Bifunctional naringenin-laden gelatin methacryloyl scaffolds with osteogenic and anti-inflammatory properties

Bibliographic Details
Main Author: Cardoso, Lais M.
Publication Date: 2024
Other Authors: de Carvalho, Ana Beatriz G. [UNESP], Anselmi, Caroline [UNESP], Mahmoud, Abdel H., Dal-Fabbro, Renan, Basso, Fernanda G. [UNESP], Bottino, Marco C.
Format: Article
Language: eng
Source: Repositório Institucional da UNESP
Download full: http://dx.doi.org/10.1016/j.dental.2024.06.019
https://hdl.handle.net/11449/299493
Summary: Objective: To fabricate and characterize an innovative gelatin methacryloyl/GelMA electrospun scaffold containing the citrus flavonoid naringenin/NA with osteogenic and anti-inflammatory properties. Methods: GelMA scaffolds (15 % w/v) containing 0/Control, 5, 10, or 20 % of NA w/w were obtained via electrospinning. The chemical composition, fiber morphology/diameter, swelling/degradation profile, and NA release were investigated. Cytotoxicity, cell proliferation, adhesion and spreading, total protein/TP production, alkaline phosphatase/ALP activity, osteogenic genes expression (OCN, OPN, RUNX2), and mineralized nodules deposition/MND with human alveolar bone-derived mesenchymal stem cells (aBMSCs) seeded on the scaffolds were assessed. Moreover, aBMSCs seeded on the scaffolds and stimulated with tumor necrosis factor-alpha/TNF-α were submitted to collagen, nitric oxide/NO, interleukin/IL-1α, and IL-6 production assessment. Data were analyzed using ANOVA and t-student/post-hoc tests (α = 5 %). Results: NA-laden scaffolds presented increased fiber diameter, lower swelling capacity, and faster degradation profile over 28 days (p < 0.05). NA release was detected over time. Cell adhesion and spreading, and TP production were similar between GelMA and GelMA+NA5 % scaffolds, while cell proliferation, ALP activity, OCN/OPN/RUNX2 gene expression, and MND were higher for GelMA+NA5 % scaffolds (p < 0.05). Cells seeded on control scaffolds and TNF-α-stimulated presented higher levels of NO, IL-1α/IL-6, and lower levels of collagen (p < 0.05). In contrast, cells seeded on GelMA+NA5 % scaffolds showed downregulation of inflammatory markers and higher collagen synthesis (p < 0.05). Significance: GelMA+NA5 % scaffold was cytocompatible, stimulated aBMSCs proliferation and differentiation, and downregulated inflammatory mediators’ synthesis, suggesting its therapeutic effect as a multi-target bifunctional scaffold with osteogenic and anti-inflammatory properties for bone tissue engineering.
id UNSP_72f4608f6592c0ba715212d5b3f922fc
oai_identifier_str oai:repositorio.unesp.br:11449/299493
network_acronym_str UNSP
network_name_str Repositório Institucional da UNESP
repository_id_str 2946
spelling Bifunctional naringenin-laden gelatin methacryloyl scaffolds with osteogenic and anti-inflammatory propertiesBoneElectrospinningFlavonoidsGelatin methacryloylInflammationRegenerationObjective: To fabricate and characterize an innovative gelatin methacryloyl/GelMA electrospun scaffold containing the citrus flavonoid naringenin/NA with osteogenic and anti-inflammatory properties. Methods: GelMA scaffolds (15 % w/v) containing 0/Control, 5, 10, or 20 % of NA w/w were obtained via electrospinning. The chemical composition, fiber morphology/diameter, swelling/degradation profile, and NA release were investigated. Cytotoxicity, cell proliferation, adhesion and spreading, total protein/TP production, alkaline phosphatase/ALP activity, osteogenic genes expression (OCN, OPN, RUNX2), and mineralized nodules deposition/MND with human alveolar bone-derived mesenchymal stem cells (aBMSCs) seeded on the scaffolds were assessed. Moreover, aBMSCs seeded on the scaffolds and stimulated with tumor necrosis factor-alpha/TNF-α were submitted to collagen, nitric oxide/NO, interleukin/IL-1α, and IL-6 production assessment. Data were analyzed using ANOVA and t-student/post-hoc tests (α = 5 %). Results: NA-laden scaffolds presented increased fiber diameter, lower swelling capacity, and faster degradation profile over 28 days (p < 0.05). NA release was detected over time. Cell adhesion and spreading, and TP production were similar between GelMA and GelMA+NA5 % scaffolds, while cell proliferation, ALP activity, OCN/OPN/RUNX2 gene expression, and MND were higher for GelMA+NA5 % scaffolds (p < 0.05). Cells seeded on control scaffolds and TNF-α-stimulated presented higher levels of NO, IL-1α/IL-6, and lower levels of collagen (p < 0.05). In contrast, cells seeded on GelMA+NA5 % scaffolds showed downregulation of inflammatory markers and higher collagen synthesis (p < 0.05). Significance: GelMA+NA5 % scaffold was cytocompatible, stimulated aBMSCs proliferation and differentiation, and downregulated inflammatory mediators’ synthesis, suggesting its therapeutic effect as a multi-target bifunctional scaffold with osteogenic and anti-inflammatory properties for bone tissue engineering.Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)National Institutes of HealthFundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)Department of Cariology Restorative Sciences and Endodontics University of Michigan–School of Dentistry, 1011 N. University AvenueDepartment of Dental Materials and Prosthodontics São Paulo State University (UNESP)–São Jose dos Campos School of Dentistry, Eng. Francisco Jose Longo 777, SPDepartment of Morphology and Pediatric Dentistry São Paulo State University (UNESP)–Araraquara School of Dentistry, Humaitá 1680, SPDepartment of Oral Biology and Pathology Stony Brook University–School of Dental Medicine, 100 Nicolls RoadDepartment of Phisiology and Pathology São Paulo State University (UNESP) Araraquara School of Dentistry, SPDepartment of Biomedical Engineering College of Engineering University of MichiganDepartment of Dental Materials and Prosthodontics São Paulo State University (UNESP)–São Jose dos Campos School of Dentistry, Eng. Francisco Jose Longo 777, SPDepartment of Morphology and Pediatric Dentistry São Paulo State University (UNESP)–Araraquara School of Dentistry, Humaitá 1680, SPDepartment of Phisiology and Pathology São Paulo State University (UNESP) Araraquara School of Dentistry, SPFAPESP: #2019/16886-4FAPESP: #2022/03788-7CNPq: 303574/2022-4University of Michigan–School of DentistryUniversidade Estadual Paulista (UNESP)Stony Brook University–School of Dental MedicineUniversity of MichiganCardoso, Lais M.de Carvalho, Ana Beatriz G. [UNESP]Anselmi, Caroline [UNESP]Mahmoud, Abdel H.Dal-Fabbro, RenanBasso, Fernanda G. [UNESP]Bottino, Marco C.2025-04-29T18:42:33Z2024-09-01info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/article1353-1363http://dx.doi.org/10.1016/j.dental.2024.06.019Dental Materials, v. 40, n. 9, p. 1353-1363, 2024.0109-5641https://hdl.handle.net/11449/29949310.1016/j.dental.2024.06.0192-s2.0-85196028382Scopusreponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengDental Materialsinfo:eu-repo/semantics/openAccess2025-05-01T05:46:48Zoai:repositorio.unesp.br:11449/299493Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestrepositoriounesp@unesp.bropendoar:29462025-05-01T05:46:48Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false
dc.title.none.fl_str_mv Bifunctional naringenin-laden gelatin methacryloyl scaffolds with osteogenic and anti-inflammatory properties
title Bifunctional naringenin-laden gelatin methacryloyl scaffolds with osteogenic and anti-inflammatory properties
spellingShingle Bifunctional naringenin-laden gelatin methacryloyl scaffolds with osteogenic and anti-inflammatory properties
Cardoso, Lais M.
Bone
Electrospinning
Flavonoids
Gelatin methacryloyl
Inflammation
Regeneration
title_short Bifunctional naringenin-laden gelatin methacryloyl scaffolds with osteogenic and anti-inflammatory properties
title_full Bifunctional naringenin-laden gelatin methacryloyl scaffolds with osteogenic and anti-inflammatory properties
title_fullStr Bifunctional naringenin-laden gelatin methacryloyl scaffolds with osteogenic and anti-inflammatory properties
title_full_unstemmed Bifunctional naringenin-laden gelatin methacryloyl scaffolds with osteogenic and anti-inflammatory properties
title_sort Bifunctional naringenin-laden gelatin methacryloyl scaffolds with osteogenic and anti-inflammatory properties
author Cardoso, Lais M.
author_facet Cardoso, Lais M.
de Carvalho, Ana Beatriz G. [UNESP]
Anselmi, Caroline [UNESP]
Mahmoud, Abdel H.
