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Improving effects of chitosan nanofiber scaffolds on osteoblast proliferation and maturation.
Ho, Ming-Hua; Liao, Mei-Hsiu; Lin, Yi-Ling; Lai, Chien-Hao; Lin, Pei-I; Chen, Ruei-Ming.
Afiliação
  • Ho MH; Department of Chemical Engineering, National Taiwan University of Science and Technology, Taipei, Taiwan ; Cell Physiology and Molecular Image Research Center and Department of Anesthesiology, Wan Fang Hospital, Taipei, Taiwan.
  • Liao MH; Graduate Institute of Medical Sciences, Taipei Medical University, Taipei, Taiwan.
  • Lin YL; Cell Physiology and Molecular Image Research Center and Department of Anesthesiology, Wan Fang Hospital, Taipei, Taiwan.
  • Lai CH; Graduate Institute of Medical Sciences, Taipei Medical University, Taipei, Taiwan.
  • Lin PI; Graduate Institute of Medical Sciences, Taipei Medical University, Taipei, Taiwan.
  • Chen RM; Cell Physiology and Molecular Image Research Center and Department of Anesthesiology, Wan Fang Hospital, Taipei, Taiwan ; Graduate Institute of Medical Sciences, Taipei Medical University, Taipei, Taiwan ; Anesthetics and Toxicology Research Center, Taipei Medical University Hospital, Taipei, Taiwan
Int J Nanomedicine ; 9: 4293-304, 2014.
Article em En | MEDLINE | ID: mdl-25246786
ABSTRACT
Osteoblast maturation plays a key role in regulating osteogenesis. Electrospun nanofibrous products were reported to possess a high surface area and porosity. In this study, we developed chitosan nanofibers and examined the effects of nanofibrous scaffolds on osteoblast maturation and the possible mechanisms. Macro- and micro observations of the chitosan nanofibers revealed that these nanoproducts had a flat surface and well-distributed fibers with nanoscale diameters. Mouse osteoblasts were able to attach onto the chitosan nanofiber scaffolds, and the scaffolds degraded in a time-dependent manner. Analysis by scanning electron microscopy further showed mouse osteoblasts adhered onto the scaffolds along the nanofibers, and cell-cell communication was also detected. Mouse osteoblasts grew much better on chitosan nanofiber scaffolds than on chitosan films. In addition, human osteoblasts were able to adhere and grow on the chitosan nanofiber scaffolds. Interestingly, culturing human osteoblasts on chitosan nanofiber scaffolds time-dependently increased DNA replication and cell proliferation. In parallel, administration of human osteoblasts onto chitosan nanofibers significantly induced osteopontin, osteocalcin, and alkaline phosphatase (ALP) messenger (m)RNA expression. As to the mechanism, chitosan nanofibers triggered runt-related transcription factor 2 mRNA and protein syntheses. Consequently, results of ALP-, alizarin red-, and von Kossa-staining analyses showed that chitosan nanofibers improved osteoblast mineralization. Taken together, results of this study demonstrate that chitosan nanofibers can stimulate osteoblast proliferation and maturation via runt-related transcription factor 2-mediated regulation of osteoblast-associated osteopontin, osteocalcin, and ALP gene expression.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Osteoblastos / Materiais Biocompatíveis / Diferenciação Celular / Quitosana / Proliferação de Células / Nanofibras Limite: Animals / Humans Idioma: En Revista: Int J Nanomedicine Ano de publicação: 2014 Tipo de documento: Article País de afiliação: Taiwan

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Osteoblastos / Materiais Biocompatíveis / Diferenciação Celular / Quitosana / Proliferação de Células / Nanofibras Limite: Animals / Humans Idioma: En Revista: Int J Nanomedicine Ano de publicação: 2014 Tipo de documento: Article País de afiliação: Taiwan