4.8 Article

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

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NATURE CELL BIOLOGY
卷 7, 期 9, 页码 870-U16

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NATURE PUBLISHING GROUP
DOI: 10.1038/ncb1288

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资金

  1. NCI NIH HHS [R01 CA095287, P01 CA72006, R01 CA099948, R01 CA95287, R01 CA095287-05, R01 CA109390-01, P01 CA072006-07, R01 CA99948, R01 CA109390, P01 CA072006] Funding Source: Medline
  2. NHLBI NIH HHS [T32 HL007731, 5T32HL007731] Funding Source: Medline

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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 beta(+) ( platelet- derived growth factor receptor beta) 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 beta(+) PPCs is recruited from bone marrow to perivascular sites in tumours. Specific inhibition of PDGFR beta signalling eliminates PDGFR beta(+) 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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