Bone regeneration: The influence of composite HA/TCP scaffolds and electrical stimulation on TGF/BMP and RANK/RANKL/OPG pathways
Main Author: | |
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Publication Date: | 2025 |
Other Authors: | , , , |
Format: | Article |
Language: | eng |
Source: | Repositório Institucional da UNESP |
Download full: | http://dx.doi.org/10.1016/j.injury.2025.112158 https://hdl.handle.net/11449/298625 |
Summary: | The repair of critical-sized bone defects represents significant clinical challenge. An alternative approach is the use of 3D composite scaffolds to support bone regeneration. Hydroxyapatite (HA) and tri-calcium phosphate (β-TCP), combined with polycaprolactone (PCL), offer promising mechanical resistance and biocompatibility. Bioelectrical stimulation (ES) at physiological levels is proposed to reestablishes tissue bioeletrocity and modulates cell signaling communication, such as the BMP/TGF-β and the RANK/RANK-L/OPG pathways. This study aimed to evaluate the use HA/TCP scaffolds and ES therapy for bone regeneration and their impact on the TGF-β/BMP pathway, alongside their relationship with the RANK/RANKL/OPG pathway in critical bone defects. The scaffolds were implanted at the bone defect in animal model (calvarial bone) and the area was subjected to ES application twice a week at 10 µA intensity of current for 5 min each session. Samples were collected for histomorphometry, immunohistochemistry, and molecular analysis. The TGF-β/BMP pathway study showed the HA/TCP+ES group increased BMP-7 gene expression at 30 and 60 days, and also greater endothelial vascular formation. Moreover, the HA/TCP and HA/TCP+ES groups exhibited a bone remodeling profile, indicated by RANKL/OPG ratio. HA/TCP scaffolds with ES enhanced vascular formation and mineralization initially, while modulation of the BMP/TGF pathway maintained bone homeostasis, controlling resorption via ES with HA/TCP. |
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Bone regeneration: The influence of composite HA/TCP scaffolds and electrical stimulation on TGF/BMP and RANK/RANKL/OPG pathwaysBioprintingElectrical stimulationMicrocurrentTGF pathwayTissue engineeringThe repair of critical-sized bone defects represents significant clinical challenge. An alternative approach is the use of 3D composite scaffolds to support bone regeneration. Hydroxyapatite (HA) and tri-calcium phosphate (β-TCP), combined with polycaprolactone (PCL), offer promising mechanical resistance and biocompatibility. Bioelectrical stimulation (ES) at physiological levels is proposed to reestablishes tissue bioeletrocity and modulates cell signaling communication, such as the BMP/TGF-β and the RANK/RANK-L/OPG pathways. This study aimed to evaluate the use HA/TCP scaffolds and ES therapy for bone regeneration and their impact on the TGF-β/BMP pathway, alongside their relationship with the RANK/RANKL/OPG pathway in critical bone defects. The scaffolds were implanted at the bone defect in animal model (calvarial bone) and the area was subjected to ES application twice a week at 10 µA intensity of current for 5 min each session. Samples were collected for histomorphometry, immunohistochemistry, and molecular analysis. The TGF-β/BMP pathway study showed the HA/TCP+ES group increased BMP-7 gene expression at 30 and 60 days, and also greater endothelial vascular formation. Moreover, the HA/TCP and HA/TCP+ES groups exhibited a bone remodeling profile, indicated by RANKL/OPG ratio. HA/TCP scaffolds with ES enhanced vascular formation and mineralization initially, while modulation of the BMP/TGF pathway maintained bone homeostasis, controlling resorption via ES with HA/TCP.Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)University Center of Hermínio Ometto Foundation FHO, Araras 13607-339, SPDivision of Dermatology Department of Internal Medicine Ribeirao Preto Medical School University of Sao Paulo, 05508-060Singapore Centre for 3D Printing School of Mechanical and Aerospace Engineering Nanyang Technological UniversityGraduate Program of Orthodontics University Center of Hermínio Ometto Foundation FHO, Araras 13607-339, SPDepartment of Social and Pediatric Dentistry Institute of Science and Technology São Paulo State University - Unesp, São José dos Campos, 12245-000Department of Social and Pediatric Dentistry Institute of Science and Technology São Paulo State University - Unesp, São José dos Campos, 12245-000FAPESP: 2018/21167–4CNPq: 423710/2018-4FHOUniversidade de São Paulo (USP)Nanyang Technological UniversityUniversidade Estadual Paulista (UNESP)Helaehil, Júlia VenturiniHuang, BoyangBartolo, PauloSantamaria-JR, Milton [UNESP]Caetano, Guilherme Ferreira2025-04-29T18:37:39Z2025-02-01info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articlehttp://dx.doi.org/10.1016/j.injury.2025.112158Injury, v. 56, n. 2, 2025.1879-02670020-1383https://hdl.handle.net/11449/29862510.1016/j.injury.2025.1121582-s2.0-85215101244Scopusreponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengInjuryinfo:eu-repo/semantics/openAccess2025-04-30T14:24:04Zoai:repositorio.unesp.br:11449/298625Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestrepositoriounesp@unesp.bropendoar:29462025-04-30T14:24:04Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false |
