Journal
FASEB JOURNAL
Volume 24, Issue 6, Pages 1824-1837Publisher
FEDERATION AMER SOC EXP BIOL
DOI: 10.1096/fj.09-148072
Keywords
insulin signaling; diabetes mellitus; fluorescence microscopy; biosensors
Categories
Funding
- Karolinska Institutet
- Swedish Diabetes Association
- Swedish Research Council
- Novo Nordisk Foundation, Eurodia [FP6-518153]
- Berth von Kantzow Foundation
- Juvenile Diabetes Research Foundation
- Family Erling-Persson Foundation
- MRC [G0500936] Funding Source: UKRI
- Medical Research Council [G0500936] Funding Source: researchfish
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Phosphatidylinositide 3-kinases (PI3Ks) play central roles in insulin signal transduction. While the contribution of class Ia PI3K members has been extensively studied, the role of class II members remains poorly understood. The diverse actions of class II PI3K-C2 alpha have been attributed to its lipid product PI(3) P. By applying pharmacological inhibitors, transient overexpression and small-interfering RNA-based knockdown of PI3K and PKB/Akt isoforms, together with PI-lipid profiling and live-cell confocal and total internal reflection fluorescence microscopy, we now demonstrate that in response to insulin, PI3K-C2 alpha generates PI(3,4) P-2, which allows the selective activation of PKB alpha/Akt1. Knockdown of PI3K-C2 alpha expression and subsequent reduction of PKB alpha/Akt1 activity in the pancreatic beta-cell impaired glucose-stimulated insulin release, at least in part, due to reduced glucokinase expression and increased AS160 activity. Hence, our results identify signal transduction via PI3K-C2 alpha as a novel pathway whereby insulin activates PKB/Akt and thus discloses PI3K-C2 alpha as a potential drugable target in type 2 diabetes. The high degree of codistribution of PI3K-C2 alpha and PKB alpha/Akt1 with insulin receptor B type, but not A type, in the same plasma membrane microdomains lends further support to the concept that selectivity in insulin signaling is achieved by the spatial segregation of signaling events.-Leibiger, B., Moede, T., Uhles, S., Barker, C. J., Creveaux, M., Domin, J., Berggren, P.-O., Leibiger, I. B. Insulin-feedback via PI3K-C2 alpha activated PKB alpha/Akt1 is required for glucose-stimulated insulin secretion. FASEB J. 24, 1824-1837 (2010). www.fasebj.org
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