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Superwettable and injectable GelMA-MSC microspheres promote cartilage repair in temporomandibular joints

Temporomandibular disorders (TMD) can be treated by promoting cartilage regeneration with biomaterials. However, there are deficiencies in the infiltration function of bone filler biological materials. In this study, stems cells were loaded onto gelatin methacryloyl (GelMA) hydrogel microspheres end...

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Autores principales: Yang, Yue, Huang, Chenyan, Zheng, Huimin, Meng, Zhaoqiang, Heng, Boon Chin, Zhou, Tuanfeng, Jiang, Shengjie, Wei, Yan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9549523/
https://www.ncbi.nlm.nih.gov/pubmed/36225601
http://dx.doi.org/10.3389/fbioe.2022.1026911
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author Yang, Yue
Huang, Chenyan
Zheng, Huimin
Meng, Zhaoqiang
Heng, Boon Chin
Zhou, Tuanfeng
Jiang, Shengjie
Wei, Yan
author_facet Yang, Yue
Huang, Chenyan
Zheng, Huimin
Meng, Zhaoqiang
Heng, Boon Chin
Zhou, Tuanfeng
Jiang, Shengjie
Wei, Yan
author_sort Yang, Yue
collection PubMed
description Temporomandibular disorders (TMD) can be treated by promoting cartilage regeneration with biomaterials. However, there are deficiencies in the infiltration function of bone filler biological materials. In this study, stems cells were loaded onto gelatin methacryloyl (GelMA) hydrogel microspheres endowed with superwettable properties and TGF-β sustained-release function, which can quickly infiltrate the irregular surface of the temporomandibular joint (TMJ) bone defect area and accelerate cartilage healing. First, to improve cell adhesion and spreading function, the BMSCs-coated GelMA microspheres were endowed with superwetting property. At the same time, the swelling adsorption characteristics of gelatin microspheres could be used to load recombinant TGF-β within the microspheres, which could in turn promote the chondrogenic differentiation of multi-potent bone marrow mesenchymal stem cells. The SEM imaging demonstrated that BMSCs-coated GelMA microsphere has superwettable and superhydrophilic property, which enabled rapid adaptation to the bone defect surface morphology, which is conducive to tissue repair. Furthermore, the cartilage defect model showed that rBMSCs-coated GelMA microspheres promote temporomandibular joint arthritis repair. In conclusion, our study established that BMSC-coated GelMA microspheres endowed with superwetting properties, can colonize the bone defect repair site better with sustained release of growth factors, thus providing an innovative strategy for promoting cartilage regeneration.
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spelling pubmed-95495232022-10-11 Superwettable and injectable GelMA-MSC microspheres promote cartilage repair in temporomandibular joints Yang, Yue Huang, Chenyan Zheng, Huimin Meng, Zhaoqiang Heng, Boon Chin Zhou, Tuanfeng Jiang, Shengjie Wei, Yan Front Bioeng Biotechnol Bioengineering and Biotechnology Temporomandibular disorders (TMD) can be treated by promoting cartilage regeneration with biomaterials. However, there are deficiencies in the infiltration function of bone filler biological materials. In this study, stems cells were loaded onto gelatin methacryloyl (GelMA) hydrogel microspheres endowed with superwettable properties and TGF-β sustained-release function, which can quickly infiltrate the irregular surface of the temporomandibular joint (TMJ) bone defect area and accelerate cartilage healing. First, to improve cell adhesion and spreading function, the BMSCs-coated GelMA microspheres were endowed with superwetting property. At the same time, the swelling adsorption characteristics of gelatin microspheres could be used to load recombinant TGF-β within the microspheres, which could in turn promote the chondrogenic differentiation of multi-potent bone marrow mesenchymal stem cells. The SEM imaging demonstrated that BMSCs-coated GelMA microsphere has superwettable and superhydrophilic property, which enabled rapid adaptation to the bone defect surface morphology, which is conducive to tissue repair. Furthermore, the cartilage defect model showed that rBMSCs-coated GelMA microspheres promote temporomandibular joint arthritis repair. In conclusion, our study established that BMSC-coated GelMA microspheres endowed with superwetting properties, can colonize the bone defect repair site better with sustained release of growth factors, thus providing an innovative strategy for promoting cartilage regeneration. Frontiers Media S.A. 2022-09-20 /pmc/articles/PMC9549523/ /pubmed/36225601 http://dx.doi.org/10.3389/fbioe.2022.1026911 Text en Copyright © 2022 Yang, Huang, Zheng, Meng, Heng, Zhou, Jiang and Wei. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Bioengineering and Biotechnology
Yang, Yue
Huang, Chenyan
Zheng, Huimin
Meng, Zhaoqiang
Heng, Boon Chin
Zhou, Tuanfeng
Jiang, Shengjie
Wei, Yan
Superwettable and injectable GelMA-MSC microspheres promote cartilage repair in temporomandibular joints
title Superwettable and injectable GelMA-MSC microspheres promote cartilage repair in temporomandibular joints
title_full Superwettable and injectable GelMA-MSC microspheres promote cartilage repair in temporomandibular joints
title_fullStr Superwettable and injectable GelMA-MSC microspheres promote cartilage repair in temporomandibular joints
title_full_unstemmed Superwettable and injectable GelMA-MSC microspheres promote cartilage repair in temporomandibular joints
title_short Superwettable and injectable GelMA-MSC microspheres promote cartilage repair in temporomandibular joints
title_sort superwettable and injectable gelma-msc microspheres promote cartilage repair in temporomandibular joints
topic Bioengineering and Biotechnology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9549523/
https://www.ncbi.nlm.nih.gov/pubmed/36225601
http://dx.doi.org/10.3389/fbioe.2022.1026911
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