Literature DB >> 2995601

Evidence for shifting connections during development of the chick retinotectal projection.

S C McLoon.   

Abstract

The pattern in which optic axons invade the tectum and begin synaptogenesis was studied in the chick. The anterogradely transported marker, horseradish peroxidase, was injected into one eye of embryos between 5 and 16 days of development (E5 to E16). This labeled the optic axons in the brain. The first retinal axons arrived in the most superficial lamina of the tectum on E6. They entered the tectum at the rostroventral margin. During the next 6 days of development the axons grew over the tectal surface. First they filled the rostral tectum, the oldest portion of the tectum, and then they spread to the caudal pole. Shortly after the first axons entered the tectum on E6, labeled retinal axons were found penetrating from the surface into deeper tectal layers. In any given area of the tectum, optic axons were seen penetrating deeper layers shortly after arriving in that area. Electron microscopic examination showed that at least some of the labeled axons in rostral tectum formed synapses with tectal cells by E7. These results show two things which contrast with results from previous studies. First, there is no delay between the time the retinal axons enter the tectum and the time they penetrate into synaptic layers of the tectum. Second, the first retinotectal connections are formed in rostral tectum and not central tectum. Retrograde tracing showed the first optic axons that arrived in the tectum were from ganglion cells in central retina. Previous studies have shown that the ganglion cells of central retina project to the central tectum in the mature chick. This opens the possibility that the optic axons from central retina, which connect to rostral tectum in the young embryo, shift their connections to central tectum during subsequent development. As they enter the tectum the growth cones of retinal axons appear to be associated with the external limiting membrane. During the time that connections would begin to shift in the tectum a second population of axons appears at the bottom of stratum opticum, some with characteristics of growth cones. This late-appearing population may represent axons shifting their connections. These results have implications for theories on how the retinotopic pattern of retinotectal connections develops.

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Year:  1985        PMID: 2995601      PMCID: PMC6565133     

Source DB:  PubMed          Journal:  J Neurosci        ISSN: 0270-6474            Impact factor:   6.167


  9 in total

1.  The initial stages of development of the retinocollicular projection in the wallaby (Macropus eugenii): distribution of ganglion cells in the retina and their axons in the superior colliculus.

Authors:  Y Ding; L R Marotte
Journal:  Anat Embryol (Berl)       Date:  1996-09

2.  Retroviral misexpression of engrailed genes in the chick optic tectum perturbs the topographic targeting of retinal axons.

Authors:  G C Friedman; D D O'Leary
Journal:  J Neurosci       Date:  1996-09-01       Impact factor: 6.167

3.  Spatio-temporal pattern of neuronal differentiation in the Drosophila visual system: A user's guide to the dynamic morphology of the developing optic lobe.

Authors:  Kathy T Ngo; Ingrid Andrade; Volker Hartenstein
Journal:  Dev Biol       Date:  2017-05-19       Impact factor: 3.582

4.  Stabilization of growing retinal axons by the combined signaling of nitric oxide and brain-derived neurotrophic factor.

Authors:  A F Ernst; G Gallo; P C Letourneau; S C McLoon
Journal:  J Neurosci       Date:  2000-02-15       Impact factor: 6.167

5.  Transformations of the retinal topography along the visual pathway of the chicken.

Authors:  U Rager; G Rager; A Kabiersch
Journal:  Anat Embryol (Berl)       Date:  1988

6.  In vitro guidance of retinal axons by a tectal lamina-specific glycoprotein Nel.

Authors:  Yulan Jiang; Hiroya Obama; Soh Leh Kuan; Ritsuko Nakamura; Chizu Nakamoto; Zhufeng Ouyang; Masaru Nakamoto
Journal:  Mol Cell Neurosci       Date:  2009-02-26       Impact factor: 4.314

7.  Neuronal specificity of the alpha 7 nicotinic acetylcholine receptor promoter develops during morphogenesis of the central nervous system.

Authors:  L Matter-Sadzinski; M C Hernandez; T Roztocil; M Ballivet; J M Matter
Journal:  EMBO J       Date:  1992-12       Impact factor: 11.598

8.  Expression of neuronal nicotinic acetylcholine receptor genes in the developing chick visual system.

Authors:  J M Matter; L Matter-Sadzinski; M Ballivet
Journal:  EMBO J       Date:  1990-04       Impact factor: 11.598

9.  Overexpression of a neural-specific rho family GTPase, cRac1B, selectively induces enhanced neuritogenesis and neurite branching in primary neurons.

Authors:  C Albertinazzi; D Gilardelli; S Paris; R Longhi; I de Curtis
Journal:  J Cell Biol       Date:  1998-08-10       Impact factor: 10.539

  9 in total

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