Deubiquitinase USP7 Regulates Neutrophil Extracellular Trap Formation and Inflammation in Lipopolysaccharide-Treated Mice Through ICAM-1 Expression.

Λεπτομέρειες βιβλιογραφικής εγγραφής
Τίτλος: Deubiquitinase USP7 Regulates Neutrophil Extracellular Trap Formation and Inflammation in Lipopolysaccharide-Treated Mice Through ICAM-1 Expression.
Συγγραφείς: Xu H; Department of Emergency, Shanghai Ninth People's Hospital Affiliated to Shanghai Jiaotong University School of Medicine, Shanghai, China., Wang Q; Department of Emergency, Shanghai Ninth People's Hospital Affiliated to Shanghai Jiaotong University School of Medicine, Shanghai, China., Fan JX; Department of Emergency, Shanghai Ninth People's Hospital Affiliated to Shanghai Jiaotong University School of Medicine, Shanghai, China., Xu YF; Department of Emergency, Shanghai Ninth People's Hospital Affiliated to Shanghai Jiaotong University School of Medicine, Shanghai, China., Yu J; Department of Emergency, Shanghai Ninth People's Hospital Affiliated to Shanghai Jiaotong University School of Medicine, Shanghai, China.
Πηγή: The Kaohsiung journal of medical sciences [Kaohsiung J Med Sci] 2026 May; Vol. 42 (5), pp. e70133. Date of Electronic Publication: 2025 Oct 31.
Τύπος έκδοσης: Journal Article
Γλώσσα: English
Στοιχεία περιοδικού: Publisher: Department of Public Health, Kaohsiung Medical University Country of Publication: China (Republic : 1949- ) NLM ID: 100960562 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 2410-8650 (Electronic) Linking ISSN: 1607551X NLM ISO Abbreviation: Kaohsiung J Med Sci Subsets: MEDLINE
Imprint Name(s): Publication: 2019- : [Kaohsiung City, Taiwan] : Department of Public Health, Kaohsiung Medical University
Original Publication: [Kaohsiung City, Taiwan, Republic of China : Kaohsiung Medical College, 1996-
Ιατρικοί όροι (MeSH): Intercellular Adhesion Molecule-1*/metabolism , Intercellular Adhesion Molecule-1*/genetics , Extracellular Traps*/metabolism , Ubiquitin-Specific Peptidase 7*/metabolism , Ubiquitin-Specific Peptidase 7*/genetics , Sepsis*/metabolism , Sepsis*/chemically induced , Sepsis*/pathology , Sepsis*/genetics , Neutrophils*/metabolism , Inflammation*/metabolism , Inflammation*/pathology , Lipopolysaccharides*, Macrophages/metabolism ; Animals ; Mice ; Mice, Knockout ; Male ; Mice, Inbred C57BL ; Disease Models, Animal ; Ubiquitination
Περίληψη: Sepsis is typified by organ failure due to an unchecked host reaction to infection. This study aims to explore the mechanism of ubiquitin-specific peptidase 7 (USP7) in sepsis with the involvement of intercellular adhesion molecule-1 (ICAM-1). A sepsis model was established using lipopolysaccharide (LPS) induction in WT and USP7-/- mice, and various assays were conducted to evaluate survival rates, organ damage, inflammatory markers, and protein interactions. The results revealed that USP7 expression increased in LPS-treated WT mice, and its interaction with ICAM-1 stabilized ICAM-1 through deubiquitination. USP7 knockout significantly elevated survival rates of septic mice. USP7 knockout reduced pulmonary inflammation, neutrophil extracellular trap (NET) formation, and myeloperoxidase and Cit-H3 levels in septic mice. Moreover, USP7 knockout lowered the levels of organ injury markers (creatine kinase-MB [CK-MB], troponin-I, and blood urea nitrogen [BUN]), liver enzymes (ALT and AST), and inflammatory markers (TNF-α, IL-1β, IL-6, and IL-8). Co-culture of bone marrow-derived macrophages (BMDMs) from WT mice with ICAM-1+ neutrophils elevated levels of TNF-α, IL-1β, and IL-6. These findings suggest that USP7 plays a critical role in driving sepsis-induced NET formation and inflammation by stabilizing ICAM-1. Targeting USP7 may represent a potential therapeutic approach to mitigate sepsis-related inflammation and organ damage.
