Cognitive integrity in Non‐Demented Individuals with Alzheimer's Neuropathology is associated with preservation and remodeling of dendritic spines

Author:

Guptarak Jutatip1,Scaduto Pietro1,Tumurbaatar Batbayar1,Zhang Wen Ru1,Jupiter Daniel2,Taglialatela Giulio1ORCID,Fracassi Anna1

Affiliation:

1. Department of Neurology, Mitchell Center for Neurodegenerative Disease, University of Texas Medical Branch at Galveston Galveston Texas USA

2. Department of Biostatistics and Data Science, University of Texas Medical Branch at Galveston Galveston Texas USA

Abstract

AbstractINTRODUCTIONIndividuals referred to as Non‐Demented with Alzheimer's Neuropathology (NDAN) exhibit cognitive resilience despite presenting Alzheimer's disease (AD) histopathological signs. Investigating the mechanisms behind this resilience may unveil crucial insights into AD resistance.METHODSDiI labeling technique was used to analyze dendritic spine morphology in control (CTRL), AD, and NDAN post mortem frontal cortex, particularly focusing on spine types near and far from amyloid beta (Aβ) plaques.RESULTSNDAN subjects displayed a higher spine density in regions distant from Aβ plaques versus AD patients. In distal areas from the plaques, NDAN individuals exhibited more immature spines, while AD patients had a prevalence of mature spines. Additionally, our examination of levels of Peptidyl‐prolyl cis‐trans isomerase NIMA‐interacting 1 (Pin1), a protein associated with synaptic plasticity and AD, showed significantly lower expression in AD versus NDAN and CTRL.DISCUSSIONThese results suggest that NDAN individuals undergo synaptic remodeling, potentially facilitated by Pin1, serving as a compensatory mechanism to preserve cognitive function despite AD pathology.Highlights Spine density is reduced near Aβ plaques compared to the distal area in CTRL, AD, and NDAN dendrites. NDAN shows higher spine density than AD in areas far from Aβ plaques. Far from Aβ plaques, NDAN has a higher density of immature spines, AD a higher density of mature spines. AD individuals show significantly lower levels of Pin1 compared to NDAN and CTRL.

Publisher

Wiley

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