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The Osteogenic Differentiation Effect of the FN Type 10-Peptide Amphiphile on PCL Fiber

The fibronectin type 10-peptide amphiphile (FNIII10-PA) was previously genetically engineered and showed osteogenic differentiation activity on rat bone marrow stem cells (rBMSCs). In this study, we investigated whether FNIII10-PA demonstrated cellular activity on polycaprolactone (PCL) fibers. FNII...

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Detalles Bibliográficos
Autores principales: Yun, Ye-Rang, Kim, Hae-Won, Jang, Jun-Hyeog
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5796102/
https://www.ncbi.nlm.nih.gov/pubmed/29300346
http://dx.doi.org/10.3390/ijms19010153
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author Yun, Ye-Rang
Kim, Hae-Won
Jang, Jun-Hyeog
author_facet Yun, Ye-Rang
Kim, Hae-Won
Jang, Jun-Hyeog
author_sort Yun, Ye-Rang
collection PubMed
description The fibronectin type 10-peptide amphiphile (FNIII10-PA) was previously genetically engineered and showed osteogenic differentiation activity on rat bone marrow stem cells (rBMSCs). In this study, we investigated whether FNIII10-PA demonstrated cellular activity on polycaprolactone (PCL) fibers. FNIII10-PA significantly increased protein production and cell adhesion activity on PCL fibers in a dose-dependent manner. In cell proliferation results, there was no effect on cell proliferation activity by FNIII10-PA; however, FNIII10-PA induced the osteogenic differentiation of MC3T3-E1 cells via upregulation of bone sialoprotein (BSP), collagen type I (Col I), osteocalcin (OC), osteopontin (OPN), and runt-related transcription factor 2 (Runx2) mitochondrial RNA (mRNA) levels; it did not increase the alkaline phosphatase (ALP) mRNA level. These results indicate that FNIII10-PA has potential as a new biomaterial for bone tissue engineering applications.
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spelling pubmed-57961022018-02-09 The Osteogenic Differentiation Effect of the FN Type 10-Peptide Amphiphile on PCL Fiber Yun, Ye-Rang Kim, Hae-Won Jang, Jun-Hyeog Int J Mol Sci Article The fibronectin type 10-peptide amphiphile (FNIII10-PA) was previously genetically engineered and showed osteogenic differentiation activity on rat bone marrow stem cells (rBMSCs). In this study, we investigated whether FNIII10-PA demonstrated cellular activity on polycaprolactone (PCL) fibers. FNIII10-PA significantly increased protein production and cell adhesion activity on PCL fibers in a dose-dependent manner. In cell proliferation results, there was no effect on cell proliferation activity by FNIII10-PA; however, FNIII10-PA induced the osteogenic differentiation of MC3T3-E1 cells via upregulation of bone sialoprotein (BSP), collagen type I (Col I), osteocalcin (OC), osteopontin (OPN), and runt-related transcription factor 2 (Runx2) mitochondrial RNA (mRNA) levels; it did not increase the alkaline phosphatase (ALP) mRNA level. These results indicate that FNIII10-PA has potential as a new biomaterial for bone tissue engineering applications. MDPI 2018-01-04 /pmc/articles/PMC5796102/ /pubmed/29300346 http://dx.doi.org/10.3390/ijms19010153 Text en © 2018 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Yun, Ye-Rang
Kim, Hae-Won
Jang, Jun-Hyeog
The Osteogenic Differentiation Effect of the FN Type 10-Peptide Amphiphile on PCL Fiber
title The Osteogenic Differentiation Effect of the FN Type 10-Peptide Amphiphile on PCL Fiber
title_full The Osteogenic Differentiation Effect of the FN Type 10-Peptide Amphiphile on PCL Fiber
title_fullStr The Osteogenic Differentiation Effect of the FN Type 10-Peptide Amphiphile on PCL Fiber
title_full_unstemmed The Osteogenic Differentiation Effect of the FN Type 10-Peptide Amphiphile on PCL Fiber
title_short The Osteogenic Differentiation Effect of the FN Type 10-Peptide Amphiphile on PCL Fiber
title_sort osteogenic differentiation effect of the fn type 10-peptide amphiphile on pcl fiber
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5796102/
https://www.ncbi.nlm.nih.gov/pubmed/29300346
http://dx.doi.org/10.3390/ijms19010153
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