Glia engulf degenerating axons during developmental axon pruning

被引:181
作者
Watts, RJ
Schuldiner, O
Perrino, J
Larsen, C
Luo, LQ [1 ]
机构
[1] Stanford Univ, Dept Biol Sci, Stanford, CA 94305 USA
[2] Stanford Univ, Program Neurosci, Stanford, CA 94305 USA
[3] Stanford Univ, Cell Sci Imaging Facil, Stanford, CA 94305 USA
[4] Natl Inst Med Res, London NW7 1AA, England
关键词
D O I
10.1016/j.cub.2004.03.035
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
Developmental axon pruning is widely used in constructing the nervous system. Accordingly, diverse mechanisms are likely employed for various forms of axon pruning [1-7]. In the Drosophila mushroom bodies (MB),gamma neurons initially extend axon branches into both the dorsal and medial MB axon lobes in larvae. Through a well-orchestrated set of developmental events during metamorphosis, axon branches to both lobes degenerate prior to the formation of adult connections [6,8]. Here, we analyze ultrastructural changes underlying axon pruning by using a genetically encoded electron microscopic (EM) marker to selectively label gamma neurons. By inhibiting axon pruning in combination with the use of this EM marker, we demonstrate a causal link between observed cellular events and axon pruning. These events include changes in axon ultrastructure, synaptic degeneration, and engulfment of degenerating axon fragments by glia for their subsequent breakdown via the endosomal-lysosomal pathway. Interestingly, glia selectively invade MB axon lobes at the onset of metamorphosis; this increase in cell number is independent of axon fragmentation. Our study reveals a key role for glia in the removal of axon fragments during developmental axon pruning.
引用
收藏
页码:678 / 684
页数:7
相关论文
共 34 条
[1]   Engulfing action of glial cells is required for programmed axon pruning during Drosophila metamorphosis [J].
Awasaki, T ;
Ito, K .
CURRENT BIOLOGY, 2004, 14 (08) :668-677
[2]   Stereotyped pruning of long hippocampal axon branches triggered by retraction inducers of the semaphorin family [J].
Bagri, A ;
Cheng, HJ ;
Yaron, A ;
Pleasure, SJ ;
Tessier-Lavigne, M .
CELL, 2003, 113 (03) :285-299
[3]   THE DEVELOPMENT OF THE CORPUS-CALLOSUM IN CATS - A LIGHT-MICROSCOPIC AND ELECTRON-MICROSCOPIC STUDY [J].
BERBEL, P ;
INNOCENTI, GM .
JOURNAL OF COMPARATIVE NEUROLOGY, 1988, 276 (01) :132-156
[4]  
CAMPBELL G, 1994, DEVELOPMENT, V120, P2957
[5]   Glial cells phagocytose neuronal debris during the metamorphosis of the central nervous system in Drosophila melanogaster [J].
Cantera, R ;
Technau, GM .
DEVELOPMENT GENES AND EVOLUTION, 1996, 206 (04) :277-280
[6]   Destination 'Lysosome':: a target organelle for tumour cell killing? [J].
Castino, R ;
Démoz, M ;
Isidoro, C .
JOURNAL OF MOLECULAR RECOGNITION, 2003, 16 (05) :337-348
[7]   Unwrapping glial biology: Gcm target genes regulating glial development, diversification, and function [J].
Freeman, MR ;
Delrow, J ;
Kim, J ;
Johnson, E ;
Doe, CQ .
NEURON, 2003, 38 (04) :567-580
[8]   GLIAL-CELLS MISSING - A BINARY SWITCH BETWEEN NEURONAL AND GLIAL DETERMINATION IN DROSOPHILA [J].
HOSOYA, T ;
TAKIZAWA, K ;
NITTA, K ;
HOTTA, Y .
CELL, 1995, 82 (06) :1025-1036
[9]   DISTRIBUTION, CLASSIFICATION, AND DEVELOPMENT OF DROSOPHILA GLIAL-CELLS IN THE LATE EMBRYONIC AND EARLY LARVAL VENTRAL NERVE CORD [J].
ITO, K ;
URBAN, J ;
TECHNAU, GM .
ROUXS ARCHIVES OF DEVELOPMENTAL BIOLOGY, 1995, 204 (05) :284-307
[10]   GLIAL-CELLS MISSING - A GENETIC SWITCH THAT CONTROLS GLIAL VERSUS NEURONAL FATE [J].
JONES, BW ;
FETTER, RD ;
TEAR, G ;
GOODMAN, CS .
CELL, 1995, 82 (06) :1013-1023