(© 2025 The Author(s). The Kaohsiung Journal of Medical Sciences published by John Wiley & Sons Australia, Ltd on behalf of Kaohsiung Medical University.)
References: Biomolecules. 2021 Jul 10;11(7):. (PMID: 34356636)
FASEB J. 2020 Jul;34(7):9771-9786. (PMID: 32506691)
Bioengineered. 2022 May;13(5):13366-13383. (PMID: 36700466)
Br Poult Sci. 2023 Oct;64(5):614-624. (PMID: 37334824)
Front Immunol. 2024 Mar 06;15:1392734. (PMID: 38515740)
Biochim Biophys Acta Rev Cancer. 2023 May;1878(3):188903. (PMID: 37127084)
APMIS. 2021 Mar;129(3):152-162. (PMID: 33241864)
iScience. 2024 Apr 05;27(6):109667. (PMID: 38966570)
Int J Mol Sci. 2023 Oct 31;24(21):. (PMID: 37958788)
Cell Chem Biol. 2024 Dec 19;31(12):2085-2095.e4. (PMID: 39631397)
J Cell Mol Med. 2021 Jan;25(2):990-1000. (PMID: 33332749)
Naunyn Schmiedebergs Arch Pharmacol. 2024 May;397(5):3425-3435. (PMID: 37962585)
Am Fam Physician. 2020 Apr 1;101(7):409-418. (PMID: 32227831)
Clin Chim Acta. 2023 Aug 1;548:117487. (PMID: 37442359)
Front Chem. 2022 Sep 15;10:1005727. (PMID: 36186590)
J Leukoc Biol. 2020 Sep;108(3):787-799. (PMID: 32182390)
Theranostics. 2022 Jan 1;12(2):976-998. (PMID: 34976224)
Kaohsiung J Med Sci. 2026 May;42(5):e70133. (PMID: 41170880)
Inflammation. 2025 Aug;48(4):2503-2515. (PMID: 39707013)
Hum Gene Ther. 2022 Oct;33(19-20):1073-1090. (PMID: 35686454)
Front Immunol. 2022 Aug 12;13:900243. (PMID: 36032091)
Int Immunopharmacol. 2024 Jul 30;136:112346. (PMID: 38850785)
J Clin Med. 2019 Dec 14;8(12):. (PMID: 31847346)
Exp Mol Med. 2020 Aug;52(8):1310-1325. (PMID: 32778797)
Theranostics. 2023 Jun 26;13(11):3761-3780. (PMID: 37441604)
Int J Biol Sci. 2022 May 9;18(8):3337-3357. (PMID: 35637949)
DNA Repair (Amst). 2019 Apr;76:30-39. (PMID: 30807924)
Cytokine Growth Factor Rev. 2025 Feb;81:27-39. (PMID: 39681501)
Cell Rep. 2024 Nov 26;43(11):114872. (PMID: 39412987)
J Mol Med (Berl). 2020 Jun;98(6):907-921. (PMID: 32440780)
Int J Mol Sci. 2024 Jun 13;25(12):. (PMID: 38928206)
Acta Clin Croat. 2022 Jun;61(Suppl 1):67-72. (PMID: 36304809)
Grant Information: ZT202110 Shanghai Jiao Tong University School of Medicine Technology Transfer Project; 2022hbyjxys-cyb Shanghai Ninth Hospital Research Physician Training Project
Contributed Indexing: Keywords: intercellular adhesion molecule‐1; neutrophil extracellular traps; sepsis; ubiquitin‐specific peptidase 7
Substance Nomenclature: 126547-89-5 (Intercellular Adhesion Molecule-1)
0 (Lipopolysaccharides)
EC 3.4.19.12 (Ubiquitin-Specific Peptidase 7)
0 (Icam1 protein, mouse)
Entry Date(s): Date Created: 20251031 Date Completed: 20260509 Latest Revision: 20260813
Update Code: 20260813
PubMed Central ID: PMC13182596
DOI: 10.1002/kjm2.70133
PMID: 41170880
Βάση Δεδομένων: MEDLINE