Xu Zhengyang, Kunala Karteek, Murphy Peter, Patak Laura, Puthussery Teresa, McGregor Juliette
Institute of Optics, University of Rochester, Rochester, New York, UNITED STATES.
Center for Visual Science, University of Rochester Medical Center, Rochester, New York, UNITED STATES.
bioRxiv. 2024 Feb 24:2023.05.30.542908. doi: 10.1101/2023.05.30.542908.
Physiological changes in retinal ganglion cells (RGCs) have been reported in rodent models of photoreceptor (PR) loss but this has not been investigated in primates. By expressing both a calcium indicator (GCaMP6s) and an optogenetic actuator (ChrimsonR) in foveal RGCs of the macaque, we reactivated RGCs and assessed their response in the weeks and years following PR loss.
We used an calcium imaging approach to record optogenetically evoked activity in deafferented RGCs in primate fovea. Cellular scale recordings were made longitudinally over a 10 week period following photoreceptor ablation and compared to responses from RGCs that had lost photoreceptor input more than two years prior.
Three eyes received photoreceptor ablation, OD of a male (M1), OS of a female (M2) and OD of a male (M3). Two animals were used for recording, one for histological assessment.
Cones were ablated with an ultrafast laser delivered through an adaptive optics scanning light ophthalmoscope (AOSLO). A 0.5 s pulse of 25Hz 660nm light optogenetically stimulated RGCs, and the resulting GCaMP fluorescence signal was recorded using AOSLO. Measurements were repeated over 10 weeks immediately after PR ablation, at 2.3 years and in control RGCs.
The calcium rise time, decay constant and sensitivity index of optogenetic mediated RGC were derived from GCaMP fluorescence recordings from 221 RGCs (Animal M1) and 218 RGCs (Animal M2) .
Following photoreceptor ablation, the mean decay constant of the calcium response in RGCs decreased 1.5 fold (1.6±0.5 s to 0.6±0.3 s SD) over the 10 week observation period in subject 1 and 2.1 fold (2.5±0.5 s to 1.2±0.2 s SD) within 8 weeks in subject 2. Calcium rise time and sensitivity index were stable. Optogenetic reactivation remained possible 2.3 years after PR ablation.
Altered calcium dynamics developed in primate foveal RGCs in the weeks after photoreceptor ablation. The mean decay constant of optogenetic mediated calcium responses decreased 1.5 - 2-fold. This is the first report of this phenomenon in primate retina and further work is required to understand the role these changes play in cell survival and activity.
在光感受器(PR)丧失的啮齿动物模型中已报道了视网膜神经节细胞(RGCs)的生理变化,但尚未在灵长类动物中进行研究。通过在猕猴的中央凹RGCs中同时表达钙指示剂(GCaMP6s)和光遗传学激活器(ChrimsonR),我们重新激活了RGCs,并评估了它们在PR丧失后的数周和数年中的反应。
我们采用钙成像方法来记录灵长类动物中央凹中去传入RGCs的光遗传学诱发活动。在光感受器消融后的10周内纵向进行细胞尺度记录,并与两年多前失去光感受器输入的RGCs的反应进行比较。
三只眼睛接受了光感受器消融,一只雄性的右眼(M1)、一只雌性的左眼(M2)和一只雄性的右眼(M3)。两只动物用于记录,一只用于组织学评估。
通过自适应光学扫描激光检眼镜(AOSLO)发射的超快激光消融视锥细胞。用25Hz 660nm光的0.5秒脉冲对RGCs进行光遗传学刺激,并使用AOSLO记录产生的GCaMP荧光信号。在PR消融后立即、2.3年以及对照RGCs中,在10周内重复进行测量。
光遗传学介导的RGC的钙上升时间、衰减常数和敏感性指数来自221个RGCs(动物M1)和218个RGCs(动物M2)的GCaMP荧光记录。
在光感受器消融后,在第1个受试者的10周观察期内,RGCs中钙反应的平均衰减常数下降了1.5倍(标准差从1.6±0.5秒降至0.6±0.3秒),在第2个受试者的8周内下降了2.1倍(标准差从2.5±0.5秒降至1.2±0.2秒)。钙上升时间和敏感性指数保持稳定。在PR消融2.3年后仍可进行光遗传学重新激活。
在光感受器消融后的数周内,灵长类动物中央凹RGCs中出现了钙动力学改变。光遗传学介导的钙反应的平均衰减常数下降了1.5至2倍。这是在灵长类动物视网膜中首次报道这一现象,需要进一步开展工作以了解这些变化在细胞存活和活动中所起的作用。