Journal Article

TRIM40 is a pathogenic driver of inflammatory bowel disease subverting intestinal barrier integrity

Kang, Sujin, Park, Hyun Woo, Kim, Jaekyung, Choi, Myung Kyung, Lee, Taeyun A., Kim, Hyung Jin, Park, Jae Hyung, Lee, Eunhye, Han, Heonjong, Cheon, Jae Hee, Cho, Hyun-Soo, Park, Boyoun, Park, Gayoung, Kim, Yongbo, Park, Areum, Koh, Minsoo, Lee, Sungwook, Shin, Wonji

2023

Overview

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. The cortical actin cytoskeleton plays a role in maintaining intestinal epithelial integrity. Here the authors report that TRIM40, an E3 ligase, disrupts cortical actin formation and leads to loss of epithelial barrier integrity, and that genetic loss of TRIM40 is protective against experimental colitis in male mice.

• Publisher: Nature Publishing Group UK,Nature Publishing Group,Nature Portfolio
• Subject: 14 / 14/19 / 38/35 / 631/80/128/1276 / 631/80/79/2028 / 82/51 / 82/80 / 96 / 96/95 / Actin / Actins - metabolism / Animals / Cell junctions / Colitis / Colitis - chemically induced / Colitis - genetics / Colitis - metabolism / Cytoskeleton / Dextran / Dextran sulfate / Dextran Sulfate - toxicity / Dextrans / Disease Models, Animal / Humanities and Social Sciences / Humans / Inflammatory bowel disease / Inflammatory bowel diseases / Inflammatory Bowel Diseases - pathology / Inflammatory response / Integrity / Intestinal Mucosa - metabolism / Intestine / Intestines / Kinases / Male / Males / Mice / Mice, Inbred C57BL / multidisciplinary / Phosphorylation / Proteins / Science / Science (multidisciplinary) / Tripartite Motif Proteins - genetics / Tripartite Motif Proteins - metabolism / Ubiquitin-protein ligase