Literature DB >> 19288186

Brn-3a deficiency transiently increases expression of calbindin D-28 k and calretinin in the trigeminal ganglion during embryonic development.

Hiroyuki Ichikawa1, Ruji Terayama, Tomoichiro Yamaai, David M Jacobowitz, Feng Qiu, Mengging Xiang, Tomosada Sugimoto.   

Abstract

Immunohistochemistry for neuron-specific nuclear protein (NeuN), caspase-3, calcitonin gene-related peptide (CGRP), and calcium-binding proteins was performed on the trigeminal ganglion (TG) in wild type and Brn-3a knockout mice at embryonic days 12.5-16.5 (E12.5-E16.5). In Brn-3a knockout mice, the number of NeuN-immunoreactive (ir) neuron profiles increased at E14.5 (40.0% increase) and decreased at E16.5 (28.3% reduction) compared to wild type mice. Caspase-3-ir neuron profiles were abundant in the TG of wild type mice at E12.5-E16.5. However, the loss of Brn-3a decreased the number of caspase-3-ir neuron profiles at E12.5 (69.7% reduction) and E14.5 (51.7% reduction). At E16.5, the distribution of caspase-3-ir neuron profiles was barely affected by the deficiency. CGRP-ir neuron profiles were observed in the TG of wild type mice but not knockout mice at E12.5. At E14.5 and E16.5, CGRP-ir neuron profiles were abundant in both wild type and knockout mice. Calbindin D-28 k (CB)-ir neuron profiles decreased in the TG of mutant mice at E12.5 compared to wild type mice (56.4% reduction). At E14.5, however, Brn-3a deficiency transiently increased CB-ir neuron profiles (169.4% increase as compared to wild type mice). Calretinin (CR)-ir neuron profiles could not be detected in the TG of wild type mice at E12.5-16.5. However, numerous CR-ir neuron profiles transiently appeared in the knockout mouse at E14.5. Parvalbumin (PV)-ir neurons appeared in wild type and knockout mice at E14.5. At this stage, the number of large (>50 mum(2)) PV-ir neuron profiles in knockout mice was fewer than that in wild type mice. The number and cell size of PV-ir neuron profiles were barely affected by the deficiency at E16.5. The present study indicates that the loss of Brn-3a causes increase of TG neurons at E14.5 and decrease of TG neurons at E16.5. It is also suggested that Brn-3a deficiency affects the number and cell size of CGRP- and calcium-binding protein-containing neurons at E12.5 and E14.5. Caspase-3-dependent cell death of CB- and CR-ir neurons may be suppressed by the deficiency at E14.5.

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Year:  2009        PMID: 19288186     DOI: 10.1007/s10571-009-9383-5

Source DB:  PubMed          Journal:  Cell Mol Neurobiol        ISSN: 0272-4340            Impact factor:   5.046


  15 in total

1.  Induction of activated caspase-3-immunoreactivity and apoptosis in the trigeminal ganglion neurons by neonatal peripheral nerve injury.

Authors:  Tomosada Sugimoto; Haiwei Jin; Masako Fijita; Tomohiro Fukunaga; Noriyuki Nagaoka; Tomoichiro Yamaai; Hiroyuki Ichikawa
Journal:  Brain Res       Date:  2004-08-13       Impact factor: 3.252

2.  Peptidergic innervation of the temporomandibular disk in the rat.

Authors:  H Ichikawa; S Wakisaka; S Matsuo; M Akai
Journal:  Experientia       Date:  1989-03-15

Review 3.  The Brn-3a transcription factor.

Authors:  D S Latchman
Journal:  Int J Biochem Cell Biol       Date:  1998-11       Impact factor: 5.085

4.  Requirement for Brn-3.0 in differentiation and survival of sensory and motor neurons.

Authors:  R J McEvilly; L Erkman; L Luo; P E Sawchenko; A F Ryan; M G Rosenfeld
Journal:  Nature       Date:  1996-12-12       Impact factor: 49.962

5.  The Brn-3a transcription factor induces neuronal process outgrowth and the coordinate expression of genes encoding synaptic proteins.

Authors:  M D Smith; S J Dawson; D S Latchman
Journal:  Mol Cell Biol       Date:  1997-01       Impact factor: 4.272

6.  Coordinate induction of the three neurofilament genes by the Brn-3a transcription factor.

Authors:  M D Smith; P J Morris; S J Dawson; M L Schwartz; W W Schlaepfer; D S Latchman
Journal:  J Biol Chem       Date:  1997-08-22       Impact factor: 5.157

7.  Coordinated regulation of gene expression by Brn3a in developing sensory ganglia.

Authors:  S Raisa Eng; Jason Lanier; Natalia Fedtsova; Eric E Turner
Journal:  Development       Date:  2004-07-14       Impact factor: 6.868

8.  Defects in sensory axon growth precede neuronal death in Brn3a-deficient mice.

Authors:  S R Eng; K Gratwick; J M Rhee; N Fedtsova; L Gan; E E Turner
Journal:  J Neurosci       Date:  2001-01-15       Impact factor: 6.167

9.  Bcl-2 transcription from the proximal P2 promoter is activated in neuronal cells by the Brn-3a POU family transcription factor.

Authors:  M D Smith; E A Ensor; R S Coffin; L M Boxer; D S Latchman
Journal:  J Biol Chem       Date:  1998-07-03       Impact factor: 5.157

10.  The Brn-3 family of POU-domain factors: primary structure, binding specificity, and expression in subsets of retinal ganglion cells and somatosensory neurons.

Authors:  M Xiang; L Zhou; J P Macke; T Yoshioka; S H Hendry; R L Eddy; T B Shows; J Nathans
Journal:  J Neurosci       Date:  1995-07       Impact factor: 6.167

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  1 in total

1.  Genetic interplay between transcription factor Pou4f1/Brn3a and neurotrophin receptor Ret in retinal ganglion cell type specification.

Authors:  Vladimir Vladimirovich Muzyka; Tudor Constantin Badea
Journal:  Neural Dev       Date:  2021-09-21       Impact factor: 3.842

  1 in total

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