Literature DB >> 2108873

Morphological classification and retinal distribution of large ganglion cells in the retina of Bufo marinus.

C Straznicky1, P Tóth, V S Nguyen.   

Abstract

The retrograde transport of horseradish peroxidase (HRP) and cobaltic-lysine complex (CLC) was used to morphologically characterize large ganglion cells (GCs) and to determine their distribution in retinal wholemounts and in sectioned material in the retina of Bufo marinus. Large GCs, amounting to about 0.5% of total GC population, were defined to be those with very large dendritic field sizes varying between 0.1 mm2 to 0.6 mm2 and cell soma sizes of between 100 microns 2 to 400 microns 2. These cells were subdivided into 3 major groups, Types I, II and III, on the basis of their dendritic field sizes, aborization patterns and the strata of dendritic branching within the inner plexiform layer (IPL). The majority of large neurons (about 90%) were classified as Type I GCs with symmetrical dendritic arbor. These cells had either bistratified branching in the scleral and vitreal sublamina of the IPL (65% of Type I Cells) or unistratified branching in the scleral (26%) or in the vitreal (9%) sublamina. Their dendritic field sizes increased linearly from the retinal centre from 0.13 mm +/- 0.02 mm2 (mean and S.D.) to 0.58 +/- 0.11 mm2 in the retinal periphery. Type II GCs (about 9% of large GC population) were characterized by an asymmetrical dendritic aborization directed towards the ciliary margin with unistratified branching in the scleral sublamina of the IPL. The mean dendritic field sizes of these cells were 0.26 +/- 0.09 mm2. Type III GCs, the least frequent (about 1%) category of large GCs had sparsely branching, elongated dendritic branching aligned approximately parallel with the nasotemporal axis of the retina. The unistratified dendritic branches of these neurons were located in the vitreal sublamina of the IPL with a mean dendritic field size of 0.42 +/- 0.11 mm2. The dendritic field sizes of Types II and III GCs did not increase with retinal eccentricity. Type I GCs were distributed unevenly across the retina, the density being greatest in the visual streak, along the nasotemporal meridian of the retina. The dendritic field sizes of these cells increased towards the retinal periphery, resulting in a constant dendritic field coverage factor across the retina. Each retinal point was covered by the dendritic fields of 4-5 adjacent GCs. In contrast, Types II and III GCs had only discontinuous dendritic coverage. The identification of morphological types of large GCs with previously described functional classes of GCs in the anuran retina is discussed.

Entities:  

Mesh:

Substances:

Year:  1990        PMID: 2108873     DOI: 10.1007/bf00608244

Source DB:  PubMed          Journal:  Exp Brain Res        ISSN: 0014-4819            Impact factor:   1.972


  30 in total

1.  Technical considerations on the use of horseradish peroxidase as a neuronal marker.

Authors:  J C Adams
Journal:  Neuroscience       Date:  1977       Impact factor: 3.590

2.  Role of the accessory optic system in the optokinetic nystagmus of the frog.

Authors:  G Lázár
Journal:  Brain Behav Evol       Date:  1972       Impact factor: 1.808

3.  Biplexiform cells: ganglion cells of the primate retina that contact photoreceptors.

Authors:  A P Mariani
Journal:  Science       Date:  1982-06-04       Impact factor: 47.728

4.  A morphometric study of the retinal ganglion cell layer and optic nerve from metamorphosis in Xenopus laevis.

Authors:  S A Dunlop; L D Beazley
Journal:  Vision Res       Date:  1984       Impact factor: 1.886

5.  Changing retinal ganglion cell distribution in the frog Heleioporus eyrei.

Authors:  S A Dunlop; L D Beazley
Journal:  J Comp Neurol       Date:  1981-10-20       Impact factor: 3.215

6.  Amacrine cells, bipolar cells and ganglion cells of the cat retina: a Golgi study.

Authors:  H Kolb; R Nelson; A Mariani
Journal:  Vision Res       Date:  1981       Impact factor: 1.886

7.  Ganglion cell death within the developing retina: a regulatory role for retinal dendrites?

Authors:  R Linden; V H Perry
Journal:  Neuroscience       Date:  1982       Impact factor: 3.590

8.  The development of retinal ganglion cells in a tetraploid strain of Xenopus laevis: a morphological study utilizing intracellular dye injection.

Authors:  D S Sakaguchi; R K Murphey; R K Hunt; R Tompkins
Journal:  J Comp Neurol       Date:  1984-04-01       Impact factor: 3.215

9.  A small population of retinal ganglion cells projecting to the retina of the other eye. An experimental study in the rat and the rabbit.

Authors:  M Müller; H Holländer
Journal:  Exp Brain Res       Date:  1988       Impact factor: 1.972

10.  Anatomy and physiology of vision in the frog (Rana pipiens).

Authors:  H R MATURANA; J Y LETTVIN; W S MCCULLOCH; W H PITTS
Journal:  J Gen Physiol       Date:  1960-07       Impact factor: 4.086

View more
  5 in total

1.  Microtubule-associated protein 2 (MAP2)-immunoreactive neurons in the retina of Bufo marinus: colocalisation with tyrosine hydroxylase and serotonin in amacrine cells.

Authors:  R Gábriel; M Wilhelm; C Straznicky
Journal:  Cell Tissue Res       Date:  1992-07       Impact factor: 5.249

2.  The morphology and distribution of photoreceptors in the retina of Bufo marinus.

Authors:  Y D Zhang; C Straznicky
Journal:  Anat Embryol (Berl)       Date:  1991

3.  Dendritic morphology and retinal distribution of tyrosine hydroxylase-like immunoreactive amacrine cells in Bufo marinus.

Authors:  B Zhu; C Straznicky
Journal:  Anat Embryol (Berl)       Date:  1990

Review 4.  Dorsal raphe nucleus projecting retinal ganglion cells: Why Y cells?

Authors:  Gary E Pickard; Kwok-Fai So; Mingliang Pu
Journal:  Neurosci Biobehav Rev       Date:  2015-08-05       Impact factor: 8.989

5.  The generation and changing retinal distribution of displaced amacrine cells in Bufo marinus from metamorphosis to adult.

Authors:  S K Chng; C Straznicky
Journal:  Anat Embryol (Berl)       Date:  1992-07
  5 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.