Nanoscale hybrid implant surfaces and Osterix-mediated osseointegration

Detalhes bibliográficos
Autor(a) principal: Morandini Rodrigues, Laís [UNESP]
Data de Publicação: 2022
Outros Autores: Lima Zutin, Elis A. [UNESP], Sartori, Elisa M. [UNESP], Rizzante, Fabio A. P., Mendonça, Daniela B. S., Krebsbach, Paul H., Jepsen, Karl J., Cooper, Lyndon F., Vasconcellos, Luana M. R. [UNESP], Mendonça, Gustavo
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UNESP
Texto Completo: http://dx.doi.org/10.1002/jbm.a.37323
http://hdl.handle.net/11449/222679
Resumo: Endosseous implant surface topography directly affects adherent cell responses following implantation. The aim of this study was to examine the impact of nanoscale topographic modification of titanium implants on Osterix gene expression since this gene has been reported as key factor for bone formation. Titanium implants with smooth and nanoscale topographies were implanted in the femurs of Osterix-Cherry mice for 1–21 days. Implant integration was evaluated using scanning electron microscopy (SEM) to evaluate cell adhesion on implant surfaces, histology, and nanotomography (NanoCT) to observe and quantify the formed bone-to-implant interface, flow cytometry to quantify of Osterix expressing cells in adjacent tissues, and real-time PCR (qPCR) to quantify the osteoinductive and osteogenic gene expression of the implant-adherent cells. SEM revealed topography-dependent adhesion of cells at early timepoints. NanoCT demonstrated greater bone formation at nanoscale implants and interfacial osteogenesis was confirmed histologically at 7 and 14 days for both smooth and nanosurface implants. Flow cytometry revealed greater numbers of Osterix positive cells in femurs implanted with nanoscale versus smooth implants. Compared to smooth surface implants, nanoscale surface adherent cells expressed higher levels of Osterix (Osx), Alkaline phosphatase (Alp), Paired related homeobox (Prx1), Dentin matrix protein 1 (Dmp1), Bone sialoprotein (Bsp), and Osteocalcin (Ocn). In conclusion, nanoscale surface implants demonstrated greater bone formation associated with higher levels of Osterix expression over the 21-day healing period with direct evidence of surface-associated gene regulation involving a nanoscale-mediated osteoinductive pathway that utilizes Osterix to direct adherent cell osteoinduction.
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spelling Nanoscale hybrid implant surfaces and Osterix-mediated osseointegrationEndosseous implant surface topography directly affects adherent cell responses following implantation. The aim of this study was to examine the impact of nanoscale topographic modification of titanium implants on Osterix gene expression since this gene has been reported as key factor for bone formation. Titanium implants with smooth and nanoscale topographies were implanted in the femurs of Osterix-Cherry mice for 1–21 days. Implant integration was evaluated using scanning electron microscopy (SEM) to evaluate cell adhesion on implant surfaces, histology, and nanotomography (NanoCT) to observe and quantify the formed bone-to-implant interface, flow cytometry to quantify of Osterix expressing cells in adjacent tissues, and real-time PCR (qPCR) to quantify the osteoinductive and osteogenic gene expression of the implant-adherent cells. SEM revealed topography-dependent adhesion of cells at early timepoints. NanoCT demonstrated greater bone formation at nanoscale implants and interfacial osteogenesis was confirmed histologically at 7 and 14 days for both smooth and nanosurface implants. Flow cytometry revealed greater numbers of Osterix positive cells in femurs implanted with nanoscale versus smooth implants. Compared to smooth surface implants, nanoscale surface adherent cells expressed higher levels of Osterix (Osx), Alkaline phosphatase (Alp), Paired related homeobox (Prx1), Dentin matrix protein 1 (Dmp1), Bone sialoprotein (Bsp), and Osteocalcin (Ocn). In conclusion, nanoscale surface implants demonstrated greater bone formation associated with higher levels of Osterix expression over the 21-day healing period with direct evidence of surface-associated gene regulation involving a nanoscale-mediated osteoinductive pathway that utilizes Osterix to direct adherent cell osteoinduction.Academy of OsseointegrationInternational Association for Dental ResearchNational Institute of Arthritis and Musculoskeletal and Skin DiseasesDepartment of Biosciences and Oral Diagnosis Institute of Science and Technology São Paulo State University (Unesp)Department of Oral Surgery and Integrated Clinics) School of Dentistry São Paulo State University (Unesp)Department of Comprehensive Dentistry School of Dental Medicine Case Western Reserve UniversityDepartment of Biological and Material Sciences & Prosthodontics School of Dentistry University of MichiganSection of Periodontics School of Dentistry University of CaliforniaDepartment of Orthopedic Surgery School of Medicine University of MichiganDepartment of Oral Biology College of Dentistry University of Illinois at ChicagoDepartment of Biosciences and Oral Diagnosis Institute of Science and Technology São Paulo State University (Unesp)Department of Oral Surgery and Integrated Clinics) School of Dentistry São Paulo State University (Unesp)National Institute of Arthritis and Musculoskeletal and Skin Diseases: P30 AR069620Universidade Estadual Paulista (UNESP)Case Western Reserve