Okutsu Rie, Rai Tatemitsu, Kikuchi Akira, Ohno Mayuko, Uchida Keiko, Sasaki Sei, Uchida Shinichi
Department of Nephrology, Graduate School of Medicine, Tokyo Medical and Dental University, Tokyo, Japan.
Kidney Int. 2008 Dec;74(11):1429-33. doi: 10.1038/ki.2008.402. Epub 2008 Aug 13.
During dehydration, protein kinase A phosphorylates aquaporin 2 (AQP2) at serine 256 and this is essential for apical membrane sorting of AQP2 in the collecting ducts. A-kinase anchoring proteins (AKAPs) bind protein kinase A and protein phosphatases conferring substrate specificity to these enzymes and localize them to the appropriate intracellular compartment. We found that AKAP220 bound to AQP2 in a yeast two-hybrid screen. Further, it was highly localized to the papilla compared to other regions of the kidney. Using double immunofluorescence and immunoelectron microscopy we found that AKAP220 co-localized with AQP2 in the cytosol of the inner medullary collecting ducts. Forskolin-mediated phosphorylation of AQP2, transiently expressed in COS cells, was increased by AKAP220 co-expression. Our results suggest that AKAP220 may be involved in the phosphorylation of AQP2 by recruiting protein kinase A.
在脱水过程中,蛋白激酶A使水通道蛋白2(AQP2)的丝氨酸256位点磷酸化,这对于集合管中AQP2的顶端膜分选至关重要。A激酶锚定蛋白(AKAPs)结合蛋白激酶A和蛋白磷酸酶,赋予这些酶底物特异性,并将它们定位到适当的细胞内区室。我们在酵母双杂交筛选中发现AKAP220与AQP2结合。此外,与肾脏的其他区域相比,它在乳头中高度定位。使用双重免疫荧光和免疫电子显微镜,我们发现AKAP220在内髓集合管的细胞质中与AQP2共定位。在COS细胞中瞬时表达的AQP2,其佛司可林介导的磷酸化通过与AKAP220共表达而增加。我们的结果表明,AKAP220可能通过募集蛋白激酶A参与AQP2的磷酸化。