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Maintenance of Hepatic Nuclear Factor 6 in Postnatal Islets Impairs Terminal Differentiation and Function of ß-Cells

¹ Department of Medicine, Division of Diabetes, Endocrinology, and Metabolism, Vanderbilt University Medical Center, Nashville, Tennessee
² Department of Molecular Physiology and Biophysics, Vanderbilt University Medical Center, Nashville, Tennessee
³ Institute of Physiology, University of Lausanne, Lausanne, Switzerland
⁴ VA Tennessee Valley Healthcare System, Nashville, Tennessee

Address correspondence and reprint requests to Maureen Gannon, Department of Medicine, Division of Diabetes, Endocrinology, and Metabolism, Vanderbilt University Medical Center, 2220 Pierce Ave., 746 PRB, Nashville, TN 37232-6303. E-mail: maureen.gannon{at}vanderbilt.edu

Abbreviations: GSIS, glucose-stimulated insulin secretion; HNF, hepatic nuclear factor; IBMX, isobutylmethylxanthine; IPGTT, intraperitoneal glucose tolerance test; SCB, sodium cacodylate buffer

The Onecut homeodomain transcription factor hepatic nuclear factor 6 (Hnf6) is necessary for proper development of islet ß-cells. Hnf6 is initially expressed throughout the pancreatic epithelium but is downregulated in endocrine cells at late gestation and is not expressed in postnatal islets. Transgenic mice in which Hnf6 expression is maintained in postnatal islets (pdx1^PBHnf6) show overt diabetes and impaired glucose-stimulated insulin secretion (GSIS) at weaning. We now define the mechanism whereby maintenance of Hnf6 expression postnatally leads to ß-cell dysfunction. We provide evidence that continued expression of Hnf6 impairs GSIS by altering insulin granule biosynthesis, resulting in a reduced response to secretagogues. Sustained expression of Hnf6 also results in downregulation of the ß-cell–specific transcription factor MafA and a decrease in total pancreatic insulin. These results suggest that downregulation of Hnf6 expression in ß-cells during development is essential to achieve a mature, glucose-responsive ß-cell.

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