Axons of callosal neurons bifurcate transiently at the white matter before consolidating an interhemispheric projection

被引:11
作者
Garcez, Patricia P.
Henrique, Narjara P.
Furtado, Danilo A.
Bolz, Juergen
Lent, Roberto
Uziel, Daniela [1 ]
机构
[1] Univ Fed Rio de Janeiro, Inst Ciencias Biomed, Dept Anat, BR-21941590 Rio De Janeiro, Brazil
[2] Univ Jena, Inst Allgemeine Zool & Tierphysiol, D-6900 Jena, Germany
关键词
axon branching; axon pathfinding; corpus callosum; cortex development; mouse;
D O I
10.1111/j.1460-9568.2007.05387.x
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The main alternative output routes of adult cortical axons are the internal capsule and the corpus callosum. How do callosal axons choose their trajectories? We hypothesized that bifurcation followed by elimination of one branch is a developmental strategy for accomplishing this aim. Using embryonic and postnatal mice, we labelled cortical projecting neurons and quantified their axonal bifurcations in correlation with the mediolateral position of their somata. Bifurcating axons were numerous in the younger brains but declined during further development. Most bifurcating axons pertained to neurons located in the dorsolateral cortex. Moreover, callosal neurons bifurcate more often than subcortically projecting cells. We then quantified bifurcations formed by dissociated green fluorescent cells plated onto cortical slices. Cells grown over dorsolateral cortex bifurcated more often than those grown over medial cortex, irrespective of their positional origin in the donor. Removal of intermediate targets from the slices prevented bifurcation. We concluded that transient bifurcation and elimination of the lateral branch is a strategy employed by developing callosal axons in search of their targets. As cell body position and intermediate targets determine axon behaviour, we suggest that bifurcations are regulated by cues expressed in the environment.
引用
收藏
页码:1384 / 1394
页数:11
相关论文
共 62 条
[11]   Netrin-1 and semaphorin 3A promote or inhibit cortical axon branching, respectively, by reorganization of the cytoskeleton [J].
Dent, EW ;
Barnes, AM ;
Tang, FJ ;
Kalil, K .
JOURNAL OF NEUROSCIENCE, 2004, 24 (12) :3002-3012
[12]   Neuronal circuits of the neocortex [J].
Douglas, RJ ;
Martin, KAC .
ANNUAL REVIEW OF NEUROSCIENCE, 2004, 27 :419-451
[13]   BIHEMISPHERIC COLLATERALIZATION OF THE CORTICAL AND SUBCORTICAL AFFERENTS TO THE RATS VISUAL-CORTEX [J].
DREHER, B ;
DEHAY, C ;
BULLIER, J .
EUROPEAN JOURNAL OF NEUROSCIENCE, 1990, 2 (04) :317-331
[14]   Area specificity and topography of thalamocortical projections are controlled by ephrin/Eph genes [J].
Dufour, A ;
Seibt, J ;
Passante, L ;
Depaepe, V ;
Ciossek, T ;
Frisén, J ;
Kullander, K ;
Flanagan, JG ;
Polleux, F ;
Vanderhaeghen, P .
NEURON, 2003, 39 (03) :453-465
[15]   Phenotype of mice lacking functional Deleted in colorectal cancer (Dcc) gene [J].
Fazeli, A ;
Dickinson, SL ;
Hermiston, ML ;
Tighe, RV ;
Steen, RG ;
Small, CG ;
Stoeckli, ET ;
KeinoMasu, K ;
Masu, M ;
Rayburn, H ;
Simons, J ;
Bronson, RT ;
Gordon, JI ;
TessierLavigne, M ;
Weinberg, RA .
NATURE, 1997, 386 (6627) :796-804
[16]   INTERHEMISPHERIC AND SUBCORTICAL COLLATERALS OF MEDIAL PREFRONTAL CORTICAL-NEURONS IN THE RAT [J].
FERINO, F ;
THIERRY, AM ;
SAFFROY, M ;
GLOWINSKI, J .
BRAIN RESEARCH, 1987, 417 (02) :257-266
[17]   Postnatal differentiation of firing properties and morphological characteristics in layer V pyramidal neurons of the sensorimotor cortex [J].
Franceschetti, S ;
Sancini, G ;
Panzica, F ;
Radici, C ;
Avanzini, G .
NEUROSCIENCE, 1998, 83 (04) :1013-1024
[18]  
FRANTZ GD, 1994, J NEUROSCI, V14, P5725
[19]   DENDRITIC MORPHOLOGY AND AXON COLLATERALS OF CORTICOTECTAL, CORTICOPONTINE, AND CALLOSAL NEURONS IN LAYER-V OF PRIMARY VISUAL-CORTEX OF THE HOODED RAT [J].
HALLMAN, LE ;
SCHOFIELD, BR ;
LIN, CS .
JOURNAL OF COMPARATIVE NEUROLOGY, 1988, 272 (01) :149-160
[20]   Morphogenesis of callosal arbors in the parietal cortex of hamsters [J].
Hedin-Pereira, C ;
Lent, R ;
Jhaveri, S .
CEREBRAL CORTEX, 1999, 9 (01) :50-64