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Tie2-Expressing Monocytes and Tumor Angiogenesis: Regulation by Hypoxia and Angiopoietin-2

Claire E. Lewis, Michele De Palma and Luigi Naldini
Claire E. Lewis
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Michele De Palma
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Luigi Naldini
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DOI: 10.1158/0008-5472.CAN-07-1684 Published September 2007
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    Figure 1.

    TEM recruitment to tumors. A, a human glioblastoma orthotopically injected in the mouse brain shows several TEMs (labeled by green fluorescent protein, green) associated with the tumor blood vessels (red, stained by an anti-CD31 monoclonal antibody). B, a human gastric adenocarcinoma stained with an anti-Tie2 monoclonal antibody. Note the Tie2+ blood vessels and the presence of scattered Tie2+ mononuclear cells (TEMs, arrows) in the stroma. Section was counterstained by H&E. C, a human colon carcinoma stained with a fluorescent anti-Tie2 monoclonal antibody (red) shows Tie2+ blood vessels and scattered Tie2+CD14+ TEMs (arrows). Green, CD14+ monocytes were stained with a FITC-conjugated anti-CD14 monoclonal antibody. Double-positive cells (i.e., TEMs) appear yellow. Bar, 50 μm.

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Cancer Research: 67 (18)
September 2007
Volume 67, Issue 18
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Tie2-Expressing Monocytes and Tumor Angiogenesis: Regulation by Hypoxia and Angiopoietin-2
Claire E. Lewis, Michele De Palma and Luigi Naldini
Cancer Res September 15 2007 (67) (18) 8429-8432; DOI: 10.1158/0008-5472.CAN-07-1684

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Tie2-Expressing Monocytes and Tumor Angiogenesis: Regulation by Hypoxia and Angiopoietin-2
Claire E. Lewis, Michele De Palma and Luigi Naldini
Cancer Res September 15 2007 (67) (18) 8429-8432; DOI: 10.1158/0008-5472.CAN-07-1684
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    • Abstract
    • Bone Marrow–Derived Cells Regulate Tumor Angiogenesis
    • Identification of TEMs
    • Role of TEMs in Tumor Angiogenesis: Insights from Mouse Tumor Models
    • Regulation of TEMs by the Tumor Microenvironment
    • Concluding Remarks
    • Acknowledgments
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