https://doi.org/10.4081/ejh.2024.4101
Deubiquitinase USP14 is upregulated in Crohn's disease and inhibits the NOD2 pathway mediated inflammatory response in vitro
Submitted: 8 July 2024
Accepted: 16 August 2024
Published: 9 September 2024
Accepted: 16 August 2024
Abstract Views: 377
PDF: 132
HTML: 1
HTML: 1
Publisher's note
All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article or claim that may be made by its manufacturer is not guaranteed or endorsed by the publisher.
All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article or claim that may be made by its manufacturer is not guaranteed or endorsed by the publisher.
Authors
The nucleotide binding oligomerization domain containing 2 (NOD2) protein and its ligand N-acetyl muramyl dipeptide (MDP) are crucially involved in Crohn’s disease (CD). However, the mechanism by which NOD2 signaling is regulated in CD patients remains unclear. Ubiquitin specific protease (USP14) is a deubiquitylase that plays an important role in immunity. This study aimed to investigate the mechanism by which UPS14 regulates NOD2 induced inflammatory response in CD and inflammatory bowel diseases (IBD). Our results showed that USP14 protein and mRNA levels in intestinal tissues of CD patients were significantly higher than those in healthy controls. In addition, USP14 was upregulated in IBD mouse model. While treatment with MDP, TNF-α or the Toll-like receptor 1/2 agonist Pam3CSK4 all led to significantly higher mRNA levels of TNF-α, IL-8 and IL-1β in THP-1 cells, pretreatment with USP14 inhibitor IU1 could stimulate further upregulation of TNF-α, IL-8 and IL-1β. In particular, MDP promoted the activation of JNK, ERK1/2 and p38 as well as NF-kB in THP-1 cells, and IU1 significantly enhanced the MDP-induced activation of these proteins without effects on USP14 protein level. Furthermore, the JNK inhibitor sp600125, ERK1/2 inhibitor U0126 or P38 MAPK inhibitor PD169316 significantly decreased the mRNA levels of TNF-α, IL-8 and IL-1β in THP-1 cells stimulated by both IU1 and MDP. In conclusion, our findings suggest that USP14 could inhibit MDP-induced activation of MAPK signaling and the inflammation response involved in IBD, and that USP14 is a potential therapeutic target for IBD.
Kaser A, Zeissig S, Blumberg RS. Inflammatory bowel disease. Annu Rev Immunol 2010;28:573-621.
DOI: https://doi.org/10.1146/annurev-immunol-030409-101225
De Souza HSP, Fiocchi C, Iliopoulos D. The IBD interactome: an integrated view of aetiology, pathogenesis and therapy. Nat Rev Gastroenterol Hepatol 2017;14:739-49.
DOI: https://doi.org/10.1038/nrgastro.2017.110
Ananthakrishnan AN. Epidemiology and risk factors for IBD. Nat Rev Gastroenterol Hepatol 2015;12:205-17.
DOI: https://doi.org/10.1038/nrgastro.2015.34
Fritz T, Niederreiter L, Adolph T, Blumberg RS, Kaser A. Crohn's disease: NOD2, autophagy and ER stress converge. Gut 2011;60:1580-8.
DOI: https://doi.org/10.1136/gut.2009.206466
Ashton JJ, Seaby EG, Beattie RM, Ennis S. NOD2 in Crohn's disease-unfinished business. J Crohns Colitis. 2023;17:450-8.
DOI: https://doi.org/10.1093/ecco-jcc/jjac124
Sun Y, Qin Z, Li Q, Wan JJ, Cheng MH, Wang PY, et al. MicroRNA-124 negatively regulates LPS-induced TNF-α production in mouse macrophages by decreasing protein stability. Acta Pharmacol Sin. 2016;37:889-97.
DOI: https://doi.org/10.1038/aps.2016.16
Li H, Zhao Z, Ling J, Pan L, Zhao X, Zhu H, et al. USP14 promotes K63-linked RIG-I deubiquitination and suppresses antiviral immune responses. Eur J Immunol 2019;49:42-53.
