Pleiotrophin is involved in the amniotic epithelial cell-induced differentiation of human umbilical cord blood-derived mesenchymal stem cells into dopaminergic neuron-like cells

► PTN was synthesized and released by AECs. ► hUCB-MSCs were cultured in ACM, rPTN or control medium. ► ACM or rPTN induced more hUCB-MSCs to differentiate into DA neuron-like cells. ► ACM might be a potential inducer to obtain DA neuron-like cells from hUCB-MSCs. We have reported that human umbilic...

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Veröffentlicht in:Neuroscience letters 2013-02, Vol.539, p.86-91
Hauptverfasser: Yang, Shu, Xue, Dan-dan, Wu, Bo, Sun, Hai-mei, Li, Xiao-shuang, Dong, Fang, Li, Wen-shuai, Ji, Feng-qing, Zhou, De-shan
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container_end_page 91
container_issue
container_start_page 86
container_title Neuroscience letters
container_volume 539
creator Yang, Shu
Xue, Dan-dan
Wu, Bo
Sun, Hai-mei
Li, Xiao-shuang
Dong, Fang
Li, Wen-shuai
Ji, Feng-qing
Zhou, De-shan
description ► PTN was synthesized and released by AECs. ► hUCB-MSCs were cultured in ACM, rPTN or control medium. ► ACM or rPTN induced more hUCB-MSCs to differentiate into DA neuron-like cells. ► ACM might be a potential inducer to obtain DA neuron-like cells from hUCB-MSCs. We have reported that human umbilical cord blood-derived mesenchymal stem cells (hUCB-MSCs) are capable of differentiating into dopaminergic (DA) neuron-like cells upon being induced by amniotic epithelial cells (AECs). However, what factor(s) is involved in the differentiation process has not been explored out thoroughly. Because pleiotrophin (PTN) is known to exert important trophic effects on DA neurons, in the present study, we investigated whether PTN is released by AECs and whether it is involved in the differentiation of hUCB-MSCs into DA neuron-like cells. The expression and secretion of PTN by AECs were detected by immunofluorescence, RT-PCR and ELISA. The hUCB-MSCs were isolated and treated with AEC-conditioned medium (ACM) or recombinant human PTN. Compared to the controls, a higher proportion of treated cells differentiated into DA neuron-like cells, indicated by the increased expression of TH and DAT and the increased dopamine content. These results indicate that PTN released by AECs acts as a synergetic factor with other neurotrophic factors and is involved in the differentiation of hUCB-MSCs into DA neuron-like cells. We suggest that ACM, which contains PTN and other neurotrophic factors, could potentially be used as an agent to promote the differentiation of DA neuron-like cells from hUCB-MSCs for cell therapy of Parkinson's disease without creating legal or ethical issues.
doi_str_mv 10.1016/j.neulet.2013.01.046
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We have reported that human umbilical cord blood-derived mesenchymal stem cells (hUCB-MSCs) are capable of differentiating into dopaminergic (DA) neuron-like cells upon being induced by amniotic epithelial cells (AECs). However, what factor(s) is involved in the differentiation process has not been explored out thoroughly. Because pleiotrophin (PTN) is known to exert important trophic effects on DA neurons, in the present study, we investigated whether PTN is released by AECs and whether it is involved in the differentiation of hUCB-MSCs into DA neuron-like cells. The expression and secretion of PTN by AECs were detected by immunofluorescence, RT-PCR and ELISA. The hUCB-MSCs were isolated and treated with AEC-conditioned medium (ACM) or recombinant human PTN. Compared to the controls, a higher proportion of treated cells differentiated into DA neuron-like cells, indicated by the increased expression of TH and DAT and the increased dopamine content. These results indicate that PTN released by AECs acts as a synergetic factor with other neurotrophic factors and is involved in the differentiation of hUCB-MSCs into DA neuron-like cells. We suggest that ACM, which contains PTN and other neurotrophic factors, could potentially be used as an agent to promote the differentiation of DA neuron-like cells from hUCB-MSCs for cell therapy of Parkinson's disease without creating legal or ethical issues.</description><identifier>ISSN: 0304-3940</identifier><identifier>EISSN: 1872-7972</identifier><identifier>DOI: 10.1016/j.neulet.2013.01.046</identifier><identifier>PMID: 23403104</identifier><language>eng</language><publisher>Ireland: Elsevier Ireland Ltd</publisher><subject>Amnion - cytology ; Amnion - metabolism ; Amniotic epithelial cell ; Blood ; Carrier Proteins - metabolism ; Carrier Proteins - pharmacology ; Cell Differentiation ; Cells, Cultured ; Culture Media, Conditioned ; Cytokines - metabolism ; Cytokines - pharmacology ; Dopaminergic neurons ; Dopaminergic Neurons - cytology ; Dopaminergic Neurons - drug effects ; Dopaminergic Neurons - metabolism ; Epithelial Cells - cytology ; Epithelial Cells - drug effects ; Epithelial Cells - metabolism ; Fetal Blood - cytology ; Fetal Blood - metabolism ; Human umbilical cord blood-derived mesenchymal stem cell ; Humans ; Mesenchymal Stromal Cells - cytology ; Mesenchymal Stromal Cells - drug effects ; Mesenchymal Stromal Cells - metabolism ; Pleiotrophin ; Recombinant Proteins - pharmacology</subject><ispartof>Neuroscience letters, 2013-02, Vol.539, p.86-91</ispartof><rights>2013 Elsevier Ireland Ltd</rights><rights>Copyright © 2013 Elsevier Ireland Ltd. