Charting the Drosophila neuropile:: a strategy for the standardised characterisation of genetically amenable neurites

被引:122
作者
Landgraf, M
Sánchez-Soriano, N
Technau, GM
Urban, J
Prokop, A
机构
[1] Univ Mainz, Inst Genet, D-55128 Mainz, Germany
[2] Univ Cambridge, Dept Zool, Cambridge CB2 3EJ, England
基金
英国惠康基金;
关键词
dendrites; mapping; neurites; synapse; development; neurogenesis; neuropeptides; insects; manipulations; imaging;
D O I
10.1016/S0012-1606(03)00215-X
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Insect neurons are individually identifiable and have been used successfully to study principles of the formation and function of neuronal circuits. In the fruitfly Drosophila, studies on identifiable neurons can be combined with efficient genetic approaches. However, to capitalise on this potential for studies of circuit formation in the CNS of Drosophila embryos or larvae, we need to identify pre- and postsynaptic elements of such circuits and describe the neuropilar territories they occupy. Here, we present a strategy for neurite mapping, using a set of evenly distributed landmarks labelled by commercially available anti-Fasciclin2 antibodies which remain comparatively constant between specimens and over developmental time. By applying this procedure to neurites labelled by three Gal4 lines, we show that neuritic territories are established in the embryo and maintained throughout larval life, although the complexity of neuritic arborisations increases during this period. Using additional immunostainings or dye fills, we can assign Gal4-targeted neurites to individual neurons and characterise them further as a reference for future experiments on circuit formation. Using the Fasciclin2-based mapping procedure as a standard (e.g., in a common database) would facilitate studies on the functional architecture of the neuropile and the identification of candiate circuit elements. (C) 2003 Elsevier Science (USA). All rights reserved.
引用
收藏
页码:207 / 225
页数:19
相关论文
共 77 条
[1]   wishful thinking encodes a BMP type II receptor that regulates synaptic growth in Drosophila [J].
Aberle, H ;
Haghighi, AP ;
Fetter, RD ;
McCabe, BD ;
Magalhaes, TR ;
Goodman, CS .
NEURON, 2002, 33 (04) :545-558
[2]   A role for drosophila Drac1 in neurite outgrowth and synaptogenesis in the giant fiber system [J].
Allen, MJ ;
Shan, XL ;
Murphey, RK .
MOLECULAR AND CELLULAR NEUROSCIENCE, 2000, 16 (06) :754-765
[3]   Postsynaptic expression of tetanus toxin light chain blocks synaptogenesis in Drosophila [J].
Baines, RA ;
Robinson, SG ;
Fujioka, M ;
Jaynes, JB ;
Bate, M .
CURRENT BIOLOGY, 1999, 9 (21) :1267-1270
[4]  
BATE M, 1993, DEV DROSOPHILA METAN, V2, P1013
[5]  
Bhat KM, 1998, INT J DEV BIOL, V42, P127
[6]   MORPHOLOGICAL-DIFFERENTIATION OF THE EMBRYONIC PERIPHERAL NEURONS IN DROSOPHILA [J].
BODMER, R ;
JAN, YN .
ROUXS ARCHIVES OF DEVELOPMENTAL BIOLOGY, 1987, 196 (02) :69-77
[7]   Axon routing across the midline controlled by the Drosophila Derailed receptor [J].
Bonkowsky, JL ;
Yoshikawa, S ;
O'Keefe, DD ;
Scully, AL ;
Thomas, JB .
NATURE, 1999, 402 (6761) :540-544
[8]  
BOSSING T, 1994, DEVELOPMENT, V120, P1895
[9]   THE GRASSHOPPER, DROSOPHILA AND NEURONAL HOMOLOGY (ADVANTAGES OF THE INSECT NERVOUS-SYSTEM FOR THE NEUROSCIENTIST) [J].
BOYAN, GS ;
BALL, EE .
PROGRESS IN NEUROBIOLOGY, 1993, 41 (06) :657-682
[10]  
BRAND AH, 1993, DEVELOPMENT, V118, P401