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<Articles JournalTitle="International Journal of Hematology-Oncology and Stem Cell Research">
  <Article>
    <Journal>
      <PublisherName>Tehran University of Medical Sciences</PublisherName>
      <JournalTitle>International Journal of Hematology-Oncology and Stem Cell Research</JournalTitle>
      <Issn>2008-2207</Issn>
      <Volume>5</Volume>
      <Issue>3</Issue>
      <PubDate PubStatus="epublish">
        <Year>2011</Year>
        <Month>09</Month>
        <Day>15</Day>
      </PubDate>
    </Journal>
    <title locale="en_US">Studying the Anti-aging Effect of Nitric Oxide on the Cell Proliferation and Telomerase Activity of Human Cord Blood Hematopoietic Stem Cells</title>
    <FirstPage>1</FirstPage>
    <LastPage>10</LastPage>
    <AuthorList>
      <Author>
        <FirstName>Abdolkhaleg</FirstName>
        <LastName>Deezagi</LastName>
        <affiliation locale="en_US">Department of Biochemistry, National Institute of Genetic Engineering and Biotechnology, Tehran-Iran</affiliation>
      </Author>
      <Author>
        <FirstName>Neda</FirstName>
        <LastName>Vaseli-hagh</LastName>
        <affiliation locale="en_US">Department of Biochemistry, National Institute of Genetic Engineering and Biotechnology, Tehran-Iran</affiliation>
      </Author>
      <Author>
        <FirstName>Masoumeh</FirstName>
        <LastName>Nouri</LastName>
        <affiliation locale="en_US">Department of Biochemistry, National Institute of Genetic Engineering and Biotechnology, Tehran-Iran</affiliation>
      </Author>
    </AuthorList>
    <History>
      <PubDate PubStatus="received">
        <Year>2015</Year>
        <Month>10</Month>
        <Day>01</Day>
      </PubDate>
    </History>
    <abstract locale="en_US">Introduction: Accumulating evidences indicated that during increasing of the animals' age, the number and the functional properties of hematopoietic stem cells (HSCs) become altered because of a gradual decrease in replication potential.&#xA0; The efficient factors in this process are DNA damaging, reduced telomerase activity, shortening of telomeres and oxidative stresses. For overcoming these factors, using of the anti-oxidants and activating of telomerase would be effective. The aim of this research was to study the effect of Nitric Oxide (NO) as an anti-oxidant on the cell proliferation, cell viability and telomerase activity of HSCs in vitro.
Methods: HSCs were isolated from human cord bloods.&#xA0; Cells were treated by L-Arginine and Sodium Nitro-Pruscide (as NO donors) in a dose dependent manner. The cell viability and proliferation were assayed by trypan blue, MTT and BrdU methods. The profile of aging was assayed by senescence sensitive &#x3B2;-Galactosidase staining and telomerase activity was assayed by TRAP-PCR E ISA method. Finally, Nitric Oxide Synthatase mRNA expression level was analyzed by RT-PCR.
Result: HSCs those treated with SNP exhibited an increase 3-7 fold (400-1000 &#xB5;mol) in NO production in comparison to untreated control cells (140&#xB5;mol).Treatment of cells by L-Arg resulted lower release of NO (Up to 200 &#xB5;mol) in comparison to SNP. Increasing NO production resulted to the inducing of cells growth potential and proliferation parameters up to 40% which accompanied&#xA0; by the increasing of telomerase activity up to 25% in the presence of 100 &#xB5;M of SNP or&#xA0; 1.0 mM of L-Arg in comparison to untreated control cells.
Discussion: The present work demonstrates that NO affect telomerase activity and cellular replicative capacity in human hematopoietic stem cells. A significant behavior was observed on the telomerase activity and cell proliferation after treatment of cells. Induction of cell proliferation&#xA0; was accompanied by a slight inhibition of HSCs senescence. Finally the telomerase induction and reduction in cell enescence were accompanied by increasing&#xA0; of the cell proliferation parameters.</abstract>
    <web_url>https://ijhoscr.tums.ac.ir/index.php/ijhoscr/article/view/280</web_url>
    <pdf_url>https://ijhoscr.tums.ac.ir/index.php/ijhoscr/article/download/280/273</pdf_url>
  </Article>
</Articles>
