TY - JOUR
T1 - ApoER2 expression increases Aβ production while decreasing Amyloid Precursor Protein (APP) endocytosis
T2 - Possible role in the partitioning of APP into lipid rafts and in the regulation of γ-secretase activity
AU - Fuentealba, Rodrigo A.
AU - Barría, Maria Ines
AU - Lee, Jiyeon
AU - Cam, Judy
AU - Araya, Claudia
AU - Escudero, Claudia A.
AU - Inestrosa, Nibaldo C.
AU - Bronfman, Francisca C.
AU - Bu, Guojun
AU - Marzolo, Maria Paz
PY - 2007/8/13
Y1 - 2007/8/13
N2 - Background: The generation of the amyloid-β peptide (Aβ) through the proteolytic processing of the amyloid precursor protein (APP) is a central event in the pathogenesis of Alzheimer's disease (AD). Recent studies highlight APP endocytosis and localization to lipid rafts as important events favoring amyloidogenic processing. However, the precise mechanisms underlying these events are poorly understood. ApoER2 is a member of the low density lipoprotein receptor (LDL-R) family exhibiting slow endocytosis rate and a significant association with lipid rafts. Despite the important neurophysiological roles described for ApoER2, little is known regarding how ApoER2 regulates APP trafficking and processing. Results: Here, we demonstrate that ApoER2 physically interacts and co-localizes with APP. Remarkably, we found that ApoER2 increases cell surface APP levels and APP association with lipid rafts. The increase of cell surface APP requires the presence of ApoER2 cytoplasmic domain and is a result of decreased APP internalization rate. Unexpectedly, ApoER2 expression correlated with a significant increase in Aβ production and reduced levels of APP-CTFs. The increased Aβ production was dependent on the integrity of the NPxY endocytosis motif of ApoER2. We also found that expression of ApoER2 increased APP association with lipid rafts and increased y-secretase activity, both of which might contribute to increased Aβ production. Conclusion: These findings show that ApoER2 negatively affects APP internalization. However, ApoER2 expression stimulates Aβ production by shifting the proportion of APP from the non-rafts to the raft membrane domains, thereby promoting β-secretase and γ-secretase mediated amyloidogenic processing and also by incrementing the activity of γ-secretase.
AB - Background: The generation of the amyloid-β peptide (Aβ) through the proteolytic processing of the amyloid precursor protein (APP) is a central event in the pathogenesis of Alzheimer's disease (AD). Recent studies highlight APP endocytosis and localization to lipid rafts as important events favoring amyloidogenic processing. However, the precise mechanisms underlying these events are poorly understood. ApoER2 is a member of the low density lipoprotein receptor (LDL-R) family exhibiting slow endocytosis rate and a significant association with lipid rafts. Despite the important neurophysiological roles described for ApoER2, little is known regarding how ApoER2 regulates APP trafficking and processing. Results: Here, we demonstrate that ApoER2 physically interacts and co-localizes with APP. Remarkably, we found that ApoER2 increases cell surface APP levels and APP association with lipid rafts. The increase of cell surface APP requires the presence of ApoER2 cytoplasmic domain and is a result of decreased APP internalization rate. Unexpectedly, ApoER2 expression correlated with a significant increase in Aβ production and reduced levels of APP-CTFs. The increased Aβ production was dependent on the integrity of the NPxY endocytosis motif of ApoER2. We also found that expression of ApoER2 increased APP association with lipid rafts and increased y-secretase activity, both of which might contribute to increased Aβ production. Conclusion: These findings show that ApoER2 negatively affects APP internalization. However, ApoER2 expression stimulates Aβ production by shifting the proportion of APP from the non-rafts to the raft membrane domains, thereby promoting β-secretase and γ-secretase mediated amyloidogenic processing and also by incrementing the activity of γ-secretase.
UR - http://www.scopus.com/inward/record.url?scp=34547670388&partnerID=8YFLogxK
U2 - 10.1186/1750-1326-2-14
DO - 10.1186/1750-1326-2-14
M3 - Article
AN - SCOPUS:34547670388
SN - 1750-1326
VL - 2
JO - Molecular Neurodegeneration
JF - Molecular Neurodegeneration
IS - 1
M1 - 14
ER -