Myeloperoxidase regulates hypoxia-induced inflammation and oxidative stress in liver-spleen axis

BACKGROUND: High-altitude hypobaric hypoxia induces inflammation and oxidative stress, yet the role of myeloperoxidase (MPO) in this pathology remains incompletely understood. This study aimed to investigate whether MPO mediates injury to the liverspleen axis under hypoxic conditions. RESULTS: mice displayed aggravated histopathological injury, accompanied by excessive phagocyte recruitment and elevated expression of key chemokines (KC, MCP1, MIP2) and proinflammatory mediators (TNFα, IL1β, IL17A). At the molecular level, MPO absence increased splenic protein expression of NFκB, NLRP3, and iNOS, while dysregulating the antioxidant response via the NRF2/HO1 pathway. CONCLUSIONS: These results reveal a novel protective role for MPO during hypoxic stress, where it functions to moderate the innate immune response and limit collateral tissue damage in the liverspleen axis. The study provides new insights into the complex immunomodulatory functions of MPO and suggests its activity is essential for maintaining immune homeostasis during acute hypoxia.

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Publication Details

Journal
Journal of Inflammation
Published
2026-05-02
DOI
https://doi.org/10.1186/s12950-026-00503-y
Primary Topic
High Altitude and Hypoxia
Type
article
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article

Myeloperoxidase regulates hypoxia-induced inflammation and oxidative stress in liver-spleen axis

Lingming Zhang, Yonggui Li, Zeyi Zuo, Xiaoluan Li et al.
Journal of Inflammation
High Altitude and Hypoxia
article

Myeloperoxidase regulates hypoxia-induced inflammation and oxidative stress in liver-spleen axis

Lingming Zhang, Yonggui Li, Zeyi Zuo, Xiaoluan Li, Qiao Gao, Xiaoli Liu, Qinfang Zhu
article en

Abstract

BACKGROUND: High-altitude hypobaric hypoxia induces inflammation and oxidative stress, yet the role of myeloperoxidase (MPO) in this pathology remains incompletely understood. This study aimed to investigate whether MPO mediates injury to the liverspleen axis under hypoxic conditions. RESULTS: mice displayed aggravated histopathological injury, accompanied by excessive phagocyte recruitment and elevated expression of key chemokines (KC, MCP1, MIP2) and proinflammatory mediators (TNFα, IL1β, IL17A). At the molecular level, MPO absence increased splenic protein expression of NFκB, NLRP3, and iNOS, while dysregulating the antioxidant response via the NRF2/HO1 pathway. CONCLUSIONS: These results reveal a novel protective role for MPO during hypoxic stress, where it functions to moderate the innate immune response and limit collateral tissue damage in the liverspleen axis. The study provides new insights into the complex immunomodulatory functions of MPO and suggests its activity is essential for maintaining immune homeostasis during acute hypoxia.

Journal of Inflammation
Qinghai University (CN), Qinghai Provincial Peoples Hospital (CN)
Good health and well-being
Openalex Percentile: Top 12%
High Altitude and Hypoxia
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