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c395t-93fa8f1ab269e0957ff489f0e6d02fd43c62374854a3fb306e20d5c849dbd52d3</citedby><cites>FETCH-LOGICAL-c395t-93fa8f1ab269e0957ff489f0e6d02fd43c62374854a3fb306e20d5c849dbd52d3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.neulet.2013.01.046$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,780,784,3549,27923,27924,45994</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/23403104$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Yang, Shu</creatorcontrib><creatorcontrib>Xue, Dan-dan</creatorcontrib><creatorcontrib>Wu, Bo</creatorcontrib><creatorcontrib>Sun, Hai-mei</creatorcontrib><creatorcontrib>Li, Xiao-shuang</creatorcontrib><creatorcontrib>Dong, Fang</creatorcontrib><creatorcontrib>Li, Wen-shuai</creatorcontrib><creatorcontrib>Ji, Feng-qing</creatorcontrib><creatorcontrib>Zhou, De-shan</creatorcontrib><title>Pleiotrophin is involved in the amniotic epithelial cell-induced differentiation of human umbilical cord blood-derived mesenchymal stem cells into dopaminergic neuron-like cells</title><title>Neuroscience letters</title><addtitle>Neurosci Lett</addtitle><description>► PTN was synthesized and released by AECs. ► hUCB-MSCs were cultured in ACM, rPTN or control medium. ► ACM or rPTN induced more hUCB-MSCs to differentiate into DA neuron-like cells. ► ACM might be a potential inducer to obtain DA neuron-like cells from hUCB-MSCs. 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These results indicate that PTN released by AECs acts as a synergetic factor with other neurotrophic factors and is involved in the differentiation of hUCB-MSCs into DA neuron-like cells. 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We have reported that human umbilical cord blood-derived mesenchymal stem cells (hUCB-MSCs) are capable of differentiating into dopaminergic (DA) neuron-like cells upon being induced by amniotic epithelial cells (AECs). However, what factor(s) is involved in the differentiation process has not been explored out thoroughly. Because pleiotrophin (PTN) is known to exert important trophic effects on DA neurons, in the present study, we investigated whether PTN is released by AECs and whether it is involved in the differentiation of hUCB-MSCs into DA neuron-like cells. The expression and secretion of PTN by AECs were detected by immunofluorescence, RT-PCR and ELISA. The hUCB-MSCs were isolated and treated with AEC-conditioned medium (ACM) or recombinant human PTN. Compared to the controls, a higher proportion of treated cells differentiated into DA neuron-like cells, indicated by the increased expression of TH and DAT and the increased dopamine content. These results indicate that PTN released by AECs acts as a synergetic factor with other neurotrophic factors and is involved in the differentiation of hUCB-MSCs into DA neuron-like cells. We suggest that ACM, which contains PTN and other neurotrophic factors, could potentially be used as an agent to promote the differentiation of DA neuron-like cells from hUCB-MSCs for cell therapy of Parkinson's disease without creating legal or ethical issues.</abstract><cop>Ireland</cop><pub>Elsevier Ireland Ltd</pub><pmid>23403104</pmid><doi>10.1016/j.neulet.2013.01.046</doi><tpages>6</tpages></addata></record>
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subjects Amnion - cytology
Amnion - metabolism
Amniotic epithelial cell
Blood
Carrier Proteins - metabolism
Carrier Proteins - pharmacology
Cell Differentiation
Cells, Cultured
Culture Media, Conditioned
Cytokines - metabolism
Cytokines - pharmacology
Dopaminergic neurons
Dopaminergic Neurons - cytology
Dopaminergic Neurons - drug effects
Dopaminergic Neurons - metabolism
Epithelial Cells - cytology
Epithelial Cells - drug effects
Epithelial Cells - metabolism
Fetal Blood - cytology
Fetal Blood - metabolism
Human umbilical cord blood-derived mesenchymal stem cell
Humans
Mesenchymal Stromal Cells - cytology
Mesenchymal Stromal Cells - drug effects
Mesenchymal Stromal Cells - metabolism
Pleiotrophin
Recombinant Proteins - pharmacology
title Pleiotrophin is involved in the amniotic epithelial cell-induced differentiation of human umbilical cord blood-derived mesenchymal stem cells into dopaminergic neuron-like cells
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