Hesperidin Promotes Osteogenesis and Modulates Collagen Matrix Organization and Mineralization In Vitro and In Vivo

This study evaluated the direct effect of a phytochemical, hesperidin, on pre-osteoblast cell function as well as osteogenesis and collagen matrix quality, as there is little known about hesperidin’s influence in mineralized tissue formation and regeneration. Hesperidin was added to a culture of MC3...

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Main Authors: Patricia A. Miguez, Stephen A. Tuin, Adam G. Robinson, Joyce Belcher, Prapaporn Jongwattanapisan, Kimberly Perley, Vinicius de Paiva Gonҫalves, Arash Hanifi, Nancy Pleshko, Elisabeth R. Barton
Format: Article
Language:English
Published: MDPI AG 2021-03-01
Series:International Journal of Molecular Sciences
Subjects:
Online Access:https://www.mdpi.com/1422-0067/22/6/3223
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spelling doaj-4583b073466344608598d6e005a9f9fb2021-03-23T00:04:11ZengMDPI AGInternational Journal of Molecular Sciences1661-65961422-00672021-03-01223223322310.3390/ijms22063223Hesperidin Promotes Osteogenesis and Modulates Collagen Matrix Organization and Mineralization In Vitro and In VivoPatricia A. Miguez0Stephen A. Tuin1Adam G. Robinson2Joyce Belcher3Prapaporn Jongwattanapisan4Kimberly Perley5Vinicius de Paiva Gonҫalves6Arash Hanifi7Nancy Pleshko8Elisabeth R. Barton9Division of Comprehensive Oral Health, School of Dentistry, University of North Carolina at Chapel Hill, Chapel Hill, NC 27599, USAOral and Craniofacial Health Sciences, University of North Carolina at Chapel Hill, Chapel Hill, NC 27599, USAOral and Craniofacial Health Sciences, University of North Carolina at Chapel Hill, Chapel Hill, NC 27599, USACabrini University, Philadelphia, PA 19019, USAOral and Craniofacial Health Sciences, University of North Carolina at Chapel Hill, Chapel Hill, NC 27599, USADepartment of Periodontics, School of Dental Medicine, University of Pennsylvania, Philadelphia, PA 19104, USADivision of Comprehensive Oral Health, School of Dentistry, University of North Carolina at Chapel Hill, Chapel Hill, NC 27599, USADepartment of Bioengineering, Temple University, Philadelphia, PA 19122, USADepartment of Bioengineering, Temple University, Philadelphia, PA 19122, USADepartment of Applied Physiology and Kinesiology, University of Florida, Gainesville, FL 32611, USAThis study evaluated the direct effect of a phytochemical, hesperidin, on pre-osteoblast cell function as well as osteogenesis and collagen matrix quality, as there is little known about hesperidin’s influence in mineralized tissue formation and regeneration. Hesperidin was added to a culture of MC3T3-E1 cells at various concentrations. Cell proliferation, viability, osteogenic gene expression and deposited collagen matrix analyses were performed. Treatment with hesperidin showed significant upregulation of osteogenic markers, particularly with lower doses. Mature and compact collagen fibrils in hesperidin-treated cultures were observed by picrosirius red staining (PSR), although a thinner matrix layer was present for the higher dose of hesperidin compared to osteogenic media alone. Fourier-transform infrared spectroscopy indicated a better mineral-to-matrix ratio and matrix distribution in cultures exposed to hesperidin and confirmed less collagen deposited with the 100-µM dose of hesperidin. In vivo, hesperidin combined with a suboptimal dose of bone morphogenetic protein 2 (BMP2) (dose unable to promote healing of a rat mandible critical-sized bone defect) in a collagenous scaffold promoted a well-controlled (not ectopic) pattern of bone formation as compared to a large dose of BMP2 (previously defined as optimal in healing the critical-sized defect, although of ectopic nature). PSR staining of newly formed bone demonstrated that hesperidin can promote maturation of bone organic matrix. Our findings show, for the first time, that hesperidin has a modulatory role in mineralized tissue formation via not only osteoblast cell differentiation but also matrix organization and matrix-to-mineral ratio and could be a potential adjunct in regenerative bone therapies.https://www.mdpi.com/1422-0067/22/6/3223collagenboneosteogenesishesperidinextracellular matrixregeneration
