Expression Analysis of cPLA2 Alpha Interacting TIP60 in Diabetic KKAy and Non-Diabetic C57BL Wild-Type Mice: No Impact of Transient and Stable TIP60 Overexpression on Glucose-Stimulated Insulin Secretion in Pancreatic Beta-Cells

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Abstract
The Review of Diabetic Studies,2007,4,3,147-158.
Published:November 2007
Type:Original Article
Authors:
Author(s) affiliations:

2Institute of Human Genetics, The Bartholin Building, University of Aarhus, DK-8000 Aarhus C, Denmark.

3Department of Molecular Biology, Aarhus University, C.F. Møllers Allé 130, DK-8000 Aarhus C, Denmark.

Abstract:

In the present study we investigate the expression levels of cytosolic phospholipase A2 α (cPLA2α) interacting histone acetyl transferase proteins TIP60α and TIP60β in nondiabetic C57BL wild-type mice and obese type 2 diabetic KKAy model mice. The aim was to test our hypothesis that TIP60 plays a regulatory role in glucose-stimulated insulin secretion from pancreatic β-cells. Materials and Methods: Ten obese diabetic KKAy mice and ten nondiabetic C57BL mice were fed a standard chow diet. After nine weeks, islet RNA was purified and used to measure TIP60 expression. We investigated the effect of TIP60α and TIP60β on glucose-stimulated insulin secretion by transient and stable overexpression in the pancreatic mouse β-cell line MIN6 and the rat β-cell line INS-1E. Results: We found that non-diabetic C57BL mice and diabetic KKAy mice have the same level of both the α and β splice forms of TIP60. Furthermore, we demonstrated that transient and stable expression of TIP60 in INS-1E cells affects neither glucose-stimulated insulin secretion, insulin output nor cell insulin content. Also susceptibility to developing glucotoxicity was unaffected. Conclusion: TIP60 overexpression does not affect glucose stimulated insulin secretion, insulin content or abnormal β-cell function during glucotoxicity.