Isolation and characterization of endothelial progenitor cells from Rhesus monkeys

Background: Endothelial progenitor cells (EPCs) are increasingly becoming a major focus of regenerative medicine research and practice. The present study was undertaken to establish an appropriate procedure for isolation and characterization of EPCs from Rhesus monkeys for regenerative med...

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Main Authors: Sun Wen, Zheng Lily, Han Pengfei, Kang Y James
Format: Article
Language:English
Published: EDP Sciences 2014-01-01
Series:Regenerative Medicine Research
Subjects:
Online Access:https://www.regenmedres-journal.org/articles/rmr/pdf/2014/01/rmr-2014-2-5.pdf
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spelling doaj-1e9944079f9a440b966cfb703d71002c2020-11-24T22:13:21ZengEDP SciencesRegenerative Medicine Research2050-490X2014-01-012510.1186/2050-490X-2-5rmr-2014-2-5Isolation and characterization of endothelial progenitor cells from Rhesus monkeysSun WenZheng LilyHan PengfeiKang Y JamesBackground: Endothelial progenitor cells (EPCs) are increasingly becoming a major focus of regenerative medicine research and practice. The present study was undertaken to establish an appropriate procedure for isolation and characterization of EPCs from Rhesus monkeys for regenerative medicine research. Result: Selective CD34+ and nonselective mononuclear EPCs were isolated from bone marrow and cultured under varying conditions. The results showed that nonselective mononuclear EPCs were a better choice for high yield of the target cells. The cells grew in M 200 better than in EGM-2, and supplementation with fetal bovine serum promoted cell proliferation; but serum level at 7.5% was better than at 10%. In addition, surface coating of the culture dishes with human fibronectin significantly improved the proliferation and ontogeny of the isolated EPCs. Immunocytochemistry including detection of markers CD34, CD133 and CD31 and double-staining for Ac-LDL and lectin verified the purity of the cultured mononuclear EPCs. Conclusion: By a thorough analysis, we established a practical procedure for isolation and propagation of EPCs from Rhesus monkeys. This procedure would help using these valuable cells for regenerative medicine research.https://www.regenmedres-journal.org/articles/rmr/pdf/2014/01/rmr-2014-2-5.pdfEPCsIsolationCell cultureCell proliferationCharacterizationMonkey
collection DOAJ
language English
format Article
sources DOAJ
author Sun Wen
Zheng Lily
Han Pengfei
Kang Y James
spellingShingle Sun Wen
Zheng Lily
Han Pengfei
Kang Y James
Isolation and characterization of endothelial progenitor cells from Rhesus monkeys
Regenerative Medicine Research
EPCs
Isolation
Cell culture
Cell proliferation
Characterization
Monkey
author_facet Sun Wen
Zheng Lily
Han Pengfei
Kang Y James
author_sort Sun Wen
title Isolation and characterization of endothelial progenitor cells from Rhesus monkeys
title_short Isolation and characterization of endothelial progenitor cells from Rhesus monkeys
title_full Isolation and characterization of endothelial progenitor cells from Rhesus monkeys
title_fullStr Isolation and characterization of endothelial progenitor cells from Rhesus monkeys
title_full_unstemmed Isolation and characterization of endothelial progenitor cells from Rhesus monkeys
title_sort isolation and characterization of endothelial progenitor cells from rhesus monkeys
publisher EDP Sciences
series Regenerative Medicine Research
issn 2050-490X
publishDate 2014-01-01
description Background: Endothelial progenitor cells (EPCs) are increasingly becoming a major focus of regenerative medicine research and practice. The present study was undertaken to establish an appropriate procedure for isolation and characterization of EPCs from Rhesus monkeys for regenerative medicine research. Result: Selective CD34+ and nonselective mononuclear EPCs were isolated from bone marrow and cultured under varying conditions. The results showed that nonselective mononuclear EPCs were a better choice for high yield of the target cells. The cells grew in M 200 better than in EGM-2, and supplementation with fetal bovine serum promoted cell proliferation; but serum level at 7.5% was better than at 10%. In addition, surface coating of the culture dishes with human fibronectin significantly improved the proliferation and ontogeny of the isolated EPCs. Immunocytochemistry including detection of markers CD34, CD133 and CD31 and double-staining for Ac-LDL and lectin verified the purity of the cultured mononuclear EPCs. Conclusion: By a thorough analysis, we established a practical procedure for isolation and propagation of EPCs from Rhesus monkeys. This procedure would help using these valuable cells for regenerative medicine research.
topic EPCs
Isolation
Cell culture
Cell proliferation
Characterization
Monkey
url https://www.regenmedres-journal.org/articles/rmr/pdf/2014/01/rmr-2014-2-5.pdf
work_keys_str_mv AT sunwen isolationandcharacterizationofendothelialprogenitorcellsfromrhesusmonkeys
AT zhenglily isolationandcharacterizationofendothelialprogenitorcellsfromrhesusmonkeys
AT hanpengfei isolationandcharacterizationofendothelialprogenitorcellsfromrhesusmonkeys
AT kangyjames isolationandcharacterizationofendothelialprogenitorcellsfromrhesusmonkeys
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