Literature DB >> 3944621

Prenatal development of retinal ganglion cell axons: segregation into eye-specific layers within the cat's lateral geniculate nucleus.

D W Sretavan, C J Shatz.   

Abstract

The morphological changes in individual retinal ganglion cell axons associated with the formation of the eye-specific layers in the dorsal lateral geniculate nucleus (LGN) were studied during the prenatal development of the cat's visual system. Previous work has shown that the pattern of segregated eye inputs found in the adult arises from an immature state in which inputs from the two eyes are intermixed within the nucleus (Shatz, 1983). Here, this developmental process is examined at its fundamental unit of connectivity--the individual retinal ganglion cell axon. To do so, an in vitro method was used to label fetal cat optic tract axons with HRP at various times during development between embryonic day 38 (E38) and postnatal day 2 (P2) (gestation = 65 d). The results presented here are based on reconstructions of 172 axons. During the initial period of intermixing (E38-43), axons are relatively simple in morphology. Many axons studied at the earliest ages (E38) end in growth cones and have very few branches along the main axon trunk as they traverse the nucleus. By E43, the number of side branches given off along the main axon trunk has increased and most axons also have a simple terminal arbor. Over the next 2 weeks (E43-55), the majority of axons are studded with side branches and the terminal arbor is well defined. Then, between E55 and birth, axons lose their side branches and the eye-specific layers appear. By birth, nearly all axons have a smooth trunk and an elaborate terminal arbor restricted to the LGN layer appropriate to the eye of axon origin. When the number of side branches per axon was quantified, the time course of appearance and subsequent loss of side branches was found to parallel the time course of the initial intermixing of inputs and subsequent reduction in territory shared by the two eyes as determined from previous intraocular injection experiments. Our results also showed that the side branches along each axon were located primarily within LGN territory destined to be occupied by the other eye. Thus, the side branches are likely to represent a morphological substrate for the intermixing of inputs from the two eyes. These observations suggest that the segregation of eye input to the LGN involves two fundamental and simultaneous events. One event is the remodeling of the branching pattern along the length of the main axon trunk so that the side branches present early on are eliminated and the main axon trunk becomes smooth.(ABSTRACT TRUNCATED AT 400 WORDS)

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Year:  1986        PMID: 3944621      PMCID: PMC6568631     

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


  38 in total

1.  Emergence of ocular dominance columns in cat visual cortex by 2 weeks of age.

Authors:  M C Crair; J C Horton; A Antonini; M P Stryker
Journal:  J Comp Neurol       Date:  2001-02-05       Impact factor: 3.215

2.  Development of topography within song control circuitry of zebra finches during the sensitive period for song learning.

Authors:  S Iyengar; S S Viswanathan; S W Bottjer
Journal:  J Neurosci       Date:  1999-07-15       Impact factor: 6.167

3.  Dynamic regulation of cpg15 during activity-dependent synaptic development in the mammalian visual system.

Authors:  R A Corriveau; C J Shatz; E Nedivi
Journal:  J Neurosci       Date:  1999-09-15       Impact factor: 6.167

Review 4.  Molecular analysis of developmental plasticity in neocortex.

Authors:  E Nedivi
Journal:  J Neurobiol       Date:  1999-10

5.  Necessity for afferent activity to maintain eye-specific segregation in ferret lateral geniculate nucleus.

Authors:  B Chapman
Journal:  Science       Date:  2000-03-31       Impact factor: 47.728

6.  Functional requirement for class I MHC in CNS development and plasticity.

Authors:  G S Huh; L M Boulanger; H Du; P A Riquelme; T M Brotz; C J Shatz
Journal:  Science       Date:  2000-12-15       Impact factor: 47.728

7.  Development of individual axon arbors in a thalamocortical circuit necessary for song learning in zebra finches.

Authors:  Soumya Iyengar; Sarah W Bottjer
Journal:  J Neurosci       Date:  2002-02-01       Impact factor: 6.167

8.  Postnatal refinement of auditory nerve projections to the cochlear nucleus in cats.

Authors:  Patricia A Leake; Russell L Snyder; Gary T Hradek
Journal:  J Comp Neurol       Date:  2002-06-17       Impact factor: 3.215

9.  Auditory experience refines cortico-basal ganglia inputs to motor cortex via remapping of single axons during vocal learning in zebra finches.

Authors:  Vanessa C Miller-Sims; Sarah W Bottjer
Journal:  J Neurophysiol       Date:  2011-12-07       Impact factor: 2.714

10.  Ephrin-As and neural activity are required for eye-specific patterning during retinogeniculate mapping.

Authors:  Cory Pfeiffenberger; Tyler Cutforth; Georgia Woods; Jena Yamada; René C Rentería; David R Copenhagen; John G Flanagan; David A Feldheim
Journal:  Nat Neurosci       Date:  2005-07-17       Impact factor: 24.884

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