UniversityUniversity of MichiganUniversity of CaliforniaUniversity of Illinois at ChicagoMorandini Rodrigues, Laís [UNESP]Lima Zutin, Elis A. [UNESP]Sartori, Elisa M. [UNESP]Rizzante, Fabio A. P.Mendonça, Daniela B. S.Krebsbach, Paul H.Jepsen, Karl J.Cooper, Lyndon F.Vasconcellos, Luana M. R. [UNESP]Mendonça, Gustavo2022-04-28T19:46:04Z2022-04-28T19:46:04Z2022-03-01info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/article696-707http://dx.doi.org/10.1002/jbm.a.37323Journal of Biomedical Materials Research - Part A, v. 110, n. 3, p. 696-707, 2022.1552-49651549-3296http://hdl.handle.net/11449/22267910.1002/jbm.a.373232-s2.0-85117359918Scopusreponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengJournal of Biomedical Materials Research - Part Ainfo:eu-repo/semantics/openAccess2022-04-28T19:46:04Zoai:repositorio.unesp.br:11449/222679Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestopendoar:29462024-08-06T00:02:16.905572Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false
dc.title.none.fl_str_mv Nanoscale hybrid implant surfaces and Osterix-mediated osseointegration
title Nanoscale hybrid implant surfaces and Osterix-mediated osseointegration
spellingShingle Nanoscale hybrid implant surfaces and Osterix-mediated osseointegration
Morandini Rodrigues, Laís [UNESP]
title_short Nanoscale hybrid implant surfaces and Osterix-mediated osseointegration
title_full Nanoscale hybrid implant surfaces and Osterix-mediated osseointegration
title_fullStr Nanoscale hybrid implant surfaces and Osterix-mediated osseointegration
title_full_unstemmed Nanoscale hybrid implant surfaces and Osterix-mediated osseointegration
title_sort Nanoscale hybrid implant surfaces and Osterix-mediated osseointegration
author Morandini Rodrigues, Laís [UNESP]
author_facet Morandini Rodrigues, Laís [UNESP]
Lima Zutin, Elis A. [UNESP]
Sartori, Elisa M. [UNESP]
Rizzante, Fabio A. P.
Mendonça, Daniela B. S.
Krebsbach, Paul H.
Jepsen, Karl J.
Cooper, Lyndon F.
Vasconcellos, Luana M. R. [UNESP]
Mendonça, Gustavo
author_role author
author2 Lima Zutin, Elis A. [UNESP]
Sartori, Elisa M. [UNESP]
Rizzante, Fabio A. P.
Mendonça, Daniela B. S.
Krebsbach, Paul H.
Jepsen, Karl J.
Cooper, Lyndon F.
Vasconcellos, Luana M. R. [UNESP]
Mendonça, Gustavo
author2_role author
author
author
author
author
author
author
author
author
dc.contributor.none.fl_str_mv Universidade Estadual Paulista (UNESP)
Case Western Reserve University
University of Michigan
University of California
University of Illinois at Chicago
dc.contributor.author.fl_str_mv Morandini Rodrigues, Laís [UNESP]
Lima Zutin, Elis A. [UNESP]
Sartori, Elisa M. [UNESP]
Rizzante, Fabio A. P.
Mendonça, Daniela B. S.
Krebsbach, Paul H.
Jepsen, Karl J.
Cooper, Lyndon F.
Vasconcellos, Luana M. R. [UNESP]
Mendonça, Gustavo
description Endosseous implant surface topography directly affects adherent cell responses following implantation. The aim of this study was to examine the impact of nanoscale topographic modification of titanium implants on Osterix gene expression since this gene has been reported as key factor for bone formation. Titanium implants with smooth and nanoscale topographies were implanted in the femurs of Osterix-Cherry mice for 1–21 days. Implant integration was evaluated using scanning electron microscopy (SEM) to evaluate cell adhesion on implant surfaces, histology, and nanotomography (NanoCT) to observe and quantify the formed bone-to-implant interface, flow cytometry to quantify of Osterix expressing cells in adjacent tissues, and real-time PCR (qPCR) to quantify the osteoinductive and osteogenic gene expression of the implant-adherent cells. SEM revealed topography-dependent adhesion of cells at early timepoints. NanoCT demonstrated greater bone formation at nanoscale implants and interfacial osteogenesis was confirmed histologically at 7 and 14 days for both smooth and nanosurface implants. Flow cytometry revealed greater numbers of Osterix positive cells in femurs implanted with nanoscale versus smooth implants. Compared to smooth surface implants, nanoscale surface adherent cells expressed higher levels of Osterix (Osx), Alkaline phosphatase (Alp), Paired related homeobox (Prx1), Dentin matrix protein 1 (Dmp1), Bone sialoprotein (Bsp), and Osteocalcin (Ocn). In conclusion, nanoscale surface implants demonstrated greater bone formation associated with higher levels of Osterix expression over the 21-day healing period with direct evidence of surface-associated gene regulation involving a nanoscale-mediated osteoinductive pathway that utilizes Osterix to direct adherent cell osteoinduction.
publishDate 2022
dc.date.none.fl_str_mv 2022-04-28T19:46:04Z
2022-04-28T19:46:04Z
2022-03-01
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/10.1002/jbm.a.37323
Journal of Biomedical Materials Research - Part A, v. 110, n. 3, p. 696-707, 2022.
1552-4965
1549-3296
http://hdl.handle.net/11449/222679
10.1002/jbm.a.37323
2-s2.0-85117359918
url http://dx.doi.org/10.1002/jbm.a.37323
http://hdl.handle.net/11449/222679
identifier_str_mv Journal of Biomedical Materials Research - Part A, v. 110, n. 3, p. 696-707, 2022.
1552-4965
1549-3296
10.1002/jbm.a.37323
2-s2.0-85117359918
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Journal of Biomedical Materials Research - Part A
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv 696-707
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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