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Changes of neural markers expression during late neurogenic differentiation of human adipose-derived stem cells
BACKGROUND: Different studies have been done to obtain sufficient number of neural cells for treatment of neurodegenerative diseases, spinal cord, and traumatic brain injury because neural stem cells are limited in central nerves system. Recently, several studies have shown that adipose-derived stem...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Medknow Publications & Media Pvt Ltd
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4627175/ https://www.ncbi.nlm.nih.gov/pubmed/26605238 http://dx.doi.org/10.4103/2277-9175.166146 |
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author | Razavi, Shahnaz Khosravizadeh, Zahra Bahramian, Hamid Kazemi, Mohammad |
author_facet | Razavi, Shahnaz Khosravizadeh, Zahra Bahramian, Hamid Kazemi, Mohammad |
author_sort | Razavi, Shahnaz |
collection | PubMed |
description | BACKGROUND: Different studies have been done to obtain sufficient number of neural cells for treatment of neurodegenerative diseases, spinal cord, and traumatic brain injury because neural stem cells are limited in central nerves system. Recently, several studies have shown that adipose-derived stem cells (ADSCs) are the appropriate source of multipotent stem cells. Furthermore, these cells are found in large quantities. The aim of this study was an assessment of proliferation and potential of neurogenic differentiation of ADSCs with passing time. MATERIALS AND METHODS: Neurosphere formation was used for neural induction in isolated human ADSCs (hADSCs). The rate of proliferation was determined by 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide assay and potential of neural differentiation of induced hADSCs was evaluated by immunocytochemical and real-time reverse transcription polymerase chain reaction analysis after 10 and 14 days post-induction. RESULTS: The rate of proliferation of induced hADSCs increased after 14 days while the expression of nestin, glial fibrillary acidic protein, and microtubule-associated protein 2 was decreased with passing time during neurogenic differentiation. CONCLUSION: These findings showed that the proliferation of induced cells increased with passing time, but in early neurogenic differentiation of hADSCs, neural expression was higher than late of differentiation. Thus, using of induced cells in early differentiation may be suggested for in vivo application. |
format | Online Article Text |
id | pubmed-4627175 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Medknow Publications & Media Pvt Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-46271752015-11-24 Changes of neural markers expression during late neurogenic differentiation of human adipose-derived stem cells Razavi, Shahnaz Khosravizadeh, Zahra Bahramian, Hamid Kazemi, Mohammad Adv Biomed Res Original Article BACKGROUND: Different studies have been done to obtain sufficient number of neural cells for treatment of neurodegenerative diseases, spinal cord, and traumatic brain injury because neural stem cells are limited in central nerves system. Recently, several studies have shown that adipose-derived stem cells (ADSCs) are the appropriate source of multipotent stem cells. Furthermore, these cells are found in large quantities. The aim of this study was an assessment of proliferation and potential of neurogenic differentiation of ADSCs with passing time. MATERIALS AND METHODS: Neurosphere formation was used for neural induction in isolated human ADSCs (hADSCs). The rate of proliferation was determined by 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide assay and potential of neural differentiation of induced hADSCs was evaluated by immunocytochemical and real-time reverse transcription polymerase chain reaction analysis after 10 and 14 days post-induction. RESULTS: The rate of proliferation of induced hADSCs increased after 14 days while the expression of nestin, glial fibrillary acidic protein, and microtubule-associated protein 2 was decreased with passing time during neurogenic differentiation. CONCLUSION: These findings showed that the proliferation of induced cells increased with passing time, but in early neurogenic differentiation of hADSCs, neural expression was higher than late of differentiation. Thus, using of induced cells in early differentiation may be suggested for in vivo application. Medknow Publications & Media Pvt Ltd 2015-09-28 /pmc/articles/PMC4627175/ /pubmed/26605238 http://dx.doi.org/10.4103/2277-9175.166146 Text en Copyright: © 2015 Advanced Biomedical Research http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 3.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as the author is credited and the new creations are licensed under the identical terms. |
spellingShingle | Original Article Razavi, Shahnaz Khosravizadeh, Zahra Bahramian, Hamid Kazemi, Mohammad Changes of neural markers expression during late neurogenic differentiation of human adipose-derived stem cells |
title | Changes of neural markers expression during late neurogenic differentiation of human adipose-derived stem cells |
title_full | Changes of neural markers expression during late neurogenic differentiation of human adipose-derived stem cells |
title_fullStr | Changes of neural markers expression during late neurogenic differentiation of human adipose-derived stem cells |
title_full_unstemmed | Changes of neural markers expression during late neurogenic differentiation of human adipose-derived stem cells |
title_short | Changes of neural markers expression during late neurogenic differentiation of human adipose-derived stem cells |
title_sort | changes of neural markers expression during late neurogenic differentiation of human adipose-derived stem cells |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4627175/ https://www.ncbi.nlm.nih.gov/pubmed/26605238 http://dx.doi.org/10.4103/2277-9175.166146 |
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