具有增益控制的光感受器的动态自适应。

IF 2 4区 生物学 Q4 BIOCHEMISTRY & MOLECULAR BIOLOGY
Miguel Castillo García, Eugenio Urdapilleta
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引用次数: 1

摘要

视网膜承载着将外部视觉刺激转化为神经编码所需的所有过程。光的光导及其转化为电信号涉及生化级联、离子调节和不同类型的耦合以及其他相关过程。这些创建了非线性处理方案和依赖于光的自适应响应。近年来提出的动态适应模型是将所有这些现象恢复到单一前馈处理方案中的一个很好的现象学候选者。在这项工作中,我们在高度非线性的条件下分析了这种描述,并发现响应与非常详细的微观模型所产生的结果不匹配,该模型是为了在水平细胞上复制电生理记录而开发的。当延迟的光依赖性增益因子纳入描述时,对于简单和复杂的刺激,即使在光强度、对比度和持续时间上跨越几个数量级,响应也是非常一致的。该扩展模型可能有助于视网膜功能的研究,使微观领域与信号处理特性的理解联系起来,并进一步纳入空间扩展的视网膜网络。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Dynamical adaptation in photoreceptors with gain control.

The retina hosts all processes needed to convert external visual stimuli into a neural code. Light phototransduction and its conversion into an electrical signal involve biochemical cascades, ionic regulations, and different kinds of coupling, among other relevant processes. These create a nonlinear processing scheme and light-dependent adaptive responses. The dynamical adaptation model formulated in recent years is an excellent phenomenological candidate to resume all these phenomena into a single feedforward processing scheme. In this work, we analyze this description in highly nonlinear conditions and find that responses do not match those resulting from a very detailed microscopic model, developed to reproduce electrophysiological recordings on horizontal cells. When a delayed light-dependent gain factor incorporates into the description, responses are in excellent agreement, even when spanning several orders of magnitude in light intensity, contrast, and duration, for simple and complex stimuli. This extended model may be instrumental for studies of the retinal function, enabling the linking of the microscopic domain to the understanding of signal processing properties, and further incorporated in spatially extended retinal networks.

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来源期刊
Physical biology
Physical biology 生物-生物物理
CiteScore
4.20
自引率
0.00%
发文量
50
审稿时长
3 months
期刊介绍: Physical Biology publishes articles in the broad interdisciplinary field bridging biology with the physical sciences and engineering. This journal focuses on research in which quantitative approaches – experimental, theoretical and modeling – lead to new insights into biological systems at all scales of space and time, and all levels of organizational complexity. Physical Biology accepts contributions from a wide range of biological sub-fields, including topics such as: molecular biophysics, including single molecule studies, protein-protein and protein-DNA interactions subcellular structures, organelle dynamics, membranes, protein assemblies, chromosome structure intracellular processes, e.g. cytoskeleton dynamics, cellular transport, cell division systems biology, e.g. signaling, gene regulation and metabolic networks cells and their microenvironment, e.g. cell mechanics and motility, chemotaxis, extracellular matrix, biofilms cell-material interactions, e.g. biointerfaces, electrical stimulation and sensing, endocytosis cell-cell interactions, cell aggregates, organoids, tissues and organs developmental dynamics, including pattern formation and morphogenesis physical and evolutionary aspects of disease, e.g. cancer progression, amyloid formation neuronal systems, including information processing by networks, memory and learning population dynamics, ecology, and evolution collective action and emergence of collective phenomena.
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