Reelin Proteolysis Affects Signaling Related to Normal Synapse Function and Neurodegeneration

被引:25
|
作者
Lussier, April L. [1 ]
Weeber, Edwin J. [1 ]
Rebeck, G. William [2 ]
机构
[1] Univ S Florida, Hlth Byrd Alzheimers Dis Inst, Dept Mol Pharmacol & Physiol, Tampa, FL USA
[2] Georgetown Univ, Dept Neurosci, Washington, DC USA
来源
FRONTIERS IN CELLULAR NEUROSCIENCE | 2016年 / 10卷
关键词
Reelin; Alzheimer's disease; neurodegeneration; proteolysis; learning and memory; AMYLOID PRECURSOR PROTEIN; LONG-TERM POTENTIATION; DEPRESSION-LIKE BEHAVIOR; ALZHEIMERS-DISEASE MICE; CAJAL-RETZIUS CELLS; ADULT DENTATE GYRUS; APOE RECEPTOR 2; NEURONAL MIGRATION; BIPOLAR DISORDER; IN-VIVO;
D O I
10.3389/fncel.2016.00075
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Reelin is a neurodevelopmental protein important in adult synaptic plasticity and learning and memory. Recent evidence points to the importance for Reelin proteolysis in normal signaling and in cognitive function. Support for the dysfunction of Reelin proteolysis in neurodegeneration and cognitive dysfunction comes from postmortem analysis of Alzheimer's diseases (AD) tissues including cerebral spinal fluid (CSF), showing that levels of Reelin fragments are altered in AD compared to control. Potential key proteases involved Reelin proteolysis have recently been defind, identifying processes that could be altered in neurodegeneration. Introduction of full-length Reelin and its proteolytic fragments into several mouse models of neurodegeneration and neuropsychiatric disorders quickly promote learning and memory. These findings of these processes are important to harness the potential of pathway in treating congnitive symptoms in neuropsychiatric and neurodegenerative diseases.
引用
收藏
页数:8
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