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Cognitive integrity in Non-Demented Individuals with Alzheimer's Neuropathology is associated with preservation and remodeling of dendritic spines
被引:5
作者:
Guptarak, Jutatip
[1
]
Scaduto, Pietro
[1
]
Tumurbaatar, Batbayar
[1
]
Zhang, Wen Ru
[1
]
Jupiter, Daniel
[2
]
Taglialatela, Giulio
[1
]
Fracassi, Anna
[1
]
机构:
[1] Univ Texas Med Branch Galveston, Mitchell Ctr Neurodegenerat Dis, Dept Neurol, 301 Univ Blvd, Galveston, TX 77555 USA
[2] Univ Texas Med Branch Galveston, Dept Biostat & Data Sci, Galveston, TX USA
基金:
美国国家卫生研究院;
关键词:
Alzheimer's disease;
amyloid beta;
cognitive resilience;
dendritic spines;
neurodegeneration;
Non-Demented with Alzheimer's Neuropathology;
Pin1;
synaptic plasticity;
AMYLOID-BETA;
DISEASE NEUROPATHOLOGY;
PIN1;
TAU;
DYNAMICS;
PROTEIN;
SYNAPSES;
PROVIDE;
D O I:
10.1002/alz.13900
中图分类号:
R74 [神经病学与精神病学];
学科分类号:
摘要:
INTRODUCTION: Individuals 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. METHODS: DiI 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 (A beta) plaques. RESULTS: NDAN subjects displayed a higher spine density in regions distant from A beta 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. DISCUSSION: These 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 A beta plaques compared to the distal area in CTRL, AD, and NDAN dendrites. NDAN shows higher spine density than AD in areas far from A beta plaques. Far from A beta 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.
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页码:4677 / 4691
页数:15
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