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Apolipoprotein E is a pancreatic extracellular factor that maintains mature ß-cell gene expression.
Mahmoud, Ahmed I; Galdos, Francisco X; Dinan, Katherine A; Jedrychowski, Mark P; Davis, Jeffrey C; Vujic, Ana; Rachmin, Inbal; Shigley, Christian; Pancoast, James R; Lee, Samuel; Hollister-Lock, Jennifer; MacGillivray, Catherine M; Gygi, Steven P; Melton, Douglas A; Weir, Gordon C; Lee, Richard T.
Affiliation
  • Mahmoud AI; Department of Stem Cell and Regenerative Biology and the Harvard Stem Cell Institute, Harvard University, Cambridge, MA, United States of America.
  • Galdos FX; Department of Stem Cell and Regenerative Biology and the Harvard Stem Cell Institute, Harvard University, Cambridge, MA, United States of America.
  • Dinan KA; Department of Stem Cell and Regenerative Biology and the Harvard Stem Cell Institute, Harvard University, Cambridge, MA, United States of America.
  • Jedrychowski MP; Department of Cell Biology, Harvard Medical School, Boston, MA, United States of America.
  • Davis JC; Department of Stem Cell and Regenerative Biology and the Harvard Stem Cell Institute, Harvard University, Cambridge, MA, United States of America.
  • Vujic A; Department of Stem Cell and Regenerative Biology and the Harvard Stem Cell Institute, Harvard University, Cambridge, MA, United States of America.
  • Rachmin I; Department of Stem Cell and Regenerative Biology and the Harvard Stem Cell Institute, Harvard University, Cambridge, MA, United States of America.
  • Shigley C; Department of Stem Cell and Regenerative Biology and the Harvard Stem Cell Institute, Harvard University, Cambridge, MA, United States of America.
  • Pancoast JR; Department of Stem Cell and Regenerative Biology and the Harvard Stem Cell Institute, Harvard University, Cambridge, MA, United States of America.
  • Lee S; Department of Stem Cell and Regenerative Biology and the Harvard Stem Cell Institute, Harvard University, Cambridge, MA, United States of America.
  • Hollister-Lock J; Islet Cell and Regenerative Biology Section, Joslin Diabetes Center, Harvard Stem Cell Institute, Harvard Medical School, Boston, MA, United States of America.
  • MacGillivray CM; Department of Stem Cell and Regenerative Biology and the Harvard Stem Cell Institute, Harvard University, Cambridge, MA, United States of America.
  • Gygi SP; Department of Cell Biology, Harvard Medical School, Boston, MA, United States of America.
  • Melton DA; Department of Stem Cell and Regenerative Biology and the Harvard Stem Cell Institute, Harvard University, Cambridge, MA, United States of America.
  • Weir GC; Islet Cell and Regenerative Biology Section, Joslin Diabetes Center, Harvard Stem Cell Institute, Harvard Medical School, Boston, MA, United States of America.
  • Lee RT; Department of Stem Cell and Regenerative Biology and the Harvard Stem Cell Institute, Harvard University, Cambridge, MA, United States of America.
PLoS One ; 13(10): e0204595, 2018.
Article in En | MEDLINE | ID: mdl-30303984
The in vivo microenvironment of tissues provides myriad unique signals to cells. Thus, following isolation, many cell types change in culture, often preserving some but not all of their in vivo characteristics in culture. At least some of the in vivo microenvironment may be mimicked by providing specific cues to cultured cells. Here, we show that after isolation and during maintenance in culture, adherent rat islets reduce expression of key ß-cell transcription factors necessary for ß-cell function and that soluble pancreatic decellularized matrix (DCM) can enhance ß-cell gene expression. Following chromatographic fractionation of pancreatic DCM, we performed proteomics to identify soluble factors that can maintain ß-cell stability and function. We identified Apolipoprotein E (ApoE) as an extracellular protein that significantly increased the expression of key ß-cell genes. The ApoE effect on beta cells was mediated at least in part through the JAK/STAT signaling pathway. Together, these results reveal a role for ApoE as an extracellular factor that can maintain the mature ß-cell gene expression profile.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Apolipoproteins E / Gene Expression Regulation / Insulin-Secreting Cells / Extracellular Space Type of study: Prognostic_studies Limits: Animals Language: En Journal: PLoS One Journal subject: CIENCIA / MEDICINA Year: 2018 Document type: Article Affiliation country: United States Country of publication: United States

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Apolipoproteins E / Gene Expression Regulation / Insulin-Secreting Cells / Extracellular Space Type of study: Prognostic_studies Limits: Animals Language: En Journal: PLoS One Journal subject: CIENCIA / MEDICINA Year: 2018 Document type: Article Affiliation country: United States Country of publication: United States