September 2023
Volume 23, Issue 11
Open Access
Optica Fall Vision Meeting Abstract  |   September 2023
Contributed Session III: In vivo calcium imaging of macaque foveolar retinal ganglion cells reveals spatiochromatic receptive field properties
Author Affiliations
  • Tyler Godat
    University of Rochester
  • Nicolas P. Cottaris
    University of Pennsylvania
  • Sara Patterson
    University of Rochester
  • Kendall Kohout
    University of Rochester
  • Keith Parkins
    University of Rochester
  • Qiang Yang
    University of Rochester
  • Jennifer M. Strazzeri
    University of Rochester Medical Center
  • Juliette E. McGregor
    University of Rochester
  • David H. Brainard
    University of Pennsylvania
  • William H. Merigan
    University of Rochester
  • David R. Williams
    University of Rochester
Journal of Vision September 2023, Vol.23, 32. doi:https://doi.org/10.1167/jov.23.11.32
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      Tyler Godat, Nicolas P. Cottaris, Sara Patterson, Kendall Kohout, Keith Parkins, Qiang Yang, Jennifer M. Strazzeri, Juliette E. McGregor, David H. Brainard, William H. Merigan, David R. Williams; Contributed Session III: In vivo calcium imaging of macaque foveolar retinal ganglion cells reveals spatiochromatic receptive field properties. Journal of Vision 2023;23(11):32. https://doi.org/10.1167/jov.23.11.32.

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      © ARVO (1962-2015); The Authors (2016-present)

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Abstract

Here, we optically record responses to spatial and chromatic stimuli using a calcium indicator in the living macaque eye to characterize the receptive field (RF) properties of retinal ganglion cells (RGCs) serving the foveal center. GCaMP6s was expressed in three female macaques. Adaptive optics ophthalmoscopy was used to image fluorescence (488nm ex, 520/35nm em) from RGCs whose RF centers were driven by cones in the central 36 arcmin of the fovea and additional RGCs driven by cones in the central 6 arcmin of the foveola. Using cone isolating and luminance flicker (1.3deg, 0.15Hz, LED 420nm, 530nm, 660nm), we derived cone weights in over 250 RGCs. Using drifting gratings (1.9deg, 6Hz, 4-50c/deg, 561nm), we derived the spatial frequency responses of 15 L vs. M cone opponent RGCs at the foveolar center. Employing computational modeling (ISETbio), we inferred the full spatial difference of gaussians center and surround structure for those 15 cells. Of the 34 foveolar RGCs, 44% exhibited L vs. M cone opponency, 15% were L+M ON, 6% were -L-M OFF, and 35% showed only L or only M responses. The spatial frequency response functions of 12/15 L vs. M opponent cells peaked at high spatial frequencies (25-40c/deg) and had a strong bandpass characteristic. Our model indicates that the responses of all 15 L vs. M opponent cells are consistent with single cone input to their RF centers and that our data are consistent with extrafoveal data when the blurring of the optics is accounted for.

Footnotes
 Funding: Funding: This work was supported by the National Eye Institute through grants NIH EY007125, NIH U01EY025497, NIH EY031467, NIH EY021166, and through an unrestricted grant to the Flaum Eye Institute from Research to Prevent Blindness.
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