Title of article :
Glioblastoma Stem Cells Generate Vascular Pericytes to Support Vessel Function and Tumor Growth
Author/Authors :
Lin Cheng، نويسنده , , Zhi Huang، نويسنده , , Wenchao Zhou، نويسنده , , Qiulian Wu، نويسنده , , Shannon Donnola، نويسنده , , James K. Liu، نويسنده , , Xiaoguang Fang، نويسنده , , Andrew E. Sloan، نويسنده , , Yubin Mao، نويسنده , , Justin D. Lathia، نويسنده , , Wang Min، نويسنده , , Roger E. McLendon، نويسنده , , Jeremy N. Rich، نويسنده , , Shideng Bao، نويسنده ,
Issue Information :
هفته نامه با شماره پیاپی سال 2013
Pages :
14
From page :
139
To page :
152
Abstract :
Glioblastomas (GBMs) are highly vascular and lethal brain tumors that display cellular hierarchies containing self-renewing tumorigenic glioma stem cells (GSCs). Because GSCs often reside in perivascular niches and may undergo mesenchymal differentiation, we interrogated GSC potential to generate vascular pericytes. Here, we show that GSCs give rise to pericytes to support vessel function and tumor growth. In vivo cell lineage tracing with constitutive and lineage-specific fluorescent reporters demonstrated that GSCs generate the majority of vascular pericytes. Selective elimination of GSC-derived pericytes disrupts the neovasculature and potently inhibits tumor growth. Analysis of human GBM specimens showed that most pericytes are derived from neoplastic cells. GSCs are recruited toward endothelial cells via the SDF-1/CXCR4 axis and are induced to become pericytes predominantly by transforming growth factor β. Thus, GSCs contribute to vascular pericytes that may actively remodel perivascular niches. Therapeutic targeting of GSC-derived pericytes may effectively block tumor progression and improve antiangiogenic therapy.
Journal title :
CELL
Serial Year :
2013
Journal title :
CELL
Record number :
1021642
Link To Document :
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