Helen Wills Neuroscience Institute, University of California, Berkeley, Berkeley, CA 94720, USA.
Department of Molecular and Cell Biology, University of California, Berkeley, Berkeley, CA 94720, USA.
Curr Biol. 2019 Dec 2;29(23):4024-4035.e5. doi: 10.1016/j.cub.2019.10.025. Epub 2019 Nov 7.
Detection of ambient illumination in the developing retina prior to maturation of conventional photoreceptors is mediated by intrinsically photosensitive retinal ganglion cells (ipRGCs) and is critical for driving several physiological processes, including light aversion, pupillary light reflexes, and photoentrainment of circadian rhythms. The strategies by which ipRGCs encode variations in ambient light intensity at these early ages are not known. Using unsupervised clustering of two-photon calcium responses followed by inspection of anatomical features, we found that the population activity of the neonatal retina could be modeled as six functional groups that were composed of mixtures of ipRGC subtypes and non-ipRGC cell types. By combining imaging, whole-cell recording, pharmacology, and anatomical techniques, we found that functional mixing of cell types is mediated in part by gap junction coupling. Together, these data show that both cell-autonomous intrinsic light responses and gap junction coupling among ipRGCs contribute to the proper encoding of light intensity in the developing retina.
在传统感光细胞成熟之前,发育中的视网膜中环境光照的检测是由内在光敏视网膜神经节细胞(ipRGC)介导的,这对于驱动几种生理过程至关重要,包括避光、瞳孔对光反射和昼夜节律的光驯化。目前尚不清楚 ipRGC 如何在这些早期阶段对环境光强度的变化进行编码。通过对双光子钙反应进行无监督聚类,然后检查解剖特征,我们发现新生儿视网膜的群体活动可以模拟为六个功能组,这些组由 ipRGC 亚型和非 ipRGC 细胞类型的混合物组成。通过结合成像、全细胞记录、药理学和解剖学技术,我们发现细胞类型的功能混合部分是由缝隙连接耦合介导的。总之,这些数据表明,细胞自主内在光反应和 ipRGC 之间的缝隙连接耦合都有助于在发育中的视网膜中对光强度进行适当编码。