Literature DB >> 8330536

Differential reaction of crossing and non-crossing rat retinal axons on cell membrane preparations from the chiasm midline: an in vitro study.

A Wizenmann1, S Thanos, Y von Boxberg, F Bonhoeffer.   

Abstract

In the rat, a small subpopulation of retinal ganglion cell axons forms a persistent projection to the ipsilateral half of the brain. These fibres originate almost exclusively from the ventrotemporal margin of the retina. In contrast to all other retinal axons they seem to be deflected from the midline of the optic chiasm and thereby led into the ipsilateral optic tract. In order to analyse the interactions between growing fibres and chiasm midline, we have developed the following in vitro model. Axons of the embryonic rat retina are grown on a carpet of tectal cell membranes used as a general growth-permissive substratum. At a certain distance from the explant (200-450 microns), the advancing fibres are confronted with two stripes of cell membranes prepared from the chiasm midline. Such chiasm membranes are shown to act as a barrier for the presumptive non-crossing axons, while they do not influence growth of fibres originating from any other regions of the retina, including the dorsotemporal part. The repulsion of non-crossing fibres by chiasm membranes is observed in vitro only when retinal explants from embryonic day (E) 17/18 and chiasm preparations from E14/15 are used. Fibres and tissue from different regions of the brain as well as from different developmental ages, and even from different species, can be combined in this assay system. In a first attempt to characterize the molecular basis of the repulsive effect of chiasm membranes on ventrotemporal fibres, similar assays were performed with membranes derived from other regions of the central nervous system midline, some of which are known to have repulsive properties against certain axon populations. Since these cell membranes did not act as a barrier for the ventrotemporal retinal axons, we suggest that the guidance cues at the chiasm are very specific. Our results are consistent with the hypothesis that certain cells at the chiasm midline (very likely radial glial cells) express 'repulsive or inhibitory' molecules, which act in a specific way on ipsilaterally projecting axons.

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Year:  1993        PMID: 8330536     DOI: 10.1242/dev.117.2.725

Source DB:  PubMed          Journal:  Development        ISSN: 0950-1991            Impact factor:   6.868


  14 in total

1.  Genesis, neurotrophin responsiveness, and apoptosis of a pronounced direct connection between the two eyes of the chick embryo: a natural error or a meaningful developmental event?

Authors:  S Thanos
Journal:  J Neurosci       Date:  1999-05-15       Impact factor: 6.167

2.  Embryonic neurons of the developing optic chiasm express L1 and CD44, cell surface molecules with opposing effects on retinal axon growth.

Authors:  D W Sretavan; L Feng; E Puré; L F Reichardt
Journal:  Neuron       Date:  1994-05       Impact factor: 17.173

3.  A role for tectal midline glia in the unilateral containment of retinocollicular axons.

Authors:  D Y Wu; G E Schneider; J Silver; M Poston; S Jhaveri
Journal:  J Neurosci       Date:  1998-10-15       Impact factor: 6.167

4.  Randomized retinal ganglion cell axon routing at the optic chiasm of GAP-43-deficient mice: association with midline recrossing and lack of normal ipsilateral axon turning.

Authors:  D W Sretavan; K Kruger
Journal:  J Neurosci       Date:  1998-12-15       Impact factor: 6.167

Review 5.  Axonal commissures in the central nervous system: how to cross the midline?

Authors:  Homaira Nawabi; Valérie Castellani
Journal:  Cell Mol Life Sci       Date:  2011-05-03       Impact factor: 9.261

6.  The ganglionic eminence may be an intermediate target for corticofugal and thalamocortical axons.

Authors:  C Métin; P Godement
Journal:  J Neurosci       Date:  1996-05-15       Impact factor: 6.167

7.  Ephrin-B regulates the Ipsilateral routing of retinal axons at the optic chiasm.

Authors:  S Nakagawa; C Brennan; K G Johnson; D Shewan; W A Harris; C E Holt
Journal:  Neuron       Date:  2000-03       Impact factor: 17.173

8.  Organization of pioneer retinal axons within the optic tract of the rhesus monkey.

Authors:  C Meissirel; L M Chalupa
Journal:  Proc Natl Acad Sci U S A       Date:  1994-04-26       Impact factor: 11.205

9.  Changing patterns of peanut agglutinin labelling in the dorsal cochlear nucleus correspond to axonal ingrowth.

Authors:  G H Riggs; L Schweitzer
Journal:  J Anat       Date:  1994-10       Impact factor: 2.610

10.  The winged helix transcription factor Foxg1 facilitates retinal ganglion cell axon crossing of the ventral midline in the mouse.

Authors:  Thomas Pratt; Natasha M M-L Tian; T Ian Simpson; John O Mason; David J Price
Journal:  Development       Date:  2004-07-07       Impact factor: 6.868

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