z-logo
open-access-imgOpen Access
Angiopoietin-1 protects against endotoxin-induced neonatal lung injury and alveolar simplification in mice
Author(s) -
Umar Salimi,
Heather Menden,
Sherry M Mabry,
Xia Sheng,
Venkatesh Sampath
Publication year - 2021
Publication title -
pediatric research
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.056
H-Index - 150
eISSN - 1530-0447
pISSN - 0031-3998
DOI - 10.1038/s41390-021-01544-0
Subject(s) - lung , inflammation , medicine , sepsis , immunology , bronchopulmonary dysplasia , endothelial stem cell , biology , in vitro , pregnancy , biochemistry , genetics , gestational age
Sepsis in premature newborns is a risk factor for bronchopulmonary dysplasia (BPD), but underlying mechanisms of lung injury remain unclear. Aberrant expression of endothelial cell (EC) angiopoietin 2 (ANGPT2) disrupts angiopoietin 1 (ANGPT1)/TIE2-mediated endothelial quiescence, and is implicated in sepsis-induced acute respiratory distress syndrome in adults. We hypothesized that recombinant ANGPT1 will mitigate sepsis-induced ANGPT2 expression, inflammation, acute lung injury (ALI), and alveolar remodeling in the saccular lung.

The content you want is available to Zendy users.

Already have an account? Click here to sign in.
Having issues? You can contact us here