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  <controlfield tag="005">20240124152850.0</controlfield>
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    <subfield code="2">doi</subfield>
    <subfield code="a">10.1089/bio.2012.0015</subfield>
  </datafield>
  <datafield tag="024" ind1="8" ind2=" ">
    <subfield code="2">sideral</subfield>
    <subfield code="a">92401</subfield>
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  <datafield tag="037" ind1=" " ind2=" ">
    <subfield code="a">ART-2012-92401</subfield>
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  <datafield tag="041" ind1=" " ind2=" ">
    <subfield code="a">eng</subfield>
  </datafield>
  <datafield tag="100" ind1=" " ind2=" ">
    <subfield code="a">Solanas, E</subfield>
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  <datafield tag="245" ind1=" " ind2=" ">
    <subfield code="a">Incubation with dimethyl sulfoxide prior to cryopreservation improves functionality of thawed human primary hepatocytes</subfield>
  </datafield>
  <datafield tag="260" ind1=" " ind2=" ">
    <subfield code="c">2012</subfield>
  </datafield>
  <datafield tag="520" ind1="3" ind2=" ">
    <subfield code="a">Background: Efficient cryopreservation of human hepatocytes is essential for their use in cell therapy. This study investigated the effects of adding melatonin and/or dimethyl sulfoxide (DMSO) to pre-incubation and/or freezing solutions on the viability and function of thawed human hepatocytes.

Methods: Isolated human hepatocytes were pre-incubated for 90 min at 4°C in Williams' Medium E (WEM), WEM containing 5 mM melatonin dissolved in DMSO, or WEM containing the equivalent amount of DMSO (1%). The hepatocytes were frozen in University of Wisconsin solution (UW) and 10% DMSO, with or without 5 mM melatonin. After thawing, viability, plating efficiency, mitochondrial dehydrogenase activity (MTT), and albumin and urea production were analyzed.

Results: Viability and plating efficiency were not affected by melatonin or DMSO in pre-incubation media. Unexpectedly, hepatocytes pre-incubated with DMSO had significantly higher MTT (29.7% vs. control, p&lt;0.01), albumin (82.8% vs. control, p&lt;0.05), and urea amounts (26.2% vs. control, p=0.06) than those incubated only with WEM. Hepatocytes pre-incubated in media containing melatonin had amounts between those of cells incubated with DMSO or only with WEM (p&lt;0.05 for MTT and p>0.05 for albumin and urea values). Also, the addition of melatonin to the freezing media did not significantly improve any of the studied parameters (p>0.05).

Discussion: Adding 1% DMSO to pre-incubation media prior to the cryopreservation of human hepatocytes preserves hepatocyte function after thawing. These findings could be considered in current hepatocyte cryopreservation protocols.</subfield>
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    <subfield code="9">info:eu-repo/semantics/closedAccess</subfield>
    <subfield code="a">All rights reserved</subfield>
    <subfield code="u">http://www.europeana.eu/rights/rr-f/</subfield>
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  <datafield tag="590" ind1=" " ind2=" ">
    <subfield code="a">1.5</subfield>
    <subfield code="b">2012</subfield>
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  <datafield tag="591" ind1=" " ind2=" ">
    <subfield code="a">MEDICAL LABORATORY TECHNOLOGY</subfield>
    <subfield code="b">16 / 31 = 0.516</subfield>
    <subfield code="c">2012</subfield>
    <subfield code="d">Q3</subfield>
    <subfield code="e">T2</subfield>
  </datafield>
  <datafield tag="591" ind1=" " ind2=" ">
    <subfield code="a">CELL BIOLOGY</subfield>
    <subfield code="b">157 / 183 = 0.858</subfield>
    <subfield code="c">2012</subfield>
    <subfield code="d">Q4</subfield>
    <subfield code="e">T3</subfield>
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  <datafield tag="655" ind1=" " ind2="4">
    <subfield code="a">info:eu-repo/semantics/article</subfield>
    <subfield code="v">info:eu-repo/semantics/publishedVersion</subfield>
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  <datafield tag="700" ind1=" " ind2=" ">
    <subfield code="a">Sostres, C</subfield>
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  <datafield tag="700" ind1=" " ind2=" ">
    <subfield code="a">Serrablo, A</subfield>
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  <datafield tag="700" ind1=" " ind2=" ">
    <subfield code="a">García-Gil, A</subfield>
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  <datafield tag="700" ind1=" " ind2=" ">
    <subfield code="a">Aranguren, F</subfield>
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  <datafield tag="700" ind1=" " ind2=" ">
    <subfield code="a">Jimenez, P</subfield>
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  <datafield tag="700" ind1=" " ind2=" ">
    <subfield code="a">Serrano, MT.</subfield>
    <subfield code="u">Universidad de Zaragoza</subfield>
    <subfield code="0">(orcid)0000-0002-7119-2244</subfield>
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  <datafield tag="710" ind1="2" ind2=" ">
    <subfield code="1">1007</subfield>
    <subfield code="2">610</subfield>
    <subfield code="a">Universidad de Zaragoza</subfield>
    <subfield code="b">Dpto. Medicina, Psiqu. y Derm.</subfield>
    <subfield code="c">Area Medicina</subfield>
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  <datafield tag="773" ind1=" " ind2=" ">
    <subfield code="g">10, 5 (2012), 446-53</subfield>
    <subfield code="p">BIOPRESERVATION AND BIOBANKING</subfield>
    <subfield code="t">BIOPRESERVATION AND BIOBANKING</subfield>
    <subfield code="x">1947-5535</subfield>
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  <datafield tag="856" ind1="4" ind2=" ">
    <subfield code="s">207062</subfield>
    <subfield code="u">http://zaguan.unizar.es/record/130263/files/texto_completo.pdf</subfield>
    <subfield code="y">Versión publicada</subfield>
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    <subfield code="u">http://zaguan.unizar.es/record/130263/files/texto_completo.jpg?subformat=icon</subfield>
    <subfield code="x">icon</subfield>
    <subfield code="y">Versión publicada</subfield>
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    <subfield code="o">oai:zaguan.unizar.es:130263</subfield>
    <subfield code="p">articulos</subfield>
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    <subfield code="a">2024-01-24-14:57:54</subfield>
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