Wolfram syndrome 1 and adenylyl cyclase 8 interact at the plasma membrane to regulate insulin production and secretion
Program in Gene Function and Expression
Medical Subject Headings
Calmodulin-Binding Proteins; Membrane Proteins; Adenylate Cyclase; Cell Membrane; Insulin
Biochemistry, Biophysics, and Structural Biology | Genetics and Genomics
Endoplasmic reticulum (ER) stress causes pancreatic beta-cell dysfunction and contributes to beta-cell loss and the progression of type 2 diabetes. Wolfram syndrome 1 (WFS1) has been shown to be an important regulator of the ER stress signalling pathway; however, its role in beta-cell function remains unclear. Here we provide evidence that WFS1 is essential for glucose- and glucagon-like peptide 1 (GLP-1)-stimulated cyclic AMP production and regulation of insulin biosynthesis and secretion. Stimulation with glucose causes WFS1 translocation from the ER to the plasma membrane, where it forms a complex with adenylyl cyclase 8 (AC8), an essential cAMP-generating enzyme in the beta-cell that integrates glucose and GLP-1 signalling. ER stress and mutant WFS1 inhibit complex formation and activation of AC8, reducing cAMP synthesis and insulin secretion. These findings reveal that an ER-stress-related protein has a distinct role outside the ER regulating both insulin biosynthesis and secretion. The reduction of WFS1 protein on the plasma membrane during ER stress is a contributing factor for beta-cell dysfunction and progression of type 2 diabetes.
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Citation: Nat Cell Biol. 2012 Sep 16. doi: 10.1038/ncb2578. Link to article on publisher's site
Fonseca, Sonya G.; Urano, Fumihiko; Weir, Gordon C.; Gromada, Jesper; and Burcin, Mark, "Wolfram syndrome 1 and adenylyl cyclase 8 interact at the plasma membrane to regulate insulin production and secretion" (2012). Program in Gene Function and Expression Publications and Presentations. Paper 204.