| Literature DB >> 30127922 |
Koichi Kawamoto1,2, Tomofumi Ohashi1, Masamitsu Konno2, Naohiro Nishida1,2, Jun Koseki3, Hidetoshi Matsui4, Daisuke Sakai2, Toshihiro Kudo2, Hidetoshi Eguchi1, Taroh Satoh2, Yuichiro Doki1,2,3, Masaki Mori1,2,3, Hideshi Ishii2,3.
Abstract
There are several obstacles to overcome prior to achieving cellular reprogramming of pancreatic β cells in vitro and in vivo. The present study demonstrated that the transfer of epigenetic phenotypes was achieved in the cell-free conditioned medium (CM) of pancreatic insulinoma MIN6 cell cultures. The comparison of a subpopulation of MIN6, m14 and m9 cells indicated that MIN6-m14 cells were more prone to cellular reprogramming. Epigenetic profiling revealed that the transcription factor pancreas/duodenum homeobox protein 1 (Pdx1) was differentially associated among the clones. The culture of differentiated adipocytes in the CM of MIN6-m14 cells resulted in the induction of insulin mRNA expression, and was accompanied by epigenetic events of Pdx1 binding. The epigenetic profiling indicated that Pdx1 is preferentially associated with a previously uncharacterized region of the endoplasmic reticulum (ER) disulfide oxidase, ER oxidoreductin 1 gene. Therefore, the results of the present study indicated that the CM of MIN6 cells was able to induce a pancreatic β cell-like phenotype in differentiated adipocytes. These data provide additional support for the utility of cell-free CM for cellular reprogramming.Entities:
Keywords: conditioned medium; epigenetic reprogramming; pancreatic β cell
Year: 2018 PMID: 30127922 PMCID: PMC6096232 DOI: 10.3892/ol.2018.9008
Source DB: PubMed Journal: Oncol Lett ISSN: 1792-1074 Impact factor: 2.967