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Neurospheres Induced from Human Adipose-Derived Stem Cells as a New Source of Neural Progenitor Cells
Human adipose-derived stem cells are used in regenerative medicine for treating various diseases including osteoarthritis, degenerative arthritis, cartilage or tendon injury, etc. However, their use in neurological disorders is limited, probably due to the lack of a quick and efficient induction met...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
SAGE Publications
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7016463/ https://www.ncbi.nlm.nih.gov/pubmed/31813268 http://dx.doi.org/10.1177/0963689719888619 |
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author | Peng, Chunyang Lu, Li Li, Yajiao Hu, Jingqiong |
author_facet | Peng, Chunyang Lu, Li Li, Yajiao Hu, Jingqiong |
author_sort | Peng, Chunyang |
collection | PubMed |
description | Human adipose-derived stem cells are used in regenerative medicine for treating various diseases including osteoarthritis, degenerative arthritis, cartilage or tendon injury, etc. However, their use in neurological disorders is limited, probably due to the lack of a quick and efficient induction method of transforming these cells into neural stem or progenitor cells. In this study, we reported a highly efficient and simple method to induce adipose-derived stem cells into neural progenitor cells within 12 hours, using serum-free culture combined with a well-defined induction medium (epidermal growth factor 20 ng/ml and basic fibroblast growth factor, both at 20 ng/ml, with N2 and B27 supplements). These adipose-derived stem cell-derived neural progenitor cells grow as neurospheres, can self-renew to form secondary neurospheres, and can be induced to become neurons and glial cells. Real-time polymerase chain reaction showed significantly upregulated expression of neurogenic genes Sox2 and Nestin with a moderate increase in stemness gene expression. Raybio human growth factor analysis showed a significantly upregulated expression of multiple neurogenic and angiogenic cytokines such as brain-derived neurotrophic factor, glial cell line-derived neurotrophic growth factor, nerve growth factor, basic fibroblast growth factor and vascular endothelial growth factor etc. Therefore, adipose-derived stem cell-derived neurospheres can be a new source of neural progenitor cells and hold great potential for future cell replacement therapy for treatment of various refractory neurological diseases. |
format | Online Article Text |
id | pubmed-7016463 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | SAGE Publications |
record_format | MEDLINE/PubMed |
spelling | pubmed-70164632020-02-27 Neurospheres Induced from Human Adipose-Derived Stem Cells as a New Source of Neural Progenitor Cells Peng, Chunyang Lu, Li Li, Yajiao Hu, Jingqiong Cell Transplant Original Articles Human adipose-derived stem cells are used in regenerative medicine for treating various diseases including osteoarthritis, degenerative arthritis, cartilage or tendon injury, etc. However, their use in neurological disorders is limited, probably due to the lack of a quick and efficient induction method of transforming these cells into neural stem or progenitor cells. In this study, we reported a highly efficient and simple method to induce adipose-derived stem cells into neural progenitor cells within 12 hours, using serum-free culture combined with a well-defined induction medium (epidermal growth factor 20 ng/ml and basic fibroblast growth factor, both at 20 ng/ml, with N2 and B27 supplements). These adipose-derived stem cell-derived neural progenitor cells grow as neurospheres, can self-renew to form secondary neurospheres, and can be induced to become neurons and glial cells. Real-time polymerase chain reaction showed significantly upregulated expression of neurogenic genes Sox2 and Nestin with a moderate increase in stemness gene expression. Raybio human growth factor analysis showed a significantly upregulated expression of multiple neurogenic and angiogenic cytokines such as brain-derived neurotrophic factor, glial cell line-derived neurotrophic growth factor, nerve growth factor, basic fibroblast growth factor and vascular endothelial growth factor etc. Therefore, adipose-derived stem cell-derived neurospheres can be a new source of neural progenitor cells and hold great potential for future cell replacement therapy for treatment of various refractory neurological diseases. SAGE Publications 2019-12-08 2019-12 /pmc/articles/PMC7016463/ /pubmed/31813268 http://dx.doi.org/10.1177/0963689719888619 Text en © The Author(s) 2019 https://creativecommons.org/licenses/by-nc/4.0/ This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (https://creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage). |
spellingShingle | Original Articles Peng, Chunyang Lu, Li Li, Yajiao Hu, Jingqiong Neurospheres Induced from Human Adipose-Derived Stem Cells as a New Source of Neural Progenitor Cells |
title | Neurospheres Induced from Human Adipose-Derived Stem Cells as a New Source of Neural Progenitor Cells |
title_full | Neurospheres Induced from Human Adipose-Derived Stem Cells as a New Source of Neural Progenitor Cells |
title_fullStr | Neurospheres Induced from Human Adipose-Derived Stem Cells as a New Source of Neural Progenitor Cells |
title_full_unstemmed | Neurospheres Induced from Human Adipose-Derived Stem Cells as a New Source of Neural Progenitor Cells |
title_short | Neurospheres Induced from Human Adipose-Derived Stem Cells as a New Source of Neural Progenitor Cells |
title_sort | neurospheres induced from human adipose-derived stem cells as a new source of neural progenitor cells |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7016463/ https://www.ncbi.nlm.nih.gov/pubmed/31813268 http://dx.doi.org/10.1177/0963689719888619 |
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