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3D-HA Scaffold Functionalized by Extracellular Matrix of Stem Cells Promotes Bone Repair

BACKGROUND AND PURPOSE: The extracellular matrix (ECM) derived from bone marrow mesenchymal stem cells (BMSCs) has been used in regenerative medicine because of its good biological activity; however, its poor mechanical properties limit its application in bone regeneration. The purpose of this study...

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Autores principales: Chi, Hui, Chen, Guanghua, He, Yixin, Chen, Guanghao, Tu, Hualei, Liu, Xiaoqi, Yan, Jinglong, Wang, Xiaoyan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7418460/
https://www.ncbi.nlm.nih.gov/pubmed/32821104
http://dx.doi.org/10.2147/IJN.S259678
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author Chi, Hui
Chen, Guanghua
He, Yixin
Chen, Guanghao
Tu, Hualei
Liu, Xiaoqi
Yan, Jinglong
Wang, Xiaoyan
author_facet Chi, Hui
Chen, Guanghua
He, Yixin
Chen, Guanghao
Tu, Hualei
Liu, Xiaoqi
Yan, Jinglong
Wang, Xiaoyan
author_sort Chi, Hui
collection PubMed
description BACKGROUND AND PURPOSE: The extracellular matrix (ECM) derived from bone marrow mesenchymal stem cells (BMSCs) has been used in regenerative medicine because of its good biological activity; however, its poor mechanical properties limit its application in bone regeneration. The purpose of this study is to construct a three dimensional-printed hydroxyapatite (3D-HA)/BMSC-ECM composite scaffold that not only has biological activity but also sufficient mechanical strength and reasonably distributed spatial structure. METHODS: A BMSC-ECM was first extracted and formed into micron-sized particles, and then the ECM particles were modified onto the surface of 3D-HA scaffolds using an innovative linking method to generate composite 3D-HA/BMSC-ECM scaffolds. The 3D-HA scaffolds were used as the control group. The basic properties, biocompatibility and osteogenesis ability of both scaffolds were tested in vitro. Finally, a critical skull defect rat model was created and the osteogenesis effect of the scaffolds was evaluated in vivo. RESULTS: The compressive modulus of the composite scaffolds reached 9.45±0.32 MPa, which was similar to that of the 3D-HA scaffolds (p>0.05). The pore size of the two scaffolds was 305±47 um and 315±34 um (p>0.05), respectively. A CCK-8 assay indicated that the scaffolds did not have cytotoxicity. The composite scaffolds had good cell adhesion ability, with a cell adhesion rate of up to 76.00±6.17% after culturing for 7 hours, while that of the 3D-HA scaffolds was 51.85±4.77% (p<0.01). In addition, the composite scaffold displayed higher alkaline phosphatase (ALP) activity, osteogenesis-related mRNA expression, and calcium nodule formation, thus confirming that the composite scaffolds had good osteogenic activity. The composite scaffolds exhibited good bone repair in vivo and were superior to the 3D-HA scaffolds. CONCLUSION: We conclude that BMSC-ECM is a good osteogenic material and that the composite scaffolds have good osteogenic ability, which provides a new method and concept for the repair of bone defects.
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spelling pubmed-74184602020-08-19 3D-HA Scaffold Functionalized by Extracellular Matrix of Stem Cells Promotes Bone Repair Chi, Hui Chen, Guanghua He, Yixin Chen, Guanghao Tu, Hualei Liu, Xiaoqi Yan, Jinglong Wang, Xiaoyan Int J Nanomedicine Original Research BACKGROUND AND PURPOSE: The extracellular matrix (ECM) derived from bone marrow mesenchymal stem cells (BMSCs) has been used in regenerative medicine because of its good biological activity; however, its poor mechanical properties limit its application in bone regeneration. The purpose of this study is to construct a three dimensional-printed hydroxyapatite (3D-HA)/BMSC-ECM composite scaffold that not only has biological activity but also sufficient mechanical strength and reasonably distributed spatial structure. METHODS: A BMSC-ECM was first extracted and formed into micron-sized particles, and then the ECM particles were modified onto the surface of 3D-HA scaffolds using an innovative linking method to generate composite 3D-HA/BMSC-ECM scaffolds. The 3D-HA scaffolds were used as the control group. The basic properties, biocompatibility and osteogenesis ability of both scaffolds were tested in vitro. Finally, a critical skull defect rat model was created and the osteogenesis effect of the scaffolds was evaluated in vivo. RESULTS: The compressive modulus of the composite scaffolds reached 9.45±0.32 MPa, which was similar to that of the 3D-HA scaffolds (p>0.05). The pore size of the two scaffolds was 305±47 um and 315±34 um (p>0.05), respectively. A CCK-8 assay indicated that the scaffolds did not have cytotoxicity. The composite scaffolds had good cell adhesion ability, with a cell adhesion rate of up to 76.00±6.17% after culturing for 7 hours, while that of the 3D-HA scaffolds was 51.85±4.77% (p<0.01). In addition, the composite scaffold displayed higher alkaline phosphatase (ALP) activity, osteogenesis-related mRNA expression, and calcium nodule formation, thus confirming that the composite scaffolds had good osteogenic activity. The composite scaffolds exhibited good bone repair in vivo and were superior to the 3D-HA scaffolds. CONCLUSION: We conclude that BMSC-ECM is a good osteogenic material and that the composite scaffolds have good osteogenic ability, which provides a new method and concept for the repair of bone defects. Dove 2020-08-06 /pmc/articles/PMC7418460/ /pubmed/32821104 http://dx.doi.org/10.2147/IJN.S259678 Text en © 2020 Chi et al. http://creativecommons.org/licenses/by-nc/3.0/ This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php).
spellingShingle Original Research
Chi, Hui
Chen, Guanghua
He, Yixin
Chen, Guanghao
Tu, Hualei
Liu, Xiaoqi
Yan, Jinglong
Wang, Xiaoyan
3D-HA Scaffold Functionalized by Extracellular Matrix of Stem Cells Promotes Bone Repair
title 3D-HA Scaffold Functionalized by Extracellular Matrix of Stem Cells Promotes Bone Repair
title_full 3D-HA Scaffold Functionalized by Extracellular Matrix of Stem Cells Promotes Bone Repair
title_fullStr 3D-HA Scaffold Functionalized by Extracellular Matrix of Stem Cells Promotes Bone Repair
title_full_unstemmed 3D-HA Scaffold Functionalized by Extracellular Matrix of Stem Cells Promotes Bone Repair
title_short 3D-HA Scaffold Functionalized by Extracellular Matrix of Stem Cells Promotes Bone Repair
title_sort 3d-ha scaffold functionalized by extracellular matrix of stem cells promotes bone repair
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7418460/
https://www.ncbi.nlm.nih.gov/pubmed/32821104
http://dx.doi.org/10.2147/IJN.S259678
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