Cargando…

F-actin Regulates Osteoblastic Differentiation of Mesenchymal Stem Cells on TiO(2) Nanotubes Through MKL1 and YAP/TAZ

Titanium and titanium alloys are widely used in orthopedic implants. Modifying the nanotopography provides a new strategy to improve osseointegration of titanium substrates. Filamentous actin (F-actin) polymerization, as a mechanical loading structure, is generally considered to be involved in cell...

Descripción completa

Detalles Bibliográficos
Autores principales: Tong, Zhicheng, Liu, Yanchang, Xia, Runzhi, Chang, Yongyun, Hu, Yi, Liu, Pengcheng, Zhai, Zanjing, Zhang, Jingwei, Li, Huiwu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer US 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7511505/
https://www.ncbi.nlm.nih.gov/pubmed/32965618
http://dx.doi.org/10.1186/s11671-020-03415-9
_version_ 1783585966044217344
author Tong, Zhicheng
Liu, Yanchang
Xia, Runzhi
Chang, Yongyun
Hu, Yi
Liu, Pengcheng
Zhai, Zanjing
Zhang, Jingwei
Li, Huiwu
author_facet Tong, Zhicheng
Liu, Yanchang
Xia, Runzhi
Chang, Yongyun
Hu, Yi
Liu, Pengcheng
Zhai, Zanjing
Zhang, Jingwei
Li, Huiwu
author_sort Tong, Zhicheng
collection PubMed
description Titanium and titanium alloys are widely used in orthopedic implants. Modifying the nanotopography provides a new strategy to improve osseointegration of titanium substrates. Filamentous actin (F-actin) polymerization, as a mechanical loading structure, is generally considered to be involved in cell migration, endocytosis, cell division, and cell shape maintenance. Whether F-actin is involved and how it functions in nanotube-induced osteogenic differentiation of mesenchymal stem cells (MSCs) remain to be elucidated. In this study, we fabricated TiO(2) nanotubes on the surface of a titanium substrate by anodic oxidation and characterized their features by scanning electron microscopy (SEM), X-ray energy dispersive analysis (EDS), and atomic force microscopy (AFM). Alkaline phosphatase (ALP) staining, Western blotting, qRT-PCR, and immunofluorescence staining were performed to explore the osteogenic potential, the level of F-actin, and the expression of MKL1 and YAP/TAZ. Our results showed that the inner diameter and roughness of TiO(2) nanotubes increased with the increase of the anodic oxidation voltage from 30 to 70 V, while their height was 2 μm consistently. Further, the larger the tube diameter, the stronger the ability of TiO(2) nanotubes to promote osteogenic differentiation of MSCs. Inhibiting F-actin polymerization by Cyto D inhibited osteogenic differentiation of MSCs as well as the expression of proteins contained in focal adhesion complexes such as vinculin (VCL) and focal adhesion kinase (FAK). In contrast, after Jasp treatment, polymerization of F-actin enhanced the expression of RhoA and transcription factors YAP/TAZ. Based on these data, we concluded that TiO(2) nanotubes facilitated the osteogenic differentiation of MSCs, and this ability was enhanced with the increasing diameter of the nanotubes within a certain range (30–70 V). F-actin mediated this process through MKL1 and YAP/TAZ.
format Online
Article
Text
id pubmed-7511505
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher Springer US
record_format MEDLINE/PubMed
spelling pubmed-75115052020-10-08 F-actin Regulates Osteoblastic Differentiation of Mesenchymal Stem Cells on TiO(2) Nanotubes Through MKL1 and YAP/TAZ Tong, Zhicheng Liu, Yanchang Xia, Runzhi Chang, Yongyun Hu, Yi Liu, Pengcheng Zhai, Zanjing Zhang, Jingwei Li, Huiwu Nanoscale Res Lett Nano Express Titanium and titanium alloys are widely used in orthopedic implants. Modifying the nanotopography provides a new strategy to improve osseointegration of titanium substrates. Filamentous actin (F-actin) polymerization, as a mechanical loading structure, is generally considered to be involved in cell migration, endocytosis, cell division, and cell shape maintenance. Whether F-actin is involved and how it