首页> 美国卫生研究院文献>Journal of Neuropathology and Experimental Neurology >From the Entorhinal Region via the Prosubiculum to the Dentate Fascia: Alzheimer Disease-Related Neurofibrillary Changes in the Temporal Allocortex
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From the Entorhinal Region via the Prosubiculum to the Dentate Fascia: Alzheimer Disease-Related Neurofibrillary Changes in the Temporal Allocortex

机译:从内脏区通过前尿到齿状筋膜:颞异位中与阿尔茨海默病相关的神经原纤维变化

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摘要

The pathological process underlying Alzheimer disease (AD) unfolds predominantly in the cerebral cortex with the gradual appearance and regional progression of abnormal tau. Intraneuronal tau pathology progresses from the temporal transentorhinal and entorhinal regions into neocortical fields/areas of the temporal allocortex. Here, based on 95 cases staged for AD-related neurofibrillary changes, we propose an ordered progression of abnormal tau in the temporal allocortex. Initially, abnormal tau was limited to distal dendritic segments followed by tau in cell bodies of projection neurons of the transentorhinal/entorhinal layer pre-α. Next, abnormal distal dendrites accumulated in the prosubiculum and extended into the CA1 stratum oriens and lacunosum. Subsequently, altered dendrites developed in the CA2/CA3 stratum oriens and stratum lacunosum-moleculare, combined with tau-positive thorny excrescences of CA3/CA4 mossy cells. Finally, granule cells of the dentate fascia became involved. Such a progression might recapitulate a sequence of transsynaptic spreading of abnormal tau from 1 projection neuron to the next: From pre-α cells to distal dendrites in the prosubiculum and CA1; then, from CA1 or prosubicular pyramids to CA2 principal cells and CA3/CA4 mossy cells; finally, from CA4 mossy cells to dentate granule cells. The lesions are additive: Those from the previous steps persist.
机译:阿尔茨海默氏病(AD)的病理过程主要在大脑皮层中展开,并伴有异常tau的逐渐出现和区域性进展。神经内tau病理学从颞跨肠和内嗅区域发展为颞皮质的新皮质区/区域。在此,根据针对AD相关的神经原纤维变化分期进行的95例病例,我们提出了时间分配区中tau异常的有序进展。最初,异常tau仅限于远端树突状节段,然后是跨肠膜/肠膜前层α的投射神经元细胞体中的tau。接下来,异常的远侧树突聚集在前房中,并延伸到原始的CA1层和腔隙中。随后,在CA2 / CA3层和层状分子中形成了改变的树突,并与CA3 / CA4苔藓细胞的tau阳性棘手异常结合。最终,齿状筋膜的颗粒细胞开始受累。这样的进展可能概括了异常tau从1个投射神经元到下一个投射神经元的突触传播序列:从前α细胞到前房和CA1中的远端树突;然后,从CA1或前亚锥体到CA2主细胞和CA3 / CA4苔藓细胞;最后,从CA4苔藓细胞到齿状颗粒细胞。病变是累加性的:先前步骤中的病变持续存在。

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