Department of Pharmacology & the Key Laboratory of Smart Drug Delivery, Ministry of Education, School of Pharmacy, Fudan University, Shanghai, China.
Department of Radiation Oncology, Fudan University Shanghai Cancer Center, Shanghai, China.
Pharmacol Res. 2024 Apr;202:107128. doi: 10.1016/j.phrs.2024.107128. Epub 2024 Mar 2.
The damage of integrated epithelial epithelium is a key pathogenic factor and closely associated with the recurrence of ulcerative colitis (UC). Here, we reported that vanillic acid (VA) exerted potent therapeutic effects on DSS-induced colitis by restoring intestinal epithelium homeostasis via the inhibition of ferroptosis. By the CETSA assay and DARTS assay, we identified carbonic anhydrase IX (CAIX, CA9) as the direct target of VA. The binding of VA to CA9 causes insulin-induced gene-2 (INSIG2) to interact with stromal interaction molecule 1 (STIM1), rather than SREBP cleavage-activating protein (SCAP), leading to the translocation of SCAP-SREBP1 from the endoplasmic reticulum (ER) to the Golgi apparatus for cleavage into mature SREBP1. The activation of SREBP1 induced by VA then significantly facilitated the transcription of stearoyl-CoA desaturase 1 (SCD1) to exert an inhibitory effect on ferroptosis. By inhibiting the excessive death of intestinal epithelial cells caused by ferroptosis, VA effectively preserved the integrity of intestinal barrier and prevented the progression of unresolved inflammation. In conclusion, our study demonstrated that VA could alleviate colitis by restoring intestinal epithelium homeostasis through CA9/STIM1-mediated inhibition of ferroptosis, providing a promising therapeutic candidate for UC.
整合上皮损伤是溃疡性结肠炎(UC)复发的关键致病因素,与溃疡的复发密切相关。在这里,我们报道了香草酸(VA)通过抑制铁死亡来恢复肠道上皮稳态,从而对 DSS 诱导的结肠炎发挥强大的治疗作用。通过 CETSA 测定和 DARTS 测定,我们确定碳酸酐酶 IX(CAIX,CA9)是 VA 的直接靶标。VA 与 CA9 的结合导致胰岛素诱导基因 2(INSIG2)与基质相互作用分子 1(STIM1)相互作用,而不是 SREBP 切割激活蛋白(SCAP),导致 SCAP-SREBP1 从内质网(ER)易位到高尔基体进行切割成成熟的 SREBP1。VA 诱导的 SREBP1 激活然后显著促进硬脂酰辅酶 A 去饱和酶 1(SCD1)的转录,从而对铁死亡发挥抑制作用。通过抑制铁死亡引起的肠道上皮细胞过度死亡,VA 有效地保持了肠道屏障的完整性,防止了未解决的炎症的进展。总之,我们的研究表明,VA 可以通过 CA9/STIM1 介导的抑制铁死亡来恢复肠道上皮稳态,从而减轻结肠炎,为 UC 提供了一种有前途的治疗候选药物。