DOI: https://doi.org/10.1002/eji.201847603
Arbab A-a-I, Yin C, Lu X, Liang Y, Abdalla I-M, Idris A-A, et al. Metformin alleviates LTA-induced inflammatory response through PPARγ/MAPK/NF-κB signaling pathway in bovine mammary epithelial cells. Biocell 2022;46:2443-54.
DOI: https://doi.org/10.32604/biocell.2022.020865
Zhang H, Wang M, Xu Y. Understanding the mechanisms underlying obesity in remodeling the breast tumor immune microenvironment: from the perspective of inflammation. Cancer Biol Med 2023;20:268-86.
DOI: https://doi.org/10.20892/j.issn.2095-3941.2022.0547
Long Y, Zhao Y, Ma X, Zeng Y, Hu T, Wu W, et al. Endoplasmic reticulum stress contributed to inflammatory bowel disease by activating p38 MAPK pathway. Eur J Histochem 2022;66:3415.
DOI: https://doi.org/10.4081/ejh.2022.3415
Liu Y, Chen H, Li G, Zhang J, Yao K, Wu C, et al. Radiotherapy delays malignant transformation and prolongs survival in patients with IDH-mutant gliomas. Cancer Biol Med 2022;19:1477-86.
DOI: https://doi.org/10.20892/j.issn.2095-3941.2022.0472
Kitaura H, Ishida M, Kimura K, Sugisawa H, Kishikawa A, Shima K, et al. Role of muramyl dipeptide in lipopolysaccharide-mediated biological activity and osteoclast Activity. Anal Cell Pathol (Amst) 2018;2018:8047610.
DOI: https://doi.org/10.1155/2018/8047610
da Paz Martins AS, Campos SBG, Goulart MOF, Moura FA. Extraintestinal manifestations of inflammatory bowel disease, nitroxidative stress and dysbiosis: What is the link between them? Biocell 2021; 45:461–81.
DOI: https://doi.org/10.32604/biocell.2021.014332
Lu J, Traub B, Kornmann M. The role of interleukin 13 receptor alpha 2 in inflammatory bowel disease and colorectal cancer. Transl Surg Oncol 2023;1:3-9.
Zhao Y, Zong F. Inhibiting USP14 ameliorates inflammatory responses in trophoblast cells by suppressing MAPK/NF-κB signaling. Immun Inflamm Dis. 2021;9:1016-24.
DOI: https://doi.org/10.1002/iid3.465
Neurath MF. Cytokines in inflammatory bowel disease. Nat Rev Immunol 2014;14:329-42.
DOI: https://doi.org/10.1038/nri3661
Darling NJ, Cook SJ. The role of MAPK signaling pathways in the response to endoplasmic reticulum stress. Biochim Biophys Acta 2014;1843:2150-63.
DOI: https://doi.org/10.1016/j.bbamcr.2014.01.009
Hu T, Zhao Y, Long Y, Ma X, Zeng Y, Wu W, et al. TLR4 promoted endoplasmic reticulum stress induced inflammatory bowel disease via the activation of p38 MAPK pathway. Biosci Rep. 2022;42:BSR20220307.
DOI: https://doi.org/10.1042/BSR20220307
Woo SM, Kwon TK. E3 ubiquitin ligases and deubiquitinases as modulators of TRAIL-mediated extrinsic apoptotic signaling pathway. BMB Rep 2019;52:119-26.
DOI: https://doi.org/10.5483/BMBRep.2019.52.2.011
Zhu D, Zhang L, Shi X, Gao S, Yue C, Zhang L, et al. RNF43 is a novel tumor-suppressor and prognostic indicator in clear cell renal cell carcinoma. Oncol Res. 2022;29:159-74.
DOI: https://doi.org/10.32604/or.2022.03458
Zhang Y, Liu L, Luo B, Tang H, Yu X, Bao S. Calcyclin-binding protein contributes to cholangiocarcinoma progression by inhibiting ubiquitination of MCM2. Oncol Res 2023;31:317-31.
DOI: https://doi.org/10.32604/or.2023.028418
Zou M, Zeng QS, Nie J, Yang JH, Luo ZY, Gan HT. The role of E3 ubiquitin ligases and deubiquitinases in inflammatory bowel disease: friend or foe? Front Immunol 2021;12:769167.
