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Obligatory participation of macrophages in an angiopoietin 2-mediated cell death switch
Author(s) -
Sujata Rao,
Ivan B. Lobov,
Jefferson E. Vallance,
Kaoru Tsujikawa,
Ichiro Shiojima,
Shailaja Akunuru,
Kenneth Walsh,
Laura E. Benjamin,
Richard A. Lang
Publication year - 2007
Publication title -
development
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.754
H-Index - 325
eISSN - 1477-9129
pISSN - 0950-1991
DOI - 10.1242/dev.012187
Subject(s) - biology , microbiology and biotechnology , macrophage , wnt signaling pathway , angiopoietin receptor , signal transduction , angiopoietin , programmed cell death , cell cycle , ligand (biochemistry) , cell , downregulation and upregulation , function (biology) , receptor , apoptosis , cancer research , genetics , gene , vascular endothelial growth factor , vegf receptors , in vitro
Macrophages have a critical function in the recognition and engulfment of dead cells. In some settings, macrophages also actively signal programmed cell death. Here we show that during developmentally scheduled vascular regression, resident macrophages are an obligatory participant in a signaling switch that favors death over survival. This switch occurs when the signaling ligand angiopoietin 2 has the dual effect of suppressing survival signaling in vascular endothelial cells (VECs) and stimulating Wnt ligand production by macrophages. In response to the Wnt ligand, VECs enter the cell cycle and in the absence of survival signals, die from G1 phase of the cell cycle. We propose that this mechanism represents an adaptation to ensure that the macrophage and its disposal capability are on hand when cell death occurs.

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