Literature DB >> 21340602

A simple model can unify a broad range of phenomena in retinotectal map development.

Hugh D Simpson1, Geoffrey J Goodhill.   

Abstract

A paradigm model system for studying the development of patterned connections in the nervous system is the topographic map formed by retinal axons in the optic tectum/superior colliculus. Starting in the 1970s, a series of computational models have been proposed to explain map development in both normal conditions, and perturbed conditions where the retina and/or tectum/superior colliculus are altered. This stands in contrast to more recent models that have often been simpler than older ones, and tend to address more limited data sets, but include more recent genetic manipulations. The original exploration of many of the early models was one-dimensional and limited by the computational resources of the time. This leaves open the ability of these early models to explain both map development in two dimensions, and the genetic manipulation data that have only appeared more recently. In this article, we show that a two-dimensional and updated version of the XBAM model (eXtended Branch Arrow Model), first proposed in 1982, reproduces a range of surgical map manipulations not yet demonstrated by more modern models. A systematic exploration of the parameter space of this model in two dimensions also reveals richer behavior than that apparent from the original one-dimensional versions. Furthermore, we show that including a specific type of axon-axon interaction can account for the map collapse recently observed when particular receptor levels are genetically manipulated in a subset of retinal ganglion cells. Together these results demonstrate that balancing multiple influences on map development seems to be necessary to explain many biological phenomena in retinotectal map formation, and suggest important constraints on the underlying biological variables.

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Year:  2011        PMID: 21340602     DOI: 10.1007/s00422-011-0417-y

Source DB:  PubMed          Journal:  Biol Cybern        ISSN: 0340-1200            Impact factor:   2.086


  9 in total

1.  Genetic dissection of EphA receptor signaling dynamics during retinotopic mapping.

Authors:  Nicholas Bevins; Greg Lemke; Michaël Reber
Journal:  J Neurosci       Date:  2011-07-13       Impact factor: 6.167

Review 2.  A role for correlated spontaneous activity in the assembly of neural circuits.

Authors:  Lowry A Kirkby; Georgeann S Sack; Alana Firl; Marla B Feller
Journal:  Neuron       Date:  2013-12-04       Impact factor: 17.173

3.  Toward understanding the neural code of the brain.

Authors:  Christoph von der Malsburg
Journal:  Biol Cybern       Date:  2021-10       Impact factor: 2.086

4.  Regulation of ephrin-A expression in compressed retinocollicular maps.

Authors:  Tizeta Tadesse; Qi Cheng; Mei Xu; Deborah J Baro; Larry J Young; Sarah L Pallas
Journal:  Dev Neurobiol       Date:  2012-11-28       Impact factor: 3.964

5.  Retinocollicular mapping explained?

Authors:  David C Sterratt; J J Johannes Hjorth
Journal:  Vis Neurosci       Date:  2013-08-23       Impact factor: 3.241

6.  On the Importance of Countergradients for the Development of Retinotopy: Insights from a Generalised Gierer Model.

Authors:  David C Sterratt
Journal:  PLoS One       Date:  2013-06-27       Impact factor: 3.240

7.  Quantitative assessment of computational models for retinotopic map formation.

Authors:  J J Johannes Hjorth; David C Sterratt; Catherine S Cutts; David J Willshaw; Stephen J Eglen
Journal:  Dev Neurobiol       Date:  2014-11-14       Impact factor: 3.964

Review 8.  Theoretical Models of Neural Development.

Authors:  Geoffrey J Goodhill
Journal:  iScience       Date:  2018-09-27

9.  New insights on the modeling of the molecular mechanisms underlying neural maps alignment in the midbrain.

Authors:  Elise Laura Savier; James Dunbar; Kyle Cheung; Michael Reber
Journal:  Elife       Date:  2020-09-30       Impact factor: 8.140

  9 in total

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