Author
Listed:
- Hui Li
(Central South University
Central South University)
- Tao Liu
(Central South University
Central South University)
- Yang Wang
(Central South University
Central South University)
- Xue-Mei Miao
(Central South University
Central South University)
- Yi-Yu Xiong
(Central South University
Central South University)
- Qian Zhao
(Central South University
Central South University)
- Wei-Yun Shen
(Central South University
Central South University)
- Fu-Hong Su
(Erasmus Hospital)
- Kang Chen
(Wayne State University)
- Ru-Ping Dai
(Central South University
Central South University)
Abstract
Acute lung injury (ALI) and acute respiratory distress syndrome (ARDS) are severe conditions with high morbidity and mortality with limited effective therapies. Neuroimmune interactions play a critical role in lung homeostasis, but it remains unclear if specific brain regions regulate lung inflammation. Here, we perform anatomical tracing, chemogenetic modulation, and pharmacological interventions in male mice and identify a neural circuit from corticotropin-releasing hormone neurons in the paraventricular nucleus of the hypothalamus (CRHPVN neurons) to the lung. The activation of these neurons protects mice from ALI and promotes survival, reduces neutrophil infiltration and effector functions in the lung, whereas inhibiting CRHPVN neurons worsens ALI. The protective effect is mediated by increased sympathetic nervous activity, with locally released norepinephrine modulating neutrophil functions via β2-AR–β-arrestin2 signaling to inhibit the NF-κB pathway. These findings uncover a brain-lung neural circuit that modulates immune responses during ALI, offering a potential therapeutic target for ALI and ARDS.
Suggested Citation
Hui Li & Tao Liu & Yang Wang & Xue-Mei Miao & Yi-Yu Xiong & Qian Zhao & Wei-Yun Shen & Fu-Hong Su & Kang Chen & Ru-Ping Dai, 2025.
"Paraventricular nucleus CRH neurons regulate acute lung injury via sympathetic nerve–neutrophil axis,"
Nature Communications, Nature, vol. 16(1), pages 1-16, December.
Handle:
RePEc:nat:natcom:v:16:y:2025:i:1:d:10.1038_s41467-025-63953-7
DOI: 10.1038/s41467-025-63953-7
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