Hyaluronic acid hydrogels incorporating platelet lysate enhance human pulp cell proliferation and differentiation

Detalhes bibliográficos
Autor(a) principal: Almeida, Leopoldina D. F.
Data de Publicação: 2018
Outros Autores: Babo, Pedro S., Silva, Cristiana R., Rodrigues, Márcia T., Hebling, Josimeri, Reis, Rui L., Gomes, Manuela E.
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UNESP
Texto Completo: http://dx.doi.org/10.1007/s10856-018-6088-7
http://hdl.handle.net/11449/231417
Resumo: The restoration of dentine-pulp complex remains a challenge for dentists; nonetheless, it has been poorly addressed. An ideal system should modulate the host response, as well as enable the recruitment, proliferation and differentiation of relevant progenitor cells. Herein was proposed a photocrosslinkable hydrogel system based on hyaluronic acid (HA) and platelet lysate (PL). PL is a cocktail of growth factors (GFs) and cytokines involved in wound healing orchestration, obtained by the cryogenic processing of platelet concentrates, and was expected to provide the HA hydrogels specific biochemical cues to enhance pulp cells’ recruitment, proliferation and differentiation. Stable HA hydrogels incorporating PL (HAPL) were prepared after photocrosslinking of methacrylated HA (Met-HA) previously dissolved in PL, triggered by the Ultra Violet activated photoinitiator Irgacure 2959. Both the HAPL and plain HA hydrogels were shown to be able to recruit cells from a cell monolayer of human dental pulp stem cells (hDPSCs) isolated from permanent teeth. The hDPCs were also seeded directly over the hydrogels (5 × 104 cells/hydrogel) and cultured in osteogenic conditions. Cell metabolism and DNA quantification were higher, in all time-points, for PL supplemented hydrogels (p < 0,05). Alkaline phosphatase (ALPL) activity and calcium quantification peaks were observed for the HAPL group at 21 days (p < 0,05). The gene expression for ALPL and COLIA1 was up-regulated at 21 days to HAPL, compared with HA group (p < 0,05). Within the same time point, the gene expression for RUNX2 did not differ between the groups. Overall, data demonstrated that the HA hydrogels incorporating PL increased the cellular metabolism and stimulate the mineralized matrix deposition by hDPSCs, providing clear evidence of the potential of the proposed system for the repair of damaged pulp/dentin tissue and endodontics regeneration.
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spelling Hyaluronic acid hydrogels incorporating platelet lysate enhance human pulp cell proliferation and differentiationThe restoration of dentine-pulp complex remains a challenge for dentists; nonetheless, it has been poorly addressed. An ideal system should modulate the host response, as well as enable the recruitment, proliferation and differentiation of relevant progenitor cells. Herein was proposed a photocrosslinkable hydrogel system based on hyaluronic acid (HA) and platelet lysate (PL). PL is a cocktail of growth factors (GFs) and cytokines involved in wound healing orchestration, obtained by the cryogenic processing of platelet concentrates, and was expected to provide the HA hydrogels specific biochemical cues to enhance pulp cells’ recruitment, proliferation and differentiation. Stable HA hydrogels incorporating PL (HAPL) were prepared after photocrosslinking of methacrylated HA (Met-HA) previously dissolved in PL, triggered by the Ultra Violet activated photoinitiator Irgacure 2959. Both the HAPL and plain HA hydrogels were shown to be able to recruit cells from a cell monolayer of human dental pulp stem cells (hDPSCs) isolated from permanent teeth. The hDPCs were also seeded directly over the hydrogels (5 × 104 cells/hydrogel) and cultured in osteogenic conditions. Cell metabolism and DNA quantification were higher, in all time-points, for PL supplemented hydrogels (p < 0,05). Alkaline phosphatase (ALPL) activity and calcium quantification peaks were observed for the HAPL group at 21 days (p < 0,05). The gene expression for ALPL and COLIA1 was up-regulated at 21 days to HAPL, compared with HA group (p < 0,05). Within the same time point, the gene expression for RUNX2 did not differ between the groups. Overall, data demonstrated that the HA hydrogels incorporating PL increased the cellular metabolism and stimulate the mineralized matrix deposition by hDPSCs, providing clear evidence of the potential of the proposed system for the repair of damaged pulp/dentin tissue and endodontics regeneration.Department of Clinical and Social Dentistry Federal University of ParaíbaDepartment of Orthodontics and Pediatric Dentistry Araraquara Dental School State of São Paulo University3B’s Research Group I3Bs–Research Institute on Biomaterials Biodegradables and Biomimetics University of Minho Headquarters of the European Institute of Excellence on Tissue Engineering and Regenerative Medicine AvePark Parque de Ciência e Tecnologia Zona Industrial da Gandra, BarcoICVS/3B’s-PT Government Associate LaboratoryThe Discoveries Centre for Regenerative and Precision Medicine Headquarters at University of Minho, BarcoFederal University of ParaíbaUniversidade de São Paulo (USP)Zona Industrial da GandraICVS/3B’s-PT Government Associate LaboratoryHeadquarters at University of MinhoAlmeida, Leopoldina D. F.Babo, Pedro S.Silva, Cristiana R.Rodrigues, Márcia T.Hebling, JosimeriReis, Rui L.Gomes, Manuela E.2022-04-29T08:45:21Z2022-04-29T08:45:21Z2018-06-01info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articlehttp://dx.doi.org/10.1007/s10856-018-6088-7Journal of Materials Science: Materials in Medicine, v. 29, n. 6, 2018.1573-48380957-4530http://hdl.handle.net/11449/23141710.1007/s10856-018-6088-72-s2.0-85048626554Scopusreponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengJournal of Materials Science: Materials in Medicineinfo:eu-repo/semantics/openAccess2022-04-29T08:45:21Zoai:repositorio.unesp.br:11449/231417Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestopendoar:29462022-04-29T08:45:21Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false
dc.title.none.fl_str_mv Hyaluronic acid hydrogels incorporating platelet lysate enhance human pulp cell proliferation and differentiation
title Hyaluronic acid hydrogels incorporating platelet lysate enhance human pulp cell proliferation and differentiation
spellingShingle Hyaluronic acid hydrogels incorporating platelet lysate enhance human pulp cell proliferation and differentiation
Almeida, Leopoldina D. F.
