Macrophage PTEN controls STING-induced inflammation and necroptosis through NICD/NRF2 signaling in APAP-induced liver injury.


Journal

Cell communication and signaling : CCS
ISSN: 1478-811X
Titre abrégé: Cell Commun Signal
Pays: England
ID NLM: 101170464

Informations de publication

Date de publication:
27 06 2023
Historique:
received: 02 04 2023
accepted: 25 05 2023
medline: 29 6 2023
pubmed: 28 6 2023
entrez: 27 6 2023
Statut: epublish

Résumé

Phosphatase and tensin homolog deleted on chromosome 10 (PTEN) signaling has been known to play a critical role in maintaining cellular and tissue homeostasis, which also has an essential role in the inflammatory response. However, it remains unidentified whether and how the macrophage PTEN may govern the innate immune signaling stimulator of interferon genes (STING) mediated inflammation and hepatocyte necroptosis in APAP-induced liver injury (AILI). Myeloid-specific PTEN knockout (PTEN Here, we report that myeloid-specific PTEN knockout (PTEN Our findings demonstrate that the macrophage PTEN-NICD/NRF2-STING axis is critical to regulating oxidative stress-induced liver inflammation and necroptosis in AILI and implies the therapeutic potential for managing sterile liver inflammation. Video Abstract.

Sections du résumé

BACKGROUND
Phosphatase and tensin homolog deleted on chromosome 10 (PTEN) signaling has been known to play a critical role in maintaining cellular and tissue homeostasis, which also has an essential role in the inflammatory response. However, it remains unidentified whether and how the macrophage PTEN may govern the innate immune signaling stimulator of interferon genes (STING) mediated inflammation and hepatocyte necroptosis in APAP-induced liver injury (AILI).
METHODS
Myeloid-specific PTEN knockout (PTEN
RESULTS
Here, we report that myeloid-specific PTEN knockout (PTEN
CONCLUSIONS
Our findings demonstrate that the macrophage PTEN-NICD/NRF2-STING axis is critical to regulating oxidative stress-induced liver inflammation and necroptosis in AILI and implies the therapeutic potential for managing sterile liver inflammation. Video Abstract.

Identifiants

pubmed: 37370115
doi: 10.1186/s12964-023-01175-4
pii: 10.1186/s12964-023-01175-4
pmc: PMC10294406
doi:

Substances chimiques

NF-E2-Related Factor 2 0
Reactive Oxygen Species 0

Types de publication

Video-Audio Media Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

160

Informations de copyright

© 2023. The Author(s).

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Auteurs

Tao Yang (T)

Department of Infectious Diseases, The First Affiliated Hospital With Nanjing Medical University, Nanjing, China.
Department of Respiratory and Critical Care Medicine, The Affiliated People's Hospital of Jiangsu University, The Zhenjiang Clinical Medical College of Nanjing Medical University, Zhenjiang, China.

Xiaoye Qu (X)

Department of Liver Surgery, Renji Hospital, Shanghai Jiaotong University School of Medicine, Shanghai, China.

Jiaying Zhao (J)

Department of Infectious Diseases, The First Affiliated Hospital With Nanjing Medical University, Nanjing, China.

Xiao Wang (X)

Department of Infectious Diseases, The First Affiliated Hospital With Nanjing Medical University, Nanjing, China.

Qian Wang (Q)

Department of Infectious Diseases, The First Affiliated Hospital With Nanjing Medical University, Nanjing, China.

Jingjing Dai (J)

Department of Infectious Diseases, The First Affiliated Hospital With Nanjing Medical University, Nanjing, China.

Chuanlong Zhu (C)

Department of Infectious Diseases, The First Affiliated Hospital With Nanjing Medical University, Nanjing, China.

Jun Li (J)

Department of Infectious Diseases, The First Affiliated Hospital With Nanjing Medical University, Nanjing, China. dr-lijun@vip.sina.com.

Longfeng Jiang (L)

Department of Infectious Diseases, The First Affiliated Hospital With Nanjing Medical University, Nanjing, China. longfengjiang@njmu.edu.cn.

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Classifications MeSH