Literature DB >> 3284443

Formation of topographic maps.

S B Udin1, J W Fawcett.   

Abstract

The catalogue of data presented here form many systems demonstrates that multiple mechanisms are involved in the formation of topographic maps. We are not yet in a position to explain why a particular mechanism appears to dominate in some situations and not in others. Certain generalizations can be made, however. First, at least some form of chemospecificity can be invoked to help explain connectivity in all of the experiments we have cited. Often, the differential identities of a population of neurons can be reflected in an orderly pattern of axon outgrowth and in the actively maintained preservation of neighbor relations as the axons grow toward their targets; such orderly arrangements are not obligatory, but, where present, they facilitate the speedy establishment of orderly maps when the axons reach their target nuclei. Within a terminal zone, chemospecific cues may dominate and constrain a given axon to terminate in a specific location, but axon-axon interactions commonly supercede chemospecific matching. At least two forms of axon-axon interaction occur, one based on some sort of biochemical properties related to the axon's embryological identity and another based on the axons' electrical activity. Tasks for the future are to identify the cellular bases of each of these mechanisms and to understand the situations in which each is manifested.

Mesh:

Year:  1988        PMID: 3284443     DOI: 10.1146/annurev.ne.11.030188.001445

Source DB:  PubMed          Journal:  Annu Rev Neurosci        ISSN: 0147-006X            Impact factor:   12.449


  45 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

2.  The information content of spontaneous retinal waves.

Authors:  D A Butts; D S Rokhsar
Journal:  J Neurosci       Date:  2001-02-01       Impact factor: 6.167

3.  Mistargeting hippocampal axons by expression of a truncated Eph receptor.

Authors:  Yong Yue; Zhi-Yong Chen; Nick W Gale; Jan Blair-Flynn; Tian-Jing Hu; Xin Yue; Margaret Cooper; David P Crockett; George D Yancopoulos; Lino Tessarollo; Renping Zhou
Journal:  Proc Natl Acad Sci U S A       Date:  2002-07-17       Impact factor: 11.205

4.  Evoked pre- and post-synaptic activity in the optic tectum of the cannulated tadpole.

Authors:  E A Debski; M Constantine-Paton
Journal:  J Comp Physiol A       Date:  1990-08       Impact factor: 1.836

5.  The behavior of optic axons on substrate gradients of retinal basal lamina proteins and merosin.

Authors:  W Halfter
Journal:  J Neurosci       Date:  1996-07-15       Impact factor: 6.167

6.  Development of the tectum and diencephalon in relation to the time of arrival of the earliest optic fibres in Xenopus.

Authors:  R M Gaze; P Grant
Journal:  Anat Embryol (Berl)       Date:  1992

7.  Genes that control ray sensory neuron axon development in the Caenorhabditis elegans male.

Authors:  Lingyun Jia; Scott W Emmons
Journal:  Genetics       Date:  2006-04-19       Impact factor: 4.562

8.  Growth dynamics and morphology of regenerating optic fibers in tectum are altered by injury conditions: an in vivo imaging study in goldfish.

Authors:  Amy J Dawson; Ronald L Meyer
Journal:  Exp Neurol       Date:  2007-12-23       Impact factor: 5.330

9.  A Hebbian learning rule mediates asymmetric plasticity in aligning sensory representations.

Authors:  Ilana B Witten; Eric I Knudsen; Haim Sompolinsky
Journal:  J Neurophysiol       Date:  2008-06-04       Impact factor: 2.714

10.  Axon position within the corpus callosum determines contralateral cortical projection.

Authors:  Jing Zhou; Yunqing Wen; Liang She; Ya-Nan Sui; Lu Liu; Linda J Richards; Mu-Ming Poo
Journal:  Proc Natl Acad Sci U S A       Date:  2013-06-28       Impact factor: 11.205

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