Open Access
Open access
volume 11 issue 7 pages 3843-3853

The influence of the morphology of titania and hydroxyapatite on the proliferation and osteogenic differentiation of human mesenchymal stem cells

Yauheni U Kuvyrkou 1, 2, 3, 4, 5, 6, 7
Nadzeya Brezhneva 5, 8, 9, 10, 11
Sviatlana A Ulasevich 12, 13, 14, 15
1
 
Republican Scientific and Practical Center of Transfusiology and Medical Biotechnologies, Dolginovskiy tract 160, 220053 Minsk, Belarus
3
 
Republican Scientific and Practical Center of Transfusiology and Medical Biotechnologies
4
 
220053 Minsk
5
 
Belarus
7
 
220006 Minsk
9
 
Chemistry department
11
 
220030 Minsk
14
 
191002 St. Petersburg
15
 
Russia
Publication typeJournal Article
Publication date2021-01-20
scimago Q1
wos Q2
SJR0.777
CiteScore7.6
Impact factor4.6
ISSN20462069
PubMed ID:  35424371
General Chemistry
General Chemical Engineering
Abstract
Herein, the proliferation and osteogenic potential of human mesenchymal stem cells (hMSCs) on the disordered and ordered porous morphology of the titania surface and titania surface modified by hydroxyapatite (HA) are compared for the first time. In 5 days, the MTT-assay showed that the ordered porous morphology of electrochemically fabricated titania nanotubes (TNT) and TNT with chemically deposited hydroxyapatite (TNT-HA) was favorable for stem cell proliferation. In 14 days, RT-qPCR demonstrated that the disordered porous morphology of the sonochemically produced titania mesoporous surface (TMS) and TMS modified by the chemical deposition of HA (TMS-HA) led to the differentiation of hMSCs into the osteogenic direction in the absence of osteogenic inductors. These results originate from the mechanism of mechanotransduction, which sheds a light on the interaction of mesenchymal stem cells with the porous interface through focal adhesion, regulating the expression of genes determining stem cell self-renewal and osteogenic differentiation. The strong focal adhesion of hMSCs adjusted by the disordered TMS and TMS-HA is enough to induce osteogenic differentiation with the delay of cellular self-renewal. The weak focal adhesion of hMSCs tuned by the ordered TNT and TNT-HA affects only cellular self-renewal. The present research makes a new contribution to nanomedicine and engineering of porous implant interfaces for the replacement of bone injuries.
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Kuvyrkou Y. U. et al. The influence of the morphology of titania and hydroxyapatite on the proliferation and osteogenic differentiation of human mesenchymal stem cells // RSC Advances. 2021. Vol. 11. No. 7. pp. 3843-3853.
GOST all authors (up to 50) Copy
Kuvyrkou Y. U., Brezhneva N., Skorb E. V., Ulasevich S. A. The influence of the morphology of titania and hydroxyapatite on the proliferation and osteogenic differentiation of human mesenchymal stem cells // RSC Advances. 2021. Vol. 11. No. 7. pp. 3843-3853.
RIS |
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RIS Copy
TY - JOUR
DO - 10.1039/D0RA08271F
UR - https://xlink.rsc.org/?DOI=D0RA08271F
TI - The influence of the morphology of titania and hydroxyapatite on the proliferation and osteogenic differentiation of human mesenchymal stem cells
T2 - RSC Advances
AU - Kuvyrkou, Yauheni U
AU - Brezhneva, Nadzeya
AU - Skorb, Ekaterina V.
AU - Ulasevich, Sviatlana A
PY - 2021
DA - 2021/01/20
PB - Royal Society of Chemistry (RSC)
SP - 3843-3853
IS - 7
VL - 11
PMID - 35424371
SN - 2046-2069
ER -
BibTex |
Cite this
BibTex (up to 50 authors) Copy
@article{2021_Kuvyrkou,
author = {Yauheni U Kuvyrkou and Nadzeya Brezhneva and Ekaterina V. Skorb and Sviatlana A Ulasevich},
title = {The influence of the morphology of titania and hydroxyapatite on the proliferation and osteogenic differentiation of human mesenchymal stem cells},
journal = {RSC Advances},
year = {2021},
volume = {11},
publisher = {Royal Society of Chemistry (RSC)},
month = {jan},
url = {https://xlink.rsc.org/?DOI=D0RA08271F},
number = {7},
pages = {3843--3853},
doi = {10.1039/D0RA08271F}
}
MLA
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Kuvyrkou, Yauheni U., et al. “The influence of the morphology of titania and hydroxyapatite on the proliferation and osteogenic differentiation of human mesenchymal stem cells.” RSC Advances, vol. 11, no. 7, Jan. 2021, pp. 3843-3853. https://xlink.rsc.org/?DOI=D0RA08271F.