collection DOAJ
language English
format Article
sources DOAJ
author Patricia A. Miguez
Stephen A. Tuin
Adam G. Robinson
Joyce Belcher
Prapaporn Jongwattanapisan
Kimberly Perley
Vinicius de Paiva Gonҫalves
Arash Hanifi
Nancy Pleshko
Elisabeth R. Barton
spellingShingle Patricia A. Miguez
Stephen A. Tuin
Adam G. Robinson
Joyce Belcher
Prapaporn Jongwattanapisan
Kimberly Perley
Vinicius de Paiva Gonҫalves
Arash Hanifi
Nancy Pleshko
Elisabeth R. Barton
Hesperidin Promotes Osteogenesis and Modulates Collagen Matrix Organization and Mineralization In Vitro and In Vivo
International Journal of Molecular Sciences
collagen
bone
osteogenesis
hesperidin
extracellular matrix
regeneration
author_facet Patricia A. Miguez
Stephen A. Tuin
Adam G. Robinson
Joyce Belcher
Prapaporn Jongwattanapisan
Kimberly Perley
Vinicius de Paiva Gonҫalves
Arash Hanifi
Nancy Pleshko
Elisabeth R. Barton
author_sort Patricia A. Miguez
title Hesperidin Promotes Osteogenesis and Modulates Collagen Matrix Organization and Mineralization In Vitro and In Vivo
title_short Hesperidin Promotes Osteogenesis and Modulates Collagen Matrix Organization and Mineralization In Vitro and In Vivo
title_full Hesperidin Promotes Osteogenesis and Modulates Collagen Matrix Organization and Mineralization In Vitro and In Vivo
title_fullStr Hesperidin Promotes Osteogenesis and Modulates Collagen Matrix Organization and Mineralization In Vitro and In Vivo
title_full_unstemmed Hesperidin Promotes Osteogenesis and Modulates Collagen Matrix Organization and Mineralization In Vitro and In Vivo
title_sort hesperidin promotes osteogenesis and modulates collagen matrix organization and mineralization in vitro and in vivo
publisher MDPI AG
series International Journal of Molecular Sciences
issn 1661-6596
1422-0067
publishDate 2021-03-01
description This study evaluated the direct effect of a phytochemical, hesperidin, on pre-osteoblast cell function as well as osteogenesis and collagen matrix quality, as there is little known about hesperidin’s influence in mineralized tissue formation and regeneration. Hesperidin was added to a culture of MC3T3-E1 cells at various concentrations. Cell proliferation, viability, osteogenic gene expression and deposited collagen matrix analyses were performed. Treatment with hesperidin showed significant upregulation of osteogenic markers, particularly with lower doses. Mature and compact collagen fibrils in hesperidin-treated cultures were observed by picrosirius red staining (PSR), although a thinner matrix layer was present for the higher dose of hesperidin compared to osteogenic media alone. Fourier-transform infrared spectroscopy indicated a better mineral-to-matrix ratio and matrix distribution in cultures exposed to hesperidin and confirmed less collagen deposited with the 100-µM dose of hesperidin. In vivo, hesperidin combined with a suboptimal dose of bone morphogenetic protein 2 (BMP2) (dose unable to promote healing of a rat mandible critical-sized bone defect) in a collagenous scaffold promoted a well-controlled (not ectopic) pattern of bone formation as compared to a large dose of BMP2 (previously defined as optimal in healing the critical-sized defect, although of ectopic nature). PSR staining of newly formed bone demonstrated that hesperidin can promote maturation of bone organic matrix. Our findings show, for the first time, that hesperidin has a modulatory role in mineralized tissue formation via not only osteoblast cell differentiation but also matrix organization and matrix-to-mineral ratio and could be a potential adjunct in regenerative bone therapies.
topic collagen
bone
osteogenesis
hesperidin
extracellular matrix
regeneration
url https://www.mdpi.com/1422-0067/22/6/3223
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