期刊
JOURNAL OF CLINICAL INVESTIGATION
卷 129, 期 3, 页码 1272-1277出版社
AMER SOC CLINICAL INVESTIGATION INC
DOI: 10.1172/JCI124853
关键词
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资金
- NIH [R37AG027924, P01NS074969, R01AG035355, RF1AG051504, R21AG052423]
- Alzheimer's Association New Investigator Research Grant [2014NIRG304190]
Carrying the epsilon 4 allele of the APOE gene encoding apolipoprotein E (APOE4) markedly increases the risk for late-onset Alzheimer's disease (AD), in which APOE4 exacerbates the brain accumulation and subsequent deposition of amyloid-beta (A beta) peptides. While the LDL receptor-related protein 1 (LRP1) is a major apoE receptor in the brain, we found that its levels are associated with those of insoluble A beta depending on APOE genotype status in postmortem AD brains. Thus, to determine the functional interaction of apoE4 and LRP1 in brain A beta metabolism, we crossed neuronal LRP1-knockout mice with amyloid model APP/PS1 mice and APOE3-targeted replacement (APO3-TR) or APOE4-TR mice. Consistent with previous findings, mice expressing apoE4 had increased A beta deposition and insoluble amounts of A beta 40 and A beta 42 in the hippocampus of APP/PS1 mice compared with those expressing apoE3. Intriguingly, such effects were reversed in the absence of neuronal LRP1. Neuronal LRP1 deficiency also increased detergent-soluble apoE4 levels, which may contribute to the inhibition of A beta deposition. Together, our results suggest that apoE4 exacerbates A beta pathology through a mechanism that depends on neuronal LRP1. A better understanding of apoE isoform-specific interaction with their metabolic receptor LRP1 on A beta metabolism is crucial for defining APOE4-related risk for AD.
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