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
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