Literature DB >> 7615874

Basal expression of the inducible transcription factors c-Jun, JunB, JunD, c-Fos, FosB, and Krox-24 in the adult rat brain.

T Herdegen1, K Kovary, A Buhl, R Bravo, M Zimmermann, P Gass.   

Abstract

Jun, Fos, and Krox proteins are inducible transcription factors contributing to the control of gene expression. The elucidation of their individual expression patterns in the nervous system provides new insights into the ability of neurons to react with changes of gene expression to external stimulation under physiological or pathological conditions. The expression of c-Jun, JunB, JunD, c-Fos, FosB, and Krox-24 was investigated in the brain of untreated male Sprague-Dawley and female BDIX rats by immunocytochemistry using specific antibodies. JunD immunoreactivity (IR) labeled the highest number of neurons, being present in almost all neurons of the brain. JunD was expressed at high levels in those areas that also exhibit c-Jun, JunB, c-Fos, and FosB-IR, such as locus coeruleus, periolivary nuclei (ncl.), pontine and central gray, lateral lemniscal ncl., inferior and superior colliculi, leaflet of geniculate ncl., midline nuclei of thalamus, dorsomedial and paraventricular ncl. of hypothalamus, ncl. supraopticus, dorsolateral part of caudate putamen and lateral septal ncl. In contrast to the high number of JunD-positive neurons, c-Jun, JunB, c-Fos, and FosB proteins were detected in rather low numbers of neurons in these brain areas; the rank of the number of immunopositive neurons was c-Fos > JunB > c-Jun > FosB. Particularly high levels of expression were observed for c-Jun in medullary motoneurons, medial geniculate ncl., arcuate ncl., and dentate gyrus, and for JunB in the CA-1 area of the hippocampus and islands of Calleja. The zinc finger protein Krox-24 was expressed in many neurons of these brain areas, with only discrete Jun- and Fos-IR; additionally, many intensely labeled nuclei were present in spinal ncl. of the trigeminal ventromedial ncl. of the hypothalamus and the CA-1 area of the hippocampus. In the cerebellum, nuclear labeling was detected only for c-Jun, JunD, and Krox-24 in granule cells. JunD-IR was also found in glial cells of gray matter and fiber tracts, whereas glial c-Jun-IR was observed only in fiber tracts. Apart from a weak JunD-IR, some areas did not express Jun, Fos, and Krox proteins such as cuneate and gracile ncl., venterobasal complex of thalamus, globus pallidum, and Purkinje cells of the cerebellum. Our data indicate that inducible transcription factors of the fos, jun, and krox gene families show patterns of individual expression in untreated animals, thereby reflecting different mechanisms and/or thresholds for induction under physiological conditions.

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Year:  1995        PMID: 7615874     DOI: 10.1002/cne.903540105

Source DB:  PubMed          Journal:  J Comp Neurol        ISSN: 0021-9967            Impact factor:   3.215


  23 in total

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Authors:  Mei Wu; Ming Tang; Dirk Adriaensen; Inge Depoortere; Theo L Peeters; Jean-Pierre Timmermans
Journal:  Histochem Cell Biol       Date:  2005-02-16       Impact factor: 4.304

Review 2.  Drugs of abuse and immediate-early genes in the forebrain.

Authors:  R E Harlan; M M Garcia
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3.  Retrograde regulation of growth-associated gene expression in adult rat Purkinje cells by myelin-associated neurite growth inhibitory proteins.

Authors:  M Zagrebelsky; A Buffo; A Skerra; M E Schwab; P Strata; F Rossi
Journal:  J Neurosci       Date:  1998-10-01       Impact factor: 6.167

4.  Do centrally administered neuropeptides access cognate receptors?: an analysis in the central corticotropin-releasing factor system.

Authors:  J C Bittencourt; P E Sawchenko
Journal:  J Neurosci       Date:  2000-02-01       Impact factor: 6.167

5.  Changing and shielded magnetic fields suppress c-Fos expression in the navigation circuit: input from the magnetosensory system contributes to the internal representation of space in a subterranean rodent.

Authors:  Tomás Burger; Marcela Lucová; Regina E Moritz; Helmut H A Oelschläger; Rastislav Druga; Hynek Burda; Wolfgang Wiltschko; Roswitha Wiltschko; Pavel Nemec
Journal:  J R Soc Interface       Date:  2010-03-10       Impact factor: 4.118

6.  Effect of acute and chronic bilateral visual deafferentation on c-Fos immunoreactivity in the visual system of adult rats.

Authors:  Rhea Wiedmann; Steffen K Rosahl; Thomas Brinker; Madjid Samii; Makoto Nakamura
Journal:  Exp Brain Res       Date:  2013-07-06       Impact factor: 1.972

7.  Cyclophosphamide cystitis as a model of visceral pain in rats: minor effects at mesodiencephalic levels as revealed by the expression of c-fos, with a note on Krox-24.

Authors:  K Bon; M Lantéri-Minet; J de Pommery; J F Michiels; D Menétrey
Journal:  Exp Brain Res       Date:  1997-02       Impact factor: 1.972

8.  Regulation of c-fos, c-jun and c-myc gene expression by angiotensin II in primary cultured rat astrocytes: role of ERK1/2 MAP kinases.

Authors:  Jimmy Delaney; Roselynn Chiarello; David Villar; Umadevi Kandalam; Ana Maria Castejon; Michelle A Clark
Journal:  Neurochem Res       Date:  2007-09-01       Impact factor: 3.996

9.  Importance of ERK activation in behavioral and biochemical effects induced by MDMA in mice.

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Journal:  Br J Pharmacol       Date:  2003-09-29       Impact factor: 8.739

10.  Expression of the c-fos transcription factor in the rat auditory pathway following postnatal auditory deprivation.

Authors:  A Keilmann; T Herdegen
Journal:  Eur Arch Otorhinolaryngol       Date:  1995       Impact factor: 2.503

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