Vessel wall-derived endothelial cells rapidly proliferate because they contain a complete hierarchy of endothelial progenitor cells

David A. Ingram, Laura E. Mead, Daniel B. Moore, Wayne Woodard, Amy Fenoglio, Mervin C. Yoder

Research output: Contribution to journalArticle

419 Citations (Scopus)

Abstract

Endothelial progenitor cells (EPCs) can be isolated from adult peripheral and umbilical cord blood and expanded exponentially ex vivo. In contrast, human umbilical vein endethelial cells (HUVECs) or human aortic endethelial cells (HAECs) derived from vessel walls are widely considered to be differentiated, mature endothelial cells (ECs). However, similar to adult- and cord blood-derived EPCs, HUVECs and HAECs derived from vessel walls can be passaged for at least 40 population doublings in vitro. Based on this paradox, we tested whether EPCs reside in HUVECs or HAECs utilizing a novel single cell deposition assay that discriminates EPCs based on their proliferative and clonogenic potential. We demonstrate that a complete hierarchy of EPCs can be identified in HUVECs and HAECs derived from vessel walls and discriminated by their clonogenic and proliferative potential. This study provides evidence that a diversity of EPCs exists in human vessels and provides a conceptual framework for determining both the origin and function of EPCs in maintaining vessel integrity.

Original languageEnglish
Pages (from-to)2783-2786
Number of pages4
JournalBlood
Volume105
Issue number7
DOIs
StatePublished - Apr 1 2005

Fingerprint

Endothelial cells
Endothelial Cells
Umbilical Veins
Fetal Blood
Blood
Endothelial Progenitor Cells
Assays

ASJC Scopus subject areas

  • Hematology

Cite this

Vessel wall-derived endothelial cells rapidly proliferate because they contain a complete hierarchy of endothelial progenitor cells. / Ingram, David A.; Mead, Laura E.; Moore, Daniel B.; Woodard, Wayne; Fenoglio, Amy; Yoder, Mervin C.

In: Blood, Vol. 105, No. 7, 01.04.2005, p. 2783-2786.

Research output: Contribution to journalArticle

Ingram, David A. ; Mead, Laura E. ; Moore, Daniel B. ; Woodard, Wayne ; Fenoglio, Amy ; Yoder, Mervin C. / Vessel wall-derived endothelial cells rapidly proliferate because they contain a complete hierarchy of endothelial progenitor cells. In: Blood. 2005 ; Vol. 105, No. 7. pp. 2783-2786.
@article{4d8cf50bf21445c09ce82982feae3753,
title = "Vessel wall-derived endothelial cells rapidly proliferate because they contain a complete hierarchy of endothelial progenitor cells",
abstract = "Endothelial progenitor cells (EPCs) can be isolated from adult peripheral and umbilical cord blood and expanded exponentially ex vivo. In contrast, human umbilical vein endethelial cells (HUVECs) or human aortic endethelial cells (HAECs) derived from vessel walls are widely considered to be differentiated, mature endothelial cells (ECs). However, similar to adult- and cord blood-derived EPCs, HUVECs and HAECs derived from vessel walls can be passaged for at least 40 population doublings in vitro. Based on this paradox, we tested whether EPCs reside in HUVECs or HAECs utilizing a novel single cell deposition assay that discriminates EPCs based on their proliferative and clonogenic potential. We demonstrate that a complete hierarchy of EPCs can be identified in HUVECs and HAECs derived from vessel walls and discriminated by their clonogenic and proliferative potential. This study provides evidence that a diversity of EPCs exists in human vessels and provides a conceptual framework for determining both the origin and function of EPCs in maintaining vessel integrity.",
author = "Ingram, {David A.} and Mead, {Laura E.} and Moore, {Daniel B.} and Wayne Woodard and Amy Fenoglio and Yoder, {Mervin C.}",
year = "2005",
month = "4",
day = "1",
doi = "10.1182/blood-2004-08-3057",
language = "English",
volume = "105",
pages = "2783--2786",
journal = "Blood",
issn = "0006-4971",
publisher = "American Society of Hematology",
number = "7",

}

TY - JOUR

T1 - Vessel wall-derived endothelial cells rapidly proliferate because they contain a complete hierarchy of endothelial progenitor cells

AU - Ingram, David A.

AU - Mead, Laura E.

AU - Moore, Daniel B.

AU - Woodard, Wayne

AU - Fenoglio, Amy

AU - Yoder, Mervin C.

PY - 2005/4/1

Y1 - 2005/4/1

N2 - Endothelial progenitor cells (EPCs) can be isolated from adult peripheral and umbilical cord blood and expanded exponentially ex vivo. In contrast, human umbilical vein endethelial cells (HUVECs) or human aortic endethelial cells (HAECs) derived from vessel walls are widely considered to be differentiated, mature endothelial cells (ECs). However, similar to adult- and cord blood-derived EPCs, HUVECs and HAECs derived from vessel walls can be passaged for at least 40 population doublings in vitro. Based on this paradox, we tested whether EPCs reside in HUVECs or HAECs utilizing a novel single cell deposition assay that discriminates EPCs based on their proliferative and clonogenic potential. We demonstrate that a complete hierarchy of EPCs can be identified in HUVECs and HAECs derived from vessel walls and discriminated by their clonogenic and proliferative potential. This study provides evidence that a diversity of EPCs exists in human vessels and provides a conceptual framework for determining both the origin and function of EPCs in maintaining vessel integrity.

AB - Endothelial progenitor cells (EPCs) can be isolated from adult peripheral and umbilical cord blood and expanded exponentially ex vivo. In contrast, human umbilical vein endethelial cells (HUVECs) or human aortic endethelial cells (HAECs) derived from vessel walls are widely considered to be differentiated, mature endothelial cells (ECs). However, similar to adult- and cord blood-derived EPCs, HUVECs and HAECs derived from vessel walls can be passaged for at least 40 population doublings in vitro. Based on this paradox, we tested whether EPCs reside in HUVECs or HAECs utilizing a novel single cell deposition assay that discriminates EPCs based on their proliferative and clonogenic potential. We demonstrate that a complete hierarchy of EPCs can be identified in HUVECs and HAECs derived from vessel walls and discriminated by their clonogenic and proliferative potential. This study provides evidence that a diversity of EPCs exists in human vessels and provides a conceptual framework for determining both the origin and function of EPCs in maintaining vessel integrity.

UR - http://www.scopus.com/inward/record.url?scp=15944381205&partnerID=8YFLogxK

UR - http://www.scopus.com/inward/citedby.url?scp=15944381205&partnerID=8YFLogxK

U2 - 10.1182/blood-2004-08-3057

DO - 10.1182/blood-2004-08-3057

M3 - Article

C2 - 15585655

AN - SCOPUS:15944381205

VL - 105

SP - 2783

EP - 2786

JO - Blood

JF - Blood

SN - 0006-4971

IS - 7

ER -