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Stem cell-mediated osteogenesis: therapeutic potential for bone tissue engineering

Intervertebral disc degeneration often requires bony spinal fusion for long-term relief. Current arthrodesis procedures use bone grafts from autogenous bone, allogenic backed bone, or synthetic materials. Autogenous bone grafts can result in donor site morbidity and pain at the donor site, while all...

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Detalles Bibliográficos
Autores principales: Neman, Josh, Hambrecht, Amanda, Cadry, Cherie, Jandial, Rahul
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3324839/
https://www.ncbi.nlm.nih.gov/pubmed/22500114
http://dx.doi.org/10.2147/BTT.S22407
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author Neman, Josh
Hambrecht, Amanda
Cadry, Cherie
Jandial, Rahul
author_facet Neman, Josh
Hambrecht, Amanda
Cadry, Cherie
Jandial, Rahul
author_sort Neman, Josh
collection PubMed
description Intervertebral disc degeneration often requires bony spinal fusion for long-term relief. Current arthrodesis procedures use bone grafts from autogenous bone, allogenic backed bone, or synthetic materials. Autogenous bone grafts can result in donor site morbidity and pain at the donor site, while allogenic backed bone and synthetic materials have variable effectiveness. Given these limitations, researchers have focused on new treatments that will allow for safe and successful bone repair and regeneration. Mesenchymal stem cells have received attention for their ability to differentiate into osteoblasts, cells that synthesize new bone. With the recent advances in scaffold and biomaterial technology as well as stem cell manipulation and transplantation, stem cells and their scaffolds are uniquely positioned to bring about significant improvements in the treatment and outcomes of spinal fusion and other injuries.
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spelling pubmed-33248392012-04-12 Stem cell-mediated osteogenesis: therapeutic potential for bone tissue engineering Neman, Josh Hambrecht, Amanda Cadry, Cherie Jandial, Rahul Biologics Review Intervertebral disc degeneration often requires bony spinal fusion for long-term relief. Current arthrodesis procedures use bone grafts from autogenous bone, allogenic backed bone, or synthetic materials. Autogenous bone grafts can result in donor site morbidity and pain at the donor site, while allogenic backed bone and synthetic materials have variable effectiveness. Given these limitations, researchers have focused on new treatments that will allow for safe and successful bone repair and regeneration. Mesenchymal stem cells have received attention for their ability to differentiate into osteoblasts, cells that synthesize new bone. With the recent advances in scaffold and biomaterial technology as well as stem cell manipulation and transplantation, stem cells and their scaffolds are uniquely positioned to bring about significant improvements in the treatment and outcomes of spinal fusion and other injuries. Dove Medical Press 2012 2012-03-09 /pmc/articles/PMC3324839/ /pubmed/22500114 http://dx.doi.org/10.2147/BTT.S22407 Text en © 2012 Neman et al, publisher and licensee Dove Medical Press Ltd. This is an Open Access article which permits unrestricted noncommercial use, provided the original work is properly cited.
spellingShingle Review
Neman, Josh
Hambrecht, Amanda
Cadry, Cherie
Jandial, Rahul
Stem cell-mediated osteogenesis: therapeutic potential for bone tissue engineering
title Stem cell-mediated osteogenesis: therapeutic potential for bone tissue engineering
title_full Stem cell-mediated osteogenesis: therapeutic potential for bone tissue engineering
title_fullStr Stem cell-mediated osteogenesis: therapeutic potential for bone tissue engineering
title_full_unstemmed Stem cell-mediated osteogenesis: therapeutic potential for bone tissue engineering
title_short Stem cell-mediated osteogenesis: therapeutic potential for bone tissue engineering
title_sort stem cell-mediated osteogenesis: therapeutic potential for bone tissue engineering
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3324839/
https://www.ncbi.nlm.nih.gov/pubmed/22500114
http://dx.doi.org/10.2147/BTT.S22407
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