TY - JOUR
T1 - MiR-375 promotes redifferentiation of adult human β cells expanded in vitro
AU - Nathan, Gili
AU - Kredo-Russo, Sharon
AU - Geiger, Tamar
AU - Lenz, Ayelet
AU - Kaspi, Haggai
AU - Hornstein, Eran
AU - Efrat, Shimon
N1 - Publisher Copyright:
© 2015 Nathan et al.
PY - 2015/4/13
Y1 - 2015/4/13
N2 - In-vitro expansion of β cells fromadult human pancreatic islets could provide abundant cells for cell replacement therapy of diabetes. However, proliferation of β-cell-derived (BCD) cells is associated with dedifferentiation. Here we analyzed changes inmicroRNAs (miRNAs) during BCD cell dedifferentiation and identified miR-375 as one of them iRNAs greatly downregulated. We hypothesized that restoration ofmiR-375 expression in expanded BCD cells may contribute to their redifferentiation. Our findings demonstrate that overexpression of miR-375 alone leads to activation of β-cell gene expression, reduced cell proliferation, and a switch from N-cadherin to E-cadherin expression, which characterizes mesenchymal-epithelial transition. These effects, which are reproducible in cells derived from multiple human donors, are likely mediated by repression of PDPK1 transcripts and indirect downregulation of GSK3 activity. These findings support an important role of miR-375 in regulation of human β-cell phenotype, and suggest thatmiR-375 upregulation may facilitate the generation of functional insulin-producing cells following ex-vivo expansion of human islet cells.
AB - In-vitro expansion of β cells fromadult human pancreatic islets could provide abundant cells for cell replacement therapy of diabetes. However, proliferation of β-cell-derived (BCD) cells is associated with dedifferentiation. Here we analyzed changes inmicroRNAs (miRNAs) during BCD cell dedifferentiation and identified miR-375 as one of them iRNAs greatly downregulated. We hypothesized that restoration ofmiR-375 expression in expanded BCD cells may contribute to their redifferentiation. Our findings demonstrate that overexpression of miR-375 alone leads to activation of β-cell gene expression, reduced cell proliferation, and a switch from N-cadherin to E-cadherin expression, which characterizes mesenchymal-epithelial transition. These effects, which are reproducible in cells derived from multiple human donors, are likely mediated by repression of PDPK1 transcripts and indirect downregulation of GSK3 activity. These findings support an important role of miR-375 in regulation of human β-cell phenotype, and suggest thatmiR-375 upregulation may facilitate the generation of functional insulin-producing cells following ex-vivo expansion of human islet cells.
UR - http://www.scopus.com/inward/record.url?scp=84928901831&partnerID=8YFLogxK
U2 - 10.1371/journal.pone.0122108
DO - 10.1371/journal.pone.0122108
M3 - ???researchoutput.researchoutputtypes.contributiontojournal.article???
C2 - 25875172
AN - SCOPUS:84928901831
SN - 1932-6203
VL - 10
JO - PLoS ONE
JF - PLoS ONE
IS - 4
M1 - e0122108
ER -