Endothelial ADAM17 Promotes Neutrophil Migration and Pulmonary Microvascular Permeability in ARDS
Biedritzky, A.; Kleinmaier, C.; Fuhr, A.; Ngamsri, K.-C.; Konrad, F.; Koeppen, M.
Show abstract
Acute respiratory distress syndrome (ARDS) is characterized by profound endothelial barrier disruption, excessive neutrophil recruitment, and sustained pulmonary inflammation. A Disintegrin and Metalloproteinase 17 (ADAM17) regulates inflammatory signaling through ectodomain shedding of adhesion molecules and cytokine receptors, yet its endothelial-specific contribution to ARDS remains poorly defined. We identify endothelial ADAM17 as a central regulator of vascular permeability, neutrophil trafficking, and inflammatory amplification in LPS-induced acute pulmonary inflammation. LPS markedly increased pulmonary ADAM17 expression, whereas endothelial-specific ADAM17 deletion reduced total lung ADAM17 mRNA by 77.5%. Endothelial ADAM17 promoted disruption of endothelial junctions and protein-rich pulmonary edema by modulating JAM-A and VE-cadherin. Concomitantly, endothelial ADAM17 facilitated neutrophil transmigration into interstitial and alveolar compartments through altered expression of PSGL-1 and CD49d. Mechanistically, endothelial ADAM17 enhanced TNF receptor 1 and IL-6 receptor signaling, increasing proinflammatory mediator release. Pharmacological ADAM17 inhibition recapitulated the protective phenotype of endothelial ADAM17 deficiency, attenuating neutrophil recruitment and preserving endothelial barrier integrity. These findings establish endothelial ADAM17 as a key driver of inflammatory vascular dysfunction in ARDS and support ADAM17 as a rational therapeutic target.
Matching journals
The top 8 journals account for 50% of the predicted probability mass.
Similar papers in this journal
- Neutrophils contribute to ER stress in lung epithelial cells in the pristane-induced diffuse alveolar hemorrhage mouse model 95%
- Identification of a novel HIF-1α-αMβ2 Integrin-NETosis axis in fibrotic interstitial lung disease 95%
- Bacterial Polyphosphates Induce CXCL4 and Synergize with Complement Anaphylatoxin C5a in Lung Injury 94%
Similar papers in this journal
- Fibroblast-specific IL11 signaling is required for lung fibrosis and inflammation 95%
- The microbiota plays a critical role in the reactivity of lung immune components to innate ligands 94%
- Lipoxin A4/FPR2 signaling mitigates ferroptosis of alveolar epithelial cells via NRF2-dependent pathway during lung ischemia-reperfusion injury 93%
Similar papers in this journal
Similar papers in this journal
"Similar papers" are the closest papers from that journal in the model's embedding space. They show what the match is built on, but the ranking comes mostly from a classifier over the whole training set, not from these examples alone.