PDGFRβ+ perivascular progenitor cells in tumours regulate pericyte differentiation and vascular survival

S Song, AJ Ewald, W Stallcup, Z Werb, G Bergers - Nature cell biology, 2005 - nature.com
S Song, AJ Ewald, W Stallcup, Z Werb, G Bergers
Nature cell biology, 2005nature.com
The microvasculature consists of endothelial cells and their surrounding pericytes. Few
studies on the regulatory mechanisms of tumour angiogenesis have focused on pericytes.
Here we report the identification of tumour-derived PDGFR β+(platelet-derived growth factor
receptor β) progenitor perivascular cells (PPCs) that have the ability to differentiate into
pericytes and regulate vessel stability and vascular survival in tumours. A subset of PDGFR
β+ PPCs is recruited from bone marrow to perivascular sites in tumours. Specific inhibition of …
Abstract
The microvasculature consists of endothelial cells and their surrounding pericytes. Few studies on the regulatory mechanisms of tumour angiogenesis have focused on pericytes. Here we report the identification of tumour-derived PDGFRβ+ (platelet-derived growth factor receptor β) progenitor perivascular cells (PPCs) that have the ability to differentiate into pericytes and regulate vessel stability and vascular survival in tumours. A subset of PDGFRβ+ PPCs is recruited from bone marrow to perivascular sites in tumours. Specific inhibition of PDGFRβ signalling eliminates PDGFRβ+ PPCs and mature pericytes around tumour vessels, leading to vascular hyperdilation and endothelial cell apoptosis in pancreatic islet tumours of transgenic Rip1Tag2 mice.
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