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    <journal-meta>
      <journal-id journal-id-type="nlm-ta">Avicenna J Med Biotech</journal-id>
      <journal-id journal-id-type="publisher-id">arij002</journal-id>
      <journal-title-group>
        <journal-title>Avicenna Journal of Medical Biotechnology</journal-title>
      </journal-title-group>
      <issn pub-type="ppub">2008-2835</issn>
      <issn pub-type="epub">2008-4625</issn>
      <publisher>
        <publisher-name>Avicenna Research Institute</publisher-name>
      </publisher>
    </journal-meta>

    <article-meta>
      <article-id pub-id-type="publisher-id">ajmb60516</article-id>
      <article-id pub-id-type="doi"></article-id>
      <article-id pub-id-type="pmid"></article-id>
      <article-categories>
        <subj-group subj-group-type="heading">
             <subject></subject> 
        </subj-group>
        <subj-group>
            <subject></subject>
        </subj-group> 
      </article-categories>
      <title-group>
        <article-title>Bioactive Materials Derived from Menstrual Blood Stem Cells Enhance the Quality  of In Vitro Bovine Embryos</article-title>
      </title-group>
        <contrib-group><contrib contrib-type="author"><name><surname>Amini </surname><given-names>Mohammad Sobhan</given-names></name></contrib></contrib-group><contrib-group><contrib contrib-type="author"><name><surname>Naderi</surname><given-names>Mohammad Mehdi</given-names></name></contrib><aff>Department of Biotechnology, School of Life Sciences, Karpagam University, Coimbatore, Tamil Nadu, India</aff></contrib-group><contrib-group><contrib contrib-type="author"><name><surname>Shirazi</surname><given-names>Abolfazl</given-names></name></contrib><aff>Reproductive Biotechnology Research Center, Avicenna Research Institute, ACECR      , Tehran, Iran</aff></contrib-group><contrib-group><contrib contrib-type="author"><name><surname>Aminafshar</surname><given-names>Mehdi</given-names></name></contrib></contrib-group><contrib-group><contrib contrib-type="author"><name><surname>Borjian Boroujeni</surname><given-names>Sara</given-names></name></contrib><aff>Department of Clinical Science, Faculty of Veterinary Medicine, University of Tehran, Tehran, Iran</aff></contrib-group><contrib-group><contrib contrib-type="author"><name><surname>Pournourali </surname><given-names>Mostafa</given-names></name></contrib></contrib-group><contrib-group><contrib contrib-type="author"><name><surname>Malekpour </surname><given-names>Ali</given-names></name></contrib></contrib-group>
      <pub-date pub-type="ppub">
        <day></day>
        <month></month>
        <year></year>
      </pub-date>
      <pub-date pub-type="epub">
        <day></day>
        <month></month>
        <year></year>
      </pub-date>
      <volume>14</volume>
      <issue>4</issue>
      <fpage>287</fpage>
      <lpage>293</lpage>
      <history>
        <date date-type="received">
          <day>24</day>
          <month>1</month>
          <year>2022</year>
        </date>
        <date date-type="accepted">
          <day>11</day>
          <month>7</month>
          <year>2022</year>
        </date>
      </history>
      <abstract>
      <p>
      &lt;p style=&quot;text-align:justify&quot;&gt;&lt;span style=&quot;font-size:11pt&quot;&gt;&lt;span style=&quot;font-size:9.5pt&quot;&gt;Backgrounds:&lt;/span&gt;&lt;span style=&quot;font-size:10.0pt&quot;&gt; The aim of this study was to determine whether the addition of bioactive materials derived from Menstrual Blood Stem Cells (MenSCs) to the oocyte maturation medium may improve the quality of bovine embryos &lt;em&gt;in vitro&lt;/em&gt;. &lt;/span&gt;&lt;/span&gt;&lt;/p&gt;

&lt;p style=&quot;text-align:justify&quot;&gt;&lt;span style=&quot;font-size:11pt&quot;&gt;&lt;span style=&quot;font-size:9.5pt&quot;&gt;Methods:&lt;/span&gt;&lt;span style=&quot;font-size:10.0pt&quot;&gt; MenSCs were collected from 6 healthy women (between 26 and 36 years old) and after 3 days of culture, their bioactive materials were frozen. The bovine &lt;/span&gt;&lt;span style=&quot;font-size:10.0pt&quot;&gt;&lt;span style=&quot;background-color:white&quot;&gt;Cumulus-Oocyte-Complexes&lt;/span&gt; (COCs) were aspirated from ovarian slaughterhouse and the oocytes with more than three layers of cumulus cells were cultured &lt;em&gt;in vitro&lt;/em&gt; in media supplemented with (treatment) and without (control) 10% MenSCs&amp;rsquo; bioactive materials. After IVM/IVF, the presumptive zygotes were cultured for 8 days. &lt;/span&gt;&lt;/span&gt;&lt;/p&gt;

&lt;p style=&quot;text-align:justify&quot;&gt;&lt;span style=&quot;font-size:11pt&quot;&gt;&lt;span style=&quot;font-size:9.5pt&quot;&gt;Results:&lt;/span&gt;&lt;span style=&quot;font-size:10.0pt&quot;&gt; The blastocyst rate on day 8 in treatment group was higher than control (40.2&amp;plusmn;1.9 &lt;em&gt;vs.&lt;/em&gt; 23&amp;plusmn;4.2.3, p=0.001). The ratio of &lt;/span&gt;&lt;span style=&quot;font-size:10.0pt&quot;&gt;&lt;span style=&quot;background-color:white&quot;&gt;Trophectoderm&lt;/span&gt;&lt;/span&gt;&lt;span style=&quot;font-size:10.0pt&quot;&gt;&lt;span style=&quot;background-color:white&quot;&gt;&amp;nbsp;(TE) and&amp;nbsp;Inner Cell Mass (ICM)&lt;/span&gt; (ICM/TE) cells was also greater in treatment group compared to control (30.3&amp;plusmn;2 &lt;em&gt;vs.&lt;/em&gt; 14.9&amp;plusmn;1; p=0.001). The re-expansion of vitrified blastocysts, 24 hours after warming, in treatment group was higher than control (93.3&amp;plusmn;2.5 &lt;em&gt;vs.&lt;/em&gt; 66.2&amp;plusmn;8.8; p=0.01). The expression of some genes related to pluripotency and implantation (&lt;em&gt;OCT4, CDX2&lt;/em&gt;, and &lt;em&gt;IFNT&lt;/em&gt;) were increased in treatment group compared to control (p&amp;lt;0/05). &lt;/span&gt;&lt;/span&gt;&lt;/p&gt;

&lt;p style=&quot;text-align:justify&quot;&gt;&lt;span style=&quot;font-size:11pt&quot;&gt;&lt;span style=&quot;font-size:9.5pt&quot;&gt;Conclusion:&lt;/span&gt;&lt;span style=&quot;font-size:10.0pt&quot;&gt; In conclusion, the addition of MenSCs&amp;rsquo; bioactive materials during &lt;em&gt;in vitro&lt;/em&gt; maturation of bovine oocytes could improve the quantity and quality of bovine IVP embryos. Also, the expression of some genes associated with pluripotency and implantation in the blastocyst would be increased.&lt;/span&gt;&lt;/span&gt;&lt;/p&gt;

      </p>
      </abstract>
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