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Mechanisms Underlying the Antiproliferative and Prodifferentiative Effects of Psoralen on Adult Neural Stem Cells via DNA Microarray

Adult neural stem cells (NSCs) persist throughout life to replace mature cells that are lost during turnover, disease, or injury. The investigation of NSC creates novel treatments for central nervous system (CNS) injuries and neurodegenerative disorders. The plasticity and reparative potential of NS...

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Autores principales: Ning, You, Huang, Jian-Hua, Xia, Shi-Jin, Bian, Qin, Chen, Yang, Zhang, Xin-Min, Dong, Jing-Cheng, Shen, Zi-Yin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3745865/
https://www.ncbi.nlm.nih.gov/pubmed/23983781
http://dx.doi.org/10.1155/2013/452948
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author Ning, You
Huang, Jian-Hua
Xia, Shi-Jin
Bian, Qin
Chen, Yang
Zhang, Xin-Min
Dong, Jing-Cheng
Shen, Zi-Yin
author_facet Ning, You
Huang, Jian-Hua
Xia, Shi-Jin
Bian, Qin
Chen, Yang
Zhang, Xin-Min
Dong, Jing-Cheng
Shen, Zi-Yin
author_sort Ning, You
collection PubMed
description Adult neural stem cells (NSCs) persist throughout life to replace mature cells that are lost during turnover, disease, or injury. The investigation of NSC creates novel treatments for central nervous system (CNS) injuries and neurodegenerative disorders. The plasticity and reparative potential of NSC are regulated by different factors, which are critical for neurological regenerative medicine research. We investigated the effects of Psoralen, which is the mature fruit of Psoralea corylifolia L., on NSC behaviors and the underlying mechanisms. The self-renewal and proliferation of NSC were examined. We detected neuron- and/or astrocyte-specific markers using immunofluorescence and Western blotting, which could evaluate NSC differentiation. Psoralen treatment significantly inhibited neurosphere formation in a dose-dependent manner. Psoralen treatment increased the expression of the astrocyte-specific marker but decreased neuron-specific marker expression. These results suggested that Psoralen was a differentiation inducer in astrocyte. Differential gene expression following Psoralen treatment was screened using DNA microarray and confirmed by quantitative real-time PCR. Our microarray study demonstrated that Psoralen could effectively regulate the specific gene expression profile of NSC. The genes involved in the classification of cellular differentiation, proliferation, and metabolism, the transcription factors belonging to Ets family, and the hedgehog pathway may be closely related to the regulation.
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spelling pubmed-37458652013-08-27 Mechanisms Underlying the Antiproliferative and Prodifferentiative Effects of Psoralen on Adult Neural Stem Cells via DNA Microarray Ning, You Huang, Jian-Hua Xia, Shi-Jin Bian, Qin Chen, Yang Zhang, Xin-Min Dong, Jing-Cheng Shen, Zi-Yin Evid Based Complement Alternat Med Research Article Adult neural stem cells (NSCs) persist throughout life to replace mature cells that are lost during turnover, disease, or injury. The investigation of NSC creates novel treatments for central nervous system (CNS) injuries and neurodegenerative disorders. The plasticity and reparative potential of NSC are regulated by different factors, which are critical for neurological regenerative medicine research. We investigated the effects of Psoralen, which is the mature fruit of Psoralea corylifolia L., on NSC behaviors and the underlying mechanisms. The self-renewal and proliferation of NSC were examined. We detected neuron- and/or astrocyte-specific markers using immunofluorescence and Western blotting, which could evaluate NSC differentiation. Psoralen treatment significantly inhibited neurosphere formation in a dose-dependent manner. Psoralen treatment increased the expression of the astrocyte-specific marker but decreased neuron-specific marker expression. These results suggested that Psoralen was a differentiation inducer in astrocyte. Differential gene expression following Psoralen treatment was screened using DNA microarray and confirmed by quantitative real-time PCR. Our microarray study demonstrated that Psoralen could effectively regulate the specific gene expression profile of NSC. The genes involved in the classification of cellular differentiation, proliferation, and metabolism, the transcription factors belonging to Ets family, and the hedgehog pathway may be closely related to the regulation. Hindawi Publishing Corporation 2013 2013-07-30 /pmc/articles/PMC3745865/ /pubmed/23983781 http://dx.doi.org/10.1155/2013/452948 Text en Copyright © 2013 You Ning 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
Ning, You
Huang, Jian-Hua
Xia, Shi-Jin
Bian, Qin
Chen, Yang
Zhang, Xin-Min
Dong, Jing-Cheng
Shen, Zi-Yin
Mechanisms Underlying the Antiproliferative and Prodifferentiative Effects of Psoralen on Adult Neural Stem Cells via DNA Microarray
title Mechanisms Underlying the Antiproliferative and Prodifferentiative Effects of Psoralen on Adult Neural Stem Cells via DNA Microarray
title_full Mechanisms Underlying the Antiproliferative and Prodifferentiative Effects of Psoralen on Adult Neural Stem Cells via DNA Microarray
title_fullStr Mechanisms Underlying the Antiproliferative and Prodifferentiative Effects of Psoralen on Adult Neural Stem Cells via DNA Microarray
title_full_unstemmed Mechanisms Underlying the Antiproliferative and Prodifferentiative Effects of Psoralen on Adult Neural Stem Cells via DNA Microarray
title_short Mechanisms Underlying the Antiproliferative and Prodifferentiative Effects of Psoralen on Adult Neural Stem Cells via DNA Microarray
title_sort mechanisms underlying the antiproliferative and prodifferentiative effects of psoralen on adult neural stem cells via dna microarray
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3745865/
https://www.ncbi.nlm.nih.gov/pubmed/23983781
http://dx.doi.org/10.1155/2013/452948
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