Beier Corinne, Hovhannisyan Anahit, Weiser Sydney, Kung Jennifer, Lee Seungjun, Lee Dae Yeong, Huie Philip, Dalal Roopa, Palanker Daniel, Sher Alexander
Electrical Engineering and
Santa Cruz Institute for Particle Physics, University of California, Santa Cruz, California 95064, and.
J Neurosci. 2017 Apr 26;37(17):4635-4644. doi: 10.1523/JNEUROSCI.2570-16.2017. Epub 2017 Apr 3.
Upon degeneration of photoreceptors in the adult retina, interneurons, including bipolar cells, exhibit a plastic response leading to their aberrant rewiring. Photoreceptor reintroduction has been suggested as a potential approach to sight restoration, but the ability of deafferented bipolar cells to establish functional synapses with photoreceptors is poorly understood. Here we use photocoagulation to selectively destroy photoreceptors in adult rabbits while preserving the inner retina. We find that rods and cones shift into the ablation zone over several weeks, reducing the blind spot at scotopic and photopic luminances. During recovery, rod and cone bipolar cells exhibit markedly different responses to deafferentation. Rod bipolar cells extend their dendrites to form new synapses with healthy photoreceptors outside the lesion, thereby restoring visual function in the deafferented retina. Secretagogin-positive cone bipolar cells did not exhibit such obvious dendritic restructuring. These findings are encouraging to the idea of photoreceptor reintroduction for vision restoration in patients blinded by retinal degeneration. At the same time, they draw attention to the postsynaptic side of photoreceptor reintroduction; various bipolar cell types, representing different visual pathways, vary in their response to the photoreceptor loss and in their consequent dendritic restructuring. Loss of photoreceptors during retinal degeneration results in permanent visual impairment. Strategies for vision restoration based on the reintroduction of photoreceptors inherently rely on the ability of the remaining retinal neurons to correctly synapse with new photoreceptors. We show that deafferented bipolar cells in the adult mammalian retina can reconnect to rods and cones and restore retinal sensitivity at scotopic and photopic luminances. Rod bipolar cells extend their dendrites to form new synapses with healthy rod photoreceptors. These findings support the idea that bipolar cells might be able to synapse with reintroduced photoreceptors, thereby restoring vision in patients blinded by retinal degeneration.
在成年视网膜的光感受器发生退化时,包括双极细胞在内的中间神经元会表现出一种可塑性反应,导致其异常重新布线。光感受器重新植入已被提议作为恢复视力的一种潜在方法,但对于去传入神经的双极细胞与光感受器建立功能性突触的能力,人们了解甚少。在这里,我们使用光凝术选择性地破坏成年兔的光感受器,同时保留视网膜内层。我们发现,视杆细胞和视锥细胞在数周内会移入消融区,减少暗视和明视亮度下的盲点。在恢复过程中,视杆双极细胞和视锥双极细胞对去传入神经的反应明显不同。视杆双极细胞会延伸其树突,与病变外健康的光感受器形成新的突触,从而恢复去传入神经视网膜的视觉功能。分泌粒蛋白阳性的视锥双极细胞没有表现出如此明显的树突重构。这些发现对于因视网膜变性而失明的患者进行光感受器重新植入以恢复视力的想法是令人鼓舞的。同时,它们也引起了人们对光感受器重新植入突触后方面的关注;代表不同视觉通路的各种双极细胞类型,对光感受器丧失的反应以及随之而来的树突重构各不相同。视网膜变性过程中光感受器的丧失会导致永久性视力损害。基于光感受器重新植入的视力恢复策略本质上依赖于剩余视网膜神经元与新光感受器正确形成突触的能力。我们表明,成年哺乳动物视网膜中去传入神经的双极细胞可以重新连接到视杆细胞和视锥细胞,并在暗视和明视亮度下恢复视网膜敏感性。视杆双极细胞会延伸其树突,与健康的视杆光感受器形成新的突触。这些发现支持了双极细胞可能能够与重新植入的光感受器形成突触,从而恢复因视网膜变性而失明患者视力的观点。