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      Foveal Retinal Ganglion Cells Develop Altered Calcium Dynamics Weeks After Photoreceptor Ablation

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          Abstract

          Purpose

          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 in vivo and assessed their response in the weeks and years after PR loss.

          Design

          We used an in vivo 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 after PR ablation and compared with responses from RGCs that had lost PR input >2 years prior.

          Participants

          Three eyes received PR ablation, the right eye of a male Macaca mulatta (M1), the left eye of a female Macaca fascicularis (M2), and the right eye of a male Macaca fascicularis (M3). Two animals were used for in vivo recording, 1 for histological assessment.

          Methods

          Cones were ablated with an ultrafast laser delivered through an adaptive optics scanning light ophthalmoscope (AOSLO). A 0.5 second pulse of 25 Hz 660 nm light optogenetically stimulated RGCs, and the resulting GCaMP fluorescence signal was recorded using an AOSLO. Measurements were repeated over 10 weeks immediately after PR ablation, at 2.3 years and in control RGCs.

          Main Outcome Measures

          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) in vivo.

          Results

          After PR ablation, the mean decay constant of the calcium response in RGCs decreased 1.5-fold (standard deviation 1.6 ± 0.5 seconds to 0.6 ± 0.3 seconds) over the 10-week observation period in subject 1 and 2.1-fold (standard deviation 2.5 ± 0.5 seconds to 1.2 ± 0.2 seconds) within 8 weeks in subject 2. Calcium rise time and sensitivity index were stable. Optogenetic reactivation remained possible 2.3 years after PR ablation.

          Conclusions

          Altered calcium dynamics developed in primate foveal RGCs in the weeks after PR ablation. The mean decay constant of optogenetic-mediated calcium responses decreased 1.5- to twofold. 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.

          Financial Disclosure(s)

          Proprietary or commercial disclosure may be found in the Footnotes and Disclosures at the end of this article.

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          Most cited references33

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          Independent Optical Excitation of Distinct Neural Populations

          Optogenetic tools enable the causal examination of how specific cell types contribute to brain circuit functions. A long-standing question is whether it is possible to independently activate two distinct neural populations in mammalian brain tissue. Such a capability would enable the examination of how different synapses or pathways interact to support computation. Here we report two new channelrhodopsins, Chronos and Chrimson, obtained through the de novo sequencing and physiological characterization of opsins from over 100 species of algae. Chrimson is 45 nm red-shifted relative to any previous channelrhodopsin, important for scenarios where red light would be preferred; we show minimal visual system mediated behavioral artifact in optogenetically stimulated Drosophila. Chronos has faster kinetics than any previous channelrhodopsin, yet is effectively more light-sensitive. Together, these two reagents enable crosstalk-free two-color activation of neural spiking and downstream synaptic transmission in independent neural populations in mouse brain slice.
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            Imaging neural activity in worms, flies and mice with improved GCaMP calcium indicators

            Genetically encoded calcium indicators (GECIs) can be used to image activity in defined neuronal populations. However, current GECIs produce inferior signals compared to synthetic indicators and recording electrodes, precluding detection of low firing rates. We developed a single-wavelength GECI based on GCaMP2 (GCaMP3), with increased baseline fluorescence (3x), dynamic range (3x), and higher affinity for calcium (1.3x). GCaMP3 fluorescence changes triggered by single action potentials were detected in pyramidal cell dendrites, with signal-to-noise ratio and photostability significantly better than GCaMP2, D3cpVenus, and TN-XXL. In Caenorhabditis elegans chemosensory neurons and the Drosophila melanogaster antennal lobe, sensory stimulation-evoked fluorescence responses were significantly enhanced with the new indicator (4–6x). In somatosensory and motor cortical neurons in the intact mouse, GCaMP3 detected calcium transients with amplitudes linearly dependent on action potential number. Long-term imaging in the motor cortex of behaving mice revealed large fluorescence changes in imaged neurons over months.
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              Partial recovery of visual function in a blind patient after optogenetic therapy

              Optogenetics may enable mutation-independent, circuit-specific restoration of neuronal function in neurological diseases. Retinitis pigmentosa is a neurodegenerative eye disease where loss of photoreceptors can lead to complete blindness. In a blind patient, we combined intraocular injection of an adeno-associated viral vector encoding ChrimsonR with light stimulation via engineered goggles. The goggles detect local changes in light intensity and project corresponding light pulses onto the retina in real time to activate optogenetically transduced retinal ganglion cells. The patient perceived, located, counted and touched different objects using the vector-treated eye alone while wearing the goggles. During visual perception, multichannel electroencephalographic recordings revealed object-related activity above the visual cortex. The patient could not visually detect any objects before injection with or without the goggles or after injection without the goggles. This is the first reported case of partial functional recovery in a neurodegenerative disease after optogenetic therapy.
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                Author and article information

                Contributors
                Journal
                Ophthalmol Sci
                Ophthalmol Sci
                Ophthalmology Science
                Elsevier
                2666-9145
                22 March 2024
                Sep-Oct 2024
                22 March 2024
                : 4
                : 5
                : 100520
                Affiliations
                [1 ]Institute of Optics, University of Rochester, Rochester, New York
                [2 ]Center for Visual Science, University of Rochester Medical Center, Rochester, New York
                [3 ]Herbert Wertheim School of Optometry & Vision Science, University of California Berkeley, Berkeley, California
                [4 ]Vision Science Graduate Program, University of California Berkeley, Berkeley, California
                [5 ]Helen Wills Neuroscience Institute, University of California Berkeley, Berkeley, California
                [6 ]Department of Ophthalmology, University of Rochester Medical Center, Rochester, New York
                Author notes
                []Correspondence: Zhengyang Xu, BSc, Box 319, 601 Elmwood Ave., Rochester, NY 14642. zxu56@ 123456ur.rochester.edu
                [∗∗ ]Juliette McGregor, PhD, Box 319, 601 Elmwood Ave., Rochester, NY 14642. jmcgrego@ 123456ur.rochester.edu
                Article
                S2666-9145(24)00056-3 100520
                10.1016/j.xops.2024.100520
                11179405
                38881601
                eb0afea5-2a4c-4a48-9295-759f026f7898
                © 2024 by the American Academy of Ophthalmology.

                This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).

                History
                : 30 June 2023
                : 28 February 2024
                : 14 March 2024
                Categories
                Original Article

                retinal ganglion cells,vision restoration,optogenetics,adaptive optics scanning light ophthalmoscopy,calcium dynamics

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