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NEDD4L mediates intestinal epithelial cell ferroptosis to restrict inflammatory bowel diseases and colorectal tumorigenesis
Jingjing Liang, … , Xiaojian Wang, Wenlong Lin
Jingjing Liang, … , Xiaojian Wang, Wenlong Lin
Published December 17, 2024
Citation Information: J Clin Invest. 2025;135(3):e173994. https://doi.org/10.1172/JCI173994.
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Research Article Cell biology Inflammation Article has an altmetric score of 8

NEDD4L mediates intestinal epithelial cell ferroptosis to restrict inflammatory bowel diseases and colorectal tumorigenesis

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Abstract

Various factors play key roles in maintaining intestine homeostasis. Disruption of the balance may lead to inflammatory bowel diseases and even colorectal cancer (CRC). Loss or gain of function of many key proteins can result in dysregulated intestinal homeostasis. Our research demonstrated that neural precursor cells expressed developmentally downregulated 4–like protein (NEDD4L, or NEDD4-2), a type of HECT family E3 ubiquitin ligase, played an important role in maintaining intestinal homeostasis. NEDD4L expression was significantly inhibited in intestinal epithelial cells (IECs) of patients with Crohn’s disease, ulcerative colitis, and CRC. Global KO of NEDD4L or its deficiency in IECs exacerbated colitis induced by dextran sulfate sodium (DSS) and 2,4,6-trinitrobenzene sulfonic acid (TNBS) and CRC induced by azoxymethane and DSS. Mechanistically, NEDD4L deficiency in IECs inhibited expression of the key ferroptosis regulator glutathione peroxidase 4 (GPX4) by reducing the protein expression of solute carrier family 3 member 2 (SLC3A2) without affecting its gene expression, ultimately promoting DSS-induced IEC ferroptosis. Importantly, ferroptosis inhibitors reduced the susceptibility of NEDD4L-deficient mice to colitis and colitis-associated CRC. Thus, NEDD4L is an important regulator in IEC ferroptosis, maintaining intestinal homeostasis, making it a potential clinical target for diagnosing and treating IBDs.

Authors

Jingjing Liang, Ning Wang, Yihan Yao, Yingmei Wang, Xiang An, Haofei Wang, Huan Liu, Yu Jiang, Hui Li, Xiaoqing Cheng, Jiaqi Xu, Xiaojing Liang, Jun Lou, Zengfeng Xin, Ting Zhang, Xiaojian Wang, Wenlong Lin

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Figure 7

NEDD4L ubiquitinates SLC3A2.

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NEDD4L ubiquitinates SLC3A2.
(A) Immunoblot analysis of NEDD4L and SLC3A...
(A) Immunoblot analysis of NEDD4L and SLC3A2 coimmunoprecipitated with anti-SLC3A2 antibody from lysates of HCT116 cells treated with 2% DSS for the indicated times. (B and C) Immunoblot analysis of Myc-tagged proteins and FLAG-tagged SLC3A2 coimmunoprecipitated with anti-Myc antibody from lysates of HEK293T cells cotransfected with indicated plasmids. WCL, whole-cell lysate. (D) Immunoblot analysis of NEDD4L, SLC3A2, and Ub, which were coimmunoprecipitated with anti-Ub antibody from lysates of NEDD4L (sgNEDD4L) or negative control (sgNTC) KO HCT116 cells treated with 2% DSS for the indicated times. (E) Immunoblot analysis of total ubiquitination of FLAG-tagged SLC3A2 following coimmunoprecipitation with anti-FLAG antibody from lysates of HEK293T cells cotransfected with indicated plasmids. (F) Immunoblot analysis of Ub-linked FLAG-tagged EGFP or SLC3A2 incubated with Myc-tagged NEDD4L, Myc-tagged NEDD4L-C942A (CA), or Myc-tagged EGFP recombinant protein in the presence of the full complement of ubiquitination reaction components, including E1, E2, Ub, and ATP, in vitro. (G and H) Immunoblot analysis of ubiquitination of FLAG-tagged SLC3A2 following coimmunoprecipitation of SLC3A2 with anti-FLAG antibody from lysates of HEK293T cells cotransfected with indicated plasmids. (I) Immunoblot analysis of K63Ub, K48Ub, Ub, GPX4, TFRC, SLC3A2, NEDD4L, and actin, which were coimmunoprecipitated with anti-SLC3A2 antibody from lysates of NEDD4L (sgNEDD4L) or negative control (sgNTC) KO HCT116 cells treated with 2% DSS for the indicated times and pretreated with 20 μM MG132 for 6 hours. (J) Immunoblot analysis of total ubiquitination of FLAG-tagged SLC3A2 following coimmunoprecipitation of SLC3A2 with anti-FLAG antibody from lysates of HEK293T cells cotransfected with indicated plasmids.

Copyright © 2025 American Society for Clinical Investigation
ISSN: 0021-9738 (print), 1558-8238 (online)

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