Perez Ross M, Campbell Jay, Goswami-Sewell Debalina, Venkatraman Rajashree, Gomez Cesiah C, Bagnetto Caitlin, Lee Audrey, Mattos Marlon F, Hoon Mrinalini, Zuniga-Sanchez Elizabeth
bioRxiv. 2025 Feb 12:2025.02.11.637690. doi: 10.1101/2025.02.11.637690.
The mammalian visual system consists of two distinct pathways: rod- and cone-driven vision. The rod pathway is responsible for dim light vision whereas the cone pathway mediates daylight vision and color perception. The distinct processing of visual information begins at the first synapse of rod and cone photoreceptors. The unique composition and organization of the rod and cone synapse is what allows information to be parsed into the different visual pathways. Although this is a critical process for vision, little is known about the key molecules responsible for establishing and maintaining the distinct synaptic architecture of the rod and cone synapse. In the present study, we uncovered a new role for Ankyrins in maintaining the synaptic integrity of the rod and cone synapse. Loss of Ankyrin-B and Ankyrin-G results in connectivity defects between photoreceptors and their synaptic partners. Ultrastructure analysis of the rod and cone synapse revealed impaired synaptic innervation, abnormal terminal morphology, and disruption of synaptic connections. Consistent with these findings, functional studies revealed impaired retinal responses in animals with loss of Ankyrin-B and Ankyrin-G. Taken together, our data supports a new role for Ankyrins in maintaining synaptic integrity and organization of photoreceptor synapses in the mouse outer retina.
The first synapse in the outer retina begins to process visual information into two distinct pathways. This is largely attributed to the different composition and organization of the rod and cone synapse. Although the structural integrity of the rod and cone synapse is critical for normal vision, little is known about the key molecules responsible for maintaining the unique structure of the different photoreceptor synapses. In this study, we demonstrate a new function for the cytoskeletal scaffolding proteins, Ankryin-B and Ankyrin-G in the mouse outer retina. We found Ankyrin-B and Ankyrin-G are both required for proper retinal connectivity, where loss of these molecules leads to synaptic defects and impaired retinal responses.
哺乳动物视觉系统由两条不同的通路组成:视杆和视锥驱动的视觉。视杆通路负责暗光视觉,而视锥通路介导日光视觉和颜色感知。视觉信息的不同处理始于视杆和视锥光感受器的第一个突触。视杆和视锥突触独特的组成和组织使得信息能够被解析到不同的视觉通路中。尽管这是视觉的一个关键过程,但对于负责建立和维持视杆和视锥突触独特突触结构的关键分子知之甚少。在本研究中,我们发现锚蛋白在维持视杆和视锥突触的突触完整性方面有新作用。锚蛋白-B和锚蛋白-G的缺失导致光感受器与其突触伙伴之间的连接缺陷。对视杆和视锥突触的超微结构分析显示突触神经支配受损、终末形态异常以及突触连接中断。与这些发现一致,功能研究表明在缺乏锚蛋白-B和锚蛋白-G的动物中视网膜反应受损。综上所述,我们的数据支持锚蛋白在维持小鼠外视网膜光感受器突触的突触完整性和组织方面有新作用。
外视网膜中的第一个突触开始将视觉信息处理成两条不同的通路。这在很大程度上归因于视杆和视锥突触的不同组成和组织。尽管视杆和视锥突触的结构完整性对于正常视觉至关重要,但对于负责维持不同光感受器突触独特结构的关键分子知之甚少。在本研究中,我们证明了细胞骨架支架蛋白锚蛋白-B和锚蛋白-G在小鼠外视网膜中的新功能。我们发现锚蛋白-B和锚蛋白-G对于视网膜的正常连接都是必需的,这些分子的缺失会导致突触缺陷和视网膜反应受损。