Yerushalmi Uri, Teicher Mina
The Leslie and Susan Gonda Interdisciplinary Brain Research Center, Bar-Ilan University, Ramat-Gan, Israel.
PLoS One. 2008;3(11):e3697. doi: 10.1371/journal.pone.0003697. Epub 2008 Nov 11.
Since synaptic plasticity is regarded as a potential mechanism for memory formation and learning, there is growing interest in the study of its underlying mechanisms. Recently several evolutionary models of cellular development have been presented, but none have been shown to be able to evolve a range of biological synaptic plasticity regimes. In this paper we present a biologically plausible evolutionary cellular development model and test its ability to evolve different biological synaptic plasticity regimes. The core of the model is a genomic and proteomic regulation network which controls cells and their neurites in a 2D environment. The model has previously been shown to successfully evolve behaving organisms, enable gene related phenomena, and produce biological neural mechanisms such as temporal representations. Several experiments are described in which the model evolves different synaptic plasticity regimes using a direct fitness function. Other experiments examine the ability of the model to evolve simple plasticity regimes in a task -based fitness function environment. These results suggest that such evolutionary cellular development models have the potential to be used as a research tool for investigating the evolutionary aspects of synaptic plasticity and at the same time can serve as the basis for novel artificial computational systems.
由于突触可塑性被视为记忆形成和学习的一种潜在机制,对其潜在机制的研究兴趣与日俱增。最近提出了几种细胞发育的进化模型,但尚无模型被证明能够进化出一系列生物突触可塑性机制。在本文中,我们提出了一个具有生物学合理性的进化细胞发育模型,并测试其进化出不同生物突触可塑性机制的能力。该模型的核心是一个基因组和蛋白质组调控网络,它在二维环境中控制细胞及其神经突。该模型此前已被证明能够成功进化出行为生物体、实现基因相关现象,并产生诸如时间表征等生物神经机制。文中描述了几个实验,在这些实验中该模型使用直接适应度函数进化出不同的突触可塑性机制。其他实验则考察了该模型在基于任务的适应度函数环境中进化出简单可塑性机制的能力。这些结果表明,此类进化细胞发育模型有潜力用作研究突触可塑性进化方面的研究工具,同时可作为新型人工计算系统的基础。