ETV5 regulates ductal morphogenesis with Sox9 and is critical for regeneration from pancreatitis

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Item Type:	Article
Title:	ETV5 regulates ductal morphogenesis with Sox9 and is critical for regeneration from pancreatitis
Creators Name:	Das, K.K., Heeg, S., Pitarresi, J.R., Reichert, M., Bakir, B., Takano, S., Kopp, J.L., Wahl-Feuerstein, A., Hicks, P., Sander, M. and Rustgi, A.K.
Abstract:	BACKGROUND: The plasticity of pancreatic acinar cells to undergo acinar to ductal metaplasia (ADM) has been demonstrated to contribute to the regeneration of the pancreas in response to injury. Sox9 is critical for ductal cell fate and important in the formation of ADM, most likely in concert with a complex hierarchy of, as yet, not fully elucidated transcription factors. RESULTS: By using a mouse model of acute pancreatitis and three dimensional organoid culture of primary pancreatic ductal cells, we herein characterize the Ets-transcription factor Etv5 as a pivotal regulator of ductal cell identity and ADM that acts upstream of Sox9 and is essential for Sox9 expression in ADM. Loss of Etv5 is associated with increased severity of acute pancreatitis and impaired ADM formation leading to delayed tissue regeneration and recovery in response to injury. CONCLUSIONS: Our data provide new insights in the regulation of ADM with implications in our understanding of pancreatic homeostasis, pancreatitis and epithelial plasticity.
Keywords:	Etv5, Sox9, Pancreatitis, Acinar Ductal Metaplasia, Animals, Mice
Source:	Developmental Dynamics
ISSN:	1058-8388
Publisher:	Wiley
Volume:	247
Number:	6
Page Range:	854-866
Date:	June 2018
Additional Information:	Copyright © 2018 Wiley Periodicals, Inc.
Official Publication:	https://doi.org/10.1002/dvdy.24626
External Fulltext:	View full text on PubMed Central
PubMed:	View item in PubMed

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