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过量的突触结合蛋白 1 导致三种类型阿尔茨海默病的衰老海马体中的位置细胞功能障碍和记忆缺陷。

Excess Synaptojanin 1 Contributes to Place Cell Dysfunction and Memory Deficits in the Aging Hippocampus in Three Types of Alzheimer's Disease.

机构信息

Taub Institute for Research on Alzheimer's Disease and the Aging Brain, Columbia University Medical Center, New York, NY 10032, USA; Department of Pathology and Cell Biology, Columbia University Medical Center, New York, NY 10032, USA; Life and Health Sciences Research Institute (ICVS), School of Medicine, University of Minho, 4710-057 Braga, Portugal; ICVS/3B's, PT Government Associate Laboratory, 4806-909 Braga/Guimarães, Portugal.

Taub Institute for Research on Alzheimer's Disease and the Aging Brain, Columbia University Medical Center, New York, NY 10032, USA; Department of Pathology and Cell Biology, Columbia University Medical Center, New York, NY 10032, USA.

出版信息

Cell Rep. 2018 Jun 5;23(10):2967-2975. doi: 10.1016/j.celrep.2018.05.011.

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.

摘要

磷酸肌醇磷酸酶突触结合蛋白 1(SYNJ1)是调节突触功能的关键蛋白。我们首先研究了 SYNJ1 是否会引起家族性阿尔茨海默病(FAD)的表型变化,并发现 SYNJ1 多态性与早发性和晚发性人类 FAD 队列的发病年龄有关。接着,我们探究了 SYNJ1 水平是否会直接影响记忆。我们发现,唐氏综合征(DS/AD)患者尸检大脑中的 SYNJ1 水平升高与突触小泡蛋白水平呈负相关,而突触小泡蛋白是突触完整性的直接指标。我们还报告了在过表达人类散发性 AD 中观察到的小鼠 Synj1 水平的小鼠模型中,年龄依赖性认知能力下降,这是通过海马过度兴奋和位置场空间重现性缺陷引发的。总之,我们的研究结果表明,SYNJ1 会导致各种形式的 AD 中衰老海马体的记忆缺陷。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5acc/6040810/cde523de77cc/nihms-976402-f0002.jpg

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