Takami K, Terai K, Matsuo A, Walker D G, McGeer P L
Pharmaceutical Development Division, Takeda Chemical Industries, Ltd., Osaka, Japan.
Brain Res. 1997 Feb 14;748(1-2):122-30. doi: 10.1016/s0006-8993(96)01274-7.
Recently, new genetic linkages have been identified for early-onset familial Alzheimer's disease (AD). Mutations have been found in the presenilin (PS)-1 (S182) gene on chromosome 14 and the PS-2 (STM2/E5-a) gene on chromosome 1. We have investigated the distribution of gene expression of both presenilins in normal rat brain, and in human control and AD cases using in situ hybridization histochemistry. In normal rat brain, intense PS-1 mRNA expression was observed predominantly in neurons, particularly hippocampal pyramidal and dentate granular neurons and cerebellar Purkinje and granular neurons. The distribution of intensely expressing PS-2 mRNA cells was similar to that of PS-1, but additional groups in the brain stem and cortex were identified. Faint but significant mRNA expression of both PS genes was detected in white matter. In control human cases, the same neuronal cell types as seen in rat brain expressed both PS mRNAs in the hippocampus and cerebellum. In AD cases, the expression of both mRNAs was markedly decreased in the hippocampus but not in the cerebellum. In addition, PS-2 hybridization showed increased mRNA expression in astrocyte-like cells in affected areas of AD cases. The present data indicate that the PS genes may play important roles in specific neurons in normal brain, and that the decreased expression in neurons in sporadic AD brain may bear some relationship to the pathogenesis.
最近,早发性家族性阿尔茨海默病(AD)新的基因连锁关系已被确定。在14号染色体上的早老素(PS)-1(S182)基因和1号染色体上的PS-2(STM2/E5-a)基因中发现了突变。我们使用原位杂交组织化学方法,研究了正常大鼠脑以及人类对照和AD病例中两种早老素的基因表达分布。在正常大鼠脑中,主要在神经元中观察到强烈的PS-1 mRNA表达,特别是海马锥体细胞和齿状颗粒神经元以及小脑浦肯野细胞和颗粒神经元。强烈表达PS-2 mRNA细胞的分布与PS-1相似,但在脑干和皮质中发现了其他细胞群。在白质中检测到两种PS基因微弱但显著的mRNA表达。在人类对照病例中,与大鼠脑中所见相同的神经元细胞类型在海马体和小脑中表达两种PS mRNA。在AD病例中,两种mRNA的表达在海马体中明显降低,但在小脑中没有。此外,PS-2杂交显示AD病例受影响区域的星形胶质样细胞中mRNA表达增加。目前的数据表明,PS基因可能在正常脑的特定神经元中起重要作用,并且散发性AD脑中神经元表达的降低可能与发病机制有一定关系。