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灵长类动物黑视蛋白神经元对环境光照的编码。

Encoding of environmental illumination by primate melanopsin neurons.

机构信息

F. M. Kirby Neurobiology Center and Department of Neurology, Boston Children's Hospital and Harvard Medical School. Boston, MA 02115, USA.

Department of Molecular and Cellular Biology and Center for Brain Science, Harvard University, Cambridge, MA 02138, USA.

出版信息

Science. 2023 Jan 27;379(6630):376-381. doi: 10.1126/science.ade2024. Epub 2023 Jan 26.

Abstract

Light regulates physiology, mood, and behavior through signals sent to the brain by intrinsically photosensitive retinal ganglion cells (ipRGCs). How primate ipRGCs sense light is unclear, as they are rare and challenging to target for electrophysiological recording. We developed a method of acute identification within the live, ex vivo retina. Using it, we found that ipRGCs of the macaque monkey are highly specialized to encode irradiance (the overall intensity of illumination) by blurring spatial, temporal, and chromatic features of the visual scene. We describe mechanisms at the molecular, cellular, and population scales that support irradiance encoding across orders-of-magnitude changes in light intensity. These mechanisms are conserved quantitatively across the ~70 million years of evolution that separate macaques from mice.

摘要

光通过向大脑发送由内在感光性视网膜神经节细胞(ipRGCs)发出的信号来调节生理、情绪和行为。目前尚不清楚灵长类动物 ipRGCs 如何感知光,因为它们数量稀少,且难以进行电生理记录。我们开发了一种在活体、离体视网膜中进行急性鉴定的方法。使用该方法,我们发现猕猴的 ipRGCs 高度专门化,通过模糊视觉场景的空间、时间和颜色特征来编码辐照度(光照的整体强度)。我们描述了在跨越光强度数量级变化的分子、细胞和群体尺度上支持辐照度编码的机制。这些机制在将猕猴与老鼠分开的约 7000 万年的进化过程中在数量上是保守的。

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