Literature DB >> 8047886

Control of topographic retinal axon branching by inhibitory membrane-bound molecules.

A L Roskies1, D D O'Leary.   

Abstract

Retinotopic map development in nonmammalian vertebrates appears to be controlled by molecules that guide or restrict retinal axons to correct locations in their targets. However, the retinotopic map in the superior colliculus (SC) of the rat is developed instead by a topographic bias in collateral branching and arborization. Temporal retinal axons extending across alternating membranes from the topographically correct rostral SC or the incorrect caudal SC of embryonic rats preferentially branch on rostral membranes. Branching preference is due to an inhibitory phosphatidylinositol-linked molecule in the caudal SC. Thus, position-encoding membrane-bound molecules may establish retinotopic maps in mammals by regulating axon branching, not by directing axon growth.

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Year:  1994        PMID: 8047886     DOI: 10.1126/science.8047886

Source DB:  PubMed          Journal:  Science        ISSN: 0036-8075            Impact factor:   47.728


  23 in total

1.  Topological specificity in reinnervation of the superior colliculus by regenerated retinal ganglion cell axons in adult hamsters.

Authors:  Y Sauvé; H Sawai; M Rasminsky
Journal:  J Neurosci       Date:  2001-02-01       Impact factor: 6.167

Review 2.  Reading of concentration gradients by axonal growth cones.

Authors:  J Löschinger; F Weth; F Bonhoeffer
Journal:  Philos Trans R Soc Lond B Biol Sci       Date:  2000-07-29       Impact factor: 6.237

3.  Morphology and growth patterns of developing thalamocortical axons.

Authors:  I Skaliora; R Adams; C Blakemore
Journal:  J Neurosci       Date:  2000-05-15       Impact factor: 6.167

4.  Topographic-specific axon branching controlled by ephrin-As is the critical event in retinotectal map development.

Authors:  P A Yates; A L Roskies; T McLaughlin; D D O'Leary
Journal:  J Neurosci       Date:  2001-11-01       Impact factor: 6.167

5.  Neurite branching on deformable substrates.

Authors:  Lisa A Flanagan; Yo-El Ju; Beatrice Marg; Miriam Osterfield; Paul A Janmey
Journal:  Neuroreport       Date:  2002-12-20       Impact factor: 1.837

6.  Loss-of-function analysis of EphA receptors in retinotectal mapping.

Authors:  David A Feldheim; Masaru Nakamoto; Miriam Osterfield; Nicholas W Gale; Thomas M DeChiara; Rajat Rohatgi; George D Yancopoulos; John G Flanagan
Journal:  J Neurosci       Date:  2004-03-10       Impact factor: 6.167

7.  Brain-derived neurotrophic factor and neurotrophin-4/5 stimulate growth of axonal branches from regenerating retinal ganglion cells.

Authors:  H Sawai; D B Clarke; P Kittlerova; G M Bray; A J Aguayo
Journal:  J Neurosci       Date:  1996-06-15       Impact factor: 6.167

8.  Development of functional topography in the corticorubral projection: An in vivo assessment using synaptic potentials recorded from fetal and newborn cats.

Authors:  W J Song; F Murakami
Journal:  J Neurosci       Date:  1998-11-15       Impact factor: 6.167

9.  Regulation of topographic projection in the brain: Elf-1 in the hippocamposeptal system.

Authors:  P P Gao; J H Zhang; M Yokoyama; B Racey; C F Dreyfus; I B Black; R Zhou
Journal:  Proc Natl Acad Sci U S A       Date:  1996-10-01       Impact factor: 11.205

10.  Interstitial branches develop from active regions of the axon demarcated by the primary growth cone during pausing behaviors.

Authors:  G Szebenyi; J L Callaway; E W Dent; K Kalil
Journal:  J Neurosci       Date:  1998-10-01       Impact factor: 6.167

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