Dal-Fabbro, Renan
Basso, Fernanda G. [UNESP]
Bottino, Marco C.
author_role author
author2 de Carvalho, Ana Beatriz G. [UNESP]
Anselmi, Caroline [UNESP]
Mahmoud, Abdel H.
Dal-Fabbro, Renan
Basso, Fernanda G. [UNESP]
Bottino, Marco C.
author2_role author
author
author
author
author
author
dc.contributor.none.fl_str_mv University of Michigan–School of Dentistry
Universidade Estadual Paulista (UNESP)
Stony Brook University–School of Dental Medicine
University of Michigan
dc.contributor.author.fl_str_mv Cardoso, Lais M.
de Carvalho, Ana Beatriz G. [UNESP]
Anselmi, Caroline [UNESP]
Mahmoud, Abdel H.
Dal-Fabbro, Renan
Basso, Fernanda G. [UNESP]
Bottino, Marco C.
dc.subject.por.fl_str_mv Bone
Electrospinning
Flavonoids
Gelatin methacryloyl
Inflammation
Regeneration
topic Bone
Electrospinning
Flavonoids
Gelatin methacryloyl
Inflammation
Regeneration
description Objective: To fabricate and characterize an innovative gelatin methacryloyl/GelMA electrospun scaffold containing the citrus flavonoid naringenin/NA with osteogenic and anti-inflammatory properties. Methods: GelMA scaffolds (15 % w/v) containing 0/Control, 5, 10, or 20 % of NA w/w were obtained via electrospinning. The chemical composition, fiber morphology/diameter, swelling/degradation profile, and NA release were investigated. Cytotoxicity, cell proliferation, adhesion and spreading, total protein/TP production, alkaline phosphatase/ALP activity, osteogenic genes expression (OCN, OPN, RUNX2), and mineralized nodules deposition/MND with human alveolar bone-derived mesenchymal stem cells (aBMSCs) seeded on the scaffolds were assessed. Moreover, aBMSCs seeded on the scaffolds and stimulated with tumor necrosis factor-alpha/TNF-α were submitted to collagen, nitric oxide/NO, interleukin/IL-1α, and IL-6 production assessment. Data were analyzed using ANOVA and t-student/post-hoc tests (α = 5 %). Results: NA-laden scaffolds presented increased fiber diameter, lower swelling capacity, and faster degradation profile over 28 days (p < 0.05). NA release was detected over time. Cell adhesion and spreading, and TP production were similar between GelMA and GelMA+NA5 % scaffolds, while cell proliferation, ALP activity, OCN/OPN/RUNX2 gene expression, and MND were higher for GelMA+NA5 % scaffolds (p < 0.05). Cells seeded on control scaffolds and TNF-α-stimulated presented higher levels of NO, IL-1α/IL-6, and lower levels of collagen (p < 0.05). In contrast, cells seeded on GelMA+NA5 % scaffolds showed downregulation of inflammatory markers and higher collagen synthesis (p < 0.05). Significance: GelMA+NA5 % scaffold was cytocompatible, stimulated aBMSCs proliferation and differentiation, and downregulated inflammatory mediators’ synthesis, suggesting its therapeutic effect as a multi-target bifunctional scaffold with osteogenic and anti-inflammatory properties for bone tissue engineering.
publishDate 2024
dc.date.none.fl_str_mv 2024-09-01
2025-04-29T18:42:33Z
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/10.1016/j.dental.2024.06.019
Dental Materials, v. 40, n. 9, p. 1353-1363, 2024.
0109-5641
https://hdl.handle.net/11449/299493
10.1016/j.dental.2024.06.019
2-s2.0-85196028382
url http://dx.doi.org/10.1016/j.dental.2024.06.019
https://hdl.handle.net/11449/299493
identifier_str_mv Dental Materials, v. 40, n. 9, p. 1353-1363, 2024.
0109-5641
10.1016/j.dental.2024.06.019
2-s2.0-85196028382
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Dental Materials
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv 1353-1363
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)
repository.mail.fl_str_mv repositoriounesp@unesp.br
_version_ 1834482431357353984