dc.title.none.fl_str_mv |
Bone regeneration: The influence of composite HA/TCP scaffolds and electrical stimulation on TGF/BMP and RANK/RANKL/OPG pathways |
title |
Bone regeneration: The influence of composite HA/TCP scaffolds and electrical stimulation on TGF/BMP and RANK/RANKL/OPG pathways |
spellingShingle |
Bone regeneration: The influence of composite HA/TCP scaffolds and electrical stimulation on TGF/BMP and RANK/RANKL/OPG pathways Helaehil, Júlia Venturini Bioprinting Electrical stimulation Microcurrent TGF pathway Tissue engineering |
title_short |
Bone regeneration: The influence of composite HA/TCP scaffolds and electrical stimulation on TGF/BMP and RANK/RANKL/OPG pathways |
title_full |
Bone regeneration: The influence of composite HA/TCP scaffolds and electrical stimulation on TGF/BMP and RANK/RANKL/OPG pathways |
title_fullStr |
Bone regeneration: The influence of composite HA/TCP scaffolds and electrical stimulation on TGF/BMP and RANK/RANKL/OPG pathways |
title_full_unstemmed |
Bone regeneration: The influence of composite HA/TCP scaffolds and electrical stimulation on TGF/BMP and RANK/RANKL/OPG pathways |
title_sort |
Bone regeneration: The influence of composite HA/TCP scaffolds and electrical stimulation on TGF/BMP and RANK/RANKL/OPG pathways |
author |
Helaehil, Júlia Venturini |
author_facet |
Helaehil, Júlia Venturini Huang, Boyang Bartolo, Paulo Santamaria-JR, Milton [UNESP] Caetano, Guilherme Ferreira |
author_role |
author |
author2 |
Huang, Boyang Bartolo, Paulo Santamaria-JR, Milton [UNESP] Caetano, Guilherme Ferreira |
author2_role |
author author author author |
dc.contributor.none.fl_str_mv |
FHO Universidade de São Paulo (USP) Nanyang Technological University Universidade Estadual Paulista (UNESP) |
dc.contributor.author.fl_str_mv |
Helaehil, Júlia Venturini Huang, Boyang Bartolo, Paulo Santamaria-JR, Milton [UNESP] Caetano, Guilherme Ferreira |
dc.subject.por.fl_str_mv |
Bioprinting Electrical stimulation Microcurrent TGF pathway Tissue engineering |
topic |
Bioprinting Electrical stimulation Microcurrent TGF pathway Tissue engineering |
description |
The repair of critical-sized bone defects represents significant clinical challenge. An alternative approach is the use of 3D composite scaffolds to support bone regeneration. Hydroxyapatite (HA) and tri-calcium phosphate (β-TCP), combined with polycaprolactone (PCL), offer promising mechanical resistance and biocompatibility. Bioelectrical stimulation (ES) at physiological levels is proposed to reestablishes tissue bioeletrocity and modulates cell signaling communication, such as the BMP/TGF-β and the RANK/RANK-L/OPG pathways. This study aimed to evaluate the use HA/TCP scaffolds and ES therapy for bone regeneration and their impact on the TGF-β/BMP pathway, alongside their relationship with the RANK/RANKL/OPG pathway in critical bone defects. The scaffolds were implanted at the bone defect in animal model (calvarial bone) and the area was subjected to ES application twice a week at 10 µA intensity of current for 5 min each session. Samples were collected for histomorphometry, immunohistochemistry, and molecular analysis. The TGF-β/BMP pathway study showed the HA/TCP+ES group increased BMP-7 gene expression at 30 and 60 days, and also greater endothelial vascular formation. Moreover, the HA/TCP and HA/TCP+ES groups exhibited a bone remodeling profile, indicated by RANKL/OPG ratio. HA/TCP scaffolds with ES enhanced vascular formation and mineralization initially, while modulation of the BMP/TGF pathway maintained bone homeostasis, controlling resorption via ES with HA/TCP. |
publishDate |
2025 |
dc.date.none.fl_str_mv |
2025-04-29T18:37:39Z 2025-02-01 |
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.injury.2025.112158 Injury, v. 56, n. 2, 2025. 1879-0267 0020-1383 https://hdl.handle.net/11449/298625 10.1016/j.injury.2025.112158 2-s2.0-85215101244 |
url |
http://dx.doi.org/10.1016/j.injury.2025.112158 https://hdl.handle.net/11449/298625 |
identifier_str_mv |
Injury, v. 56, n. 2, 2025. 1879-0267 0020-1383 10.1016/j.injury.2025.112158 2-s2.0-85215101244 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
Injury |
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) |
repository.mail.fl_str_mv |
repositoriounesp@unesp.br |
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1834482865636638720 |