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Article: Strategies for derivation of endothelial lineages from human stem cells

TitleStrategies for derivation of endothelial lineages from human stem cells
Authors
KeywordsEndothelial cells
Tissue engineering
Human stem cells
3D EB formation
Issue Date2019
PublisherBioMed Central Ltd. The Journal's web site is located at http://www.stemcellres.com
Citation
Stem Cell Research & Therapy, 2019, v. 10, p. article no. 200 How to Cite?
AbstractAccumulating evidence demonstrates that pre-vascularization of tissue-engineered constructs can significantly enhance their survival and engraftment upon transplantation. Endothelial cells (ECs), the basic component of vasculatures, are indispensable to the entire process of pre-vascularization. However, the source of ECs still poses an issue. Recent studies confirmed that diverse approaches are available in the derivation of ECs for tissue engineering, such as direct isolation of autologous ECs, reprogramming of somatic cells, and induced differentiation of stem cells in typology. Herein, we discussed a variety of human stem cells (i.e., totipotent, pluripotent, multipotent, oligopotent, and unipotent stem cells), which can be induced to differentiate into ECs and reviewed the multifarious approaches for EC generation, such as 3D EB formation for embryonic stem cells (ESCs), stem cell-somatic cell co-culture, and directed endothelial differentiation with growth factors in conventional 2D culture.
Persistent Identifierhttp://hdl.handle.net/10722/308338
ISSN
2021 Impact Factor: 8.079
2020 SCImago Journal Rankings: 1.599
PubMed Central ID
ISI Accession Number ID

 

DC FieldValueLanguage
dc.contributor.authorXu, M-
dc.contributor.authorHe, J-
dc.contributor.authorZhang, C-
dc.contributor.authorXu, J-
dc.contributor.authorWang, Y-
dc.date.accessioned2021-11-26T00:55:13Z-
dc.date.available2021-11-26T00:55:13Z-
dc.date.issued2019-
dc.identifier.citationStem Cell Research & Therapy, 2019, v. 10, p. article no. 200-
dc.identifier.issn1757-6512-
dc.identifier.urihttp://hdl.handle.net/10722/308338-
dc.description.abstractAccumulating evidence demonstrates that pre-vascularization of tissue-engineered constructs can significantly enhance their survival and engraftment upon transplantation. Endothelial cells (ECs), the basic component of vasculatures, are indispensable to the entire process of pre-vascularization. However, the source of ECs still poses an issue. Recent studies confirmed that diverse approaches are available in the derivation of ECs for tissue engineering, such as direct isolation of autologous ECs, reprogramming of somatic cells, and induced differentiation of stem cells in typology. Herein, we discussed a variety of human stem cells (i.e., totipotent, pluripotent, multipotent, oligopotent, and unipotent stem cells), which can be induced to differentiate into ECs and reviewed the multifarious approaches for EC generation, such as 3D EB formation for embryonic stem cells (ESCs), stem cell-somatic cell co-culture, and directed endothelial differentiation with growth factors in conventional 2D culture.-
dc.languageeng-
dc.publisherBioMed Central Ltd. The Journal's web site is located at http://www.stemcellres.com-
dc.relation.ispartofStem Cell Research & Therapy-
dc.rightsStem Cell Research & Therapy. Copyright © BioMed Central Ltd.-
dc.rightsThis work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.-
dc.subjectEndothelial cells-
dc.subjectTissue engineering-
dc.subjectHuman stem cells-
dc.subject3D EB formation-
dc.titleStrategies for derivation of endothelial lineages from human stem cells-
dc.typeArticle-
dc.identifier.emailZhang, C: zhangcf@hku.hk-
dc.identifier.emailXu, J: xujg1982@connect.hku.hk-
dc.identifier.authorityZhang, C=rp01408-
dc.description.naturepublished_or_final_version-
dc.identifier.doi10.1186/s13287-019-1274-1-
dc.identifier.pmid31286997-
dc.identifier.pmcidPMC6615090-
dc.identifier.scopuseid_2-s2.0-85068939620-
dc.identifier.hkuros321155-
dc.identifier.volume10-
dc.identifier.spagearticle no. 200-
dc.identifier.epagearticle no. 200-
dc.identifier.isiWOS:000475605000002-
dc.publisher.placeUnited Kingdom-

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