Literature DB >> 10431919

Analysis of two types of cone bipolar cells in the retina of a New World monkey, the marmoset, Callithrix jacchus.

X Luo1, K K Ghosh, P R Martin, U Grünert.   

Abstract

Two types of cone bipolar cells, the blue cone bipolar cell and the diffuse bipolar cell (DB3), were labelled immunohistochemically and investigated in the retina of a New World monkey, the marmoset. Blue cone bipolar cells were labelled with an antiserum against cholecystokinin. Short-wavelength-sensitive (SWS) cones were labelled with an antiserum against the SWS cone opsin. The DB3 cells were labelled with antibodies to calbindin. Blue cone bipolar cells in marmoset do not form a regular mosaic but instead follow the random distribution of the SWS cones. Nevertheless, the SWS cone to blue cone bipolar cell connectivity in marmoset is very similar to that previously described for macaque. In contrast to the blue cone bipolar cells, the DB3 cells form a regular mosaic. The synaptic connectivity of DB3 cells in the inner plexiform layer was analyzed. They make output synapses onto ganglion cells and amacrine cells, and gap junctions with each other. Our results provide further evidence for the existence of parallel bipolar cell pathways in the primate retina and support the view that the retinae of Old World and New World primates have common neuronal connectivity. The random distribution of SWS cones and blue cone bipolar cells is an exception to the general rule of a regular mosaic distribution of cell populations in the retina.

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Year:  1999        PMID: 10431919     DOI: 10.1017/s0952523899164101

Source DB:  PubMed          Journal:  Vis Neurosci        ISSN: 0952-5238            Impact factor:   3.241


  11 in total

1.  Evaluation of AAV-mediated expression of Chop2-GFP in the marmoset retina.

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Review 2.  From random to regular: Variation in the patterning of retinal mosaics.

Authors:  Patrick W Keeley; Stephen J Eglen; Benjamin E Reese
Journal:  J Comp Neurol       Date:  2020-03-03       Impact factor: 3.215

3.  The primordial, blue-cone color system of the mouse retina.

Authors:  Silke Haverkamp; Heinz Wässle; Jens Duebel; Thomas Kuner; George J Augustine; Guoping Feng; Thomas Euler
Journal:  J Neurosci       Date:  2005-06-01       Impact factor: 6.167

4.  Response characteristics and receptive field widths of on-bipolar cells in the mouse retina.

Authors:  A Berntson; W R Taylor
Journal:  J Physiol       Date:  2000-05-01       Impact factor: 5.182

5.  Neural Mechanisms Mediating Motion Sensitivity in Parasol Ganglion Cells of the Primate Retina.

Authors:  Michael B Manookin; Sara S Patterson; Conor M Linehan
Journal:  Neuron       Date:  2018-03-01       Impact factor: 17.173

6.  Retinal connectivity and primate vision.

Authors:  Barry B Lee; Paul R Martin; Ulrike Grünert
Journal:  Prog Retin Eye Res       Date:  2010-09-06       Impact factor: 21.198

7.  Analysis of Parvocellular and Magnocellular Visual Pathways in Human Retina.

Authors:  Rania A Masri; Ulrike Grünert; Paul R Martin
Journal:  J Neurosci       Date:  2020-10-02       Impact factor: 6.167

8.  Network Architecture of Gap Junctional Coupling among Parallel Processing Channels in the Mammalian Retina.

Authors:  Crystal L Sigulinsky; James R Anderson; Ethan Kerzner; Christopher N Rapp; Rebecca L Pfeiffer; Taryn M Rodman; Daniel P Emrich; Kevin D Rapp; Noah T Nelson; J Scott Lauritzen; Miriah Meyer; Robert E Marc; Bryan W Jones
Journal:  J Neurosci       Date:  2020-04-24       Impact factor: 6.167

9.  Predictive encoding of motion begins in the primate retina.

Authors:  Belle Liu; Arthur Hong; Fred Rieke; Michael B Manookin
Journal:  Nat Neurosci       Date:  2021-08-02       Impact factor: 24.884

10.  AII amacrine cells in the primate fovea contribute to photopic vision.

Authors:  Enrica Strettoi; Rania A Masri; Ulrike Grünert
Journal:  Sci Rep       Date:  2018-11-06       Impact factor: 4.379

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