Neuronal sorting protein-related receptor sorLA/LR11 regulates processing of the amyloid precursor protein

被引:506
作者
Andersen, OM
Reiche, J
Schmidt, V
Gotthardt, M
Spoelgen, R
Behlke, J
von Arnim, CAF
Breiderhoff, T
Jansen, P
Wu, X
Bales, KR
Cappai, R
Masters, CL
Gliemann, J
Mufson, EJ
Hyman, BT
Paul, SM
Nykjær, A
Willnow, TE
机构
[1] Max Delbruck Ctr Mol Med, D-13125 Berlin, Germany
[2] Lilly Res Labs, Indianapolis, IN 46285 USA
[3] Massachusetts Gen Hosp, Charlestown, MA 02129 USA
[4] Rush Univ, Med Ctr, Dept Neurol Sci, Chicago, IL 60612 USA
[5] Aarhus Univ, Inst Med Biochem, DK-8000 Aarhus, Denmark
[6] Univ Melbourne, Dept Pathol, Melbourne, Vic 3010, Australia
关键词
endocytic receptors; knockout mouse; neurodegeneration; Vps10p-domain receptors;
D O I
10.1073/pnas.0503689102
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
sorLA (sorting protein-related receptor) is a type-1 membrane protein of unknown function that is expressed in neurons. Its homology to sorting receptors that shuttle between the plasma membrane, endosomes, and the Golgi suggests a related function in neuronal trafficking processes. Because expression of sorLA is reduced in the brain of patients with Alzheimer's disease (AD), we tested involvement of this receptor in intracellular transport and processing of the amyloid precursor protein (APP) to the amyloid) beta-peptide (A beta), the principal component of senile plaques. We demonstrate that sorLA interacts with APP in vitro and in living cells and that both proteins colocalize in endosomal and Golgi compartments. Overexpression of sorLA in neurons causes redistribution of APP to the Golgi and decreased processing to A beta, whereas ablation of sorLA expression in knockout mice results in increased levels of A beta in the brain similar to the situation in AD patients. Thus, sorLA acts as a sorting receptor that protects APP from processing into A beta and thereby reduces the burden of amyloidogenic peptide formation. Consequently, reduced receptor expression in the human brain may increase A beta production and plaque formation and promote spontaneous AD.
引用
收藏
页码:13461 / 13466
页数:6
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