Spatial Organization of Chromatic Pathways in the Mouse Dorsal Lateral Geniculate Nucleus

被引:36
|
作者
Denman, Daniel J. [1 ]
Siegle, Joshua H. [1 ]
Koch, Christof [1 ]
Reid, R. Clay [1 ]
Blanche, Timothy J. [1 ,2 ]
机构
[1] Allen Inst Brain Sci, 615 Westlake Ave N, Seattle, WA 98109 USA
[2] Univ Calif Berkeley, Redwood Ctr Theoret Neurosci, Berkeley, CA 94720 USA
关键词
color; LGN; mouse; vision; PRIMARY VISUAL-CORTEX; RETINAL GANGLION-CELLS; CONE PHOTORECEPTOR; MAMMALIAN RETINA; STRIATE CORTEX; PRIMATE RETINA; DUAL GRADIENT; COLOR-VISION; M OPSINS; RESPONSES;
D O I
10.1523/JNEUROSCI.1742-16.2016
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
In both dichromats and trichromats, cone opsin signals are maintained independently in cones and combined at the bipolar and retinal ganglion cell level, creating parallel color opponent pathways to the central visual system. Like other dichromats, the mouse retina expresses a short-wavelength (S) and a medium-wavelength (M) opsin, with the S-opsin shifted to peak sensitivity in the ultraviolet (UV) range. Unlike in primates, nonuniform opsin expression across the retina and coexpression in single cones creates a mostly mixed chromatic signal. Here, we describe the visuotopic and chromatic organization of spiking responses in the dorsal lateral geniculate and of the local field potentials in their recipient zone in primary visual cortex (V1). We used an immersive visual stimulus dome that allowed us to present spatiotemporally modulated UV and green luminance in any region of the visual field of an awake, head-fixed mouse. Consistent with retinal expression of opsins, we observed graded UV-to-green dominated responses from the upper to lower visual fields, with a smaller difference across azimuth. In addition, we identified a subpopulation of cells (<10%) that exhibited spectrally opponent responses along the S-M axis. Luminance signals of each wavelength and color signals project to the middle layers of V1.
引用
收藏
页码:1102 / 1116
页数:15
相关论文
共 50 条
  • [41] Lamination of the Lateral Geniculate Nucleus of Catarrhine Primates
    de Sousa, Alexandra A.
    Sherwood, Chet C.
    Hof, Patrick R.
    Zilles, Karl
    BRAIN BEHAVIOR AND EVOLUTION, 2013, 81 (02) : 93 - 108
  • [42] Binocular response modulation in the lateral geniculate nucleus
    Dougherty, Kacie
    Schmid, Michael C.
    Maier, Alexander
    JOURNAL OF COMPARATIVE NEUROLOGY, 2019, 527 (03) : 522 - 534
  • [43] Subdivisions of the dorsal raphe nucleus projecting to the lateral geniculate nucleus and primary visual cortex in the Mongolian gerbil
    Janusonis, S
    Fite, KV
    Bengston, L
    NEUROREPORT, 2003, 14 (03) : 459 - 462
  • [44] Dynamics of Temporal Integration in the Lateral Geniculate Nucleus
    Alexander, Prescott C.
    Alitto, Henry J.
    Fisher, Tucker G.
    Rathbun, Daniel L.
    Weyand, Theodore G.
    Usrey, W. Martin
    ENEURO, 2022, 9 (04)
  • [45] Developmental remodeling of relay cells in the dorsal lateral geniculate nucleus in the absence of retinal input
    Rana N. El-Danaf
    Thomas E. Krahe
    Emily K. Dilger
    Martha E. Bickford
    Michael A. Fox
    William Guido
    Neural Development, 10
  • [46] Role of GABAergic inhibition in shaping the spatial frequency tuning of neurons and its contrast dependency in the dorsal lateral geniculate nucleus of cat
    Kimura, Akihiro
    Shimegi, Satoshi
    Hara, Shin'ichiro
    Okamoto, Masahiro
    Sato, Hiromichi
    EUROPEAN JOURNAL OF NEUROSCIENCE, 2013, 37 (08) : 1270 - 1283
  • [47] Short Wavelengths Contribution to Light-induced Responses and Irradiance Coding in the Rat Dorsal Lateral Geniculate Nucleus - An In vivo Electrophysiological Approach
    Jeczmien-Lazur, Jagoda Stanislawa
    Orlowska-Feuer, Patrycja
    Kustron, Anna
    Lewandowski, Marian Henryk
    NEUROSCIENCE, 2021, 468 : 220 - 234
  • [48] Visual responses in the lateral geniculate evoked by Cx36-independent rod pathways
    Brown, Timothy M.
    Allen, Annette E.
    Wynne, Jonathan
    Paul, David L.
    Piggins, Hugh D.
    Lucas, Robert J.
    VISION RESEARCH, 2011, 51 (02) : 280 - 287
  • [49] Cell type- and layer-specific convergence in core and shell neurons of the dorsal lateral geniculate nucleus
    Okigawa, Sayumi
    Yamaguchi, Masahiro
    Ito, Kei N.
    Takeuchi, Ryosuke F.
    Morimoto, Nao
    Osakada, Fumitaka
    JOURNAL OF COMPARATIVE NEUROLOGY, 2021, 529 (08) : 2099 - 2124
  • [50] Heterochrony of postnatal accumulation of nonphosphorylated heavy-chain neurofilament by neurons of the cat dorsal lateral geniculate nucleus
    Mikhalkin, Aleksandr
    Nikitina, Nina
    Merkulyeva, Natalia
    JOURNAL OF COMPARATIVE NEUROLOGY, 2021, 529 (07) : 1430 - 1441