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Vascular endothelial growth factor enhances macrophage clearance of apoptotic cells
Author(s) -
M.T. Kearns,
Samay Dalal,
Sarah A. Horstmann,
Tiffany R. Richens,
Takeshi Tanaka,
Jenna M. Doe,
Darren M. Boé,
Norbert F. Voelkel,
Laimute TarasevicieneStewart,
William J. Janssen,
Chun Geun Lee,
Jack A. Elias,
Donna L. Bratton,
Rubin M. Tuder,
Peter M. Henson,
R. William Vandivier
Publication year - 2012
Publication title -
ajp lung cellular and molecular physiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.892
H-Index - 163
eISSN - 1522-1504
pISSN - 1040-0605
DOI - 10.1152/ajplung.00116.2011
Subject(s) - apoptosis , vascular endothelial growth factor , macrophage , microbiology and biotechnology , monocyte , in vivo , cell , chemistry , cancer research , biology , immunology , in vitro , vegf receptors , biochemistry
Efficient clearance of apoptotic cells from the lung by alveolar macrophages is important for the maintenance of tissue structure and function. Lung tissue from humans with emphysema contains increased numbers of apoptotic cells and decreased levels of vascular endothelial growth factor (VEGF). Mice treated with VEGF receptor inhibitors have increased numbers of apoptotic cells and develop emphysema. We hypothesized that VEGF regulates apoptotic cell clearance by alveolar macrophages (AM) via its interaction with VEGF receptor 1 (VEGF R1). Our data show that the uptake of apoptotic cells by murine AMs and human monocyte-derived macrophages is inhibited by depletion of VEGF and that VEGF activates Rac1. Antibody blockade or pharmacological inhibition of VEGF R1 activity also decreased apoptotic cell uptake ex vivo. Conversely, overexpression of VEGF significantly enhanced apoptotic cell uptake by AMs in vivo. These results indicate that VEGF serves a positive regulatory role via its interaction with VEGF R1 to activate Rac1 and enhance AM apoptotic cell clearance.

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