Amyloid beta mediates memory formation

被引:132
作者
Garcia-Osta, Ana [1 ]
Alberini, Cristina M. [1 ,2 ]
机构
[1] Mt Sinai Sch Med, Dept Neurosci, New York, NY 10029 USA
[2] Mt Sinai Sch Med, Dept Psychiat, New York, NY 10029 USA
关键词
NICOTINIC ACETYLCHOLINE-RECEPTORS; RAT BASAL FOREBRAIN; PRECURSOR PROTEIN; SYNAPTIC PLASTICITY; ALZHEIMERS-DISEASE; NATURAL OLIGOMERS; MICE LACKING; PEPTIDE; DEFICITS; BRAIN;
D O I
10.1101/lm.1310209
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The amyloid precursor protein (APP) undergoes sequential cleavages to generate various polypeptides, including the amyloid beta (1-42) peptide (A beta[1-42]), which is believed to play a major role in amyloid plaque formation in Alzheimer's disease (AD). Here we provide evidence that, in contrast with its pathological role when accumulated, endogenous Ab in normal hippocampi mediates learning and memory formation. Furthermore, hippocampal injection of picomolar concentrations of exogenous A beta(1-42) enhances memory consolidation. Correlative data suggest that Ab peptides may exert their function via nicotinic acethylcoline receptors. Hence, Ab peptides, including A beta(1-42), play an important physiological role in hippocampal memory formation.
引用
收藏
页码:267 / 272
页数:6
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