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Shelf Life Evaluation of Clinical Grade Chondrogenic Induced Aged Adult Stem Cells for Cartilage Regeneration
The study objectives include, enhancing the proliferations of aged bone marrow stem cells (BMSCs) and adipose stem cells (ADSCs); and evaluating the shelf lives of clinical grade chondrogenically induced cells from both samples. ADSCs and BMSCs from 56 patients (76 ± 8 yrs) were proliferated using b...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5847521/ https://www.ncbi.nlm.nih.gov/pubmed/29531282 http://dx.doi.org/10.1038/s41598-018-22748-1 |
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author | Ude, C. C. Seet, W. T. Sharen Aini, S. Aminuddin, B. S. Ruszymah, B. H. I. |
author_facet | Ude, C. C. Seet, W. T. Sharen Aini, S. Aminuddin, B. S. Ruszymah, B. H. I. |
author_sort | Ude, C. C. |
collection | PubMed |
description | The study objectives include, enhancing the proliferations of aged bone marrow stem cells (BMSCs) and adipose stem cells (ADSCs); and evaluating the shelf lives of clinical grade chondrogenically induced cells from both samples. ADSCs and BMSCs from 56 patients (76 ± 8 yrs) were proliferated using basal medium (FD) and at (5, 10, 15, 20 and 25) ng/ml of basal fibroblast growth factor (bFGF). They were induced to chondrogenic lineage and stored for more than 120 hrs in FD, serum, Dulbecco’s phosphate buffered saline (DPBS) and saline at 4 °C. In FD, cells stagnated and BMSCs’ population doubling time (PDT) was 137 ± 30 hrs, while ADSCs’ was 129.7 ± 40 hrs. bFGF caused PDT’s decrease to 24.5 ± 5.8 hrs in BMSCs and 22.0 ± 6.5 hrs in ADSCs (p = 0.0001). Both cells were positive to stem cell markers before inductions and thereafter, expressed significantly high chondrogenic genes (p = 0.0001). On shelf life, both cells maintained viabilities and counts above 70% in FD and serum after 120 hrs. BMSCs’ viabilities in DPBS fell below 70% after 96 hrs and saline after 72 hrs. ADSCs’ viability fell below 70% in DPBS after 24 hrs and saline within 24 hrs. Concentrations between 20 ng/ml bFGF is ideal for aged adult cells’ proliferation and delivery time of induced BMSCs and ADSCs can be 120 hrs in 4 °C serum. |
format | Online Article Text |
id | pubmed-5847521 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-58475212018-03-19 Shelf Life Evaluation of Clinical Grade Chondrogenic Induced Aged Adult Stem Cells for Cartilage Regeneration Ude, C. C. Seet, W. T. Sharen Aini, S. Aminuddin, B. S. Ruszymah, B. H. I. Sci Rep Article The study objectives include, enhancing the proliferations of aged bone marrow stem cells (BMSCs) and adipose stem cells (ADSCs); and evaluating the shelf lives of clinical grade chondrogenically induced cells from both samples. ADSCs and BMSCs from 56 patients (76 ± 8 yrs) were proliferated using basal medium (FD) and at (5, 10, 15, 20 and 25) ng/ml of basal fibroblast growth factor (bFGF). They were induced to chondrogenic lineage and stored for more than 120 hrs in FD, serum, Dulbecco’s phosphate buffered saline (DPBS) and saline at 4 °C. In FD, cells stagnated and BMSCs’ population doubling time (PDT) was 137 ± 30 hrs, while ADSCs’ was 129.7 ± 40 hrs. bFGF caused PDT’s decrease to 24.5 ± 5.8 hrs in BMSCs and 22.0 ± 6.5 hrs in ADSCs (p = 0.0001). Both cells were positive to stem cell markers before inductions and thereafter, expressed significantly high chondrogenic genes (p = 0.0001). On shelf life, both cells maintained viabilities and counts above 70% in FD and serum after 120 hrs. BMSCs’ viabilities in DPBS fell below 70% after 96 hrs and saline after 72 hrs. ADSCs’ viability fell below 70% in DPBS after 24 hrs and saline within 24 hrs. Concentrations between 20 ng/ml bFGF is ideal for aged adult cells’ proliferation and delivery time of induced BMSCs and ADSCs can be 120 hrs in 4 °C serum. Nature Publishing Group UK 2018-03-12 /pmc/articles/PMC5847521/ /pubmed/29531282 http://dx.doi.org/10.1038/s41598-018-22748-1 Text en © The Author(s) 2018 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/. |
spellingShingle | Article Ude, C. C. Seet, W. T. Sharen Aini, S. Aminuddin, B. S. Ruszymah, B. H. I. Shelf Life Evaluation of Clinical Grade Chondrogenic Induced Aged Adult Stem Cells for Cartilage Regeneration |
title | Shelf Life Evaluation of Clinical Grade Chondrogenic Induced Aged Adult Stem Cells for Cartilage Regeneration |
title_full | Shelf Life Evaluation of Clinical Grade Chondrogenic Induced Aged Adult Stem Cells for Cartilage Regeneration |
title_fullStr | Shelf Life Evaluation of Clinical Grade Chondrogenic Induced Aged Adult Stem Cells for Cartilage Regeneration |
title_full_unstemmed | Shelf Life Evaluation of Clinical Grade Chondrogenic Induced Aged Adult Stem Cells for Cartilage Regeneration |
title_short | Shelf Life Evaluation of Clinical Grade Chondrogenic Induced Aged Adult Stem Cells for Cartilage Regeneration |
title_sort | shelf life evaluation of clinical grade chondrogenic induced aged adult stem cells for cartilage regeneration |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5847521/ https://www.ncbi.nlm.nih.gov/pubmed/29531282 http://dx.doi.org/10.1038/s41598-018-22748-1 |
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