volume 28 pages 64-75

Osteogenic differentiation of human mesenchymal stem cells in the absence of osteogenic supplements: A surface-roughness gradient study.

Publication typeJournal Article
Publication date2015-12-01
scimago Q1
wos Q1
SJR2.007
CiteScore17.8
Impact factor9.6
ISSN17427061, 18787568
Biochemistry
Molecular Biology
General Medicine
Biotechnology
Biomaterials
Biomedical Engineering
Abstract
The use of biomaterials to direct osteogenic differentiation of human mesenchymal stem cells (hMSCs) in the absence of osteogenic supplements is thought to be part of the next generation of orthopedic implants. We previously engineered surface-roughness gradients of average roughness (Ra) varying from the sub-micron to the micrometer range (∼0.5-4.7 μm), and mean distance between peaks (RSm) gradually varying from ∼214 μm to 33 μm. Here we have screened the ability of such surface-gradients of polycaprolactone to influence the expression of alkaline phosphatase (ALP), collagen type 1 (COL1) and mineralization by hMSCs cultured in dexamethasone (Dex)-deprived osteogenic induction medium (OIM) and in basal growth medium (BGM). Ra∼1.53 μm/RSm∼79 μm in Dex-deprived OI medium, and Ra∼0.93 μm/RSm∼135 μm in BGM consistently showed higher effectiveness at supporting the expression of the osteogenic markers ALP, COL1 and mineralization, compared to the tissue culture polystyrene (TCP) control in complete OIM. The superior effectiveness of specific surface-roughness revealed that this strategy may be used as a compelling alternative to soluble osteogenic inducers in orthopedic applications featuring the clinically relevant biodegradable polymer polycaprolactone.Biodegradable polymers, such as polycaprolactone (PCL), are promising materials in the field of tissue engineering and regenerative medicine, which aims at creating viable options to replace permanent orthopedic implants. The material, cells, and growth-stimulating factors are often referred to as the key components of engineered tissues. In this article, we studied the hypothesis of specific surface modification of PCL being capable of inducing mesenchymal stem cell differentiation in bone cells in the absence of cell-differentiating factors. The systematic investigation of the linearly varying surface-roughness gradient showed that an average PCL roughness of 0.93 μm alone can serve as a compelling alternative to soluble osteogenic inducers in orthopedic applications featuring the clinically relevant biodegradable polymer polycaprolactone.
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Faia Torres A. B. et al. Osteogenic differentiation of human mesenchymal stem cells in the absence of osteogenic supplements: A surface-roughness gradient study. // Acta Biomaterialia. 2015. Vol. 28. pp. 64-75.
GOST all authors (up to 50) Copy
Goren T., Guimond-Lischer S., Rottmar M., Maniura-Weber K., Spencer N. D., Keller B., Neves N. M. Osteogenic differentiation of human mesenchymal stem cells in the absence of osteogenic supplements: A surface-roughness gradient study. // Acta Biomaterialia. 2015. Vol. 28. pp. 64-75.
RIS |
Cite this
RIS Copy
TY - JOUR
DO - 10.1016/j.actbio.2015.09.028
UR - https://doi.org/10.1016/j.actbio.2015.09.028
TI - Osteogenic differentiation of human mesenchymal stem cells in the absence of osteogenic supplements: A surface-roughness gradient study.
T2 - Acta Biomaterialia
AU - Goren, Tolga
AU - Guimond-Lischer, Stefanie
AU - Rottmar, Markus
AU - Maniura-Weber, Katharina
AU - Spencer, Nicholas D.
AU - Keller, Beat
AU - Neves, Nuno M.
PY - 2015
DA - 2015/12/01
PB - Elsevier
SP - 64-75
VL - 28
PMID - 26432440
SN - 1742-7061
SN - 1878-7568
ER -
BibTex
Cite this
BibTex (up to 50 authors) Copy
@article{2015_Faia Torres,
author = {Tolga Goren and Stefanie Guimond-Lischer and Markus Rottmar and Katharina Maniura-Weber and Nicholas D. Spencer and Beat Keller and Nuno M. Neves},
title = {Osteogenic differentiation of human mesenchymal stem cells in the absence of osteogenic supplements: A surface-roughness gradient study.},
journal = {Acta Biomaterialia},
year = {2015},
volume = {28},
publisher = {Elsevier},
month = {dec},
url = {https://doi.org/10.1016/j.actbio.2015.09.028},
pages = {64--75},
doi = {10.1016/j.actbio.2015.09.028}
}