Literature DB >> 3772437

Quantitative correlation between barrel-field size and the sensory innervation of the whiskerpad: a comparative study in six strains of mice bred for different patterns of mystacial vibrissae.

E Welker, H Van der Loos.   

Abstract

In mice from 6 strains bred for different patterns of mystacial vibrissae, we studied the consequences of the presence of supernumerary whiskers for the sensory innervation of the vibrissal follicles and their cortical representation in the barrel field. The parameters were number of axons innervating individual vibrissal follicles, tangential area of individual barrels, and thickness of the layers in the barrel cortex. These parameters are highly constant for animals within a strain but may differ greatly between strains. For all strains, the innervation of a follicle depends on its position on the whiskerpad, the highest innervation density being at the posterolateral corner. This matches the wave of development that travels over this part of the face during embryogenesis. Although large differences exist between strains in the number of axons innervating the whiskerpad, the relative number of axons innervating the "standard" follicles of 1 row is remarkably constant. The thickness of the barrel cortex increases from posteromedial to anterolateral for all strains. This increase is due to variations in thickness of the cortical output layers (II and III, V and VI). For individual barrel-follicle pairs, we calculated the ratio between cortical barrel area and axon number. The major findings were that supernumerary follicles are innervated and, given a threshold number of axons, represented by barrels; barrel area per peripheral axon differs between follicles within a row and is highest for the supernumerary elements; and for each strain there is a direct, linear correlation between axon number and barrel size, which differs significantly among certain, but not all, strains. The data allowed us tentatively to define some of the factors that play a role in the formation of brain maps and pointed to the existence of major genetic differences between mouse strains with respect to these factors.

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Mesh:

Year:  1986        PMID: 3772437      PMCID: PMC6568481     

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


  52 in total

Review 1.  Neural activity: sculptor of 'barrels' in the neocortex.

Authors:  R S Erzurumlu; P C Kind
Journal:  Trends Neurosci       Date:  2001-10       Impact factor: 13.837

Review 2.  Somatosensory cortical plasticity: recruiting silenced barrels by active whiskers.

Authors:  Reha S Erzurumlu
Journal:  Exp Neurol       Date:  2003-12       Impact factor: 5.330

Review 3.  The barrel cortex--integrating molecular, cellular and systems physiology.

Authors:  Carl C H Petersen
Journal:  Pflugers Arch       Date:  2003-09-19       Impact factor: 3.657

4.  Time course of embryonic midbrain and thalamic auditory connection development in mice as revealed by carbocyanine dye tracing.

Authors:  Bina Gurung; Bernd Fritzsch
Journal:  J Comp Neurol       Date:  2004-11-15       Impact factor: 3.215

Review 5.  The sense of touch in the star-nosed mole: from mechanoreceptors to the brain.

Authors:  Kenneth C Catania
Journal:  Philos Trans R Soc Lond B Biol Sci       Date:  2011-11-12       Impact factor: 6.237

Review 6.  Development and critical period plasticity of the barrel cortex.

Authors:  Reha S Erzurumlu; Patricia Gaspar
Journal:  Eur J Neurosci       Date:  2012-05       Impact factor: 3.386

7.  Precision mapping of the vibrissa representation within murine primary somatosensory cortex.

Authors:  Per M Knutsen; Celine Mateo; David Kleinfeld
Journal:  Philos Trans R Soc Lond B Biol Sci       Date:  2016-10-05       Impact factor: 6.237

8.  Plasticity in the barrel cortex of the adult mouse: effects of peripheral deprivation on GAD-immunoreactivity.

Authors:  E Welker; E Soriano; H Van der Loos
Journal:  Exp Brain Res       Date:  1989       Impact factor: 1.972

9.  Continuous spike-waves during slow-wave sleep in a mouse model of focal cortical dysplasia.

Authors:  Qian-Quan Sun; Chen Zhou; Weiguo Yang; Daniel Petrus
Journal:  Epilepsia       Date:  2016-08-16       Impact factor: 5.864

10.  EphA4 is necessary for spatially selective peripheral somatosensory topography.

Authors:  H A North; A Karim; M F Jacquin; M J Donoghue
Journal:  Dev Dyn       Date:  2010-02       Impact factor: 3.780

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