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<ArticleSet>
  <Article>
    <Journal>
      <PublisherName>Academy of Medical Sciences of I.R. Iran</PublisherName>
      <JournalTitle>Archives of Iranian Medicine</JournalTitle>
      <Issn>1029-2977</Issn>
      <Volume>19</Volume>
      <Issue>8</Issue>
      <PubDate PubStatus="ppublish">
        <Year>2016</Year>
        <Month>08</Month>
        <DAY>01</DAY>
      </PubDate>
    </Journal>
    <ArticleTitle>Dopaminergic Induction of Umbilical Cord Mesenchymal Stem Cells by Conditioned Medium of Choroid Plexus Epithelial Cells Reduces Apomorphine-Induced Rotation in Parkinsonian Rats</ArticleTitle>
    <FirstPage>0</FirstPage>
    <LastPage>0</LastPage>
    <Language>EN</Language>
    <AuthorList>
      <Author>
        <FirstName>A</FirstName>
        <LastName>Aliaghaei</LastName>
      </Author>
      <Author>
        <FirstName>Mossa</FirstName>
        <LastName>Gardaneh</LastName>
      </Author>
      <Author>
        <FirstName>Nader</FirstName>
        <LastName>Maghsoudi</LastName>
      </Author>
      <Author>
        <FirstName>Parvin</FirstName>
        <LastName>Salehinejad</LastName>
      </Author>
      <Author>
        <FirstName>Ehsan</FirstName>
        <LastName>Gharib</LastName>
      </Author>
    </AuthorList>
    <PublicationType>Journal Article</PublicationType>
    <ArticleIdList>
      <ArticleId IdType="doi">
      </ArticleId>
    </ArticleIdList>
    <History>
    </History>
    <Abstract> BACKGROUND/OBJECTIVE: Degeneration of dopaminergic neurons in Parkinson’s disease (PD) implies cell replacement using potentially differentiable sources as a promising therapeutic solution. We tested the capacity of conditioned medium from choroid plexus epithelial cells (CPECs-CM) to induce the dopaminergic potential of umbilical cord matrix mesenchymal stem cells (UCMSCs). METHODS: We isolated UCMSCs from human umbilical cord and CPECs from rat brain. Following expansion and characterization, CPECs-CM were collected, tested for expression of various growth factors, and applied to UCMSCs. Differentiation was examined and UCMSCs were injected into 6-OHDA-leasioned striatum to test their survival and function. RESULTS: RT-PCR and immuno-staining demonstrated neuronal/dopaminergic signaling in UCMSCs induced by CPECs-CM and accelerated by addition of retinoic acid (RA) and fibroblast growth factor-2. Expression of β–tubulin-3, Nestin and MAP2 confirmed neuronal differentiation whereas tyrosine hydroxylase, aromatic acid decarboxylase and dopamine transporter were expressed as signs of dopaminergic differentiation. Post-transplantation, the UCMSCs survived, showed reduced rate of apoptosis and led to animals’ recovery from apomorphine-induced rotations. CONCLUSION: The combination of neurotrophic factors present in CPECs-CM and RA can synergize to maximize dopaminergic differentiation of potential cell sources including UCMSCs. Our study may have implications for PD cell replacement therapy.</Abstract>
  </Article>
</ArticleSet>