Centre for Ophthalmology, Institute for Ophthalmic Research, University of Tübingen, Elfriede-Aulhorn-Str. 5-7, D-72076 Tübingen, Germany.
J Neural Eng. 2018 Aug;15(4):045004. doi: 10.1088/1741-2552/aac811. Epub 2018 Jun 19.
A feasibility study for a transmitter based subretinal prosthesis, generating visual responses in blind mouse retina is presented.
Degenerated rd1 mouse retina were stimulated in subretinal configuration by local glutamate (Glu) or NMDA application via micropipettes (~1.5 μm) and thereby the outer retinal activity was recorded by calcium-imaging or the ganglion cell (GC) activity was recorded by the multi-electrode array system. The network mediated activation of GC via bipolar cells was approved by the administration of Glu receptor blockers.
Data of the degenerated and blind rd1 mouse retina reveals that the outer retina is Glu sensitive and that the subretinal Glu stimulation promotes network mediated GC responses. Analysis of the spatial activity-spread indicates that the Glu induced cell activation radius in the outer retina (12.5 μm) and postsynaptically activated GC (40 μm) is focal to the stimulation pipette tip. Moreover, the application of NMDA in subretinal space also evoked network mediated GC responses. The Glu-activated GC were identified as ON-OFF, OFF and two ON cells types.
This study evaluates the prerequisite for the function of a transmitter based implant, that after the loss of the photoreceptors, the remnant blind retinal network is Glu sensitive and functional, positively. The differential activation of ON (hyperpolarisation) and OFF (depolarisation) bipolar cells by transmitter Glu is a unique feature and of high interest for retinal implants. Therefore, the respective bipolar cell types could only be driven by glutamatergic stimulation accurately and not by electrical stimulation. The preserved functionality of the blind retina at the onset of complete blindness is motivating to continue research on a transmitter-based prosthesis. Since the artificial Glu stimulation mimics the natural retinal input, early implantation of a Glu-prosthesis might delay the devastating retinal remodelling positively, due to the neuronal-plasticity.
提出了一种基于发射器的视网膜下假体的可行性研究,该假体可在盲鼠视网膜中产生视觉反应。
通过微管(约 1.5 μm)在视网膜下配置中刺激变性 rd1 鼠视网膜,通过钙成像记录外视网膜活动,或通过多电极阵列系统记录节细胞 (GC) 活动。通过施用谷氨酸受体阻滞剂证实了通过双极细胞的网络介导的 GC 激活。
变性和盲 rd1 鼠视网膜的数据表明,外视网膜对谷氨酸敏感,并且视网膜下谷氨酸刺激促进了网络介导的 GC 反应。对空间活动传播的分析表明,谷氨酸诱导的外视网膜细胞激活半径(约 12.5 μm)和突触后激活的 GC(约 40 μm)与刺激微管尖端呈焦点状。此外,NMDA 在视网膜下空间的应用也引起了网络介导的 GC 反应。谷氨酸激活的 GC 被鉴定为 ON-OFF、OFF 和两种 ON 细胞类型。
这项研究评估了基于递质的植入物功能的前提条件,即在光感受器丧失后,残留的盲视网膜网络对递质谷氨酸呈正谷氨酸敏感和功能性。递质谷氨酸对 ON(超极化)和 OFF(去极化)双极细胞的不同激活是视网膜植入物的一个独特特征,具有很高的研究价值。因此,只有谷氨酸能刺激才能准确地驱动相应的双极细胞类型,而不能通过电刺激。完全失明时盲视网膜保留的功能是令人鼓舞的,因为这促使人们继续研究基于递质的假体。由于人工谷氨酸刺激模拟了自然视网膜输入,因此早期植入谷氨酸假体可能会由于神经元可塑性而积极地延迟破坏性的视网膜重塑。