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Aberrant presenilin-1 expression downregulates LDL receptor-related protein (LRP): Is LRP central to Alzheimer's disease pathogenesis?
被引:32
|作者:
Van Uden, E
[1
]
Carlson, G
St George-Hyslop, P
Westaway, D
Orlando, R
Mallory, M
Rockenstein, E
Masliah, E
机构:
[1] Univ Calif San Diego, Sch Med, Dept Neurosci, La Jolla, CA 92093 USA
[2] Univ Calif San Diego, Sch Med, Dept Pathol, La Jolla, CA 92093 USA
[3] McLaughlin Res Inst, Great Falls, MT 59405 USA
[4] Univ Toronto, Dept Med, Ctr Res Neurodegenerat Dis, Toronto, ON, Canada
[5] Univ Toronto, Dept Pathol, Toronto, ON, Canada
关键词:
D O I:
10.1006/mcne.1999.0772
中图分类号:
Q189 [神经科学];
学科分类号:
071006 ;
摘要:
Low density lipoprotein receptor-related protein (LRP) polymorphisms have recently been associated with an increased susceptibility of Alzheimer's disease (AD). Furthermore, LRP has been linked to molecules that confer susceptibility to AD (apolipoprotein E, alpha-2-macroglobulin, amyloid precursor protein), previously with the exception of the presenilins. Here we report that aberrant presenilin-1 expression in vivo and in vitro downregulates LRP. Specifically, transgenic mice overexpressing the M146L or L286V presenilin-1 mutation show decreased levels of LRP expression in neuronal populations where presenilin-1 and LRP are closely colocalized or coexpressed. Moreover, cell lines transfected with presenilin-1 also expressed decreased levels of LRP. These findings suggest that LRP may be central to AD pathogenesis since all proteins genetically associated with AD can now be linked via a single pathway to LRP.
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页码:129 / 140
页数:12
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