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Kang, Sujin; Kim, Jaekyung; Park, Areum; Koh, Minsoo; Shin, Wonji; Park, Gayoung; Lee, Taeyun A; Kim, Hyung Jin; Han, Heonjong; Kim, Yongbo; Choi, Myung Kyung; Park, Jae Hyung; Lee, Eunhye; Cho, Hyun-Soo; Park, Hyun Woo; Cheon, Jae Hee; Lee, Sungwook; Park, Boyoun
Nature communications, 02/2023, Volume: 14, Issue: 1Journal Article
The cortical actin cytoskeleton plays a critical role in maintaining intestinal epithelial integrity, and the loss of this architecture leads to chronic inflammation, as seen in inflammatory bowel disease (IBD). However, the exact mechanisms underlying aberrant actin remodeling in pathological states remain largely unknown. Here, we show that a subset of patients with IBD exhibits substantially higher levels of tripartite motif-containing protein 40 (TRIM40), a gene that is hardly detectable in healthy individuals. TRIM40 is an E3 ligase that directly targets Rho-associated coiled-coil-containing protein kinase 1 (ROCK1), an essential kinase involved in promoting cell-cell junctions, markedly decreasing the phosphorylation of key signaling factors critical for cortical actin formation and stabilization. This causes failure of the epithelial barrier function, thereby promoting a long-lived inflammatory response. A mutant TRIM40 lacking the RING, B-box, or C-terminal domains has impaired ability to accelerate ROCK1 degradation-driven cortical actin disruption. Accordingly, Trim40-deficient male mice are highly resistant to dextran sulfate sodium (DSS)-induced colitis. Our findings highlight that aberrant upregulation of TRIM40, which is epigenetically silenced under healthy conditions, drives IBD by subverting cortical actin formation and exacerbating epithelial barrier dysfunction.
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