Open Access
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
,
Ekaterina V. Skorb
12
,
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
|
8
9
Chemistry department
11
220030 Minsk
|
14
191002 St. Petersburg
15
Russia
|
Publication type: Journal Article
Publication date: 2021-01-20
scimago Q1
wos Q2
SJR: 0.777
CiteScore: 7.6
Impact factor: 4.6
ISSN: 20462069
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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Total citations:
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Citations from 2024:
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(50%)
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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)
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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.
Cite this
RIS
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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 -
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BibTex (up to 50 authors)
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@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}
}
Cite this
MLA
Copy
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.
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