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Recent studies have found that bone marrow-derived cells give rise to endothelial cells during states of tissue repair and
disease. We have found that one key integrin, integrin-α4β1, promotes the homing of circulating endothelial progenitor cells
(EPCs) to sites of ongoing tissue repair. This integrin facilitates the adhesion of EPCs to the vascular endothelium in inflamed
tissue or within tumors. We demonstrate how to identify, isolate, purify, and characterize EPCs. We also demonstrate in vivo analysis of the roles of bone marrow-derived cells in tumor growth and angiogenesis by demonstrating adoptive transfer, bone
marrow transplantation, tumor models, and immunohistochemistry for markers of blood and endothelial vessels. Finally, we show
how to characterize cell adhesion mechanisms regulating bone marrow-derived progenitor cell trafficking.
Affiliation(s): (3) Department of Orthopaedic Surgery, Schulthess Klinik, Zurich, Switzerland
(4) Moores UCSD Cancer Center, University of California, San Diego, California, USA
(4) Moores UCSD Cancer Center, University of California, San Diego, California, USA
Book Title: Angiogenesis Protocols: Second Edition
Series: Methods in Molecular Biology | Volume: 467 | Pub. Date: Dec-01-2008 | Page Range: 139-155 | DOI: 10.1007/978-1-59745-241-0_8
Subject: Cell Biology
Key Words: Angiogenesis - CD34 - endothelial progenitor cell - Lin−
- lymphangiogenesis - peripheral blood mononuclear cell - Sca1 - stem cell
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