Cargando…

Nanotextured silk fibroin/hydroxyapatite biomimetic bilayer tough structure regulated osteogenic/chondrogenic differentiation of mesenchymal stem cells for osteochondral repair

OBJECTIVES: Articular cartilage plays a vital role in bearing and buffering. Injured cartilage and subchondral bone repair is a crucial challenge in cartilage tissue engineering due to the peculiar structure of osteochondral unit and the requirement of osteogenic/chondrogenic bi‐directional differen...

Descripción completa

Detalles Bibliográficos
Autores principales: Shang, Lingling, Ma, Baojin, Wang, Fulei, Li, Jianhua, Shen, Song, Li, Xiaoyuan, Liu, Hong, Ge, Shaohua
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7653257/
https://www.ncbi.nlm.nih.gov/pubmed/33001510
http://dx.doi.org/10.1111/cpr.12917
_version_ 1783607867314536448
author Shang, Lingling
Ma, Baojin
Wang, Fulei
Li, Jianhua
Shen, Song
Li, Xiaoyuan
Liu, Hong
Ge, Shaohua
author_facet Shang, Lingling
Ma, Baojin
Wang, Fulei
Li, Jianhua
Shen, Song
Li, Xiaoyuan
Liu, Hong
Ge, Shaohua
author_sort Shang, Lingling
collection PubMed
description OBJECTIVES: Articular cartilage plays a vital role in bearing and buffering. Injured cartilage and subchondral bone repair is a crucial challenge in cartilage tissue engineering due to the peculiar structure of osteochondral unit and the requirement of osteogenic/chondrogenic bi‐directional differentiation. Based on the bionics principle, a nanotextured silk fibroin (SF)‐chondroitin sulphate (CS)/hydroxyapatite (HAp) nanowire tough bilayer structure was prepared for osteochondral repair. METHODS: The SF‐CS/HAp membrane was constructed by alcohol‐induced β‐sheet formation serving as the physical crosslink. Its osteochondral repairing capacity was evaluated by culturing bone marrow mesenchymal stem cells (BMSCs) in vitro and constructing a rat osteochondral defect model in vivo. RESULTS: The bilayer SF‐CS/HAp membrane with satisfactory mechanical properties similar to natural cartilage imitated the natural osteochondral unit structural layers and exerted the function of bearing and buffering timely after in vivo implantation. SF‐CS layer upregulated the expression of chondrogenesis‐related genes of BMSCs by surface nanotopography and sustained release CS. Meanwhile, nanotextured HAp layer assembled with nanowire endowed the membrane with an osteogenic differentiation tendency for BMSCs. In vivo results proved that the biomimetic bilayer structure dramatically promoted new cartilage formation and subchondral bone remodelling for osteochondral defect model after implantation. CONCLUSIONS: The SF‐CS/HAp biomimetic bilayer membrane provides a promising strategy for precise osteochondral repair.
format Online
Article
Text
id pubmed-7653257
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher John Wiley and Sons Inc.
record_format MEDLINE/PubMed
spelling pubmed-76532572020-11-16 Nanotextured silk fibroin/hydroxyapatite biomimetic bilayer tough structure regulated osteogenic/chondrogenic differentiation of mesenchymal stem cells for osteochondral repair Shang, Lingling Ma, Baojin Wang, Fulei Li, Jianhua Shen, Song Li, Xiaoyuan Liu, Hong Ge, Shaohua Cell Prolif Original Articles OBJECTIVES: Articular cartilage plays a vital role in bearing and buffering. Injured cartilage and subchondral bone repair is a crucial challenge in cartilage tissue engineering due to the peculiar structure of osteochondral unit and the requirement of osteogenic/chondrogenic bi‐directional differentiation. Based on the bionics principle, a nanotextured silk fibroin (SF)‐chondroitin sulphate (CS)/hydroxyapatite (HAp) nanowire tough bilayer structure was prepared for osteochondral repair. METHODS: The SF‐CS/HAp membrane was constructed by alcohol‐induced β‐sheet formation serving as the physical crosslink. Its osteochondral repairing capacity was evaluated by culturing bone marrow mesenchymal stem cells (BMSCs) in vitro and constructing a rat osteochondral defect model in vivo. RESULTS: The