Endocytosis and retrograde axonal traffic in motor neurons

被引:21
作者
Deinhardt, K [1 ]
Schiavo, G [1 ]
机构
[1] Canc Res UK, London Res Inst, Mol NeuroPathobiol Lab, London WC2A 3PX, England
来源
LIPIDS, RAFTS AND TRAFFIC | 2005年 / 72卷
关键词
D O I
10.1042/bss0720139
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Spinal cord motor neurons control voluntary movement by relaying messages that arrive from upper brain centres to the innervated muscles. Despite the importance of motor neurons in human health and disease, the precise control of their membrane dynamics and its effect on motor neuron homoeostasis and survival are poorly understood. In particular, the molecular basis of the coordination of specific endocytic events with the axonal retrograde transport pathway is largely unknown. To study these important vesicular trafficking events, we pioneered the use of atoxic fragments of tetanus and botulinum neurotoxins to follow endocytosis and retrograde axonal transport in motor neurons. These neurotoxins bind specifically to pre-synaptic nerve terminals, where they are internalized. Whereas botulinum neurotoxins remain at the neuromuscular junction, tetanus toxin is retrogradely transported along the axon to the cell body, where it is released into the intersynaptic space and is internalized by adjacent inhibitory interneurons. The high neurospecificity and the differential intracellular sorting make tetanus and botulinum neurotoxins tools to study neuronal physiology. In the present review, we discuss recent developments in our understanding of the internalization and trafficking of these molecules in spinal cord motor neurons. Furthermore, we describe the development of a reliable transfection method for motor neurons based on microinjection, which will be extremely useful for dissecting further the molecular basis of membrane dynamics and axonal transport in these cells.
引用
收藏
页码:139 / 150
页数:12
相关论文
共 58 条
[41]   The high-affinity binding of Clostridium botulinum type B neurotoxin to synaptotagmin II associated with gangliosides G(T1b)/G(D1a) [J].
Nishiki, T ;
Tokuyama, Y ;
Kamata, Y ;
Nemoto, Y ;
Yoshida, A ;
Sato, K ;
Sekiguchi, M ;
Takahashi, M ;
Kozaki, S .
FEBS LETTERS, 1996, 378 (03) :253-257
[42]  
PARTON RG, 1987, J NEUROCHEM, V49, P1057
[43]   DYNEIN ATPASE IS INHIBITED SELECTIVELY IN VITRO BY ERYTHRO-9-[3-2-(HYDROXYNONYL)]ADENINE [J].
PENNINGROTH, SM ;
CHEUNG, A ;
BOUCHARD, P ;
GAGNON, C ;
BARDIN, CW .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1982, 104 (01) :234-240
[44]   Lipid rafts: heterogeneity on the high seas [J].
Pike, LJ .
BIOCHEMICAL JOURNAL, 2004, 378 :281-292
[45]   Mutant dynactin in motor neuron disease [J].
Puls, I ;
Jonnakuty, C ;
LaMonte, BH ;
Holzbaur, ELF ;
Tokito, M ;
Mann, E ;
Floeter, MK ;
Bidus, K ;
Drayna, D ;
Oh, SJ ;
Brown, RH ;
Ludlow, CL ;
Fischbeck, KH .
NATURE GENETICS, 2003, 33 (04) :455-456
[46]   The HCC-domain of botulinum neurotoxins A and B exhibits a singular ganglioside binding site displaying serotype specific carbohydrate interaction [J].
Rummel, A ;
Mahrhold, S ;
Bigalke, H ;
Binz, T .
MOLECULAR MICROBIOLOGY, 2004, 51 (03) :631-643
[47]   Two carbohydrate binding sites in the Hcc-domain of tetanus neurotoxin are required for toxicity [J].
Rummel, A ;
Bade, S ;
Alves, J ;
Bigalke, H ;
Binz, T .
JOURNAL OF MOLECULAR BIOLOGY, 2003, 326 (03) :835-847
[48]   Neurotoxins affecting neuroexocytosis [J].
Schiavo, G ;
Matteoli, M ;
Montecucco, C .
PHYSIOLOGICAL REVIEWS, 2000, 80 (02) :717-766
[49]   Thy-1 is critical for normal retinal development [J].
Simon, PD ;
McConnell, J ;
Zurakowski, D ;
Vorwerk, CK ;
Naskar, R ;
Grosskreutz, CL ;
Dreyer, EB .
DEVELOPMENTAL BRAIN RESEARCH, 1999, 117 (02) :219-223
[50]   Analysis of mutants of tetanus toxin HC fragment:: ganglioside binding, cell binding and retrograde axonal transport properties [J].
Sinha, K ;
Box, M ;
Lalli, G ;
Schiavo, G ;
Schneider, H ;
Groves, M ;
Siligardi, G ;
Fairweather, N .
MOLECULAR MICROBIOLOGY, 2000, 37 (05) :1041-1051