潘尼斯电池
伤口愈合
化生
溃疡性结肠炎
上皮
细胞
病理
化学
癌症研究
医学
细胞迁移
炎症
分子生物学
杯状细胞
肠粘膜
细胞生长
细胞生物学
生物
透明质酸
细胞免疫
作者
Tomohiro Muto,Go Ito,Hiromune Katsuda,Yui Hiraguri,Satoru Fujii,Kurara Yamamoto,Joana P. Bernardes,Finn Hinrichsen,Hitoshi Uchida,Yasuhiro Nemoto,Mayumi Kinoshita,Eri Oshina,Kouhei Yamamoto,Shuji Hibiya,Sayaka Nagata,Fenja Amrei Schuran,Shiro Yui,Penelope Pelczar,Samuel Huber,Stefan Schreiber
标识
DOI:10.1038/s41467-026-71136-1
摘要
Paneth cell metaplasia (PCM) is a phenomenon in which Paneth cells, typically found in the small intestine, appear in the colonic epithelium of patients with ulcerative colitis (UC). Our study demonstrates that the PCM occurrence correlates with disease duration and active inflammation. Furthermore, we identified IL-22, an inflammation-associated cytokine, as a key regulator that promotes PCM formation in the colonic epithelium through suppression of Notch signaling and induces REG3A expression within metaplastic niches. In vitro, we show that Reg3a directly enhances cell proliferation and promotes wound healing using mouse colonic organoids. In vivo, Reg3aΔIEC mice in both acute and chronic DSS-induced colitis models exhibit delayed wound healing. Additionally, studies conducted with patient-derived human colonic organoids revealed that REG3A administration stimulates cell proliferation and accelerates wound healing. Together, these findings support a protective role of PCM-associated REG3A in the colonic epithelium of patients with UC.
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