bilayer SF‐CS/HAp membrane with satisfactory mechanical properties similar to natural cartilage imitated the natural osteochondral unit structural layers and exerted the function of bearing and buffering timely after in vivo implantation. SF‐CS layer upregulated the expression of chondrogenesis‐related genes of BMSCs by surface nanotopography and sustained release CS. Meanwhile, nanotextured HAp layer assembled with nanowire endowed the membrane with an osteogenic differentiation tendency for BMSCs. In vivo results proved that the biomimetic bilayer structure dramatically promoted new cartilage formation and subchondral bone remodelling for osteochondral defect model after implantation. CONCLUSIONS: The SF‐CS/HAp biomimetic bilayer membrane provides a promising strategy for precise osteochondral repair. John Wiley and Sons Inc. 2020-10-01 /pmc/articles/PMC7653257/ /pubmed/33001510 http://dx.doi.org/10.1111/cpr.12917 Text en © 2020 The Authors. Cell Proliferation published by John Wiley & Sons Ltd This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Articles
Shang, Lingling
Ma, Baojin
Wang, Fulei
Li, Jianhua
Shen, Song
Li, Xiaoyuan
Liu, Hong
Ge, Shaohua
Nanotextured silk fibroin/hydroxyapatite biomimetic bilayer tough structure regulated osteogenic/chondrogenic differentiation of mesenchymal stem cells for osteochondral repair
title Nanotextured silk fibroin/hydroxyapatite biomimetic bilayer tough structure regulated osteogenic/chondrogenic differentiation of mesenchymal stem cells for osteochondral repair
title_full Nanotextured silk fibroin/hydroxyapatite biomimetic bilayer tough structure regulated osteogenic/chondrogenic differentiation of mesenchymal stem cells for osteochondral repair
title_fullStr Nanotextured silk fibroin/hydroxyapatite biomimetic bilayer tough structure regulated osteogenic/chondrogenic differentiation of mesenchymal stem cells for osteochondral repair
title_full_unstemmed Nanotextured silk fibroin/hydroxyapatite biomimetic bilayer tough structure regulated osteogenic/chondrogenic differentiation of mesenchymal stem cells for osteochondral repair
title_short Nanotextured silk fibroin/hydroxyapatite biomimetic bilayer tough structure regulated osteogenic/chondrogenic differentiation of mesenchymal stem cells for osteochondral repair
title_sort nanotextured silk fibroin/hydroxyapatite biomimetic bilayer tough structure regulated osteogenic/chondrogenic differentiation of mesenchymal stem cells for osteochondral repair
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7653257/
https://www.ncbi.nlm.nih.gov/pubmed/33001510
http://dx.doi.org/10.1111/cpr.12917
work_keys_str_mv AT shanglingling nanotexturedsilkfibroinhydroxyapatitebiomimeticbilayertoughstructureregulatedosteogenicchondrogenicdifferentiationofmesenchymalstemcellsforosteochondralrepair
AT mabaojin nanotexturedsilkfibroinhydroxyapatitebiomimeticbilayertoughstructureregulatedosteogenicchondrogenicdifferentiationofmesenchymalstemcellsforosteochondralrepair
AT wangfulei nanotexturedsilkfibroinhydroxyapatitebiomimeticbilayertoughstructureregulatedosteogenicchondrogenicdifferentiationofmesenchymalstemcellsforosteochondralrepair
AT lijianhua nanotexturedsilkfibroinhydroxyapatitebiomimeticbilayertoughstructureregulatedosteogenicchondrogenicdifferentiationofmesenchymalstemcellsforosteochondralrepair
AT shensong nanotexturedsilkfibroinhydroxyapatitebiomimeticbilayertoughstructureregulatedosteogenicchondrogenicdifferentiationofmesenchymalstemcellsforosteochondralrepair
AT lixiaoyuan nanotexturedsilkfibroinhydroxyapatitebiomimeticbilayertoughstructureregulatedosteogenicchondrogenicdifferentiationofmesenchymalstemcellsforosteochondralrepair
AT liuhong nanotexturedsilkfibroinhydroxyapatitebiomimeticbilayertoughstructureregulatedosteogenicchondrogenicdifferentiationofmesenchymalstemcellsforosteochondralrepair
AT geshaohua nanotexturedsilkfibroinhydroxyapatitebiomimeticbilayertoughstructureregulatedosteogenicchondrogenicdifferentiationofmesenchymalstemcellsforosteochondralrepair