Literature DB >> 3719315

Synaptogenesis in the retina of the cat.

J Maslim, J Stone.   

Abstract

We have studied the development of synapses in the retina of the cat from E(embryonic day)21 to adulthood. The inner plexiform layer (IPL) could be distinguished by E36, but at this age no synapses had formed, although compact processes had formed in the IPL and membrane specialisations had developed in adjacent processes. Conventional synapses form in the IPL from E45 and become increasingly numerous and differentiated over subsequent weeks. Extracellular space and cellular debris were prominent during the formation of these synapses. The conventional synapses appear to form principally between amacrine cells until E56, when ganglion cell dendrites could be identified as postsynaptic processes. Ribbon synapses characteristic of bipolar cells were identified around birth, suggesting that bipolar cells do not form synapses until that age. The outer plexiform layer (OPL) could be distinguished in central retina at E56. Extracellular space, debris of degenerating cells and mounds of agranular vesicles were prominent at this age but synapses were not observed until E59, when cone pedicles formed ribbon synapses onto horizontal cell processes. The first synapses clearly formed by spherules, also onto horizontal cells, were seen at E62. The central process of the postsynaptic triad, considered to be the dendrite of a bipolar cell, was first observed in both cone pedicles and rod spherules around birth, again suggesting that bipolar cells do not enter into synaptic arrangements until that age. Synaptogenesis in the OPL shows a strong centro-peripheral gradient; its initial stages were observed centrally in the late E50's but synapse formation was not complete in the retinal periphery until P(postnatal day)7 or later. We could not detect a centro-peripheral gradient in the formation of conventional synapses in the IPL, but the formation of ribbon synapses in this layer began centrally at birth and in the mid-periphery at P5. In summary, the first synapses to form in the retina are those which spread information laterally within the plexiform layers, between amacrine cells and from receptor to horizontal cells. The cells which carry information centrally, in particular bipolar cells, enter into synaptic arrangements considerably later. Further, retinal cells seem to form synapses in a distinct sequence: first amacrines, then receptors and lastly bipolar cells.

Entities:  

Mesh:

Year:  1986        PMID: 3719315     DOI: 10.1016/0006-8993(86)90313-6

Source DB:  PubMed          Journal:  Brain Res        ISSN: 0006-8993            Impact factor:   3.252


  15 in total

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3.  Synapses of the inner plexiform layer of the area centralis of kitten retina during postnatal development: a quantitative study.

Authors:  J Crooks; J D Morrison
Journal:  J Anat       Date:  1989-04       Impact factor: 2.610

4.  Segregation of on and off bipolar cell axonal arbors in the absence of retinal ganglion cells.

Authors:  E Günhan-Agar; D Kahn; L M Chalupa
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Review 5.  Functional architecture of the retina: development and disease.

Authors:  Mrinalini Hoon; Haruhisa Okawa; Luca Della Santina; Rachel O L Wong
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6.  Retinal ganglion beta cells project transiently to the superior colliculus during development.

Authors:  A S Ramoa; G Campbell; C J Shatz
Journal:  Proc Natl Acad Sci U S A       Date:  1989-03       Impact factor: 11.205

7.  The role of GABA during development of the outer retina in the rabbit.

Authors:  E K Messersmith; D A Redburn
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8.  Immunohistological studies of metabotropic glutamate receptor subtype 6-deficient mice show no abnormality of retinal cell organization and ganglion cell maturation.

Authors:  Y Tagawa; H Sawai; Y Ueda; M Tauchi; S Nakanishi
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9.  Shank 2 expression coincides with neuronal differentiation in the developing retina.

Authors:  Jeong Hun Kim; Jin Hyoung Kim; Esther Yang; Jae Hwan Park; Young Suk Yu; Kyu Won Kim
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10.  NADPH-diaphorase reactivity in adult and developing cat retinae.

Authors:  T M Vaccaro; M D Cobcroft; J M Provis; J Mitrofanis
Journal:  Cell Tissue Res       Date:  1991-08       Impact factor: 5.249

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