Literature DB >> 8509512

Spatial and temporal differences between the expression of short- and middle-wave sensitive cone pigments in the mouse retina: a developmental study.

A Szél1, P Röhlich, K Mieziewska, G Aguirre, T van Veen.   

Abstract

In an earlier study we found a topographic separation of middlewave-sensitive (M) and shortwave-sensitive (S) cones in the adult mouse retina. In the present study we investigated the development of the two colour-specific cone types to see whether there is also a temporal difference between the expression of the specific cone visual pigments. Using two anti-cone visual pigment antibodies, COS-1 and OS-2, we compared the densities of immunopositive cone outer segments on retinal whole mounts derived from mice of various ages. The first detectable cone outer segments were the S-cones which appeared in the inferior half of the retina on postnatal day 4. At this stage, the density of the S-cones was very low (30-40 cones/retina) but increased steadily on the following days to reach a value comparable to that of adults by P30 (18,000/mm2). This cone type always remained much more abundant in the lower part of the retina throughout the whole retinal development. In the superior half of the retina, a few S-cones appeared from postnatal day 7; however, their number always remained about one order of magnitude lower than in the inferior part. In contrast, M-cone outer segments were not identifiable earlier than postnatal day 11 and were confined exclusively to the superior part of the retina during the whole developmental process. On postnatal day 12, their density was 1,900/mm2 and increased to a value of 11,000/mm2 by postnatal day 30, which represented the adult stage. As shown by comparison of isodensity lines derived from immunocytochemical reactions of whole mount retinas, the two cone types occupied complementary halves of the mouse retina with maximum density centres located in opposite retinal quadrants. We conclude that 1) in contrast to the primate retina, mouse S-cones precede the M-cones in their development, and 2) the spatial arrangements of the two cone types is maintained throughout the whole differentiation process.

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Year:  1993        PMID: 8509512     DOI: 10.1002/cne.903310411

Source DB:  PubMed          Journal:  J Comp Neurol        ISSN: 0021-9967            Impact factor:   3.215


  28 in total

1.  Retarded developmental expression and patterning of retinal cone opsins in hypothyroid mice.

Authors:  Ailing Lu; Lily Ng; Michelle Ma; Benjamin Kefas; Terry F Davies; Arturo Hernandez; Chi-Chao Chan; Douglas Forrest
Journal:  Endocrinology       Date:  2008-10-30       Impact factor: 4.736

2.  Role for Visual Experience in the Development of Direction-Selective Circuits.

Authors:  Rémi Bos; Christian Gainer; Marla B Feller
Journal:  Curr Biol       Date:  2016-05-05       Impact factor: 10.834

3.  Type 3 deiodinase, a thyroid-hormone-inactivating enzyme, controls survival and maturation of cone photoreceptors.

Authors:  Lily Ng; Arkady Lyubarsky; Sergei S Nikonov; Michelle Ma; Maya Srinivas; Benjamin Kefas; Donald L St Germain; Arturo Hernandez; Edward N Pugh; Douglas Forrest
Journal:  J Neurosci       Date:  2010-03-03       Impact factor: 6.167

4.  Transformation of cone precursors to functional rod photoreceptors by bZIP transcription factor NRL.

Authors:  Edwin C T Oh; Naheed Khan; Elena Novelli; Hemant Khanna; Enrica Strettoi; Anand Swaroop
Journal:  Proc Natl Acad Sci U S A       Date:  2007-01-22       Impact factor: 11.205

5.  Suppressing thyroid hormone signaling preserves cone photoreceptors in mouse models of retinal degeneration.

Authors:  Hongwei Ma; Arjun Thapa; Lynsie Morris; T Michael Redmond; Wolfgang Baehr; Xi-Qin Ding
Journal:  Proc Natl Acad Sci U S A       Date:  2014-02-18       Impact factor: 11.205

6.  Different patterns of retinal cone topography in two genera of rodents, Mus and Apodemus.

Authors:  A Szél; G Csorba; A R Caffé; G Szél; P Röhlich; T van Veen
Journal:  Cell Tissue Res       Date:  1994-04       Impact factor: 5.249

7.  S-opsin knockout mice with the endogenous M-opsin gene replaced by an L-opsin variant.

Authors:  Scott H Greenwald; James A Kuchenbecker; Daniel K Roberson; Maureen Neitz; Jay Neitz
Journal:  Vis Neurosci       Date:  2014-01       Impact factor: 3.241

8.  Pias3-dependent SUMOylation controls mammalian cone photoreceptor differentiation.

Authors:  Akishi Onishi; Guang-Hua Peng; Shiming Chen; Seth Blackshaw
Journal:  Nat Neurosci       Date:  2010-08-22       Impact factor: 24.884

9.  Developmental expression of thyroid hormone receptor beta2 protein in cone photoreceptors in the mouse.

Authors:  Lily Ng; Michelle Ma; Tom Curran; Douglas Forrest
Journal:  Neuroreport       Date:  2009-04-22       Impact factor: 1.837

10.  Topographical characterization of cone photoreceptors and the area centralis of the canine retina.

Authors:  Freya M Mowat; Simon M Petersen-Jones; Helen Williamson; David L Williams; Philip J Luthert; Robin R Ali; James W Bainbridge
Journal:  Mol Vis       Date:  2008-12-29       Impact factor: 2.367

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