Endothelial Progenitors: A Consensus Statement on Nomenclature.
Identifieur interne : 000D34 ( PubMed/Checkpoint ); précédent : 000D33; suivant : 000D35Endothelial Progenitors: A Consensus Statement on Nomenclature.
Auteurs : Reinhold J. Medina [Royaume-Uni] ; Chad L. Barber [États-Unis] ; Florence Sabatier [France] ; Francoise Dignat-George [France] ; Juan M. Melero-Martin [États-Unis] ; Kiarash Khosrotehrani [Australie] ; Osamu Ohneda [Japon] ; Anna M. Randi [Royaume-Uni] ; Jerry K Y. Chan [Singapour] ; Teruhide Yamaguchi [Japon] ; Victor W M. Van Hinsbergh [Pays-Bas] ; Mervin C. Yoder [États-Unis] ; Alan W. Stitt [Royaume-Uni]Source :
- Stem cells translational medicine [ 2157-6564 ] ; 2017.
Abstract
Endothelial progenitor cell (EPC) nomenclature remains ambiguous and there is a general lack of concordance in the stem cell field with many distinct cell subtypes continually grouped under the term "EPC." It would be highly advantageous to agree on standards to confirm an endothelial progenitor phenotype and this should include detailed immunophenotyping, potency assays, and clear separation from hematopoietic angiogenic cells which are not endothelial progenitors. In this review, we seek to discourage the indiscriminate use of "EPCs," and instead propose precise terminology based on defining cellular phenotype and function. Endothelial colony forming cells and myeloid angiogenic cells are examples of two distinct and well-defined cell types that have been considered EPCs because they both promote vascular repair, albeit by completely different mechanisms of action. It is acknowledged that scientific nomenclature should be a dynamic process driven by technological and conceptual advances; ergo the ongoing "EPC" nomenclature ought not to be permanent and should become more precise in the light of strong scientific evidence. This is especially important as these cells become recognized for their role in vascular repair in health and disease and, in some cases, progress toward use in cell therapy. Stem Cells Translational Medicine 2017;6:1316-1320.
DOI: 10.1002/sctm.16-0360
PubMed: 28296182
Affiliations:
- Australie, France, Japon, Pays-Bas, Royaume-Uni, Singapour, États-Unis
- Angleterre, Californie, Grand Londres, Hollande-Septentrionale, Indiana, Massachusetts, Provence-Alpes-Côte d'Azur
- Amsterdam, Londres, Marseille
- Université d'Aix-Marseille
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<front><div type="abstract" xml:lang="en">Endothelial progenitor cell (EPC) nomenclature remains ambiguous and there is a general lack of concordance in the stem cell field with many distinct cell subtypes continually grouped under the term "EPC." It would be highly advantageous to agree on standards to confirm an endothelial progenitor phenotype and this should include detailed immunophenotyping, potency assays, and clear separation from hematopoietic angiogenic cells which are not endothelial progenitors. In this review, we seek to discourage the indiscriminate use of "EPCs," and instead propose precise terminology based on defining cellular phenotype and function. Endothelial colony forming cells and myeloid angiogenic cells are examples of two distinct and well-defined cell types that have been considered EPCs because they both promote vascular repair, albeit by completely different mechanisms of action. It is acknowledged that scientific nomenclature should be a dynamic process driven by technological and conceptual advances; ergo the ongoing "EPC" nomenclature ought not to be permanent and should become more precise in the light of strong scientific evidence. This is especially important as these cells become recognized for their role in vascular repair in health and disease and, in some cases, progress toward use in cell therapy. Stem Cells Translational Medicine 2017;6:1316-1320.</div>
</front>
</TEI>
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<ArticleTitle>Endothelial Progenitors: A Consensus Statement on Nomenclature.</ArticleTitle>
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<Abstract><AbstractText>Endothelial progenitor cell (EPC) nomenclature remains ambiguous and there is a general lack of concordance in the stem cell field with many distinct cell subtypes continually grouped under the term "EPC." It would be highly advantageous to agree on standards to confirm an endothelial progenitor phenotype and this should include detailed immunophenotyping, potency assays, and clear separation from hematopoietic angiogenic cells which are not endothelial progenitors. In this review, we seek to discourage the indiscriminate use of "EPCs," and instead propose precise terminology based on defining cellular phenotype and function. Endothelial colony forming cells and myeloid angiogenic cells are examples of two distinct and well-defined cell types that have been considered EPCs because they both promote vascular repair, albeit by completely different mechanisms of action. It is acknowledged that scientific nomenclature should be a dynamic process driven by technological and conceptual advances; ergo the ongoing "EPC" nomenclature ought not to be permanent and should become more precise in the light of strong scientific evidence. This is especially important as these cells become recognized for their role in vascular repair in health and disease and, in some cases, progress toward use in cell therapy. Stem Cells Translational Medicine 2017;6:1316-1320.</AbstractText>
<CopyrightInformation>© 2017 The Authors Stem Cells Translational Medicine published by Wiley Periodicals, Inc. on behalf of AlphaMed Press.</CopyrightInformation>
</Abstract>
<AuthorList CompleteYN="Y"><Author ValidYN="Y"><LastName>Medina</LastName>
<ForeName>Reinhold J</ForeName>
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<ForeName>Chad L</ForeName>
<Initials>CL</Initials>
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<ForeName>Florence</ForeName>
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<Author ValidYN="Y"><LastName>Melero-Martin</LastName>
<ForeName>Juan M</ForeName>
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<AffiliationInfo><Affiliation>Department of Surgery, Harvard Medical School, Boston, Massachusetts, USA.</Affiliation>
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<AffiliationInfo><Affiliation>Harvard Stem Cell Institute, Cambridge, Massachusetts, USA.</Affiliation>
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<AffiliationInfo><Affiliation>University of Queensland Diamantina Institute, Translational Research Institute, Woolloongabba, Queensland, Australia.</Affiliation>
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<ForeName>Osamu</ForeName>
<Initials>O</Initials>
<AffiliationInfo><Affiliation>Lab of Regenerative Medicine and Stem Cell Biology, University of Tsukuba, Tsukuba, Japan.</Affiliation>
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