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Potential Use of Amniotic Membrane - Derived Scaffold for Cerebrospinal Fluid Applications

Scaffolds derived from decellularized tissues provide a natural microenvironment for cell culture. Embryonic cerebrospinal fluid (e-CSF) contains factors which play vital roles in the development of the nervous system. This research was aimed to survey the effect of Wistar rat e-CSF on neural differ...

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Autores principales: Dorazehi, Fereshteh, Nabiuni, Mohammad, Jalali, Hanieh
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Babol University of Medical Sciences 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6148501/
https://www.ncbi.nlm.nih.gov/pubmed/30276164
http://dx.doi.org/10.22088/IJMCM.BUMS.7.2.91
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author Dorazehi, Fereshteh
Nabiuni, Mohammad
Jalali, Hanieh
author_facet Dorazehi, Fereshteh
Nabiuni, Mohammad
Jalali, Hanieh
author_sort Dorazehi, Fereshteh
collection PubMed
description Scaffolds derived from decellularized tissues provide a natural microenvironment for cell culture. Embryonic cerebrospinal fluid (e-CSF) contains factors which play vital roles in the development of the nervous system. This research was aimed to survey the effect of Wistar rat e-CSF on neural differentiation of bone marrow derived mesenchymal stem cells (BM-MSCs) cultured on the human amniotic membrane (AM). BM-MSCs were collected from femurs and tibias, and were cultured in Dulbecco's Modified Eagle's Medium. The placenta was harvested from healthy women during cesarean section and AM was acellularized using EDTA and physical scrubbing. e- CSF was harvested from rat fetuses at E17. Adequate numbers of BM-MSCs were cultured on acellularized membrane, and were treated with E17 CSF for 7 days. MTT (3-(4, 5-dimethylthiazol-2-yl)-2.5-diphenyltetrazolium bromide) assay confirmed the survival and proliferation of BM-MSCs cultured on AM derived scaffold. Hematoxylin/eosin staining and scanning electron microscopy showed the morphological and the structural changes of BM-MSCs throughout the culture and treatment with e-CSF. The results of immunocytochemistry showed that microtubule associated protein 2 and beta-III tubulin were expressed in BM-MSCs cultured on acellular amnion scaffold and treated with e-CSF. Our results showed for the first time that the combination of acellular AM as a natural scaffold and e-CSF as a source of neurological factors could effectively improve the BM-MSCs cultivation and differentiation
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spelling pubmed-61485012018-10-01 Potential Use of Amniotic Membrane - Derived Scaffold for Cerebrospinal Fluid Applications Dorazehi, Fereshteh Nabiuni, Mohammad Jalali, Hanieh Int J Mol Cell Med Original Article Scaffolds derived from decellularized tissues provide a natural microenvironment for cell culture. Embryonic cerebrospinal fluid (e-CSF) contains factors which play vital roles in the development of the nervous system. This research was aimed to survey the effect of Wistar rat e-CSF on neural differentiation of bone marrow derived mesenchymal stem cells (BM-MSCs) cultured on the human amniotic membrane (AM). BM-MSCs were collected from femurs and tibias, and were cultured in Dulbecco's Modified Eagle's Medium. The placenta was harvested from healthy women during cesarean section and AM was acellularized using EDTA and physical scrubbing. e- CSF was harvested from rat fetuses at E17. Adequate numbers of BM-MSCs were cultured on acellularized membrane, and were treated with E17 CSF for 7 days. MTT (3-(4, 5-dimethylthiazol-2-yl)-2.5-diphenyltetrazolium bromide) assay confirmed the survival and proliferation of BM-MSCs cultured on AM derived scaffold. Hematoxylin/eosin staining and scanning electron microscopy showed the morphological and the structural changes of BM-MSCs throughout the culture and treatment with e-CSF. The results of immunocytochemistry showed that microtubule associated protein 2 and beta-III tubulin were expressed in BM-MSCs cultured on acellular amnion scaffold and treated with e-CSF. Our results showed for the first time that the combination of acellular AM as a natural scaffold and e-CSF as a source of neurological factors could effectively improve the BM-MSCs cultivation and differentiation Babol University of Medical Sciences 2018 2018-08-19 /pmc/articles/PMC6148501/ /pubmed/30276164 http://dx.doi.org/10.22088/IJMCM.BUMS.7.2.91 Text en This is an Open Access article distributed under the terms of the Creative Commons Attribution License, (http://creativecommons.org/licenses/by/3.0/) which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Dorazehi, Fereshteh
Nabiuni, Mohammad
Jalali, Hanieh
Potential Use of Amniotic Membrane - Derived Scaffold for Cerebrospinal Fluid Applications
title Potential Use of Amniotic Membrane - Derived Scaffold for Cerebrospinal Fluid Applications
title_full Potential Use of Amniotic Membrane - Derived Scaffold for Cerebrospinal Fluid Applications
title_fullStr Potential Use of Amniotic Membrane - Derived Scaffold for Cerebrospinal Fluid Applications
title_full_unstemmed Potential Use of Amniotic Membrane - Derived Scaffold for Cerebrospinal Fluid Applications
title_short Potential Use of Amniotic Membrane - Derived Scaffold for Cerebrospinal Fluid Applications
title_sort potential use of amniotic membrane - derived scaffold for cerebrospinal fluid applications
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6148501/
https://www.ncbi.nlm.nih.gov/pubmed/30276164
http://dx.doi.org/10.22088/IJMCM.BUMS.7.2.91
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