Department of Biomedical Engineering, The University of Melbourne, Melbourne, VIC, Australia.
Centre for Neural Engineering, The University of Melbourne, Melbourne, VIC, Australia.
Front Neural Circuits. 2019 Mar 14;13:13. doi: 10.3389/fncir.2019.00013. eCollection 2019.
Increasing evidence supports the hypothesis that the visual system employs a sparse code to represent visual stimuli, where information is encoded in an efficient way by a small population of cells that respond to sensory input at a given time. This includes simple cells in primary visual cortex (V1), which are defined by their linear spatial integration of visual stimuli. Various models of sparse coding have been proposed to explain physiological phenomena observed in simple cells. However, these models have usually made the simplifying assumption that inputs to simple cells already incorporate linear spatial summation. This overlooks the fact that these inputs are known to have strong non-linearities such the separation of ON and OFF pathways, or separation of excitatory and inhibitory neurons. Consequently these models ignore a range of important experimental phenomena that are related to the emergence of linear spatial summation from non-linear inputs, such as segregation of ON and OFF sub-regions of simple cell receptive fields, the push-pull effect of excitation and inhibition, and phase-reversed cortico-thalamic feedback. Here, we demonstrate that a two-layer model of the visual pathway from the lateral geniculate nucleus to V1 that incorporates these biological constraints on the neural circuits and is based on sparse coding can account for the emergence of these experimental phenomena, diverse shapes of receptive fields and contrast invariance of orientation tuning of simple cells when the model is trained on natural images. The model suggests that sparse coding can be implemented by the V1 simple cells using neural circuits with a simple biologically plausible architecture.
越来越多的证据支持这样一种假设,即视觉系统采用稀疏编码来表示视觉刺激,其中信息通过一小部分对给定时间内的感官输入做出反应的细胞以有效的方式进行编码。这包括初级视觉皮层 (V1) 中的简单细胞,其特征是对视觉刺激的线性空间整合。已经提出了各种稀疏编码模型来解释在简单细胞中观察到的生理现象。然而,这些模型通常做出了简化的假设,即简单细胞的输入已经包含了线性空间求和。这忽略了这样一个事实,即这些输入具有很强的非线性,例如 ON 和 OFF 途径的分离,或兴奋性和抑制性神经元的分离。因此,这些模型忽略了一系列与线性空间求和从非线性输入中出现相关的重要实验现象,例如简单细胞感受野的 ON 和 OFF 子区域的分离、兴奋和抑制的推拉效应,以及相位反转的皮质丘脑反馈。在这里,我们证明了一种从外侧膝状体到 V1 的视觉通路的两层模型,该模型将这些对神经回路的生物学限制纳入其中,并基于稀疏编码,可以解释这些实验现象、感受野的不同形状以及简单细胞的方位调谐的对比度不变性,当模型在自然图像上进行训练时。该模型表明,稀疏编码可以通过具有简单生物学上合理架构的 V1 简单细胞的神经回路来实现。