Department of Gastroenterology, The First Affiliated Hospital, Sun Yat-sen University, 58 Zhongshan II Road, Guangzhou, 510080, People's Republic of China.
Dig Dis Sci. 2021 Oct;66(10):3375-3390. doi: 10.1007/s10620-020-06697-2. Epub 2020 Nov 13.
DNA damage-regulated autophagy modulator 1 (DRAM1) is required for induction of autophagy and apoptosis. However, the influence of DRAM1 on the pathogenesis of inflammatory bowel disease (IBD) has not been explored.
DRAM1 expression was examined in the intestinal mucosa of patients with IBD and colons of colitis mice. We used a recombinant adeno-associated virus carrying small hairpain DRAM1 to knock down the DRAM1 gene to treat colitis in the mice. The effect of DRAM1 on autophagy and apoptosis of intestinal epithelial cells was explored. DRAM1-mediated interaction with the c-Jun N-terminal kinase (JNK) pathway was also examined.
DRAM1 expression in the intestinal mucosa of the IBD patients was higher than that in the control participates. DRAM1 expression in the inflammatory cells in patients with Crohn's disease (CD) was lower than that in patients with ulcerative colitis (UC). Additionally, DRAM1 expression was correlated with the Simple Endoscopic Score for CD and the Mayo endoscopic score for UC. Serum levels of DRAM1 in the IBD group were substantially higher than those in the normal group. The knockdown of DRAM1 could alleviate colitis symptoms in mice. In in vitro experiments, knocking down DRAM1 could reduce autophagy and apoptosis levels. Mechanistically, DRAM1 may participate in the regulation of these two processes by positively regulating JNK activation.
During intestinal inflammation, the upregulation of DRAM1 may promote the activation of JNK and further aggravate intestinal epithelium damage.
DNA 损伤调控自噬调节剂 1(DRAM1)是诱导自噬和细胞凋亡所必需的。然而,DRAM1 对炎症性肠病(IBD)发病机制的影响尚未被探索。
检测 IBD 患者的肠黏膜和结肠炎小鼠结肠中的 DRAM1 表达。我们使用携带短发夹 RNA DRAM1 的重组腺相关病毒来敲低 DRAM1 基因,以治疗小鼠结肠炎。探索了 DRAM1 对肠上皮细胞自噬和凋亡的影响。还检查了 DRAM1 介导的与 c-Jun N 端激酶(JNK)途径的相互作用。
IBD 患者肠黏膜中的 DRAM1 表达高于对照组。CD 患者炎症细胞中的 DRAM1 表达低于 UC 患者。此外,DRAM1 表达与 CD 的简单内镜评分和 UC 的 Mayo 内镜评分相关。IBD 组的血清 DRAM1 水平明显高于正常组。DRAM1 的敲低可减轻小鼠的结肠炎症状。在体外实验中,敲低 DRAM1 可降低自噬和凋亡水平。从机制上讲,DRAM1 可能通过正调控 JNK 激活来参与这两个过程的调节。
在肠道炎症过程中,DRAM1 的上调可能会促进 JNK 的激活,从而进一步加重肠道上皮损伤。