周细胞
生物
血管生成
祖细胞
细胞生物学
壁细胞
血小板源性生长因子受体
癌症研究
骨髓
血小板衍生生长因子
病理
生长因子
干细胞
内皮干细胞
受体
免疫学
医学
生物化学
体外
作者
Steven Song,Andrew J. Ewald,William B. Stallcup,Zena Werb,Gabriele Bergers
摘要
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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