Exp Clin Endocrinol Diabetes 2007; 115(10): 654-661
DOI: 10.1055/s-2007-982514
Article

© J. A. Barth Verlag in Georg Thieme Verlag KG Stuttgart · New York

Sustained Expression of Hepatocyte Nuclear Factor-6 Leads to Loss of Pancreatic Beta-cells by Apoptosis

M. Hara 1 , J. Shen 1 , W. Pugh 1 , K. S. Polonsky 1 , M. M. Le Beau 1 , G. I. Bell 1
  • 1Department of Medicine, University of Chicago, Chicago, Illinois, United States
Further Information

Publication History

received 12.02.2007 first decision 07.04.2007

accepted 24.05.2007

Publication Date:
30 November 2007 (online)

Abstract

Hepatocyte nuclear factor-6 (HNF-6) is the ONECUT-homeodomain transcription factor that is enriched in liver and also present in pancreas and central nervous system. It is expressed in the pancreatic bud at E10.5. In adult pancreas, its expression is restricted to the exocrine pancreas and duct cells. Since duct cells are thought to be precursors of endocrine cells and HNF-6 is involved in the regulation of the expression of HNF-4α and -1β, genes that cause maturity onset diabetes of the young (MODY), we hypothesized that the sustained expression of HNF-6 would affect beta-cell function. We generated transgenic mice over-expressing human HNF-6 using the mouse insulin I promoter (MIP). We obtained one female founder in which the transgene had been incorporated into two sites; the chromosome (Ch) 14 and the X chromosome. The integration site of the latter was within centromeric heterochromatin and the transgene was inactivated. Studies on mice in which the transgene was integrated into Ch14 showed beta-cell specific defects functionally and pathologically. The insulin secretory response to glucose and arginine in the in situ-perfused pancreas was also significantly impaired in these mice. Immunohistochemical analysis revealed that the islets were smaller and had an abnormal architecture with an inverted ratio of alpha- and beta-cells resulting from beta-cell loss to 30% by 6-wk of age. The decreased number of beta-cells was quantified first time by fluorescent activated cell sorting using entire pancreata from the transgenic mice crossed with MIP-green fluorescent protein (GFP) mice. This severe loss of beta-cells involved programmed cell death.

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Correspondence

Dr. M. HaraDDS, PhD 

Department of Medicine

University of Chicago

5841 S. Maryland Ave.

MC1027

Chicago

60637 Illinois

United States

Phone: +773/702/37 27

Fax: +773/834/04 86

Email: mhara@midway.uchicago.edu

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