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Injectable nanoporous microgels generate vascularized constructs and support bone regeneration in critical-sized defects
Large and aberrant bone fractures require ossification and concomitant vascularization for proper healing. Evidence indicates that osteogenesis and vessel growth are coupled in bone fractures. Although the synergistic role of endothelial cells has been recognized, vascularizing large bone grafts rem...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9499928/ https://www.ncbi.nlm.nih.gov/pubmed/36138042 http://dx.doi.org/10.1038/s41598-022-19968-x |
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author | Patrick, Matthew D. Keys, Jeremy F. Suresh Kumar, Harshini Annamalai, Ramkumar T. |
author_facet | Patrick, Matthew D. Keys, Jeremy F. Suresh Kumar, Harshini Annamalai, Ramkumar T. |
author_sort | Patrick, Matthew D. |
collection | PubMed |
description | Large and aberrant bone fractures require ossification and concomitant vascularization for proper healing. Evidence indicates that osteogenesis and vessel growth are coupled in bone fractures. Although the synergistic role of endothelial cells has been recognized, vascularizing large bone grafts remains a challenge and has apprehended the clinical translation of engineered bone constructs. Here, we describe a facile method to fabricate vascularized constructs using chitosan and gelatin-based microgels that promote osteogenesis of human mesenchymal stromal cells (MSC) while supporting endothelial sprouting and network formation. The microgels are enzymatically degradable and had a high hydration rate with a volume swelling ratio of ~ 493% and a polymer density of ~ 431 mg/cm(3)(,) which is comparable to that of native skeletal tissues. AFM indentation of the surface showed an average Young’s modulus of 189 kPa, falling in a range that is conducive to both osteogenesis and vasculogenesis. The osteogenic microgel containing chitosan, gelatin, and hydroxyapatite, mimicking the bone matrix, supported robust attachment, proliferation, and differentiation of MSC. On the other hand, the vasculogenic microgels containing only gelatin, enriched endothelial phenotype and enabled vascular networks formation when embedded in 3D matrices. Combining the two types of microgels created a hybrid construct that sustained the functions of both osteogenic and vasculogenic microgels and enhanced one another. Using a murine model, we also show that the osteogenic microgels regenerate bone in a critical-sized defect with > 95% defect closure by week 12. These multifunctional microgels can be administered minimally invasively and can conformally fill large bone defects. This work lays the foundation to establish principles of designing multiphasic scaffolds with tissue-specific biophysical and biochemical properties for regenerating vascularized and interfacial tissues. |
format | Online Article Text |
id | pubmed-9499928 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-94999282022-09-24 Injectable nanoporous microgels generate vascularized constructs and support bone regeneration in critical-sized defects Patrick, Matthew D. Keys, Jeremy F. Suresh Kumar, Harshini Annamalai, Ramkumar T. Sci Rep Article Large and aberrant bone fractures require ossification and concomitant vascularization for proper healing. Evidence indicates that osteogenesis and vessel growth are coupled in bone fractures. Although the synergistic role of endothelial cells has been recognized, vascularizing large bone grafts remains a challenge and has apprehended the clinical translation of engineered bone constructs. Here, we describe a facile method to fabricate vascularized constructs using chitosan and gelatin-based microgels that promote osteogenesis of human mesenchymal stromal cells (MSC) while supporting endothelial sprouting and network formation. The microgels are enzymatically degradable and had a high hydration rate with a volume swelling ratio of ~ 493% and a polymer density of ~ 431 mg/cm(3)(,) which is comparable to that of native skeletal tissues. AFM indentation of the surface showed an average Young’s modulus of 189 kPa, falling in a range that is conducive to both osteogenesis and vasculogenesis. The osteogenic microgel containing chitosan, gelatin, and hydroxyapatite, mimicking the bone matrix, supported robust attachment, proliferation, and differentiation of MSC. On the other hand, the vasculogenic microgels containing only gelatin, enriched endothelial phenotype and enabled vascular networks formation when embedded in 3D matrices. Combining the two types of microgels created a hybrid construct that sustained the functions of both osteogenic and vasculogenic microgels and enhanced one another. Using a murine model, we also show that the osteogenic microgels regenerate bone in a critical-sized defect with > 95% defect closure by week 12. These multifunctional microgels can be administered minimally invasively and can conformally fill large bone defects. This work lays the foundation to establish principles of designing multiphasic scaffolds with tissue-specific biophysical and biochemical properties for regenerating vascularized and interfacial tissues. Nature Publishing Group UK 2022-09-22 /pmc/articles/PMC9499928/ /pubmed/36138042 http://dx.doi.org/10.1038/s41598-022-19968-x Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Patrick, Matthew D. Keys, Jeremy F. Suresh Kumar, Harshini Annamalai, Ramkumar T. Injectable nanoporous microgels generate vascularized constructs and support bone regeneration in critical-sized defects |
title | Injectable nanoporous microgels generate vascularized constructs and support bone regeneration in critical-sized defects |
title_full | Injectable nanoporous microgels generate vascularized constructs and support bone regeneration in critical-sized defects |
title_fullStr | Injectable nanoporous microgels generate vascularized constructs and support bone regeneration in critical-sized defects |
title_full_unstemmed | Injectable nanoporous microgels generate vascularized constructs and support bone regeneration in critical-sized defects |
title_short | Injectable nanoporous microgels generate vascularized constructs and support bone regeneration in critical-sized defects |
title_sort | injectable nanoporous microgels generate vascularized constructs and support bone regeneration in critical-sized defects |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9499928/ https://www.ncbi.nlm.nih.gov/pubmed/36138042 http://dx.doi.org/10.1038/s41598-022-19968-x |
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