Unknown

Dataset Information

0

Glucocorticoid Signaling Enhances Expression of Glucose-Sensing Molecules in Immature Pancreatic Beta-Like Cells Derived from Murine Embryonic Stem Cells In Vitro.


ABSTRACT: Pluripotent stem cells may serve as an alternative source of beta-like cells for replacement therapy of type 1 diabetes; however, the beta-like cells generated in many differentiation protocols are immature. The maturation of endogenous beta cells involves an increase in insulin expression starting in late gestation and a gradual acquisition of the abilities to sense glucose and secrete insulin by week 2 after birth in mice; however, what molecules regulate these maturation processes are incompletely known. In this study, we aim to identify small molecules that affect immature beta cells. A cell-based assay, using pancreatic beta-like cells derived from murine embryonic stem (ES) cells harboring a transgene containing an insulin 1-promoter driven enhanced green fluorescent protein reporter, was used to screen a compound library (NIH Clinical Collection-003). Cortisone, a glucocorticoid, was among five positive hit compounds. Quantitative reverse transcription-polymerase chain reaction analysis revealed that glucocorticoids enhance the gene expression of not only insulin 1 but also glucose transporter-2 (Glut2; Slc2a2) and glucokinase (Gck), two molecules important for glucose sensing. Mifepristone, a pharmacological inhibitor of glucocorticoid receptor (GR) signaling, reduced the effects of glucocorticoids on Glut2 and Gck expression. The effects of glucocorticoids on ES-derived cells were further validated in immature primary islets. Isolated islets from 1-week-old mice had an increased Glut2 and Gck expression in response to a 4-day treatment of exogenous hydrocortisone in vitro. Gene deletion of GR in beta cells using rat insulin 2 promoter-driven Cre crossed with GRflox/flox mice resulted in a reduced gene expression of Glut2, but not Gck, and an abrogation of insulin secretion when islets were incubated in 0.5?mM d-glucose and stimulated by 17?mM d-glucose in vitro. These results demonstrate that glucocorticoids positively regulate glucose sensors in immature murine beta-like cells.

SUBMITTER: Ghazalli N 

PROVIDER: S-EPMC6029647 | biostudies-literature | 2018 Jul

REPOSITORIES: biostudies-literature

altmetric image

Publications

Glucocorticoid Signaling Enhances Expression of Glucose-Sensing Molecules in Immature Pancreatic Beta-Like Cells Derived from Murine Embryonic Stem Cells In Vitro.

Ghazalli Nadiah N   Wu Xiaoxing X   Walker Stephanie S   Trieu Nancy N   Hsin Li-Yu LY   Choe Justin J   Chen Chialin C   Hsu Jasper J   LeBon Jeanne J   Kozlowski Mark T MT   Rawson Jeffrey J   Tirrell David A DA   Yip M L Richard MLR   Ku Hsun Teresa HT  

Stem cells and development 20180606 13


Pluripotent stem cells may serve as an alternative source of beta-like cells for replacement therapy of type 1 diabetes; however, the beta-like cells generated in many differentiation protocols are immature. The maturation of endogenous beta cells involves an increase in insulin expression starting in late gestation and a gradual acquisition of the abilities to sense glucose and secrete insulin by week 2 after birth in mice; however, what molecules regulate these maturation processes are incompl  ...[more]

Similar Datasets

| S-EPMC3547908 | biostudies-literature
| S-EPMC7678872 | biostudies-literature
| S-EPMC2586982 | biostudies-other
| S-EPMC7932895 | biostudies-literature
| S-EPMC3636645 | biostudies-literature
| S-EPMC6851018 | biostudies-literature
| S-EPMC7408589 | biostudies-literature
| S-EPMC8880991 | biostudies-literature
| S-EPMC4354927 | biostudies-literature
| S-EPMC2853211 | biostudies-literature