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阿尔茨海默病中β淀粉样蛋白前体的非同位素原位杂交:在有神经原纤维缠结的神经元及老年斑周围微环境中的表达

Nonisotopic in situ hybridization of amyloid beta protein precursor in Alzheimer's disease: expression in neurofibrillary tangle bearing neurons and in the microenvironment surrounding senile plaques.

作者信息

Hyman B T, Wenniger J J, Tanzi R E

机构信息

Neurology Service, Massachusetts General Hospital, Harvard Medical School, Boston 02114.

出版信息

Brain Res Mol Brain Res. 1993 May;18(3):253-8. doi: 10.1016/0169-328x(93)90197-w.

Abstract

We have used nonisotopic in situ hybridization techniques with biotinylated junctional oligonucleotide probes to study expression of amyloid precursor protein (APP) 695 and 751 mRNA in the hippocampal formation of Alzheimer's disease. Both mRNAs are strongly expressed in neurons of the hippocampal formation, particularly in the dentate gyrus granule cells and the pyramidal neurons of CA3. The patterns of expression of neither APP695 nor APP751 mRNA correlate well with the stereotyped topography of neurofibrillary tangles or senile plaques, which occur primarily in CA1 and subiculum. We double-labeled in situ sections with immunohistochemical reagents for neurofibrillary tangles or senile plaques. Neurons that contain neurofibrillary tangles continue to express APP mRNA. The level of APP695 and APP751 was measured semiquantitatively by optical density measurements in neurons that were close to (within 25 microns) or father from a senile plaque (more than 100 microns). There was no increase in expression in neurons in the immediate microenvironment of senile plaques. Our results suggest that no major change in distribution or type of APP mRNA accompanies neurofibrillary tangle or senile plaque development.

摘要

我们使用了生物素化的连接寡核苷酸探针的非同位素原位杂交技术,来研究阿尔茨海默病海马结构中淀粉样前体蛋白(APP)695和751 mRNA的表达。两种mRNA在海马结构的神经元中均强烈表达,特别是在齿状回颗粒细胞和CA3区的锥体细胞中。APP695和APP751 mRNA的表达模式均与主要出现在CA1区和海马下托的神经原纤维缠结或老年斑的刻板形态学特征没有很好的相关性。我们用针对神经原纤维缠结或老年斑的免疫组化试剂对原位切片进行了双重标记。含有神经原纤维缠结的神经元继续表达APP mRNA。通过光密度测量对靠近(25微米内)或远离(超过100微米)老年斑的神经元中的APP695和APP751水平进行了半定量测定。在老年斑紧邻的微环境中的神经元中,表达没有增加。我们的结果表明,在神经原纤维缠结或老年斑形成过程中,APP mRNA的分布或类型没有重大变化。

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