Dynamics of motor nerve terminal remodeling unveiled using SNARE-cleaving botulinum toxins: the extent and duration are dictated by the sites of SNAP-25 truncation

被引:103
作者
Meunier, FA
Lisk, G
Sesardic, D
Dolly, JO [1 ]
机构
[1] Univ London Imperial Coll Sci Technol & Med, Ctr Neurobiochem, Dept Biol Sci, London SW7 2AY, England
[2] Natl Inst Biol Stand & Controls, Div Bacteriol, Potters Bar EN6 3QG, Herts, England
基金
英国生物技术与生命科学研究理事会;
关键词
D O I
10.1016/S1044-7431(02)00016-7
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Nerve sprouts emerge from motor nerve terminals following blockade of exo-endocytosis for more than 3 days by botulinum neurotoxin (BoNT), and form functional synapses, albeit temporary. Upon restoration of synaptic activity to the parent terminal 7 and 90 days after exposure to BoNT/F or A respectively, a concomitant retraction of the outgrowths was observed. BoNT/E caused short-term neuroparalysis, and dramatically accelerated the recovery of BoNT/A-paralyzed muscle by further truncation of SNAP-25 and its replenishment with functional full-length SNARE. The removal of 9 C-terminal residues from SNAP-25 by BoNT/A leads to persistence of the inhibitory product due to the formation of a nonproductive SNARE complex(es) at release sites, whereas deletion of a further 17 amino acids permits replenishment and a speedy recovery. (C) 2003 Elsevier Science (USA). All rights reserved.
引用
收藏
页码:454 / 466
页数:13
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