Premium
Mint2/X11‐like colocalizes with the Alzheimer's disease amyloid precursor protein and is associated with neuritic plaques in Alzheimer's disease
Author(s) -
McLoughlin Declan M.,
Irving Nicholas G.,
Brownlees Janet,
Brion JeanPierre,
Leroy Karelle,
Miller Christopher C. J.
Publication year - 1999
Publication title -
european journal of neuroscience
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.346
H-Index - 206
eISSN - 1460-9568
pISSN - 0953-816X
DOI - 10.1046/j.1460-9568.1999.00610.x
Subject(s) - senile plaques , amyloid precursor protein , alzheimer's disease , amyloid precursor protein secretase , pathogenesis , bace1 as , microbiology and biotechnology , p3 peptide , amyloid (mycology) , transfection , biology , disease , medicine , biochemistry , pathology , gene , immunology
Aberrant metabolism of the amyloid precursor protein (APP) is believed to be at least part of the pathogenic process in Alzheimer's disease. The carboxy‐terminus of APP has been shown to interact with the Mint/X11 family of phosphotyrosine binding (PTB) domain‐bearing proteins. It is via their PTB domains that the Mints/X11s bind to APP. Here we report the cloning of full‐length mouse Mint2 and demonstrate that in primary cortical neurons, Mint2 and APP share highly similar distributions. Mint2 also colocalizes with APP in transfected CHO cells. In Mint2/APP‐cotransfected cells, Mint2 reorganizes the subcellular distribution of APP and also increases the steady‐state levels of APP. Finally, we demonstrate that Mint2 is associated with the neuritic plaques found in Alzheimer's disease but not with neurofibrillary tangles. These results are consistent with a role for Mint2 in APP metabolism and trafficking, and suggest a possible role for the Mints/X11s in the pathogenesis of Alzheimer's disease.