4.7 Article

Y-Cell Receptive Field and Collicular Projection of Parasol Ganglion Cells in Macaque Monkey Retina

期刊

JOURNAL OF NEUROSCIENCE
卷 28, 期 44, 页码 11277-11291

出版社

SOC NEUROSCIENCE
DOI: 10.1523/JNEUROSCI.2982-08.2008

关键词

primate; superior colliculus; retina; Y cell; magnocellular; spatial vision

资金

  1. Paul Kayser International Award
  2. Retina Research Foundation
  3. National Institutes of Health [EY06678]
  4. Vision Research Center [EY01730]
  5. Tissue Distribution Program of the National Primate Research Center at the University of Washington [RR00166]
  6. National Science Foundation [DBI-0551852]

向作者/读者索取更多资源

The distinctive parasol ganglion cell of the primate retina transmits a transient, spectrally nonopponent signal to the magnocellular layers of the lateral geniculate nucleus. Parasol cells show well-recognized parallels with the alpha-Y cell of other mammals, yet two key alpha-Y cell properties, a collateral projection to the superior colliculus and nonlinear spatial summation, have not been clearly established for parasol cells. Here, we show by retrograde photodynamic staining that parasol cells project to the superior colliculus. Photostained dendritic trees formed characteristic spatial mosaics and afforded unequivocal identification of the parasol cells among diverse collicular-projecting cell types. Loose-patch recordings were used to demonstrate for all parasol cells a distinct Y-cell receptive field signature marked by a nonlinear mechanism that responded to contrast-reversing gratings at twice the stimulus temporal frequency [second Fourier harmonic (F2)] independent of stimulus spatial phase. The F2 component showed high contrast gain and temporal sensitivity and appeared to originate from a region coextensive with that of the linear receptive field center. The F2 spatial frequency response peaked well beyond the resolution limit of the linear receptive field center, showing a Gaussian center radius of similar to 15 mu m. Blocking inner retinal inhibition elevated the F2 response, suggesting that amacrine circuitry does not generate this nonlinearity. Our data are consistent with a pooled-subunit model of the parasol Y-cell receptive field in which summation from an array of transient, partially rectifying cone bipolar cells accounts for both linear and nonlinear components of the receptive field.

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