteins and inflammatory cytokines were examined in 32 patients with remission UC and 22 controls. Relapse was monitored prospectively.
In Study 1, comprehensive genetic analysis using RNA sequencing revealed distinct gene profiles in the rectum and sigmoid colon of patients with remission UC. The rectum of these patients exhibited an enriched immune response and apical junction phenotype with persistent upregulation of CLDN2 gene expression. In Study 2, even in patients with remission UC, the MI values in the rectum, but not in the sigmoid colon, were significantly decreased, whereas they were negatively correlated with CLDN2, IL-1β, and IL-6 expressions.
The status of the rectum in patients with remission UC differs from that of the colon, with microinflammation and impaired mucosal barrier function, which are associated with the upregulation of CLDN2, playing a role in relapse.
溃疡性结肠炎(UC)是一种影响直肠和结肠的难治性炎症性疾病,直肠环境在复发起始中起关键作用。本研究分两个阶段进行,以检查直肠和结肠之间基因表达的差异并确定复发因素。
在研究1中,对活动期UC患者、缓解期UC患者和对照组的结肠和直肠活检组织进行RNA测序。在研究2中,检测了32例缓解期UC患者和22例对照者反映黏膜屏障功能的黏膜阻抗(MI)值以及紧密连接蛋白和炎性细胞因子的mRNA表达。对复发进行前瞻性监测。
在研究1中,使用RNA测序进行的综合基因分析揭示了缓解期UC患者直肠和乙状结肠中不同的基因谱。这些患者的直肠表现出丰富的免疫反应和顶端连接表型,CLDN2基因表达持续上调。在研究2中,即使在缓解期UC患者中,直肠而非乙状结肠的MI值也显著降低,而MI值与CLDN2、IL-1β和IL-6的表达呈负相关。
缓解期UC患者的直肠状态与结肠不同,存在微炎症和黏膜屏障功能受损,这与CLDN2上调有关,在复发中起作用。