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In-situ forming injectable GFOGER-conjugated BMSCs-laden hydrogels for osteochondral regeneration
The collagen-mimetic peptide GFOGER possesses the chondrogenic potential and has been used as a cell adhesion peptide or chondrogenic inducer. Here, we prepared an injectable in situ forming composite hydrogel system comprising methoxy polyethylene glycol-b-polycaprolactone (MPEG-PCL) and GFOGER-con...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9822921/ https://www.ncbi.nlm.nih.gov/pubmed/36609447 http://dx.doi.org/10.1038/s41536-022-00274-z |
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author | Ha, Mi Yeon Yang, Dae Hyeok You, Su Jung Kim, Hyun Joo Chun, Heung Jae |
author_facet | Ha, Mi Yeon Yang, Dae Hyeok You, Su Jung Kim, Hyun Joo Chun, Heung Jae |
author_sort | Ha, Mi Yeon |
collection | PubMed |
description | The collagen-mimetic peptide GFOGER possesses the chondrogenic potential and has been used as a cell adhesion peptide or chondrogenic inducer. Here, we prepared an injectable in situ forming composite hydrogel system comprising methoxy polyethylene glycol-b-polycaprolactone (MPEG-PCL) and GFOGER-conjugated PEG-PCL (GFOGER-PEG-PCL) with various GFOGER concentrations based on our recently patented technology. The conjugation of GFOGER to PEG-PCL was confirmed by (1)H NMR, and the particle size distribution and rheological properties for the sol-gel transition behavior of the samples with respect to the GFOGER content were evaluated systemically. In vitro experiments using rat bone marrow-derived mesenchymal stem cells (BMSCs) revealed that the GFOGER-PEG-PCL hydrogel significantly enhanced expression of integrins (β1, α2, and α11), increased expression of FAK, and induced downstream signaling of ERK and p38. Overexpression of chondrogenic markers suggested that BMSCs have the potential to differentiate into chondrogenic lineages within GFOGER-PEG-PCL samples. In vivo studies using a rat osteochondral defect model revealed that transplanted BMSCs with GFOGER(0.8)-PEG-PCL survived at the defect with strong chondrogenic expression after 4 weeks. The stem cell-laden GFOGER(0.8)-PEG-PCL hydrogel produced remarkable osteochondral regeneration at 8 weeks of transplantation, as determined by histological findings and micro-CT analysis. The histomorphological score in the GFOGER(0.8)-PEG-PCL + BMSCs group was ~1.7-, 2.6-, and 5.3-fold higher than that in the GFOGER(0.8)-PEG-PCL, MPEG-PCL, and defect groups, respectively. Taken together, these results provide an important platform for further advanced GFOGER-based stem cell research for osteochondral repair. |
format | Online Article Text |
id | pubmed-9822921 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-98229212023-01-08 In-situ forming injectable GFOGER-conjugated BMSCs-laden hydrogels for osteochondral regeneration Ha, Mi Yeon Yang, Dae Hyeok You, Su Jung Kim, Hyun Joo Chun, Heung Jae NPJ Regen Med Article The collagen-mimetic peptide GFOGER possesses the chondrogenic potential and has been used as a cell adhesion peptide or chondrogenic inducer. Here, we prepared an injectable in situ forming composite hydrogel system comprising methoxy polyethylene glycol-b-polycaprolactone (MPEG-PCL) and GFOGER-conjugated PEG-PCL (GFOGER-PEG-PCL) with various GFOGER concentrations based on our recently patented technology. The conjugation of GFOGER to PEG-PCL was confirmed by (1)H NMR, and the particle size distribution and rheological properties for the sol-gel transition behavior of the samples with respect to the GFOGER content were evaluated systemically. In vitro experiments using rat bone marrow-derived mesenchymal stem cells (BMSCs) revealed that the GFOGER-PEG-PCL hydrogel significantly enhanced expression of integrins (β1, α2, and α11), increased expression of FAK, and induced downstream signaling of ERK and p38. Overexpression of chondrogenic markers suggested that BMSCs have the potential to differentiate into chondrogenic lineages within GFOGER-PEG-PCL samples. In vivo studies using a rat osteochondral defect model revealed that transplanted BMSCs with GFOGER(0.8)-PEG-PCL survived at the defect with strong chondrogenic expression after 4 weeks. The stem cell-laden GFOGER(0.8)-PEG-PCL hydrogel produced remarkable osteochondral regeneration at 8 weeks of transplantation, as determined by histological findings and micro-CT analysis. The histomorphological score in the GFOGER(0.8)-PEG-PCL + BMSCs group was ~1.7-, 2.6-, and 5.3-fold higher than that in the GFOGER(0.8)-PEG-PCL, MPEG-PCL, and defect groups, respectively. Taken together, these results provide an important platform for further advanced GFOGER-based stem cell research for osteochondral repair. Nature Publishing Group UK 2023-01-06 /pmc/articles/PMC9822921/ /pubmed/36609447 http://dx.doi.org/10.1038/s41536-022-00274-z Text en © The Author(s) 2023 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Ha, Mi Yeon Yang, Dae Hyeok You, Su Jung Kim, Hyun Joo Chun, Heung Jae In-situ forming injectable GFOGER-conjugated BMSCs-laden hydrogels for osteochondral regeneration |
title | In-situ forming injectable GFOGER-conjugated BMSCs-laden hydrogels for osteochondral regeneration |
title_full | In-situ forming injectable GFOGER-conjugated BMSCs-laden hydrogels for osteochondral regeneration |
title_fullStr | In-situ forming injectable GFOGER-conjugated BMSCs-laden hydrogels for osteochondral regeneration |
title_full_unstemmed | In-situ forming injectable GFOGER-conjugated BMSCs-laden hydrogels for osteochondral regeneration |
title_short | In-situ forming injectable GFOGER-conjugated BMSCs-laden hydrogels for osteochondral regeneration |
title_sort | in-situ forming injectable gfoger-conjugated bmscs-laden hydrogels for osteochondral regeneration |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9822921/ https://www.ncbi.nlm.nih.gov/pubmed/36609447 http://dx.doi.org/10.1038/s41536-022-00274-z |
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