학술논문

Excess Synaptojanin 1 Contributes to Place Cell Dysfunction and Memory Deficits in the Aging Hippocampus in Three Types of Alzheimer’s Disease
Document Type
article
Source
Cell Reports. 23(10)
Subject
Biochemistry and Cell Biology
Biological Sciences
Dementia
Acquired Cognitive Impairment
Alzheimer's Disease including Alzheimer's Disease Related Dementias (AD/ADRD)
Alzheimer's Disease
Aging
Neurosciences
Brain Disorders
Neurodegenerative
Genetics
Aetiology
2.1 Biological and endogenous factors
Neurological
Alzheimer Disease
Animals
Cognition Disorders
Haplotypes
Hippocampus
Memory Disorders
Mice
Inbred C57BL
Mice
Transgenic
Mutant Proteins
Nerve Tissue Proteins
Phosphoric Monoester Hydrolases
Place Cells
Polymorphism
Single Nucleotide
Synapses
Long-term memory
SYNJ1
hyperexcitability
in vivo electrophysiology
neurodegenerative disorders
single nucleotide polymorphisms
synaptic dysfunction
Medical Physiology
Biological sciences
Language
Abstract
The phosphoinositide phosphatase synaptojanin 1 (SYNJ1) is a key regulator of synaptic function. We first tested whether SYNJ1 contributes to phenotypic variations in familial Alzheimer's disease (FAD) and show that SYNJ1 polymorphisms are associated with age of onset in both early- and late-onset human FAD cohorts. We then interrogated whether SYNJ1 levels could directly affect memory. We show that increased SYNJ1 levels in autopsy brains from adults with Down syndrome (DS/AD) are inversely correlated with synaptophysin levels, a direct readout of synaptic integrity. We further report age-dependent cognitive decline in a mouse model overexpressing murine Synj1 to the levels observed in human sporadic AD, triggered through hippocampal hyperexcitability and defects in the spatial reproducibility of place fields. Taken together, our findings suggest that SYNJ1 contributes to memory deficits in the aging hippocampus in all forms of AD.