| | |  | | | | Record from Web of Science® | | | | | | |
| Expression of VEGFR-2 and AC133 by circulating human CD34(+) cells identifies a population of functional endothelial precursors |
|
|
| Author(s): Peichev M, Naiyer AJ, Pereira D, Zhu ZP, Lane WJ, Williams M, Oz MC, Hicklin DJ, Witte L, Moore MAS, Rafii S |
| Source: BLOOD Volume: 95 Issue: 3 Pages: 952-958 Published: FEB 1 2000 |
| Times Cited: 862 References: 30 |
| Abstract: Emerging data suggest that a subset of circulating human CD34(+) cells have phenotypic features of endothelial cells. Whether these cells are sloughed mature endothelial cells or functional circulating endothelial precursors (CEPs) is not known. Using monoclonal antibodies (MoAbs) to the extracellular domain of the human Vascular endothelial receptor-2 (VEGFR-2), we have shown that 1.2 +/- 0.3% of CD34(+) cells isolated from fetal liver (FL), 2 +/- 0.5% from mobilized peripheral blood, and 1.4 +/- 0.5% from cord blood were VEGFR-2(+). In addition, most CD34(+)VEGFR-2(+) cells express hematopoietic stem cell marker AC133. Because mature endothelial cells do not express AC133, coexpression of VEGFR-2 and AC133 on CD34(+) cells phenotypically Identifies a unique population of CEPs. CD34(+)VEGFR-2(+) cells express endothelial-specific markers, including VE-cadherin and E-selectin, Also, virtually all CD34(+)VEGFR-2(+) cells express the chemokine receptor CXCR4 and migrate in response to stromal derived factor (SDF)-1 or VEGF, To quantitate the plating efficiency of CD34(+) cells that give rise to endothelial colonies, CD34(+) cells derived from FL were Incubated with VEGF and fibroblast growth factor (FGF)-2, Subsequent isolation and plating of nonadherent FL-derived VEGFR-2(+) cells with VEGF and FGF-2 resulted in differentiation of AC133(+) VEGFR-2(+) cells Into adherent AC133(-)VEGFR-2(+)Ac-LDL+ (acetylated low-density lipoprotein) colonies (plating efficiency of 3%). In an In vivo human model, we have found that the neointima formed on the surface of left ventricular assist devices is colonized with AC133(+)VEGFR-2(+) cells. These data suggest that circulating CD34(+) cells expressing VEGFR-2 and AC133 constitute a phenotypically and functionally distinct population of circulating endothelial cells that may play a role In neo-angiogenesis. (C) 2000 by The American Society of Hematology.
|
| Document Type: Article |
| Language: English |
| Reprint Address: Rafii, S (reprint author), Cornell Univ, Weill Med Coll, Div Hematol Oncol, 1300 York Ave,Room C-606, New York, NY 10021 USA |
Addresses:
1. Cornell Univ, Weill Med Coll, Div Hematol Oncol, New York, NY 10021 USA
2. ImClone Syst, Div Mol Cell Biol & Immunol, New York, NY USA
3. Columbia Presbyterian Med Ctr, Dept Cardiothorac Surg, New York, NY USA
4. Mem Sloan Kettering Canc Ctr, Div Dev Hematopoiesis, New York, NY USA |
| Publisher: AMER SOC HEMATOLOGY, 1200 19TH ST, NW, STE 300, WASHINGTON, DC 20036-2422 USA |
| Subject Category: Hematology |
| IDS Number: 278MN |
| ISSN: 0006-4971 |
|
| | | | | | | | | Record from Web of Science® | | | | | | | | | |