Macrophage Hypoxia Signaling Pathways and Their Roles in Sepsis

Evidence from laboratory and animal studies provides groundwork for understanding mechanisms and potential before human studies continue.

• Level A · Stronger Clinical Evidence
• Level B · Emerging clinical evidence with positive signals
• Level C · Early human research exploring benefits
• Level D · Scientific groundwork from lab and animal studies
• Emerging · Emerging topic under active research

Abstract (original English)

Sepsis is a severe systemic inflammatory response syndrome, and macrophages play a crucial role in its pathogenesis. In recent years, more and more attention has been paid to the molecular signaling pathways of hypoxia, especially hypoxia-inducible factor 1-alpha (HIF-1α) and its related metabolic reprogramming, which have shown their importance in regulating the inflammatory response and functional state of macrophages. At present, although a large number of studies have explored the functional changes of macrophages in sepsis, there are still many unsolved mysteries about the specific mechanism and clinical significance of the effect of hypoxia signaling pathway on macrophage function and disease progression. In this review, the metabolic pathways regulated by HIF-1α, the activation of inflammasomes, the reprogramming of cell functions, and the effects of hypoxia-related signaling pathways on macrophage function and the pathological process of sepsis were summarized. Combined with the latest single-cell transcriptomics data and molecular mechanism research, we systematically explore the potential therapeutic targets and intervention strategies, which provide theoretical basis and research direction for the precise treatment of sepsis.

Evidence level

Evidence from laboratory and animal studies provides groundwork for understanding mechanisms and potential before human studies continue.

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