In vitro study: HIF-1α-dependent glycolysis enhances NETosis in hypoxic conditions

This study provides novel insights into the interplay between metabolic reprogramming and NETosis in response to hypoxic stress. We identify HIF-1α-dependent glycolysis as a key driver of NETs formation, advancing our understanding of the mechanisms underlying hypoxia-related inflammatory diseases. These findings also suggest that targeting metabolic pathways may offer potential therapeutic strategies for modulating immune responses in hypoxia-associated disorders.

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Publication Details

Journal
Frontiers in Immunology
Published
2025-04-28
DOI
https://doi.org/10.3389/fimmu.2025.1583587
Citations
13
Primary Topic
Neutrophil, Myeloperoxidase and Oxidative Mechanisms
Type
article
Field-Weighted Citation Impact
10.37

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article

In vitro study: HIF-1α-dependent glycolysis enhances NETosis in hypoxic conditions

Yanjun Wang, Juanli Liu, Tana Wuren, Qiying Xu et al.
13 citations
Frontiers in Immunology
Neutrophil, Myeloperoxidase and Oxidative Mechanisms
10.37
article

In vitro study: HIF-1α-dependent glycolysis enhances NETosis in hypoxic conditions

Yanjun Wang, Juanli Liu, Tana Wuren, Qiying Xu, Yi Ye, Ziqi Yang, Ri-Li Ge
article en
13 citations

Abstract

This study provides novel insights into the interplay between metabolic reprogramming and NETosis in response to hypoxic stress. We identify HIF-1α-dependent glycolysis as a key driver of NETs formation, advancing our understanding of the mechanisms underlying hypoxia-related inflammatory diseases. These findings also suggest that targeting metabolic pathways may offer potential therapeutic strategies for modulating immune responses in hypoxia-associated disorders.

Frontiers in ImmunologyVol. 16
Qinghai University (CN), Qinghai University Affiliated Hospital (CN), Qinghai Provincial Peoples Hospital (CN)
National Natural Science Foundation of China, National Science and Technology Major Project
Openalex Percentile: Top 1%
Neutrophil, Myeloperoxidase and Oxidative Mechanisms
10.37
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