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dc.contributor.authorBryan, N
dc.contributor.authorLewis, FC
dc.contributor.authorBond, D
dc.contributor.authorStanley, C
dc.contributor.authorHunt, JA
dc.date.accessioned2021-05-21T15:14:21Z
dc.date.available2012-12-07
dc.date.available2021-05-21T15:14:21Z
dc.date.issued2013-01-22
dc.identifier.citationBryan N, Lewis FC, Bond D, Stanley C, Hunt JA (2013) Evaluation of a Novel Non-Destructive Catch and Release Technology for Harvesting Autologous Adult Stem Cells. PLoS ONE 8(1): e53933. doi:10.1371/journal.pone.0053933en_US
dc.identifier.urihttps://qmro.qmul.ac.uk/xmlui/handle/123456789/71988
dc.description.abstractBACKGROUND: Cell based therapies are required now to meet the critical care needs of paediatrics and healthy ageing in an increasingly long-lived human population. Repair of compromised tissue by supporting autologous regeneration is a life changing objective uniting the fields of medical science and engineering. Adipose stem cells (adSCs) are a compelling candidate for use in cell based medicine due to their plasticity and residence in numerous tissues. Adipose found in all animals contains a relatively high concentration of stem cells and is easily isolated by a minimally invasive clinical intervention; such as liposuction. METHODS: This study utilised primary rat adipose to validate a novel strategy for selecting adult stem cells. Experiments explored the use of large, very dense cell-specific antibody loaded isolation beads (diameter 5x-10x greater than target cells) which overcome the problem of endocytosis and have proved to be very effective in cell isolation from minimally processed primary tissue. The technique also benefited from pH mediated release, which enabled elution of captured cells using a simple pH shift. RESULTS: Large beads successfully captured and released adSCs from rat adipose, which were characterised using a combination of microscopy, flow cytometry and PCR. The resultant purified cell population retains minimal capture artefact facilitating autologous reperfusion or application in in vitro models. CONCLUSION: Although evidenced here for adSCs, this approach provides a technological advance at a platform level; whereby it can be applied to isolate any cell population for which there is a characterised surface antigen.en_US
dc.format.extente53933
dc.languageeng
dc.publisherPublic Library of Scienceen_US
dc.relation.ispartofPLoS One
dc.rightsThis is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
dc.subjectAdipose Tissueen_US
dc.subjectAdulten_US
dc.subjectAdult Stem Cellsen_US
dc.subjectAnimalsen_US
dc.subjectCell Counten_US
dc.subjectCell Separationen_US
dc.subjectFlow Cytometryen_US
dc.subjectHumansen_US
dc.subjectMicroscopy, Fluorescenceen_US
dc.subjectRatsen_US
dc.subjectReproducibility of Resultsen_US
dc.subjectReverse Transcriptase Polymerase Chain Reactionen_US
dc.subjectStem Cellsen_US
dc.subjectThy-1 Antigensen_US
dc.titleEvaluation of a novel non-destructive catch and release technology for harvesting autologous adult stem cells.en_US
dc.typeArticleen_US
dc.rights.holder© 2013 Bryan et al.
dc.identifier.doi10.1371/journal.pone.0053933
pubs.author-urlhttps://www.ncbi.nlm.nih.gov/pubmed/23349768en_US
pubs.issue1en_US
pubs.notesNot knownen_US
pubs.publication-statusPublisheden_US
pubs.publisher-urlhttps://doi.org/10.1371/journal.pone.0053933
pubs.volume8en_US
dcterms.dateAccepted2012-12-07
rioxxterms.funderDefault funderen_US
rioxxterms.identifier.projectDefault projecten_US


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