Mufson Elliott J, Counts Scott E, Ginsberg Stephen D
Department of Neurological Sciences, Rush Alzheimer's Disease Research Center, Rush-Presbyterian-St. Luke's Medical Center, Chicago, IL 60612, USA.
Neurochem Res. 2002 Oct;27(10):1035-48. doi: 10.1023/a:1020952704398.
Cholinergic neurons of the nucleus basalis (NB) are selectively vulnerable in Alzheimer's disease (AD), yet the molecular mechanisms associated with their dysfunction remain unknown. We used single cell RNA amplification and custom array technology to examine the expression of functional classes of mRNAs found in anterior NB neurons from normal aged and AD subjects. mRNAs encoding neurotrophin receptors, synaptic proteins, protein phosphatases, and amyloid-related proteins were evaluated. We found that trkB and trkC mRNAs were selectively down-regulated in NB neurons, whereas p75NTR mRNA levels remained stable in end stage AD. TrkA mRNA was reduced by approximately 28%, but did not reach statistical significance. There was a down-regulation of synaptophysin, synaptotagmin, and protein phosphatases PP1alpha and PP1beta mRNAs in AD. In contrast, we found a selective up-regulation of cathepsin D mRNA in NB neurons in AD brain. Thus, anterior NB neurons undergo selective alterations in gene expression in AD. These results may provide clues to the molecular pathogenesis of NB neuronal degeneration during AD.
基底核(NB)的胆碱能神经元在阿尔茨海默病(AD)中具有选择性易损性,但其功能障碍相关的分子机制仍不清楚。我们使用单细胞RNA扩增和定制阵列技术,检测正常老年和AD受试者前NB神经元中功能性mRNA类别的表达。对编码神经营养因子受体、突触蛋白、蛋白磷酸酶和淀粉样相关蛋白的mRNA进行了评估。我们发现,trkB和trkC mRNA在NB神经元中选择性下调,而在AD终末期p75NTR mRNA水平保持稳定。TrkA mRNA减少了约28%,但未达到统计学意义。AD中突触素、突触结合蛋白以及蛋白磷酸酶PP1α和PP1β mRNA表达下调。相反,我们发现AD脑内NB神经元中组织蛋白酶D mRNA选择性上调。因此,AD中前NB神经元的基因表达发生了选择性改变。这些结果可能为AD期间NB神经元变性的分子发病机制提供线索。