Differential gene expression by lithium chloride induction of adipose-derived stem cells into neural phenotype cells

<em><strong>Objective(s):</strong></em> Adipose-derived stem cells (ADSCs), with suitable and easy access, are multipotential cells that have the ability for differentiation into other mesodermal and transdifferentiate into neural phenotype cells. In this study, Lithium chlor...

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Main Authors: Samaneh Farrokhfar, Taki Tiraihi, Mansoureh Movahedin, Hossein Azizi
Format: Article
Language:English
Published: Mashhad University of Medical Sciences 2020-04-01
Series:Iranian Journal of Basic Medical Sciences
Subjects:
Online Access:http://ijbms.mums.ac.ir/article_14974_3561b8def012f06d100cedc52a199c72.pdf
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spelling doaj-6153e55914864bdda8c3fc569bc15c4b2020-11-25T02:39:04ZengMashhad University of Medical SciencesIranian Journal of Basic Medical Sciences 2008-38662008-38742020-04-0123454455010.22038/ijbms.2020.41582.982014974Differential gene expression by lithium chloride induction of adipose-derived stem cells into neural phenotype cellsSamaneh Farrokhfar0Taki Tiraihi1Mansoureh Movahedin2Hossein Azizi3Department of Anatomy, Faculty of Medical Sciences, Tarbiat Modares University, Tehran, IranDepartment of Anatomy, Faculty of Medical Sciences, Tarbiat Modares University, P.O.BOX.14115-331 Tehran, IranDepartment of Anatomy, Faculty of Medical Sciences, Tarbiat Modares University, P.O.BOX.14115-331 Tehran, IranDepartment of Physiology, Faculty of Medical Sciences, Tarbiat Modares University, P.O.BOX.14115-331 Tehran, Iran<em><strong>Objective(s):</strong></em> Adipose-derived stem cells (ADSCs), with suitable and easy access, are multipotential cells that have the ability for differentiation into other mesodermal and transdifferentiate into neural phenotype cells. In this study, Lithium chloride (LiCl) was used for <em>in vitro</em> transdifferentiation of rat ADSCs into neuron-like cells (NLCs).<br /><em><strong>Materials and Methods:</strong></em> ADSCs were isolated from the rats’ perinephric region using Dulbecco΄s Modified Eagle΄s Medium (DMEM) with Fetal Bovine Serum (FBS), cultured for 3 passages, characterized by flowcytometry and differentiation into adipogenic and osteogenic phenotypes. The ADSCs were exposed to 0.1, 0.5, 1, 1.5, 2, 5, and 10 millimolar (mM) LiCl without serum for 24 hr. The optimum dose of LiCl was selected according the maximum viability of cells. The expression of neurofilament light chain (NfL), neurofilament high chain (NfH), and nestin was evaluated by immunocytochemistry. Quantitative reverse transcription polymerase chain reaction (qRT-PCR) was used to evaluate the amount of synaptophysin, neurogenin-1, neuroD1, NfL, NfH, and nestin genes’ expression in ADSCs and NLCs.<br /><em><strong>Results:</strong></em> The optimum dose of LiCl was 1 mM in 24 hr. The transdifferentiated ADSCs showed cytoplasmic extension with synapse-like formation. Synaptophysin, neurogenin-1, neuroD1, NfL, NfH, and nestin genes were significantly expressed more in NLCs than in ADSCs.<br /><em><strong>Conclusion:</strong></em> LiCl can induce ADSCs into neural phenotype cells with higher expression of neural and neuronal genes.http://ijbms.mums.ac.ir/article_14974_3561b8def012f06d100cedc52a199c72.pdfinductionlithium chlorideneuron-like cellsstem cellstransdifferentiation
collection DOAJ
language English
format Article
sources DOAJ
author Samaneh Farrokhfar
Taki Tiraihi
Mansoureh Movahedin
Hossein Azizi
spellingShingle Samaneh Farrokhfar
Taki Tiraihi
Mansoureh Movahedin
Hossein Azizi
Differential gene expression by lithium chloride induction of adipose-derived stem cells into neural phenotype cells
Iranian Journal of Basic Medical Sciences
induction
lithium chloride
neuron-like cells
stem cells
transdifferentiation
author_facet Samaneh Farrokhfar
Taki Tiraihi
Mansoureh Movahedin
Hossein Azizi
author_sort Samaneh Farrokhfar
title Differential gene expression by lithium chloride induction of adipose-derived stem cells into neural phenotype cells
title_short Differential gene expression by lithium chloride induction of adipose-derived stem cells into neural phenotype cells
title_full Differential gene expression by lithium chloride induction of adipose-derived stem cells into neural phenotype cells
title_fullStr Differential gene expression by lithium chloride induction of adipose-derived stem cells into neural phenotype cells
title_full_unstemmed Differential gene expression by lithium chloride induction of adipose-derived stem cells into neural phenotype cells
title_sort differential gene expression by lithium chloride induction of adipose-derived stem cells into neural phenotype cells
publisher Mashhad University of Medical Sciences
series Iranian Journal of Basic Medical Sciences
issn 2008-3866
2008-3874
publishDate 2020-04-01
description <em><strong>Objective(s):</strong></em> Adipose-derived stem cells (ADSCs), with suitable and easy access, are multipotential cells that have the ability for differentiation into other mesodermal and transdifferentiate into neural phenotype cells. In this study, Lithium chloride (LiCl) was used for <em>in vitro</em> transdifferentiation of rat ADSCs into neuron-like cells (NLCs).<br /><em><strong>Materials and Methods:</strong></em> ADSCs were isolated from the rats’ perinephric region using Dulbecco΄s Modified Eagle΄s Medium (DMEM) with Fetal Bovine Serum (FBS), cultured for 3 passages, characterized by flowcytometry and differentiation into adipogenic and osteogenic phenotypes. The ADSCs were exposed to 0.1, 0.5, 1, 1.5, 2, 5, and 10 millimolar (mM) LiCl without serum for 24 hr. The optimum dose of LiCl was selected according the maximum viability of cells. The expression of neurofilament light chain (NfL), neurofilament high chain (NfH), and nestin was evaluated by immunocytochemistry. Quantitative reverse transcription polymerase chain reaction (qRT-PCR) was used to evaluate the amount of synaptophysin, neurogenin-1, neuroD1, NfL, NfH, and nestin genes’ expression in ADSCs and NLCs.<br /><em><strong>Results:</strong></em> The optimum dose of LiCl was 1 mM in 24 hr. The transdifferentiated ADSCs showed cytoplasmic extension with synapse-like formation. Synaptophysin, neurogenin-1, neuroD1, NfL, NfH, and nestin genes were significantly expressed more in NLCs than in ADSCs.<br /><em><strong>Conclusion:</strong></em> LiCl can induce ADSCs into neural phenotype cells with higher expression of neural and neuronal genes.
topic induction
lithium chloride
neuron-like cells
stem cells
transdifferentiation
url http://ijbms.mums.ac.ir/article_14974_3561b8def012f06d100cedc52a199c72.pdf
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