Please use this identifier to cite or link to this item: http://hdl.handle.net/2440/83103
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Type: Journal article
Title: Disrupted pancreatic exocrine differentiation and malabsorption in response to chronic elevated systemic glucocorticoid
Author: Wallace, K.
Flecknell, P.
Burt, A.
Wright, M.
Citation: American Journal of Pathology, 2010; 177(3):1225-1232
Publisher: Amer Soc Investigative Pathology Inc
Issue Date: 2010
ISSN: 0002-9440
1525-2191
Statement of
Responsibility: 
Karen Wallace, Paul A. Flecknell, Alastair D. Burt, Matthew C. Wright
Abstract: Glucocorticoids are antiinflammatory therapeutics that have potent effects on cell differentiation. The aim of this study was to establish whether systemic glucocorticoid exposure significantly affects pancreatic differentiation in vivo because hepatocyte-like cells have been documented to occur in the diseased rodent pancreas. Expression of hepatic markers was examined in pancreata from mice genetically modified to secrete elevated circulating endogenous glucocorticoid [Tg(Crh)]. Tg(Crh) mice with elevated glucocorticoid appeared cushingoid and by 21 weeks of age were obese, insulin-resistant, and had extensive areas of hepatic gene expression in exocrine tissue. Acinar cells from Tg(Crh) mice costained for both amylase and cyp2e1, suggesting direct acinar-hepatic transdifferentiation. Hepatic expression increased with age in the pancreas to such an extent that malabsorption and rapid weight loss occurred in a subset of aging mice; this effect was reversed by dietary porcine pancreatic enzyme supplementation. Indeed, pancreatic expression of hepatic markers was prevented by adrenalectomy, establishing a direct role for glucocorticoid. Elevated levels of circulating glucocorticoid therefore promote a transdifferentiation of adult exocrine pancreas into hepatocyte-like cells, and chronic exposure results in pancreatic malfunction. Glucocorticoids are thus capable of modulating the differentiation of terminally differentiated adult cells.
Keywords: Pancreas; Hepatocytes; Animals; Mice, Transgenic; Mice; Corticotropin-Releasing Hormone; Insulin; Blood Glucose; Glucocorticoids; Blotting, Western; Adrenalectomy; Reverse Transcriptase Polymerase Chain Reaction; Age Factors; Cell Differentiation; Gene Expression
Rights: © American Society for Investigative Pathology
RMID: 0020130515
DOI: 10.2353/ajpath.2010.100107
Appears in Collections:Medicine publications

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