4.5 Review

Endothelial progenitor cells: identity defined?

Journal

JOURNAL OF CELLULAR AND MOLECULAR MEDICINE
Volume 13, Issue 1, Pages 87-102

Publisher

WILEY
DOI: 10.1111/j.1582-4934.2008.00598.x

Keywords

endothelial progenitor cells; haematopoietic cells; CD34; CD45; CD133

Funding

  1. Fund for Scientific Research, Flanders [G.0096.05]
  2. National Institute of Neurological Disorders and Stroke [P50 NS052606]
  3. Department of Defense [NF043019]
  4. Riley Children's Foundation [W81XWH05-1-0161]
  5. National Institutes of Health [P30 CA82709, 1 P01 HL085036, 2 P01 HL05358611A1]
  6. National Institutes of Health/National Heart, Lung, and Blood Institute [R21 HL088885]
  7. NATIONAL CANCER INSTITUTE [P30CA082709] Funding Source: NIH RePORTER
  8. NATIONAL HEART, LUNG, AND BLOOD INSTITUTE [R21HL088885, P50HL085036, P01HL053586] Funding Source: NIH RePORTER
  9. NATIONAL INSTITUTE OF NEUROLOGICAL DISORDERS AND STROKE [P50NS052606] Funding Source: NIH RePORTER

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In the past decade, researchers have gained important insights on the role of bone marrow (BM)-derived cells in adult neovascularization. A subset of BM-derived cells, called endothelial progenitor cells (EPCs), has been of particular interest, as these cells were suggested to home to sites of neovascularization and neoendothelialization and differentiate into endothelial cells (ECs) in situ, a process referred to as postnatal vasculogenesis. Therefore, EPCs were proposed as a potential regenerative tool for treating human vascular disease and a possible target to restrict vessel growth in tumour pathology. However, conflicting results have been reported in the field, and the identification, characterization, and exact role of EPCs in vascular biology is still a subject of much discussion. The focus of this review is on the controversial issues in the field of EPCs which are related to the lack of a unique EPC marker, identification challenges related to the paucity of EPCs in the circulation, and the important phenotypical and functional overlap between EPCs, haematopoietic cells and mature ECs. We also discuss our recent findings on the origin of endothelial outgrowth cells (EOCs), showing that this in vitro defined EC population does not originate from circulating CD133(+) cells or CD45(+) haematopoietic cells.

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