TY - JOUR
T1 - Effects of multiwalled carbon nanotube reinforced collagen scaffolds on the osteogenic differentiation of mesenchymal stem cells
AU - Baktur, Rena
AU - Yoon, Sang Hee
AU - Kwon, Soonjo
PY - 2013
Y1 - 2013
N2 - With recent advances in nanotechnology, carbon nanotubes (CNTs) have been extensively studied as substrates for cell culture, drug delivery systems, and medical implant materials. However, surprisingly little is known about the effect of CNTs on collective cellular processes (e.g., adhesion, proliferation, and differentiation). This leads to the need for quantitative characterization of the proliferation, differentiation, and mineralization of mesenchymal stem cells (MSCs) on multiwalled CNT-s (MWCNTs-) collagen scaffolds. In here, a set of MWCNTs-collagen scaffolds where three different types of MWCNTs are, respectively, entrapped in reconstituted type I collagen at four different concentrations less than 100 ppm are prepared; the MSC differentiation thereon is investigated by monitoring the transcription factor RunX2 (RunX), transforming growth factor β (TGF-β), alkaline phosphatase (AP), osteocalcin, and mineralized nodules of extracellular matrix (ECM). In short, the MWCNT-collagen scaffolds induced significant increases in AP activity and ECM mineralization due to the increased stiffness and strength of the scaffold by entrapping MWCNTs. This offers a potential for controlling MSC differentiation using MWCNT-collagen scaffolds.
AB - With recent advances in nanotechnology, carbon nanotubes (CNTs) have been extensively studied as substrates for cell culture, drug delivery systems, and medical implant materials. However, surprisingly little is known about the effect of CNTs on collective cellular processes (e.g., adhesion, proliferation, and differentiation). This leads to the need for quantitative characterization of the proliferation, differentiation, and mineralization of mesenchymal stem cells (MSCs) on multiwalled CNT-s (MWCNTs-) collagen scaffolds. In here, a set of MWCNTs-collagen scaffolds where three different types of MWCNTs are, respectively, entrapped in reconstituted type I collagen at four different concentrations less than 100 ppm are prepared; the MSC differentiation thereon is investigated by monitoring the transcription factor RunX2 (RunX), transforming growth factor β (TGF-β), alkaline phosphatase (AP), osteocalcin, and mineralized nodules of extracellular matrix (ECM). In short, the MWCNT-collagen scaffolds induced significant increases in AP activity and ECM mineralization due to the increased stiffness and strength of the scaffold by entrapping MWCNTs. This offers a potential for controlling MSC differentiation using MWCNT-collagen scaffolds.
UR - http://www.scopus.com/inward/record.url?scp=84893821615&partnerID=8YFLogxK
U2 - 10.1155/2013/904083
DO - 10.1155/2013/904083
M3 - Article
AN - SCOPUS:84893821615
SN - 1687-4110
VL - 2013
JO - Journal of Nanomaterials
JF - Journal of Nanomaterials
M1 - 904083
ER -