Journal article Open Access

Epithelial-to-Mesenchymal Transition Generates Proliferative Human Islet Precursor Cells

Gershengorn, M. C.


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  <identifier identifierType="URL">https://zenodo.org/record/1230848</identifier>
  <creators>
    <creator>
      <creatorName>Gershengorn, M. C.</creatorName>
      <givenName>M. C.</givenName>
      <familyName>Gershengorn</familyName>
    </creator>
  </creators>
  <titles>
    <title>Epithelial-to-Mesenchymal Transition Generates Proliferative Human Islet Precursor Cells</title>
  </titles>
  <publisher>Zenodo</publisher>
  <publicationYear>2004</publicationYear>
  <dates>
    <date dateType="Issued">2004-12-24</date>
  </dates>
  <resourceType resourceTypeGeneral="Text">Journal article</resourceType>
  <alternateIdentifiers>
    <alternateIdentifier alternateIdentifierType="url">https://zenodo.org/record/1230848</alternateIdentifier>
  </alternateIdentifiers>
  <relatedIdentifiers>
    <relatedIdentifier relatedIdentifierType="DOI" relationType="IsIdenticalTo">10.1126/science.1101968</relatedIdentifier>
  </relatedIdentifiers>
  <rightsList>
    <rights rightsURI="http://creativecommons.org/publicdomain/zero/1.0/legalcode">Creative Commons Zero v1.0 Universal</rights>
    <rights rightsURI="info:eu-repo/semantics/openAccess">Open Access</rights>
  </rightsList>
  <descriptions>
    <description descriptionType="Abstract">Insulin-expressing beta cells, found in pancreatic islets, are capable of generating more beta cells even in the adult. We show that fibroblast-like cells derived from adult human islets donated postmortem proliferate readily in vitro. These mesenchymal-type cells, which exhibit no hormone expression, can then be induced to differentiate into hormone-expressing islet-like cell aggregates, which reestablishes the epithelial character typical of islet cells. Immunohistochemistry, in situ hybridization, and messenger RNA measurements in single cells and cell populations establish the transition of epithelial cells within islets to mesenchymal cells in culture and then to insulin-expressing epithelial cells. Cultured human insulin-secreting cells can be coaxed to become less differentiated and then to divide into insulin-producing cells that are potentially useful for treating diabetes. Cultured human insulin-secreting cells can be coaxed to become less differentiated and then to divide into insulin-producing cells that are potentially useful for treating diabetes.</description>
  </descriptions>
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