1. Academic Validation
  2. Loss of neutrophil Shp1 produces hemorrhagic and lethal acute lung injury

Loss of neutrophil Shp1 produces hemorrhagic and lethal acute lung injury

  • bioRxiv. 2024 May 28:2024.05.23.595575. doi: 10.1101/2024.05.23.595575.
S F Moussavi-Harami 1 2 S J Cleary 1 M Magnen 1 Y Seo 1 C Conrad 1 B C English 3 4 L Qiu 1 K M Wang 1 C L Abram 5 C A Lowell 5 M R Looney 1 5
Affiliations

Affiliations

  • 1 Division of Pulmonary, Critical Care, Allergy and Sleep Medicine, Department of Medicine, University of California, San Francisco.
  • 2 Division of Pediatric Critical Care Medicine, Department of Pediatrics, University of California, San Francisco.
  • 3 Department of Microbiology & Immunology, University of California, San Francisco.
  • 4 CoLabs, University of California, San Francisco.
  • 5 Department of Laboratory Medicine, University of California, San Francisco.
Abstract

The acute respiratory distress syndrome (ARDS) is associated with significant morbidity and mortality and neutrophils are critical to its pathogenesis. Neutrophil activation is closely regulated by inhibitory tyrosine phosphatases including Src homology region 2 domain containing phosphatase-1 (Shp1). Here, we report that loss of neutrophil Shp1 in mice produced hyperinflammation and lethal pulmonary hemorrhage in sterile inflammation and pathogen-induced models of acute lung injury (ALI) through a Syk kinase-dependent mechanism. We observed large intravascular neutrophil clusters, perivascular inflammation, and excessive neutrophil extracellular traps in neutrophil-specific Shp1 knockout mice suggesting an underlying mechanism for the observed pulmonary hemorrhage. Targeted immunomodulation through the administration of a Shp1 activator (SC43) reduced agonist-induced Reactive Oxygen Species in vitro and ameliorated ALI-induced alveolar neutrophilia and NETs in vivo. We propose that the pharmacologic activation of Shp1 has the potential to fine-tune neutrophil hyperinflammation that is central to the pathogenesis of ARDS.

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