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High-yield isolation of pure fetal endothelial colony forming cells and mesenchymal stem cells from the human full-term placenta

A need to identify a stem cell source for human endothelial colony forming cells (ECFCs) and mesenchymal stem cells (MSCs) that is high yield is crucial for their implementation in ischemia. Our lab has developed an isolation protocol to do this using full-term human villous placental tissue. This p...

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Detalles Bibliográficos
Autores principales: Nano, Rachel, Sim, Seen Ling, Shafiee, Abbas, Khosrotehrani, Kiarash, Patel, Jatin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9059155/
https://www.ncbi.nlm.nih.gov/pubmed/35509970
http://dx.doi.org/10.1016/j.xpro.2022.101354
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author Nano, Rachel
Sim, Seen Ling
Shafiee, Abbas
Khosrotehrani, Kiarash
Patel, Jatin
author_facet Nano, Rachel
Sim, Seen Ling
Shafiee, Abbas
Khosrotehrani, Kiarash
Patel, Jatin
author_sort Nano, Rachel
collection PubMed
description A need to identify a stem cell source for human endothelial colony forming cells (ECFCs) and mesenchymal stem cells (MSCs) that is high yield is crucial for their implementation in ischemia. Our lab has developed an isolation protocol to do this using full-term human villous placental tissue. This protocol describes enzymatic tissue digestion followed by MACS and FACS, achieving an 8 times greater yield versus traditional isolation techniques and delivering pure fetal stem cell colonies within 21–28 days cell culture. For complete details on the use and execution of this protocol, please refer to Patel et al. (2013) and Patel et al. (2014).
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spelling pubmed-90591552022-05-03 High-yield isolation of pure fetal endothelial colony forming cells and mesenchymal stem cells from the human full-term placenta Nano, Rachel Sim, Seen Ling Shafiee, Abbas Khosrotehrani, Kiarash Patel, Jatin STAR Protoc Protocol A need to identify a stem cell source for human endothelial colony forming cells (ECFCs) and mesenchymal stem cells (MSCs) that is high yield is crucial for their implementation in ischemia. Our lab has developed an isolation protocol to do this using full-term human villous placental tissue. This protocol describes enzymatic tissue digestion followed by MACS and FACS, achieving an 8 times greater yield versus traditional isolation techniques and delivering pure fetal stem cell colonies within 21–28 days cell culture. For complete details on the use and execution of this protocol, please refer to Patel et al. (2013) and Patel et al. (2014). Elsevier 2022-04-23 /pmc/articles/PMC9059155/ /pubmed/35509970 http://dx.doi.org/10.1016/j.xpro.2022.101354 Text en © 2022 The Author(s) https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Protocol
Nano, Rachel
Sim, Seen Ling
Shafiee, Abbas
Khosrotehrani, Kiarash
Patel, Jatin
High-yield isolation of pure fetal endothelial colony forming cells and mesenchymal stem cells from the human full-term placenta
title High-yield isolation of pure fetal endothelial colony forming cells and mesenchymal stem cells from the human full-term placenta
title_full High-yield isolation of pure fetal endothelial colony forming cells and mesenchymal stem cells from the human full-term placenta
title_fullStr High-yield isolation of pure fetal endothelial colony forming cells and mesenchymal stem cells from the human full-term placenta
title_full_unstemmed High-yield isolation of pure fetal endothelial colony forming cells and mesenchymal stem cells from the human full-term placenta
title_short High-yield isolation of pure fetal endothelial colony forming cells and mesenchymal stem cells from the human full-term placenta
title_sort high-yield isolation of pure fetal endothelial colony forming cells and mesenchymal stem cells from the human full-term placenta
topic Protocol
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9059155/
https://www.ncbi.nlm.nih.gov/pubmed/35509970
http://dx.doi.org/10.1016/j.xpro.2022.101354
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