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阿尔茨海默病和老年对照大脑中淀粉样前体样蛋白-1和淀粉样前体样蛋白-2表达的免疫组织化学及原位分析。

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.

作者信息

McNamara M J, Ruff C T, Wasco W, Tanzi R E, Thinakaran G, Hyman B T

机构信息

Alzheimer Research Unit, Massachusetts General Hospital, Harvard Medical School, Boston, MA, USA.

出版信息

Brain Res. 1998 Aug 31;804(1):45-51. doi: 10.1016/s0006-8993(98)00653-2.

Abstract

Amyloid precursor protein (APP) is a ubiquitously expressed membrane spanning glycoprotein which is endoproteolytically processed to Abeta, 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.

摘要

淀粉样前体蛋白(APP)是一种广泛表达的跨膜糖蛋白,它通过内蛋白水解作用加工成β淀粉样蛋白,这是一种由39 - 43个氨基酸组成的肽,是阿尔茨海默病(AD)中淀粉样斑块的主要成分。APP是一个高度保守的基因家族的成员,包括淀粉样前体样蛋白(APLPs)APLP1和APLP2。我们现在对AD和老年对照大脑中的APLP1和APLP2 mRNA及蛋白表达进行了特征描述。通过在对照和AD大脑的海马组织中进行原位杂交,我们发现APLP1和APLP2 mRNA主要在齿状回的颗粒细胞、CA1 - CA3区域以及海马下托中表达。免疫组织化学显示,在AD和对照病例的神经元和血管中,APLP1和APLP2均有染色。此外,在AD大脑中,一部分淀粉样斑块中的大型营养不良性神经突被APLP1和APLP2抗体显著标记。老年对照大脑中具有免疫反应性的斑块和营养不良性神经突明显较少。APLP1和APLP2的区域、细胞和亚细胞分布相互重叠,并且与APP的分布也有重叠。这些观察结果支持了这一假说,即该蛋白家族的成员可能具有相似的功能。

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