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Inducing Acute Lung Injury in Mice by Direct Intratracheal Lipopolysaccharide Instillation
Published on: July 6, 2019
The suppressive effects of Mer inhibition on inflammatory responses in the pathogenesis of LPS-induced ALI/ARDS
Masahiko Fukatsu1, Hiroshi Ohkawara1, Xintao Wang1
1Department of Hematology, Fukushima Medical University, Fukushima, Japan.
Abstract:
The pathogenesis of sepsis-induced acute lung injury (ALI)/acute respiratory distress syndrome (ARDS) has not yet been fully elucidated. Growth arrest-specific 6 (Gas6) has marked effects on hemostasis and reduces inflammation through its interaction with receptor tyrosine kinases of the TAM family: Tyro3, Axl, and Mer. Here, we found that plasma concentrations of Gas6 and soluble Mer were greater in patients with severe sepsis or septic ALI/ARDS compared with those in normal healthy donors. To determine whether the Gas6-Mer axis was critical in the pathogenesis of ALI/ARDS, we investigated the effects of intravenous administration of the selective Mer inhibitor UNC2250 on lipopolysaccharide (LPS)-induced ALI in mouse models subjected to inhalation of LPS. UNC2250 markedly inhibited the infiltration into the lungs of neutrophils and monocytes with increased amounts of Gas6 and Mer proteins, severe lung damage, and increased amounts of reactive oxygen species (ROS) in LPS-induced ALI in mice. In human pulmonary aortic endothelial cells, LPS induced decreases in the amounts of endothelial nitric oxide synthase, thrombomodulin, and vascular endothelial-cadherin, which was blocked by treatment with UNC2250. UNC2250 also inhibited the LPS-dependent increases in cell proliferation and enhanced apoptosis in HL-60 cells, a human neutrophil-like cell line, and RAW264.7 cells, a mouse monocyte/macrophage cell line. These data provide insights into the potential multiple beneficial effects of the Mer inhibitor UNC2250 as a therapeutic reagent to treat inflammatory responses in ALI/ARDS.
Insights
Growth arrest-specific 6 (Gas6) and its receptor Mer are elevated in sepsis-induced acute lung injury (ALI)/acute respiratory distress syndrome (ARDS). Inhibiting Mer with UNC2250 reduced lung inflammation and damage in mouse models.
Area of Science:
- Immunology
- Pathophysiology
- Pharmacology
Background:
- Sepsis-induced acute lung injury (ALI) and acute respiratory distress syndrome (ARDS) pathogenesis remains incompletely understood.
- Growth arrest-specific 6 (Gas6) and its receptor tyrosine kinases (TAM family: Tyro3, Axl, Mer) play roles in hemostasis and inflammation.
Purpose of the Study:
- To investigate the role of the Gas6-Mer axis in sepsis-induced ALI/ARDS.
- To evaluate the therapeutic potential of a selective Mer inhibitor, UNC2250, in ALI/ARDS models.
Main Methods:
- Measured plasma Gas6 and soluble Mer levels in patients with severe sepsis or ALI/ARDS.
- Administered UNC2250 intravenously to lipopolysaccharide (LPS)-induced ALI mouse models.
- Assessed inflammatory cell infiltration, lung damage, reactive oxygen species (ROS), and endothelial cell markers in vitro.
Main Results:
- Elevated plasma Gas6 and soluble Mer concentrations were observed in patients with severe sepsis or ALI/ARDS.
- UNC2250 treatment significantly reduced neutrophil and monocyte infiltration in LPS-induced ALI mouse lungs.
- UNC2250 protected human pulmonary aortic endothelial cells from LPS-induced damage and modulated inflammatory cell responses.
Conclusions:
- The Gas6-Mer axis is implicated in the pathogenesis of ALI/ARDS.
- Mer inhibition using UNC2250 demonstrates potential therapeutic benefits for inflammatory responses in ALI/ARDS.

