Decreased synaptic vesicle recycling efficiency and cognitive deficits in amphiphysin 1 knockout mice

被引:181
作者
Di Paolo, G
Sankaranarayanan, S
Wenk, MR
Daniell, L
Perucco, E
Caldarone, BJ
Flavell, R
Picciotto, MR
Ryan, TA
Cremona, O
De Camilli, P [1 ]
机构
[1] Yale Univ, Sch Med, Howard Hughes Med Inst, New Haven, CT 06510 USA
[2] Yale Univ, Sch Med, Dept Cell Biol, New Haven, CT 06510 USA
[3] Yale Univ, Sch Med, Immunol Sect, New Haven, CT 06510 USA
[4] Yale Univ, Sch Med, Dept Psychiat, New Haven, CT 06510 USA
[5] Cornell Univ, Weill Med Coll, Dept Biochem, New York, NY 10021 USA
[6] Univ Piemonte Orientale, Dipartimento Sci Med, I-28100 Novara, Italy
[7] Univ Vita Salute San Raffaele Milano, San Raffaele Sci Inst, I-20132 Milan, Italy
关键词
D O I
10.1016/S0896-6273(02)00601-3
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The function of the clathrin coat in synaptic vesicle endocytosis is assisted by a variety of accessory factors, among which amphiphysin (amphiphysin 1 and 2) is one of the best characterized. A putative endocytic function of amphiphysin was supported by dominant-negative interference studies. We have now generated amphiphysin 1 knockout mice and found that lack of amphiphysin 1 causes a parallel dramatic reduction of amphiphysin 2 selectively in brain. Cell-free assembly of endocytic protein scaffolds is defective in mutant brain extracts. Knockout mice exhibit defects in synaptic vesicle recycling that are unmasked by stimulation and suggest impairments at multiple stages of the cycle. These defects correlate with increased mortality due to rare irreversible seizures and with major learning deficits, suggesting a critical role of amphiphysin for higher brain functions.
引用
收藏
页码:789 / 804
页数:16
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