Immunohistochemical and in situ analysis of amyloid precursor-like protein-1 and amyloid precursor-like protein-2 expression in Alzheimer disease and aged control brains

被引:33
作者
McNamara, MJ
Ruff, CT
Wasco, W
Tanzi, RE
Thinakaran, G
Hyman, BT
机构
[1] Harvard Univ, Massachusetts Gen Hosp, Sch Med, Alzheimer Res Unit, Boston, MA USA
[2] Harvard Univ, Massachusetts Gen Hosp, Sch Med, Neurogenet Unit, Boston, MA USA
[3] Johns Hopkins Univ, Sch Med, Dept Pathol, Baltimore, MD 21205 USA
关键词
amyloid precursor-like proteins; amyloid precursor protein; Alzheimer's disease; immunohistochemistry; in situ hybridization;
D O I
10.1016/S0006-8993(98)00653-2
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Amyloid precursor protein (APP) is a ubiquitously expressed membrane spanning glycoprotein which is endoproteolytically processed to AP, a 39-43 amino acid peptide that is the main component of senile plaques in Alzheimer Disease (AD). APP is a member of a highly conserved gene family, including Amyloid Precursor-Like Proteins (APLPs) APLP1 and APLP2. We now characterize APLP1 and APLP2 mRNA and protein expression in AD and aged control brains. Using in situ hybridization in hippocampal tissue from control and AD brain, we show that APLP1 and APLP2 mRNA are expressed primarily in the granule cells of the dentate gyrus, in areas CA1-CA3, and subiculum. Immunohistochemistry reveals staining for both APLP1 and APLP2 in neurons and blood vessels in AD and control cases. In addition, in AD brain, large dystrophic neurites in a subset of senile plaques are conspicuously labeled with APLP1 and APLP2 antibodies. The aged control brains have significantly fewer immunoreactive plaques and dystrophic neurites. The regional, cellular, and subcellular distribution of APLP1 and APLP2 overlap with each other and with APP. These observations support the hypothesis that the members of this family of proteins may perform similar functions. (C) 1998 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:45 / 51
页数:7
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