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Glucocorticoid-induced pancreatic-hepatic trans-differentiation in a human cell line in vitro.

Authors :
Fairhall EA
Leitch AC
Lakey AF
Probert PME
Richardson G
De Santis C
Wright MC
Source :
Differentiation; research in biological diversity [Differentiation] 2018 Jul - Aug; Vol. 102, pp. 10-18. Date of Electronic Publication: 2018 May 22.
Publication Year :
2018

Abstract

The rodent pancreatic AR42J-B13 (B-13) cell line differentiates into non-replicative hepatocyte-like cells in response to glucocorticoid mediated via the glucocorticoid receptor (GR). The aims of this study were to identify a human cell line that responds similarly and investigate the mechanisms underpinning any alteration in differentiation. Exposing the human pancreatic adenocarcinoma (HPAC) cell line to 1-10 µM concentrations of dexamethasone (DEX) resulted an inhibition of proliferation, suppressed carcinoembryonic antigen expression, limited expression of pancreatic acinar and hepatic gene expression and significant induction of the constitutively-expressed hepatic CYP3A5 mRNA transcript. These changes were associated with a pulse of genomic DNA methylation and suppressed notch signalling activity. HPAC cells expressed high levels of GR transcript in contrast to other nuclear receptors - such as the glucocorticoid-activated pregnane X receptor (PXR) - and GR transcriptional function was activated by DEX in HPAC cells. Expression of selected hepatocyte transcripts in response to DEX was blocked by co-treatment with the GR antagonist RU486. These data indicate that the HPAC response to glucocorticoid exposure includes an inhibition in proliferation, alterations in notch signalling and a limited change in the expression of genes associated with an acinar and hepatic phenotype. This is the first demonstration of a human cell responding to similarly to the rodent B-13 cell regarding formation of hepatocyte-like cells in response to glucocorticoid. Identifying and modulating the ablating factor(s) may enhance the hepatocyte-like forming capacity of HPAC cells after exposure to glucocorticoid and generate an unlimited in vitro supply of human hepatocytes for toxicology studies and a variety of clinical applications.<br /> (Copyright © 2018 International Society of Differentiation. Published by Elsevier B.V. All rights reserved.)

Details

Language :
English
ISSN :
1432-0436
Volume :
102
Database :
MEDLINE
Journal :
Differentiation; research in biological diversity
Publication Type :
Academic Journal
Accession number :
29857331
Full Text :
https://doi.org/10.1016/j.diff.2018.05.003