Cargando…
Allogeneic Bone-Marrow Mesenchymal Stem Cell with Moldable Cryogel for Craniofacial Bone Regeneration
Allogeneic bone-marrow mesenchymal stem cells (BMSCs) can promote bone regeneration and substitute for autologous BMSCs if autologous sources are unavailable, but the efficacy of bone regeneration by allogeneic BMSCs is still inconsistent. A Lewis rat cranium defect model was used to investigate the...
Autores principales: | , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8704672/ https://www.ncbi.nlm.nih.gov/pubmed/34945798 http://dx.doi.org/10.3390/jpm11121326 |
_version_ | 1784621762916384768 |
---|---|
author | Chu, Cheng-Feng Mao, Shih-Hsuan Shyu, Victor Bong-Hang Chen, Chih-Hao Chen, Chien-Tzung |
author_facet | Chu, Cheng-Feng Mao, Shih-Hsuan Shyu, Victor Bong-Hang Chen, Chih-Hao Chen, Chien-Tzung |
author_sort | Chu, Cheng-Feng |
collection | PubMed |
description | Allogeneic bone-marrow mesenchymal stem cells (BMSCs) can promote bone regeneration and substitute for autologous BMSCs if autologous sources are unavailable, but the efficacy of bone regeneration by allogeneic BMSCs is still inconsistent. A Lewis rat cranium defect model was used to investigate the efficacy of bone regeneration between autologous and allogeneic BMSCs in gelatin-nanohydroxyapatite cryogel scaffolds. BMSCs from Wistar rats served as the allogeneic cell lineage. The full-thickness cranium defects were treated by either blank control, cryogel only, allogeneic BMSC-seeded cryogel, or autologous BMSC-seeded cryogel (n = 5). Bone regeneration was monitored by micro-computed tomography and examined histologically at week 12. In addition, we assessed the immune responses in vitro by mixed lymphocyte reaction (MLR) assay and CD(4)(+) immunochemistry staining ex vivo. The MLR showed that allogeneic BSMCs elicited a weak immune response on day 14 that progressively attenuated by day 28. In vivo, the bone regeneration in allogeneic BMSCs was inferior at week 4, but progressively matched the autologous BMSCs by week 12. Our results suggest that allogeneic BMSCs can serve as an alternative source for bone regeneration. |
format | Online Article Text |
id | pubmed-8704672 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-87046722021-12-25 Allogeneic Bone-Marrow Mesenchymal Stem Cell with Moldable Cryogel for Craniofacial Bone Regeneration Chu, Cheng-Feng Mao, Shih-Hsuan Shyu, Victor Bong-Hang Chen, Chih-Hao Chen, Chien-Tzung J Pers Med Article Allogeneic bone-marrow mesenchymal stem cells (BMSCs) can promote bone regeneration and substitute for autologous BMSCs if autologous sources are unavailable, but the efficacy of bone regeneration by allogeneic BMSCs is still inconsistent. A Lewis rat cranium defect model was used to investigate the efficacy of bone regeneration between autologous and allogeneic BMSCs in gelatin-nanohydroxyapatite cryogel scaffolds. BMSCs from Wistar rats served as the allogeneic cell lineage. The full-thickness cranium defects were treated by either blank control, cryogel only, allogeneic BMSC-seeded cryogel, or autologous BMSC-seeded cryogel (n = 5). Bone regeneration was monitored by micro-computed tomography and examined histologically at week 12. In addition, we assessed the immune responses in vitro by mixed lymphocyte reaction (MLR) assay and CD(4)(+) immunochemistry staining ex vivo. The MLR showed that allogeneic BSMCs elicited a weak immune response on day 14 that progressively attenuated by day 28. In vivo, the bone regeneration in allogeneic BMSCs was inferior at week 4, but progressively matched the autologous BMSCs by week 12. Our results suggest that allogeneic BMSCs can serve as an alternative source for bone regeneration. MDPI 2021-12-07 /pmc/articles/PMC8704672/ /pubmed/34945798 http://dx.doi.org/10.3390/jpm11121326 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Chu, Cheng-Feng Mao, Shih-Hsuan Shyu, Victor Bong-Hang Chen, Chih-Hao Chen, Chien-Tzung Allogeneic Bone-Marrow Mesenchymal Stem Cell with Moldable Cryogel for Craniofacial Bone Regeneration |
title | Allogeneic Bone-Marrow Mesenchymal Stem Cell with Moldable Cryogel for Craniofacial Bone Regeneration |
title_full | Allogeneic Bone-Marrow Mesenchymal Stem Cell with Moldable Cryogel for Craniofacial Bone Regeneration |
title_fullStr | Allogeneic Bone-Marrow Mesenchymal Stem Cell with Moldable Cryogel for Craniofacial Bone Regeneration |
title_full_unstemmed | Allogeneic Bone-Marrow Mesenchymal Stem Cell with Moldable Cryogel for Craniofacial Bone Regeneration |
title_short | Allogeneic Bone-Marrow Mesenchymal Stem Cell with Moldable Cryogel for Craniofacial Bone Regeneration |
title_sort | allogeneic bone-marrow mesenchymal stem cell with moldable cryogel for craniofacial bone regeneration |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8704672/ https://www.ncbi.nlm.nih.gov/pubmed/34945798 http://dx.doi.org/10.3390/jpm11121326 |
work_keys_str_mv | AT chuchengfeng allogeneicbonemarrowmesenchymalstemcellwithmoldablecryogelforcraniofacialboneregeneration AT maoshihhsuan allogeneicbonemarrowmesenchymalstemcellwithmoldablecryogelforcraniofacialboneregeneration AT shyuvictorbonghang allogeneicbonemarrowmesenchymalstemcellwithmoldablecryogelforcraniofacialboneregeneration AT chenchihhao allogeneicbonemarrowmesenchymalstemcellwithmoldablecryogelforcraniofacialboneregeneration AT chenchientzung allogeneicbonemarrowmesenchymalstemcellwithmoldablecryogelforcraniofacialboneregeneration |