Obligatory participation of macrophages in an angiopoietin 2-mediated cell death switch

Author:

Rao Sujata1,Lobov Ivan B.1,Vallance Jefferson E.1,Tsujikawa Kaoru2,Shiojima Ichiro3,Akunuru Shailaja4,Walsh Kenneth3,Benjamin Laura E.2,Lang Richard A.1

Affiliation:

1. Division of Pediatric Ophthalmology, Division of Developmental Biology,Children's Hospital Research Foundation and Department of Ophthalmology,University of Cincinnati, Cincinnati, OH 45229, USA.

2. Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, MA 02215, USA.

3. Whitaker Cardiovascular Institute, Boston University School of Medicine,Boston MA 02118, USA.

4. Graduate Program of Molecular and Developmental Biology, College of Medicine,University of Cincinnati, Cincinnati, OH45229, USA.

Abstract

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.

Publisher

The Company of Biologists

Subject

Developmental Biology,Molecular Biology

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