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- W2059007391 abstract "To dissect the rat receptor for advanced glycation end products (RAGE) subcellular distribution and trafficking in eukaryotic cells, an expression system coding for a fusion protein between the RAGE and an enhanced green fluorescent protein (EGFP) has been used. The RAGE–EGFP protein is expressed at the plasma membrane of CHO-k1 and Neuro-2a (N2a) cells and retains the capacity to bind Texas Red-labelled advanced glycation end products (AGEs). AGEs addition to the cell cultures induced a change in the subcellular distribution of the fluorescent RAGE–EGFP protein compatible with an internalization of the AGEs–RAGE complex. Furthermore, while N2a cells expressing the RAGE–EGFP showed an increase in ERK1/2 phosphorylation and NF-κB DNA binding in response to AGEs, pre-incubation with dansyl-cadaverine or phenylarsine oxide, inhibitors of receptors internalization, blocked the activation of ERKs and other intracellular responses mediated by AGEs. These results suggest that internalization plays a key role in the signal transduction mediated by RAGE." @default.
- W2059007391 created "2016-06-24" @default.
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- W2059007391 date "2008-10-11" @default.
- W2059007391 modified "2023-10-16" @default.
- W2059007391 title "Internalization of the Receptor for Advanced Glycation End Products (RAGE) is Required to Mediate Intracellular Responses" @default.
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- W2059007391 doi "https://doi.org/10.1093/jb/mvn137" @default.
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