Literature DB >> 33364934

Early Dendritic Dystrophy in Human Brains With Primary Age-Related Tauopathy.

Yan-Bin Shi1, Tian Tu2, Juan Jiang2, Qi-Lei Zhang2, Jia-Qi Ai2, Aihua Pan2, Jim Manavis3, Ewen Tu4, Xiao-Xin Yan2.   

Abstract

Dystrophic neurites (DNs) are found in many neurological conditions such as traumatic brain injury and age-related neurodegenerative diseases. In Alzheimer's disease (AD) specifically, senile plaques containing silver-stained DNs were already described in the original literature defining this disease. These DNs could be both axonal and dendritic in origin, while axonal dystrophy relative to plaque formation has been more extensively studied. Here, we demonstrate an early occurrence of dendritic dystrophy in the hippocampal CA1 and subicular regions in human brains (n = 23) with primary age-related tauopathy (PART), with neurofibrillary tangle (NFT) burden ranging from Braak stages I to III in the absence of cerebral β-amyloid (Aβ) deposition. In Bielschowsky's silver stain, segmented fusiform swellings on the apical dendrites of hippocampal and subicular pyramidal neurons were observed in all the cases, primarily over the stratum radiatum (s.r.). The numbers of silver-stained neuronal somata and dendritic swellings counted over CA1 to subiculum were positively correlated among the cases. Swollen dendritic processes were also detected in sections immunolabeled for phosphorylated tau (pTau) and sortilin. In aged and AD brains with both Aβ and pTau pathologies, silver- and immunolabeled dystrophic-like dendritic profiles occurred around and within individual neuritic plaques. These findings implicate that dendritic dystrophy can occur among hippocampal pyramidal neurons in human brains with PART. Therefore, as with the case of axonal dystrophy reported in literature, dendritic dystrophy can develop prior to Alzheimer-type plaque and tangle formation in the human brain.
Copyright © 2020 Shi, Tu, Jiang, Zhang, Ai, Pan, Manavis, Tu and Yan.

Entities:  

Keywords:  Alzheimer’s disease; brain aging; neuritic dystrophy; neurodegeneration; synaptic pathology

Year:  2020        PMID: 33364934      PMCID: PMC7750631          DOI: 10.3389/fnagi.2020.596894

Source DB:  PubMed          Journal:  Front Aging Neurosci        ISSN: 1663-4365            Impact factor:   5.750


  102 in total

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