TY - JOUR
T1 - Biologic Properties of Endothelial Progenitor Cells and Their Potential for Cell Therapy
AU - Young, Pampee P.
AU - Vaughan, Douglas E.
AU - Hatzopoulos, Antonis K.
N1 - Funding Information:
This work was supported by an American Heart Association grant (PPY), Veterans Affairs (PPY), and National Institutes of Health grant HL083958 (AKH).
PY - 2007/5
Y1 - 2007/5
N2 - Recent studies indicate that portions of ischemic and tumor neovasculature are derived by neovasculogenesis, whereby bone marrow (BM)-derived circulating endothelial progenitor cells (EPCs) home to sites of regenerative or malignant growth and contribute to blood vessel formation. Recent data from animal models suggest that a variety of cell types, including unfractionated BM mononuclear cells and those obtained by ex vivo expansion of human peripheral blood or enriched progenitors, can function as EPCs to promote tissue vasculogenesis, regeneration, and repair when introduced in vivo. The promising preclinical results have led to several human clinical trials using BM as a potential source of EPCs in cardiac repair as well as ongoing basic research on using EPCs in tissue engineering or as cell therapy to target tumor growth.
AB - Recent studies indicate that portions of ischemic and tumor neovasculature are derived by neovasculogenesis, whereby bone marrow (BM)-derived circulating endothelial progenitor cells (EPCs) home to sites of regenerative or malignant growth and contribute to blood vessel formation. Recent data from animal models suggest that a variety of cell types, including unfractionated BM mononuclear cells and those obtained by ex vivo expansion of human peripheral blood or enriched progenitors, can function as EPCs to promote tissue vasculogenesis, regeneration, and repair when introduced in vivo. The promising preclinical results have led to several human clinical trials using BM as a potential source of EPCs in cardiac repair as well as ongoing basic research on using EPCs in tissue engineering or as cell therapy to target tumor growth.
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U2 - 10.1016/j.pcad.2007.02.004
DO - 10.1016/j.pcad.2007.02.004
M3 - Article
C2 - 17498522
AN - SCOPUS:34247857552
SN - 0033-0620
VL - 49
SP - 421
EP - 429
JO - Progress in Cardiovascular Diseases
JF - Progress in Cardiovascular Diseases
IS - 6
ER -