functions in nanotube-induced osteogenic differentiation of mesenchymal stem cells (MSCs) remain to be elucidated. In this study, we fabricated TiO(2) nanotubes on the surface of a titanium substrate by anodic oxidation and characterized their features by scanning electron microscopy (SEM), X-ray energy dispersive analysis (EDS), and atomic force microscopy (AFM). Alkaline phosphatase (ALP) staining, Western blotting, qRT-PCR, and immunofluorescence staining were performed to explore the osteogenic potential, the level of F-actin, and the expression of MKL1 and YAP/TAZ. Our results showed that the inner diameter and roughness of TiO(2) nanotubes increased with the increase of the anodic oxidation voltage from 30 to 70 V, while their height was 2 μm consistently. Further, the larger the tube diameter, the stronger the ability of TiO(2) nanotubes to promote osteogenic differentiation of MSCs. Inhibiting F-actin polymerization by Cyto D inhibited osteogenic differentiation of MSCs as well as the expression of proteins contained in focal adhesion complexes such as vinculin (VCL) and focal adhesion kinase (FAK). In contrast, after Jasp treatment, polymerization of F-actin enhanced the expression of RhoA and transcription factors YAP/TAZ. Based on these data, we concluded that TiO(2) nanotubes facilitated the osteogenic differentiation of MSCs, and this ability was enhanced with the increasing diameter of the nanotubes within a certain range (30–70 V). F-actin mediated this process through MKL1 and YAP/TAZ. Springer US 2020-09-23 /pmc/articles/PMC7511505/ /pubmed/32965618 http://dx.doi.org/10.1186/s11671-020-03415-9 Text en © The Author(s) 2020 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Nano Express
Tong, Zhicheng
Liu, Yanchang
Xia, Runzhi
Chang, Yongyun
Hu, Yi
Liu, Pengcheng
Zhai, Zanjing
Zhang, Jingwei
Li, Huiwu
F-actin Regulates Osteoblastic Differentiation of Mesenchymal Stem Cells on TiO(2) Nanotubes Through MKL1 and YAP/TAZ
title F-actin Regulates Osteoblastic Differentiation of Mesenchymal Stem Cells on TiO(2) Nanotubes Through MKL1 and YAP/TAZ
title_full F-actin Regulates Osteoblastic Differentiation of Mesenchymal Stem Cells on TiO(2) Nanotubes Through MKL1 and YAP/TAZ
title_fullStr F-actin Regulates Osteoblastic Differentiation of Mesenchymal Stem Cells on TiO(2) Nanotubes Through MKL1 and YAP/TAZ
title_full_unstemmed F-actin Regulates Osteoblastic Differentiation of Mesenchymal Stem Cells on TiO(2) Nanotubes Through MKL1 and YAP/TAZ
title_short F-actin Regulates Osteoblastic Differentiation of Mesenchymal Stem Cells on TiO(2) Nanotubes Through MKL1 and YAP/TAZ
title_sort f-actin regulates osteoblastic differentiation of mesenchymal stem cells on tio(2) nanotubes through mkl1 and yap/taz
topic Nano Express
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7511505/
https://www.ncbi.nlm.nih.gov/pubmed/32965618
http://dx.doi.org/10.1186/s11671-020-03415-9
work_keys_str_mv AT tongzhicheng factinregulatesosteoblasticdifferentiationofmesenchymalstemcellsontio2nanotubesthroughmkl1andyaptaz
AT liuyanchang factinregulatesosteoblasticdifferentiationofmesenchymalstemcellsontio2nanotubesthroughmkl1andyaptaz
AT xiarunzhi factinregulatesosteoblasticdifferentiationofmesenchymalstemcellsontio2nanotubesthroughmkl1andyaptaz
AT changyongyun factinregulatesosteoblasticdifferentiationofmesenchymalstemcellsontio2nanotubesthroughmkl1andyaptaz
AT huyi factinregulatesosteoblasticdifferentiationofmesenchymalstemcellsontio2nanotubesthroughmkl1andyaptaz
AT liupengcheng factinregulatesosteoblasticdifferentiationofmesenchymalstemcellsontio2nanotubesthroughmkl1andyaptaz
AT zhaizanjing factinregulatesosteoblasticdifferentiationofmesenchymalstemcellsontio2nanotubesthroughmkl1andyaptaz
AT zhangjingwei factinregulatesosteoblasticdifferentiationofmesenchymalstemcellsontio2nanotubesthroughmkl1andyaptaz
AT lihuiwu factinregulatesosteoblasticdifferentiationofmesenchymalstemcellsontio2nanotubesthroughmkl1andyaptaz