Cell calcium · 2025
Abnormal calcium activity and CREB phosphorylation are associated with motor memory impairment in presenilin-1 mutant knock-in mice.
СтатьяПоддержка исследования: вне правительства СШАПоддержка NIH: внешняя программаНазвание и аннотация: Перевод в очереди
Обработка статьи · этапы, ошибки и управление
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Lin Yuan, Bai Yang, Martin-Avila Alejandro, Li Wei, Wu Xujun, Ziff Edward, Gan Wen-Biao
Аннотация
INTRODUCTION: Presenilin (PS) gene mutations cause memory impairment in early-onset familial Alzheimer's disease (FAD), but the underlying mechanisms remain unclear.
METHODS: We examined the effects of the PS1 M146V FAD mutation on motor learning, motor learning-related changes in neuronal Ca2+activity and CREB phosphorylation in the primary motor cortex.
RESULTS: We found that PS1 M146V knock-in mice displayed long-term deficiencies in motor skill learning. Ca2+ levels are altered in a cortical layer and neuron type-specific manner in PS1 mutant mice as compared to WT control mice. Notably, while running caused a significant increase of CREB phosphorylation in WT mice, it led to a significant decrease of CREB phosphorylation in layer 5 neurons of mutant mice.
DISCUSSION: These findings suggest that alterations of Ca2+ activity and CREB phosphorylation in deep cortical layers are early events leading to memory impairment in the PS1 mutation-related familial form of AD.
METHODS: We examined the effects of the PS1 M146V FAD mutation on motor learning, motor learning-related changes in neuronal Ca2+activity and CREB phosphorylation in the primary motor cortex.
RESULTS: We found that PS1 M146V knock-in mice displayed long-term deficiencies in motor skill learning. Ca2+ levels are altered in a cortical layer and neuron type-specific manner in PS1 mutant mice as compared to WT control mice. Notably, while running caused a significant increase of CREB phosphorylation in WT mice, it led to a significant decrease of CREB phosphorylation in layer 5 neurons of mutant mice.
DISCUSSION: These findings suggest that alterations of Ca2+ activity and CREB phosphorylation in deep cortical layers are early events leading to memory impairment in the PS1 mutation-related familial form of AD.