1 Ocak 2022 Dergi makalesi Açık Erişim

Sokullu, Emel; Polat, Irem; Ozkaya, Ferhat Can; El-Neketi, Mona; Ebrahim, Weaam; Sarabi, Misagh Rezapour; Sengul, Gulgun; Tasoglu, Savas

DataCite XML

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  <identifier identifierType="URL">https://aperta.ulakbim.gov.tr/record/255399</identifier>
  <creators>
    <creator>
      <creatorName>Sokullu, Emel</creatorName>
      <givenName>Emel</givenName>
      <familyName>Sokullu</familyName>
      <affiliation>Koc Univ, KUTTAM, Dept Biophys, Sch Med, TR-34450 Istanbul, Turkey</affiliation>
    </creator>
    <creator>
      <creatorName>Polat, Irem</creatorName>
      <givenName>Irem</givenName>
      <familyName>Polat</familyName>
      <affiliation>Izmir Katip Celebi Univ, Dept Nat &amp; Appl Sci, Grad Sch Nanosci &amp; Nanotechnol, TR-35620 Izmir, Turkey</affiliation>
    </creator>
    <creator>
      <creatorName>Ozkaya, Ferhat Can</creatorName>
      <givenName>Ferhat Can</givenName>
      <familyName>Ozkaya</familyName>
      <affiliation>Ege Univ, Ctr Sci &amp; Technol, EBILTEM, TR-35100 Izmir, Turkey</affiliation>
    </creator>
    <creator>
      <creatorName>El-Neketi, Mona</creatorName>
      <givenName>Mona</givenName>
      <familyName>El-Neketi</familyName>
      <affiliation>Mansoura Univ, Fac Pharm, Dept Pharmacognosy, Mansoura 35516, Egypt</affiliation>
    </creator>
    <creator>
      <creatorName>Ebrahim, Weaam</creatorName>
      <givenName>Weaam</givenName>
      <familyName>Ebrahim</familyName>
      <affiliation>Mansoura Univ, Fac Pharm, Dept Pharmacognosy, Mansoura 35516, Egypt</affiliation>
    </creator>
    <creator>
      <creatorName>Sarabi, Misagh Rezapour</creatorName>
      <givenName>Misagh Rezapour</givenName>
      <familyName>Sarabi</familyName>
      <affiliation>Koc Univ, Dept Mech Engn, TR-34450 Istanbul, Turkey</affiliation>
    </creator>
    <creator>
      <creatorName>Sengul, Gulgun</creatorName>
      <givenName>Gulgun</givenName>
      <familyName>Sengul</familyName>
      <affiliation>Ege Univ, Sch Med, Anat Dept, TR-35040 Izmir, Turkey</affiliation>
    </creator>
    <creator>
      <creatorName>Tasoglu, Savas</creatorName>
      <givenName>Savas</givenName>
      <familyName>Tasoglu</familyName>
    </creator>
  </creators>
  <titles>
    <title>3D Engineered Neural Co-Culture Model And Neurovascular Effects Of Marine Fungi-Derived Citreohybridonol</title>
  </titles>
  <publisher>Aperta</publisher>
  <publicationYear>2022</publicationYear>
  <dates>
    <date dateType="Issued">2022-01-01</date>
  </dates>
  <resourceType resourceTypeGeneral="Text">Journal article</resourceType>
  <alternateIdentifiers>
    <alternateIdentifier alternateIdentifierType="url">https://aperta.ulakbim.gov.tr/record/255399</alternateIdentifier>
  </alternateIdentifiers>
  <relatedIdentifiers>
    <relatedIdentifier relatedIdentifierType="DOI" relationType="IsIdenticalTo">10.1063/5.0100452</relatedIdentifier>
  </relatedIdentifiers>
  <rightsList>
    <rights rightsURI="http://www.opendefinition.org/licenses/cc-by">Creative Commons Attribution</rights>
    <rights rightsURI="info:eu-repo/semantics/openAccess">Open Access</rights>
  </rightsList>
  <descriptions>
    <description descriptionType="Abstract">Marine-based biomolecules are emerging metabolites that have gained attention for developing novel biomaterials, drugs, and pharmaceutical in vitro platforms. Here, we developed a 3D engineered neural co-culture model via a 3D prototyped sliding frame-platform for multi-step UV lithography and investigated the neurovascular potential of citreohybridonol in neuroblastoma treatment. Citreohybridonol was isolated from a sponge-derived fungus Penicillium atrovenetum. The model was characterized by Fourier-transform infrared spectroscopy and scanning electron microscopy analysis. Human umbilical cord vein endothelial cells (HUVECs) and neuroblastoma (SH-SY5Y) cell lines were encapsulated in gelatin methacrylate (GelMA) with and without citreohybridonol. The effect of citreohybridonol on the proliferation capacity of cells was assessed via cell viability and immunostaining assays. GelMA and 3D culture characterization indicated that the cells were successfully encapsulated as axenic and mixed with/without citreohybridonol. The cytotoxic test confirmed that the 3D microenvironment was non-toxic for cultural experiments, and it showed the inhibitory effects of citreohybridonol on SH-SY5Y cells and induced the proliferation of HUVECs. Finally, immunohistochemical staining demonstrated that citreohybridonol suppressed SH-SY5Y cells and induced vascularization of HUVECs in mixed 3D cell culture.</description>
  </descriptions>
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