DOI: https://doi.org/10.3389/fimmu.2021.769167
Pu S, Zheng H, Tao Y, Shao J, Yang M, Li S. The function of ubiquitin-specific protease 31 in intracerebral hemorrhage. Biocell 2022;46:1545-55.
DOI: https://doi.org/10.32604/biocell.2022.017544
Ethics Approval
this study was approved by Ethics Committee of Changsha Central Hospital (approval no. 2023036) and all patients provided informed consent, All animal experiments were reviewed and approved by the Institutional Animal Care Committee of University of South China (approval no. 2023094)Supporting Agencies
Natural Science Foundation of Hunan Province of ChinaHow to Cite
Li, M., Zhao, Y., Zhang, J., Jiang, W., Peng, S., Hu, J., & Shen, Y. (2024). Deubiquitinase USP14 is upregulated in Crohn’s disease and inhibits the NOD2 pathway mediated inflammatory response <i>in vitro</i>. European Journal of Histochemistry, 68(3). https://doi.org/10.4081/ejh.2024.4101
Copyright (c) 2024 The Author(s)
This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License.
PAGEPress has chosen to apply the Creative Commons Attribution NonCommercial 4.0 International License (CC BY-NC 4.0) to all manuscripts to be published.
Similar Articles
- Ewing Duque-Díaz, Hernán Hurtado Giraldo, Linda P. Rocha-Muñoz, Rafael Coveñas, Glyphosate, AMPA and glyphosate-based herbicide exposure leads to GFAP, PCNA and caspase-3 increased immunoreactive area on male offspring rat hypothalamus , European Journal of Histochemistry: Vol. 66 No. 4 (2022)
- J. Rieger, P. Janczyk, H. Hünigen, J. Plendl, Enhancement of immunohistochemical detection of Salmonella in tissues of experimentally infected pigs , European Journal of Histochemistry: Vol. 59 No. 3 (2015)
- H. Zhang, P. Yu, S. Zhong, T. Ge, S. Peng, Z. Zhou, X. Guo, Gliocyte and synapse analyses in cerebral ganglia of the Chinese mitten crab, Eriocheir sinensis: ultrastructural study , European Journal of Histochemistry: Vol. 60 No. 3 (2016)
- A Franchini, E Marchesini, R Poletti, E Ottaviania, Swiss mice CD1 fed on mussels contaminated by okadaic acid and yessotoxins: effects on thymus and spleen , European Journal of Histochemistry: Vol. 49 No. 2 (2005)
- J. Xue, H. Chen, L. Diao, X. Chen, D. Xia, Expression of Caveolin-1 in tongue squamous cell carcinoma by quantum dots , European Journal of Histochemistry: Vol. 54 No. 2 (2010)
- S. Shibata, Y. Sakamoto, O. Baba, C. Qin, G. Murakami, B.H. Cho, An immunohistochemical study of matrix proteins in the craniofacial cartilage in midterm human fetuses , European Journal of Histochemistry: Vol. 57 No. 4 (2013)
- I. Tsukamoto, M. Akagi, S. Inoue, K. Yamagishi, S. Mori, S. Asada, Expressions of local renin-angiotensin system components in chondrocytes , European Journal of Histochemistry: Vol. 58 No. 2 (2014)
- E. Akat, H. Arıkan, B. Göçmen, Histochemical and biometric study of the gastrointestinal system of Hyla orientalis (Bedriaga, 1890) (Anura, Hylidae) , European Journal of Histochemistry: Vol. 58 No. 4 (2014)
- Haixia Li, Ning Sun, Yaqiao Zhu, Wei Wang, Meihong Cai, Xiaohuan Luo, Wei Xia, Song Quan, Growth hormone inhibits the JAK/STAT3 pathway by regulating SOCS1 in endometrial cells in vitro: a clue to enhance endometrial receptivity in recurrent implantation failure , European Journal of Histochemistry: Vol. 67 No. 1 (2023)
- C Demonceau, AS Marshall, J Sales, E Heinen, Investigation of close interactions between sympathetic neural fibres and the follicular dendritic cells network in the mouse spleen , European Journal of Histochemistry: Vol. 52 No. 2 (2008)
<< < 26 27 28 29 30 31 32 33 34 35 > >>
You may also start an advanced similarity search for this article.
