Human apolipoprotein C-I expression in mice impairs learning and memory functions
Human apolipoprotein C-I expression in mice impairs learning and memory functions
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DOI:
10.1194/jlr.m700518-jlr200
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发表时间:
2008-04-01
影响因子:
6.5
通讯作者:
Mulder, Monique
中科院分区:
文献类型:
--
作者:
Abildayeva, Karlygash;Berbee, Jimmy F. P.;Mulder, Monique
The H2 allele of APOC I, giving rise to increased gene expression of apolipoprotein C-I (apoC-I), is in genetic disequilibrium with the APOE4 allele and may provide a major risk factor for Alzheimer's disease (AD). We found that apoC-I protein is present in astrocytes and endothelial cells within hippocampal regions in both human control and AD brains. Interestingly, apoC-I colocalized with R-amyloid (A beta) in plaques in AD brains, and in vitro experiments revealed that aggregation of A beta was delayed in the presence of apoC-I. Moreover, apoC-I was found to exacerbate the soluble A beta oligomer-induced neuronal death. To establish a potential role for apoC-I in cognitive functions, we used human (h) APOC1(+/0) transgenic mice that express APOC1 mRNA throughout their brains and apoC-I protein in astrocytes and endothelial cells. The hAPOC1(+/0) mice displayed impaired hippocampal-dependent learning and memory functions compared with their wild-type litter-mates, as judged from their performance in the object recognition task (P = 0.012) and in the Morris water maze task (P = 0.010). ApoC-I may affect learning as a result of its inhibitory properties toward apoE-dependent lipid metabolism. However, no differences in brain mRNA or protein levels of endogenous apoE were detected between transgenic and wild-type mice. In conclusion, human apoC-I expression impairs cognitive functions in mice independent of apoE expression, which supports the potential of a modulatory role for apoC-I during the development of AD.