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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...

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Autores principales: Lu, Wei, Zeng, Min, Liu, Wenbin, Ma, Tianliang, Fan, Xiaolei, Li, Hui, Wang, Yinan, Wang, Haoyi, Hu, Yihe, Xie, Jie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2023
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.
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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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