title_short Hyaluronic acid hydrogels incorporating platelet lysate enhance human pulp cell proliferation and differentiation
title_full Hyaluronic acid hydrogels incorporating platelet lysate enhance human pulp cell proliferation and differentiation
title_fullStr Hyaluronic acid hydrogels incorporating platelet lysate enhance human pulp cell proliferation and differentiation
title_full_unstemmed Hyaluronic acid hydrogels incorporating platelet lysate enhance human pulp cell proliferation and differentiation
title_sort Hyaluronic acid hydrogels incorporating platelet lysate enhance human pulp cell proliferation and differentiation
author Almeida, Leopoldina D. F.
author_facet Almeida, Leopoldina D. F.
Babo, Pedro S.
Silva, Cristiana R.
Rodrigues, Márcia T.
Hebling, Josimeri
Reis, Rui L.
Gomes, Manuela E.
author_role author
author2 Babo, Pedro S.
Silva, Cristiana R.
Rodrigues, Márcia T.
Hebling, Josimeri
Reis, Rui L.
Gomes, Manuela E.
author2_role author
author
author
author
author
author
dc.contributor.none.fl_str_mv Federal University of Paraíba
Universidade de São Paulo (USP)
Zona Industrial da Gandra
ICVS/3B’s-PT Government Associate Laboratory
Headquarters at University of Minho
dc.contributor.author.fl_str_mv Almeida, Leopoldina D. F.
Babo, Pedro S.
Silva, Cristiana R.
Rodrigues, Márcia T.
Hebling, Josimeri
Reis, Rui L.
Gomes, Manuela E.
description The restoration of dentine-pulp complex remains a challenge for dentists; nonetheless, it has been poorly addressed. An ideal system should modulate the host response, as well as enable the recruitment, proliferation and differentiation of relevant progenitor cells. Herein was proposed a photocrosslinkable hydrogel system based on hyaluronic acid (HA) and platelet lysate (PL). PL is a cocktail of growth factors (GFs) and cytokines involved in wound healing orchestration, obtained by the cryogenic processing of platelet concentrates, and was expected to provide the HA hydrogels specific biochemical cues to enhance pulp cells’ recruitment, proliferation and differentiation. Stable HA hydrogels incorporating PL (HAPL) were prepared after photocrosslinking of methacrylated HA (Met-HA) previously dissolved in PL, triggered by the Ultra Violet activated photoinitiator Irgacure 2959. Both the HAPL and plain HA hydrogels were shown to be able to recruit cells from a cell monolayer of human dental pulp stem cells (hDPSCs) isolated from permanent teeth. The hDPCs were also seeded directly over the hydrogels (5 × 104 cells/hydrogel) and cultured in osteogenic conditions. Cell metabolism and DNA quantification were higher, in all time-points, for PL supplemented hydrogels (p < 0,05). Alkaline phosphatase (ALPL) activity and calcium quantification peaks were observed for the HAPL group at 21 days (p < 0,05). The gene expression for ALPL and COLIA1 was up-regulated at 21 days to HAPL, compared with HA group (p < 0,05). Within the same time point, the gene expression for RUNX2 did not differ between the groups. Overall, data demonstrated that the HA hydrogels incorporating PL increased the cellular metabolism and stimulate the mineralized matrix deposition by hDPSCs, providing clear evidence of the potential of the proposed system for the repair of damaged pulp/dentin tissue and endodontics regeneration.
publishDate 2018
dc.date.none.fl_str_mv 2018-06-01
2022-04-29T08:45:21Z
2022-04-29T08:45:21Z
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://dx.doi.org/10.1007/s10856-018-6088-7
Journal of Materials Science: Materials in Medicine, v. 29, n. 6, 2018.
1573-4838
0957-4530
http://hdl.handle.net/11449/231417
10.1007/s10856-018-6088-7
2-s2.0-85048626554
url http://dx.doi.org/10.1007/s10856-018-6088-7
http://hdl.handle.net/11449/231417
identifier_str_mv Journal of Materials Science: Materials in Medicine, v. 29, n. 6, 2018.
1573-4838
0957-4530
10.1007/s10856-018-6088-7
2-s2.0-85048626554
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Journal of Materials Science: Materials in Medicine
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.source.none.fl_str_mv Scopus
reponame:Repositório Institucional da UNESP
instname:Universidade Estadual Paulista (UNESP)
instacron:UNESP
instname_str Universidade Estadual Paulista (UNESP)
instacron_str UNESP
institution UNESP
reponame_str Repositório Institucional da UNESP
collection Repositório Institucional da UNESP
repository.name.fl_str_mv Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)
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