Genetics and Cell Biology of Building Specific Synaptic Connectivity

被引:175
作者
Shen, Kang [1 ]
Scheiffele, Peter [2 ]
机构
[1] Stanford Univ, Howard Hughes Med Inst, Dept Biol & Pathol, Stanford, CA 94305 USA
[2] Univ Basel, Biozentrum, Dept Cell Biol, CH-4056 Basel, Switzerland
来源
ANNUAL REVIEW OF NEUROSCIENCE, VOL 33 | 2010年 / 33卷
关键词
recognition; trans-synaptic signaling; guidepost cell; synapse elimination; OCULAR DOMINANCE COLUMNS; CENTRAL-NERVOUS-SYSTEM; CAJAL-RETZIUS CELLS; N-TERMINAL DOMAIN; MOTOR-NEURON POOL; C-ELEGANS; NEUROMUSCULAR-JUNCTION; CAENORHABDITIS-ELEGANS; GAMMA-PROTOCADHERINS; GLUTAMATE-RECEPTOR;
D O I
10.1146/annurev.neuro.051508.135302
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The assembly of specific synaptic connections during development of the nervous system represents a remarkable example of cellular recognition and differentiation. Neurons employ several different cellular signaling strategies to solve this puzzle, which successively limit unwanted interactions and reduce the number of direct recognition events that are required to result in a specific connectivity pattern. Specificity mechanisms include the action of contact-mediated and long-range signals that support or inhibit synapse formation, which can take place directly between synaptic partners or with transient partners and transient cell populations. The molecular signals that drive the synaptic differentiation process at individual synapses in the central nervous system are similarly diverse and act through multiple, parallel differentiation pathways. This molecular complexity balances the need for central circuits to be assembled with high accuracy during development while retaining plasticity for local and dynamic regulation.
引用
收藏
页码:473 / 507
页数:35
相关论文
共 199 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]   Signaling across the synapse: a role for Wnt and Dishevelled in presynaptic assembly and neurotransmitter release [J].
Ahmad-Annuar, Azlina ;
Ciani, Lorenza ;
Simeonidis, Iordanis ;
Herreros, Judit ;
Ben Fredj, Naila ;
Rosso, Silvana B. ;
Hall, Anita ;
Brickley, Stephen ;
Salinas, Patricia C. .
JOURNAL OF CELL BIOLOGY, 2006, 174 (01) :127-139
[3]  
Altman J., 1997, RELATION ITS EVOLUTI
[4]   HETEROCHRONIC GENES AND THE TEMPORAL CONTROL OF C-ELEGANS DEVELOPMENT [J].
AMBROS, V ;
MOSS, EG .
TRENDS IN GENETICS, 1994, 10 (04) :123-127
[5]   Ankyrin-based subcellular gradient of neurofascin, an immunoglobulin family protein, directs GABAergic innervation at Purkinje axon initial segment [J].
Ango, F ;
di Cristo, G ;
Higashiyama, H ;
Bennett, V ;
Wu, P ;
Huang, ZJ .
CELL, 2004, 119 (02) :257-272
[6]   Bergmann glia and the recognition molecule CHL1 organize GABAergic axons and direct innervation of Purkinje cell dendrites [J].
Ango, Fabrice ;
Wu, Caizhi ;
Van der Want, Johannes J. ;
Wu, Priscilla ;
Schachner, Melitta ;
Huang, Z. Josh .
PLOS BIOLOGY, 2008, 6 (04) :739-756
[7]   Rapid activity-dependent modifications in synaptic structure and function require bidirectional Wnt signaling [J].
Ataman, Bulent ;
Ashley, James ;
Gorczyca, Michael ;
Ramachandran, Preethi ;
Fouquet, Wernher ;
Sigrist, Stephan J. ;
Budnik, Vivian .
NEURON, 2008, 57 (05) :705-718
[8]   The Mystery and Magic of Glia: A Perspective on Their Roles in Health and Disease [J].
Barres, Ben A. .
NEURON, 2008, 60 (03) :430-440
[9]  
BARTLETT WP, 1984, J NEUROSCI, V4, P1954
[10]   PIONEER NEURONS IN AN INSECT EMBRYO [J].
BATE, CM .
NATURE, 1976, 260 (5546) :54-56