Howard Hughes Medical Institute, Department of Biology and Pathology, Stanford University, Stanford, California 94305, USA.
Annu Rev Neurosci. 2010;33:473-507. doi: 10.1146/annurev.neuro.051508.135302.
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.
神经系统发育过程中特定突触连接的组装是细胞识别和分化的一个显著例子。神经元采用几种不同的细胞信号策略来解决这个难题,这些策略依次限制了不需要的相互作用,并减少了产生特定连接模式所需的直接识别事件的数量。特异性机制包括接触介导和远程信号的作用,这些信号支持或抑制突触形成,可以在突触伙伴之间或与短暂的伙伴和短暂的细胞群体之间直接发生。在中枢神经系统中,驱动单个突触的突触分化过程的分子信号也同样多样化,并通过多个平行的分化途径发挥作用。这种分子复杂性平衡了在发育过程中高精度组装中枢回路的需要,同时保留了局部和动态调节的可塑性。