Developmental Self-Construction and -Configuration of Functional Neocortical Neuronal Networks

被引:18
作者
Bauer, Roman [1 ,2 ]
Zubler, Frederic [1 ,3 ]
Pfister, Sabina [1 ]
Hauri, Andreas [1 ]
Pfeiffer, Michael [1 ]
Muir, Dylan R. [1 ,4 ]
Douglas, Rodney J. [1 ]
机构
[1] Univ ETH Zurich, Inst Neuroinformat, Zurich, Switzerland
[2] Newcastle Univ, Sch Comp Sci, Newcastle Upon Tyne NE1 7RU, Tyne & Wear, England
[3] Univ Bern, Univ Hosp Bern, Inselspital Bern, Dept Neurol, Bern, Switzerland
[4] Univ Basel, Biozentrum, Basel, Switzerland
关键词
TIMING-DEPENDENT PLASTICITY; GABA-IMMUNOREACTIVE NEURONS; PRIMARY VISUAL-CORTEX; INHIBITORY NEURONS; QUANTITATIVE DISTRIBUTION; INTRINSIC CONNECTIONS; SYNAPTIC PLASTICITY; EXCITATORY NEURONS; PYRAMIDAL NEURONS; RECEPTIVE-FIELDS;
D O I
10.1371/journal.pcbi.1003994
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
The prenatal development of neural circuits must provide sufficient configuration to support at least a set of core postnatal behaviors. Although knowledge of various genetic and cellular aspects of development is accumulating rapidly, there is less systematic understanding of how these various processes play together in order to construct such functional networks. Here we make some steps toward such understanding by demonstrating through detailed simulations how a competitive co-operative ('winner-take-all', WTA) network architecture can arise by development from a single precursor cell. This precursor is granted a simplified gene regulatory network that directs cell mitosis, differentiation, migration, neurite outgrowth and synaptogenesis. Once initial axonal connection patterns are established, their synaptic weights undergo homeostatic unsupervised learning that is shaped by wave-like input patterns. We demonstrate how this autonomous genetically directed developmental sequence can give rise to self-calibrated WTA networks, and compare our simulation results with biological data.
引用
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页数:18
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