Apolipoprotein E is a pancreatic extracellular factor that maintains mature β-cell gene expression.
Ahmed I MahmoudFrancisco Xavier GaldosKatherine A DinanMark P JedrychowskiJeffrey C DavisAna VujicInbal RachminChristian ShigleyJames R PancoastSamuel LeeJennifer Hollister-LockCatherine M MacGillivraySteven P GygiDouglas A MeltonGordon C WeirRichard T LeePublished in: PloS one (2018)
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 β-cell transcription factors necessary for β-cell function and that soluble pancreatic decellularized matrix (DCM) can enhance β-cell gene expression. Following chromatographic fractionation of pancreatic DCM, we performed proteomics to identify soluble factors that can maintain β-cell stability and function. We identified Apolipoprotein E (ApoE) as an extracellular protein that significantly increased the expression of key β-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 β-cell gene expression profile.
Keyphrases
- metabolic syndrome
- gene expression
- single cell
- cell therapy
- signaling pathway
- induced apoptosis
- transcription factor
- mass spectrometry
- poor prognosis
- endothelial cells
- type diabetes
- genome wide
- epithelial mesenchymal transition
- skeletal muscle
- oxidative stress
- cell death
- dna binding
- simultaneous determination
- amino acid