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


Autoria(s): Meunier, Frederic; Lisk, Godfrey; Sesardic, Dorothea; Dolly, J. Oliver
Contribuinte(s)

G. Lemke

F. S. Walshe

Data(s)

01/04/2003

Resumo

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.

Identificador

http://espace.library.uq.edu.au/view/UQ:66439

Idioma(s)

eng

Publicador

Elsvier

Palavras-Chave #Neurosciences #Neurotoxin Serotype-a #Exocytosis #Membrane #Cleavage #Identification #Paralysis #Recovery #Protein #Release #Permeabilized Chromaffin Cells #C1 #270100 Biochemistry and Cell Biology #730104 Nervous system and disorders
Tipo

Journal Article