Decellularised Extracellular Matrix Decorated Pcl Polyhipe Scaffolds for Enhanced Cellular Activity, Integration and Angiogenesis
| dc.contributor.author | Dikici, Serkan | |
| dc.contributor.author | Aldemir Dikici, Betül | |
| dc.contributor.author | MacNeil, Sheila | |
| dc.contributor.author | Claeyssens, Frederik | |
| dc.date.accessioned | 2021-11-06T09:49:31Z | |
| dc.date.available | 2021-11-06T09:49:31Z | |
| dc.date.issued | 2021 | |
| dc.description.abstract | Wound healing involves a complex series of events where cell-cell and cell-extracellular matrix (ECM) interactions play a key role. Wounding can be simple, such as the loss of the epithelial integrity, or deeper and more complex, reaching to subcutaneous tissues, including blood vessels, muscles and nerves. Rapid neovascularisation of the wounded area is crucial for wound healing as it has a key role in supplying oxygen and nutrients during the highly demanding proliferative phase and transmigration of inflammatory cells to the wound area. One approach to circumvent delayed neovascularisation is the exogenous use of pro-angiogenic factors, which is expensive, highly dose-dependent, and the delivery of them requires a very well-controlled system to avoid leaky, highly permeable and haemorrhagic blood vessel formation. In this study, we decorated polycaprolactone (PCL)-based polymerised high internal phase emulsion (PolyHIPE) scaffolds with fibroblast-derived ECM to assess fibroblast, endothelial cell and keratinocyte activity in vitro and angiogenesis in ex ovo chick chorioallantoic membrane (CAM) assays. Our results showed that the inclusion of ECM in the scaffolds increased the metabolic activity of three types of cells that play a key role in wound healing and stimulated angiogenesis in ex ovo CAM assays over 7 days. Herein, we demonstrated that fibroblast-ECM functionalised PCL PolyHIPE scaffolds appear to have great potential to be used as an active wound dressing to promote angiogenesis and wound healing. | en_US |
| dc.description.sponsorship | The authors are grateful to the Turkish Ministry of National Education for the funding SD and BAD. They also acknowledge the Engineering and Physical Sciences Research Council (EPSRC grant EP/I007695/1) and the Medical Research Council (MRC grant MR/L012669/1) for funding the equipment used in this study. | en_US |
| dc.identifier.doi | 10.1039/d1bm01262b | |
| dc.identifier.issn | 2047-4830 | |
| dc.identifier.issn | 2047-4849 | |
| dc.identifier.scopus | 2-s2.0-85117529344 | |
| dc.identifier.uri | https://doi.org/10.1039/d1bm01262b | |
| dc.identifier.uri | https://hdl.handle.net/11147/11440 | |
| dc.language.iso | en | en_US |
| dc.publisher | Royal Society of Chemistry | en_US |
| dc.relation.ispartof | Biomaterials Science | en_US |
| dc.rights | info:eu-repo/semantics/openAccess | en_US |
| dc.subject | Extracellular matrices | en_US |
| dc.subject | Angiogenesis | en_US |
| dc.subject | Polycaprolactone | en_US |
| dc.subject | PCL PolyHIPE scaffolds | en_US |
| dc.title | Decellularised Extracellular Matrix Decorated Pcl Polyhipe Scaffolds for Enhanced Cellular Activity, Integration and Angiogenesis | en_US |
| dc.type | Article | en_US |
| dspace.entity.type | Publication | |
| gdc.author.id | 0000-0001-9933-5254 | |
| gdc.author.id | 0000-0001-9933-5254 | en_US |
| gdc.author.institutional | Dikici, Serkan | |
| gdc.author.institutional | Aldemir Dikici, Betül | |
| gdc.author.wosid | Dikici, Serkan/AAL-6000-2020 | |
| gdc.bip.impulseclass | C4 | |
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| gdc.coar.access | open access | |
| gdc.coar.type | text::journal::journal article | |
| gdc.collaboration.industrial | false | |
| gdc.description.department | İzmir Institute of Technology. Bioengineering | en_US |
| gdc.description.endpage | 7310 | en_US |
| gdc.description.issue | 21 | en_US |
| gdc.description.publicationcategory | Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı | en_US |
| gdc.description.scopusquality | Q1 | |
| gdc.description.startpage | 7297 | en_US |
| gdc.description.volume | 9 | en_US |
| gdc.description.wosquality | Q2 | |
| gdc.identifier.openalex | W3203541817 | |
| gdc.identifier.pmid | 34617526 | |
| gdc.identifier.wos | WOS:000704931500001 | |
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| gdc.index.type | Scopus | |
| gdc.index.type | PubMed | |
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| gdc.oaire.keywords | Chemistry | |
| gdc.oaire.keywords | Polymers | |
| gdc.oaire.keywords | Animals | |
| gdc.oaire.keywords | Neovascularization, Physiologic | |
| gdc.oaire.keywords | Chorioallantoic Membrane | |
| gdc.oaire.keywords | Extracellular Matrix | |
| gdc.oaire.keywords | Styrenes | |
| gdc.oaire.popularity | 2.6131806E-8 | |
| gdc.oaire.publicfunded | false | |
| gdc.oaire.sciencefields | 0301 basic medicine | |
| gdc.oaire.sciencefields | 0303 health sciences | |
| gdc.oaire.sciencefields | 03 medical and health sciences | |
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| gdc.opencitations.count | 27 | |
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| local.message.claim | 2023-01-26T11:07:34.093+0300 | * |
| local.message.claim | |rp03855 | * |
| local.message.claim | |submit_approve | * |
| local.message.claim | |dc_contributor_author | * |
| local.message.claim | |None | * |
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