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    <identifier>10.57760/sciencedb.j00217.12028</identifier>
    <datestamp>2026-03-04T10:34:52Z</datestamp>
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<oai_dc:dc xmlns:oai_dc="http://www.openarchives.org/OAI/2.0/oai_dc/" xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/ http://www.openarchives.org/OAI/2.0/oai_dc.xsd">
  <dc:date>2026-03-04</dc:date>
  <dc:title>Protective effect of HUCMSCs-Exo on IFN-&amp;gamma;-mediated melanocyte injury</dc:title>
  <dc:identifier>doi:10.57760/sciencedb.j00217.12028</dc:identifier>
  <dc:language>en</dc:language>
  <dc:description>Objective To explore the protective effect of exosomes derived from human umbilical cord mesenchymal stem cells (HUCMSCs-Exo) against interferon-gamma (IFN-&amp;gamma;)-mediated melanocyte injury.Methods Human epidermal melanocytes were cultured in vitro. Melanocytes were treated with different concentrations of IFN-&amp;gamma; (100, 200, 400, 800 ng/mL) for 48 hours, and cell survival rate was detected by CCK-8 assay to screen an appropriate IFN-&amp;gamma;concentration for establishing an immunosuppressive model. Melanocytes were treated with different concentrations of HUCMSCs-Exo for 48 hours, and cell proliferation activity was detected by CCK-8 assay to determine the safe concentration of exosomes for subsequent experiments. Melanocytes were pretreated with exosomes at a safe concentration and then incubated with or without 100 ng/mL IFN-&amp;gamma; for 48 hours. Cell proliferation activity was assessed using the CCK-8 assay; mitochondrial membrane potential was detected by JC-1 staining; apoptosis was evaluated by flow cytometry; and tyrosinase activity was measured by the dopamine oxidation method.Results With the increase in IFN-&amp;gamma; concentration, cell survival rate gradually decreased. The cell survival rates in the 100, 200, 400, and 800 ng/mL IFN-&amp;gamma; groups were significantly different from those in the control group (P ＜ 0.05). 100 ng/mL IFN-&amp;gamma; was selected to establish an epidermal melanocyte immunosuppressive model. Melanocytes treated with 10 and 20 &amp;mu;g/mL exosomes for 48 hours showed significant differences compared with the control group (P ＜ 0.05), and 10 &amp;mu;g/mL exosomes were selected for subsequent experiments. Compared with the IFN-&amp;gamma; group, exosomes significantly increased cell proliferation activity.Conclusions HUCMSCs-Exo has a protective effect against IFN-&amp;gamma;-mediated immunosuppressive injury in melanocytes.</dc:description>
  <dc:subject>Interferon-gamma; Vitiligo; melanocyte; Exosome</dc:subject>
  <dc:creator>null.null</dc:creator>
  <dc:creator>null.null</dc:creator>
  <dc:creator>null.null</dc:creator>
  <dc:creator>null.null</dc:creator>
  <dc:rights>PUBLIC</dc:rights>
  <dc:rights>https://creativecommons.org/publicdomain/zero/1.0/</dc:rights>
  <dc:type>dataset</dc:type>
  <dc:publisher>Science Data Bank</dc:publisher>
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