Amyloid Precursor Protein and Presenilin1 Interact with the Adaptor GRB2 and Modulate ERK 1,2 Signaling

The amyloid precursor protein (APP) and the presenilins 1 and 2 are genetically linked to the development of familial Alzheimer disease. APP is a single-pass transmembrane protein and precursor of fibrillar and toxic amyloid-β peptides, which are considered responsible for Alzheimer disease neurodeg...

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Published inThe Journal of biological chemistry Vol. 282; no. 18; pp. 13833 - 13844
Main Authors Nizzari, Mario, Venezia, Valentina, Repetto, Emanuela, Caorsi, Valentina, Magrassi, Raffaella, Gagliani, Maria Cristina, Carlo, Pia, Florio, Tullio, Schettini, Gennaro, Tacchetti, Carlo, Russo, Tommaso, Diaspro, Alberto, Russo, Claudio
Format Journal Article
LanguageEnglish
Published United States Elsevier Inc 04.05.2007
American Society for Biochemistry and Molecular Biology
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Summary:The amyloid precursor protein (APP) and the presenilins 1 and 2 are genetically linked to the development of familial Alzheimer disease. APP is a single-pass transmembrane protein and precursor of fibrillar and toxic amyloid-β peptides, which are considered responsible for Alzheimer disease neurodegeneration. Presenilins are multipass membrane proteins, involved in the enzymatic cleavage of APP and other signaling receptors and transducers. The role of APP and presenilins in Alzheimer disease development seems to be related to the formation of amyloid-β peptides; however, their physiological function, reciprocal interaction, and molecular mechanisms leading to neurodegeneration are unclear. APP and presenilins are also involved in multiple interactions with intracellular proteins, the significance of which is under investigation. Among the different APP-interacting proteins, we focused our interest on the GRB2 adaptor protein, which connects cell surface receptors to intracellular signaling pathways. In this study we provide evidence by co-immunoprecipitation experiments, confocal and electron microscopy, and by fluorescence resonance energy transfer experiments that both APP and presenilin1 interact with GRB2 in vesicular structures at the centrosome of the cell. The final target for these interactions is ERK1,2, which is activated in mitotic centrosomes in a PS1- and APP-dependent manner. These data suggest that both APP and presenilin1 can be part of a common signaling pathway that regulates ERK1,2 and the cell cycle.
Bibliography:http://www.jbc.org/
ObjectType-Article-1
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ISSN:0021-9258
1083-351X
DOI:10.1074/jbc.M610146200