Bifunctional naringenin-laden gelatin methacryloyl scaffolds with osteogenic and anti-inflammatory properties
| Autor(a) principal: | |
|---|---|
| Data de Publicação: | 2024 |
| Outros Autores: | , , , , , |
| Tipo de documento: | Artigo |
| Idioma: | eng |
| Título da fonte: | Repositório Institucional da UNESP |
| Texto Completo: | http://dx.doi.org/10.1016/j.dental.2024.06.019 https://hdl.handle.net/11449/299493 |
Resumo: | 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. |
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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 |
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info:eu-repo/semantics/article |
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article |
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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 |
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eng |
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Dental Materials |
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info:eu-repo/semantics/openAccess |
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openAccess |
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1353-1363 |
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Scopus reponame:Repositório Institucional da UNESP instname:Universidade Estadual Paulista (UNESP) instacron:UNESP |
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Universidade Estadual Paulista (UNESP) |
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UNESP |
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Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP) |
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