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Microarray Analysis of mRNA and MicroRNA Expression Profile Reveals the Role of β-Sitosterol-D-glucoside in the Proliferation of Neural Stem Cell

Neural stem cells (NSCs) are self-regenerating cells, but their regenerative capacity is limited. The present study was conducted to investigate the effect of β-sitosterol-D-glucoside (BSSG) on the proliferation of hippocampal NSCs and to determine the corresponding molecular mechanism. Results of C...

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Autores principales: Jiang, Li-hua, Yang, Nian-yun, Yuan, Xiao-lin, Zou, Yi-jie, Jiang, Ze-qun, Zhao, Feng-ming, Chen, Jian-ping, Wang, Ming-yan, Lu, Da-xiang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3874330/
https://www.ncbi.nlm.nih.gov/pubmed/24391673
http://dx.doi.org/10.1155/2013/360302
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author Jiang, Li-hua
Yang, Nian-yun
Yuan, Xiao-lin
Zou, Yi-jie
Jiang, Ze-qun
Zhao, Feng-ming
Chen, Jian-ping
Wang, Ming-yan
Lu, Da-xiang
author_facet Jiang, Li-hua
Yang, Nian-yun
Yuan, Xiao-lin
Zou, Yi-jie
Jiang, Ze-qun
Zhao, Feng-ming
Chen, Jian-ping
Wang, Ming-yan
Lu, Da-xiang
author_sort Jiang, Li-hua
collection PubMed
description Neural stem cells (NSCs) are self-regenerating cells, but their regenerative capacity is limited. The present study was conducted to investigate the effect of β-sitosterol-D-glucoside (BSSG) on the proliferation of hippocampal NSCs and to determine the corresponding molecular mechanism. Results of CCK-8 assay showed that BSSG significantly increased NSC proliferation and the effectiveness of BSSG was similar to that of basic fibroblast growth factor and epidermal growth factor. mRNA expression profiling showed that 960 genes were differentially expressed after NSCs were treated with BSSG. Among the 960 genes, IGF1 is considered as a key regulatory gene that functionally promotes NSC proliferation. MicroRNA (miRNA) expression profiling indicated that 30 and 84 miRNAs were upregulated and downregulated, respectively. miRNA-mRNA relevance analysis revealed that numerous mRNAs including IGF1 mRNA were negatively regulated by miRNAs with decreased expression, thereby increasing the corresponding mRNA expression. The increased expression of IGF1 protein was validated by ELISA. Picropodophyllin (PPP, an inhibitor of IGF-1R) inhibition test confirmed that the proliferation-enhancing effect depended on IGF1. This study provided information about BSSG as an efficient and inexpensive growth factor alternative, of which the effect is closely involved in IGF1.
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spelling pubmed-38743302014-01-05 Microarray Analysis of mRNA and MicroRNA Expression Profile Reveals the Role of β-Sitosterol-D-glucoside in the Proliferation of Neural Stem Cell Jiang, Li-hua Yang, Nian-yun Yuan, Xiao-lin Zou, Yi-jie Jiang, Ze-qun Zhao, Feng-ming Chen, Jian-ping Wang, Ming-yan Lu, Da-xiang Evid Based Complement Alternat Med Research Article Neural stem cells (NSCs) are self-regenerating cells, but their regenerative capacity is limited. The present study was conducted to investigate the effect of β-sitosterol-D-glucoside (BSSG) on the proliferation of hippocampal NSCs and to determine the corresponding molecular mechanism. Results of CCK-8 assay showed that BSSG significantly increased NSC proliferation and the effectiveness of BSSG was similar to that of basic fibroblast growth factor and epidermal growth factor. mRNA expression profiling showed that 960 genes were differentially expressed after NSCs were treated with BSSG. Among the 960 genes, IGF1 is considered as a key regulatory gene that functionally promotes NSC proliferation. MicroRNA (miRNA) expression profiling indicated that 30 and 84 miRNAs were upregulated and downregulated, respectively. miRNA-mRNA relevance analysis revealed that numerous mRNAs including IGF1 mRNA were negatively regulated by miRNAs with decreased expression, thereby increasing the corresponding mRNA expression. The increased expression of IGF1 protein was validated by ELISA. Picropodophyllin (PPP, an inhibitor of IGF-1R) inhibition test confirmed that the proliferation-enhancing effect depended on IGF1. This study provided information about BSSG as an efficient and inexpensive growth factor alternative, of which the effect is closely involved in IGF1. Hindawi Publishing Corporation 2013 2013-12-11 /pmc/articles/PMC3874330/ /pubmed/24391673 http://dx.doi.org/10.1155/2013/360302 Text en Copyright © 2013 Li-hua Jiang et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Jiang, Li-hua
Yang, Nian-yun
Yuan, Xiao-lin
Zou, Yi-jie
Jiang, Ze-qun
Zhao, Feng-ming
Chen, Jian-ping
Wang, Ming-yan
Lu, Da-xiang
Microarray Analysis of mRNA and MicroRNA Expression Profile Reveals the Role of β-Sitosterol-D-glucoside in the Proliferation of Neural Stem Cell
title Microarray Analysis of mRNA and MicroRNA Expression Profile Reveals the Role of β-Sitosterol-D-glucoside in the Proliferation of Neural Stem Cell
title_full Microarray Analysis of mRNA and MicroRNA Expression Profile Reveals the Role of β-Sitosterol-D-glucoside in the Proliferation of Neural Stem Cell
title_fullStr Microarray Analysis of mRNA and MicroRNA Expression Profile Reveals the Role of β-Sitosterol-D-glucoside in the Proliferation of Neural Stem Cell
title_full_unstemmed Microarray Analysis of mRNA and MicroRNA Expression Profile Reveals the Role of β-Sitosterol-D-glucoside in the Proliferation of Neural Stem Cell
title_short Microarray Analysis of mRNA and MicroRNA Expression Profile Reveals the Role of β-Sitosterol-D-glucoside in the Proliferation of Neural Stem Cell
title_sort microarray analysis of mrna and microrna expression profile reveals the role of β-sitosterol-d-glucoside in the proliferation of neural stem cell
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3874330/
https://www.ncbi.nlm.nih.gov/pubmed/24391673
http://dx.doi.org/10.1155/2013/360302
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