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Human urine-derived stem cell exosomes delivered via injectable GelMA templated hydrogel accelerate bone regeneration
The key to critical bone regeneration in tissue engineering relies on an ideal bio-scaffold coated with a controlled release of growth factors. Gelatin methacrylate (GelMA) and Hyaluronic acid methacrylate (HAMA) have been a novel topic of interest in bone regeneration while introducing appropriate...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9945756/ https://www.ncbi.nlm.nih.gov/pubmed/36846309 http://dx.doi.org/10.1016/j.mtbio.2023.100569 |
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author | Lu, Wei Zeng, Min Liu, Wenbin Ma, Tianliang Fan, Xiaolei Li, Hui Wang, Yinan Wang, Haoyi Hu, Yihe Xie, Jie |
author_facet | Lu, Wei Zeng, Min Liu, Wenbin Ma, Tianliang Fan, Xiaolei Li, Hui Wang, Yinan Wang, Haoyi Hu, Yihe Xie, Jie |
author_sort | Lu, Wei |
collection | PubMed |
description | The key to critical bone regeneration in tissue engineering relies on an ideal bio-scaffold coated with a controlled release of growth factors. Gelatin methacrylate (GelMA) and Hyaluronic acid methacrylate (HAMA) have been a novel topic of interest in bone regeneration while introducing appropriate nano-hydroxyapatite (nHAP) to improve its mechanical properties. And the exosomes derived from human urine-derived stem cells (human (USC)EXOs) have also been reported to promote osteogenesis in tissue engineering. The present study aimed to design a new GelMA-HAMA/nHAP composite hydrogel as a drug delivery system. The (USC)EXOs were encapsulated and slow-released in the hydrogel for better osteogenesis. The characterization of the GelMA-based hydrogel showed excellent controlled release performance and appropriate mechanical properties. The in vitro studies showed that the (USC)EXOs/GelMA-HAMA/nHAP composite hydrogel could promote the osteogenesis of bone marrow mesenchymal stem cells (BMSCs) and the angiogenesis of endothelial progenitor cells (EPCs), respectively. Meanwhile, the in vivo results confirmed that this composite hydrogel could significantly promote the defect repair of cranial bone in the rat model. In addition, we also found that (USC)EXOs/GelMA-HAMA/nHAP composite hydrogel can promote the formation of H-type vessels in the bone regeneration area, enhancing the therapeutic effect. In conclusion, our findings suggested that this controllable and biocompatible (USC)EXOs/GelMA-HAMA/nHAP composite hydrogel may effectively promote bone regeneration by coupling osteogenesis and angiogenesis. |
format | Online Article Text |
id | pubmed-9945756 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-99457562023-02-23 Human urine-derived stem cell exosomes delivered via injectable GelMA templated hydrogel accelerate bone regeneration Lu, Wei Zeng, Min Liu, Wenbin Ma, Tianliang Fan, Xiaolei Li, Hui Wang, Yinan Wang, Haoyi Hu, Yihe Xie, Jie Mater Today Bio Full Length Article The key to critical bone regeneration in tissue engineering relies on an ideal bio-scaffold coated with a controlled release of growth factors. Gelatin methacrylate (GelMA) and Hyaluronic acid methacrylate (HAMA) have been a novel topic of interest in bone regeneration while introducing appropriate nano-hydroxyapatite (nHAP) to improve its mechanical properties. And the exosomes derived from human urine-derived stem cells (human (USC)EXOs) have also been reported to promote osteogenesis in tissue engineering. The present study aimed to design a new GelMA-HAMA/nHAP composite hydrogel as a drug delivery system. The (USC)EXOs were encapsulated and slow-released in the hydrogel for better osteogenesis. The characterization of the GelMA-based hydrogel showed excellent controlled release performance and appropriate mechanical properties. The in vitro studies showed that the (USC)EXOs/GelMA-HAMA/nHAP composite hydrogel could promote the osteogenesis of bone marrow mesenchymal stem cells (BMSCs) and the angiogenesis of endothelial progenitor cells (EPCs), respectively. Meanwhile, the in vivo results confirmed that this composite hydrogel could significantly promote the defect repair of cranial bone in the rat model. In addition, we also found that (USC)EXOs/GelMA-HAMA/nHAP composite hydrogel can promote the formation of H-type vessels in the bone regeneration area, enhancing the therapeutic effect. In conclusion, our findings suggested that this controllable and biocompatible (USC)EXOs/GelMA-HAMA/nHAP composite hydrogel may effectively promote bone regeneration by coupling osteogenesis and angiogenesis. Elsevier 2023-02-01 /pmc/articles/PMC9945756/ /pubmed/36846309 http://dx.doi.org/10.1016/j.mtbio.2023.100569 Text en © 2023 The Authors https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Full Length Article Lu, Wei Zeng, Min Liu, Wenbin Ma, Tianliang Fan, Xiaolei Li, Hui Wang, Yinan Wang, Haoyi Hu, Yihe Xie, Jie Human urine-derived stem cell exosomes delivered via injectable GelMA templated hydrogel accelerate bone regeneration |
title | Human urine-derived stem cell exosomes delivered via injectable GelMA templated hydrogel accelerate bone regeneration |
title_full | Human urine-derived stem cell exosomes delivered via injectable GelMA templated hydrogel accelerate bone regeneration |
title_fullStr | Human urine-derived stem cell exosomes delivered via injectable GelMA templated hydrogel accelerate bone regeneration |
title_full_unstemmed | Human urine-derived stem cell exosomes delivered via injectable GelMA templated hydrogel accelerate bone regeneration |
title_short | Human urine-derived stem cell exosomes delivered via injectable GelMA templated hydrogel accelerate bone regeneration |
title_sort | human urine-derived stem cell exosomes delivered via injectable gelma templated hydrogel accelerate bone regeneration |
topic | Full Length Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9945756/ https://www.ncbi.nlm.nih.gov/pubmed/36846309 http://dx.doi.org/10.1016/j.mtbio.2023.100569 |
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