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Dose-dependent effects of zoledronic acid on the osteogenic differentiation of human bone marrow stem cells (hBMSCs)

dc.contributor.authorHadad, Henrique [UNESP]
dc.contributor.authorMatheus, Henrique Rinaldi [UNESP]
dc.contributor.authorChen, Jason Evan
dc.contributor.authorJounaidi, Youssef
dc.contributor.authorSouza, Francisley Ávila [UNESP]
dc.contributor.authorGuastaldi, Fernando Pozzi Semeghini
dc.contributor.institutionHarvard School of Dental Medicine
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)
dc.contributor.institutionHarvard Medical School
dc.date.accessioned2025-04-29T20:00:51Z
dc.date.issued2023-12-01
dc.description.abstractRecent studies have shown that bisphosphonates can also impact osteoblasts besides osteoclasts. This study aimed to evaluate the effects of different concentrations of Zoledronic acid (ZA) during the osteogenic differentiation of human Bone Marrow Stem Cells (hBMSCs) in vitro. Thus, osteogenic differentiation of hBMSCs was conducted with different concentrations of Zoledronic Acid (ZA) (0, 0.1, 1.0, and 5.0 μM) for the first 3 days. Cell metabolism was quantified at 1-, 3-, 7-, and 14 days. At 7- and 14-days, the following analyses were performed: 1) mineralization nodule assay, 2) LIVE/DEAD™, 3) cell adhesion and spreading, 4) alkaline phosphatase (ALP) activity, and 5) qPCR analysis for RUNX-2), ALPL, and COL1 A1. Data were analyzed by ANOVA 2-way, followed by Tukey's post hoc test (p < 0.05). Cell metabolism (3-, 7-, and 14-days) (p < 0.001), mineralization (7-, 14-days) (p < 0.001), and ALP activity (14-days) (p < 0.001) were reduced in ZA 5.0 µM when compared to control (no ZA). Also, ZA 5.0 µM downregulated the expression of RUNX2 at 7- and 14-days (p < 0.001). It is possible to conclude that ZA (5.0 µM) can impair hBMSC differentiation into osteoblasts and interferes with its mineralization phase.en
dc.description.affiliationSkeletal Biology Research Center Department of Oral and Maxillofacial Surgery Massachusetts General Hospital Harvard School of Dental Medicine
dc.description.affiliationDepartment of Diagnosis and Surgery Oral & Maxillofacial Surgery Division São Paulo State University (UNESP) School of Dentistry, SP
dc.description.affiliationDepartment of Diagnosis and Surgery Division of Periodontics São Paulo State University (UNESP) School of Dentistry, SP
dc.description.affiliationDepartment of Anesthesia Critical Care and Pain Medicine Massachusetts General Hospital Harvard Medical School
dc.description.affiliationUnespDepartment of Diagnosis and Surgery Oral & Maxillofacial Surgery Division São Paulo State University (UNESP) School of Dentistry, SP
dc.description.affiliationUnespDepartment of Diagnosis and Surgery Division of Periodontics São Paulo State University (UNESP) School of Dentistry, SP
dc.identifierhttp://dx.doi.org/10.1016/j.jormas.2023.101479
dc.identifier.citationJournal of Stomatology, Oral and Maxillofacial Surgery, v. 124, n. 6, 2023.
dc.identifier.doi10.1016/j.jormas.2023.101479
dc.identifier.issn2468-7855
dc.identifier.scopus2-s2.0-85169817669
dc.identifier.urihttps://hdl.handle.net/11449/304803
dc.language.isoeng
dc.relation.ispartofJournal of Stomatology, Oral and Maxillofacial Surgery
dc.sourceScopus
dc.subjectHuman bone marrow stem cells
dc.subjectMedication-related osteonecrosis of the jaw
dc.subjectOsteogenic differentiation
dc.subjectZoledronic acid
dc.titleDose-dependent effects of zoledronic acid on the osteogenic differentiation of human bone marrow stem cells (hBMSCs)en
dc.typeArtigopt
dspace.entity.typePublication
unesp.author.orcid0000-0001-8554-8849[6]

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