Literature DB >> 474443

Subdivision of mouse vibrissae on an embryological basis, with descriptions of variations in the number and arrangement of sinus hairs and cortical barrels in BALB/c (nu/+; nude, nu/nu) and hairless (hr/hr) strains.

M Yamakado, T Yohro.   

Abstract

Development of vibrissae was studied in dd/y mouse embryos by scanning electron microscopy. Arrangement of vibrissae and cortical barrels were also studied by light microscopy in adult dd/y, BALB/c(nu/+), nude (BALB/c, nu/nu) and hairless (hr/hr) mice to find genetic or epigenetic variations. Rudiments of vibrissae first appear on Day 12 of pregnancy as longitudinal ridges on the developing muzzle, and each hair rudiment is represented by a dome on the ridges. The dorsal two rows (A and B; Woolsey and Van der Loos, '70) of mystacial vibrissae are on the lateral nasal prominence, while the ventral three (C, D and E) are on the maxillary prominence. Smaller hairs of mystacial vibrissae appear at the labial part of the maxillary prominenceon Day 13. The rudiments of rhinal hairs also appear at this stage on the part of the muzzle derived from the medial nasal prominence. Thus the so-called mystacial vibrissae should be subdivided into three (or 4, including the rhinal) groups on an embryological basis. They are the lateral nasal, the maxillary and the labial. A supernumerary sinus hair and a corresponding barrel was observed between D and C rows uni-or bilaterally in one third of individuals of BALB/c, nude and hairless mice. It is suggested that supernumerary hairs tend to occur between the groups of hairs as defined above. In nude and hairless mice small barrels representing labial hairs are diminished in number. The number of hair follicles, however, is normal.

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Year:  1979        PMID: 474443     DOI: 10.1002/aja.1001550202

Source DB:  PubMed          Journal:  Am J Anat        ISSN: 0002-9106


  13 in total

1.  Vibrissae-evoked behavior and conditioning before functional ontogeny of the somatosensory vibrissae cortex.

Authors:  M S Landers; R M Sullivan
Journal:  J Neurosci       Date:  1999-06-15       Impact factor: 6.167

2.  Characterizing the functional significance of the neonatal rat vibrissae prior to the onset of whisking.

Authors:  Regina M Sullivan; Margo S Landers; Jennifer Flemming; Cara Vaught; Theresa A Young; H Jonathan Polan
Journal:  Somatosens Mot Res       Date:  2003       Impact factor: 1.111

Review 3.  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

Review 4.  Molecular determinants of the face map development in the trigeminal brainstem.

Authors:  Reha S Erzurumlu; Zhou-Feng Chen; Mark F Jacquin
Journal:  Anat Rec A Discov Mol Cell Evol Biol       Date:  2006-02

Review 5.  The role of vibrissae in behavior: a status review.

Authors:  A S Ahl
Journal:  Vet Res Commun       Date:  1986-07       Impact factor: 2.459

6.  Target-derived influences on axon growth modes in cultures of trigeminal neurons.

Authors:  R S Erzurumlu; S Jhaveri; H Takahashi; R D McKay
Journal:  Proc Natl Acad Sci U S A       Date:  1993-08-01       Impact factor: 11.205

7.  From sensory periphery to cortex: the architecture of the barrelfield as modified by various early manipulations of the mouse whiskerpad.

Authors:  F L Andrés; H Van der Loos
Journal:  Anat Embryol (Berl)       Date:  1985

8.  A spatial relationship between innervation and the early differentiation of vibrissa follicles in the embryonic mouse.

Authors:  R J Van Exan; M H Hardy
Journal:  J Anat       Date:  1980-12       Impact factor: 2.610

9.  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

10.  Developmental pattern of axonal pathways in the house shrew maxillary nerve.

Authors:  K Yasui; R Arakaki; M Uemura; S Tanaka
Journal:  Anat Embryol (Berl)       Date:  1996-09
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