Literature DB >> 9050787

Comparative localization of fibroblast growth factor receptor-1, -2, and -3 mRNAs in the rat brain: in situ hybridization analysis.

N Belluardo1, G Wu, G Mudo, A C Hansson, R Pettersson, K Fuxe.   

Abstract

The present study provides a detailed comparative description in the adult rat brain of areas that express mRNAs coding for the fibroblast growth factor subtype receptors 1-3 (FGFR1-3). One observation in this analysis was a widespread expression in the brain of all three FGFR mRNAs, according to the following rank order: FGFR1, diencephalon < telencephalon < mesencephalon and metencephalon < myelencephalon; FGFR2 and FGFR3, telencephalon < diencephalon < mesencephalon and metencephalon < myelencephalon. Another observation was an apparent cellular specificity in their basal expression. Thus, the FGFR1 mRNA was expressed mainly in large and weakly stained cells, whereas FGFR2 transcripts were expressed primarily in small and strongly stained cells and in cells of brain regions devoid of neuronal cells, such as the white matter. FGFR3 mRNA was always detected in small and strongly stained cells with scattered distribution and was not expressed in the white matter. However, FGFR2 mRNA was weakly expressed also in large cells localized in some nuclei of the lower brainstem, in the diagonal band, and in the septum. Furthermore, in the medial habenula and in the nuclei of the pons, there exists a high density of cells expressing both FGFR1 and FGFR2 (60-100%). With neurotoxic lesions involving 6-hydroxydopamine microinjections in the substantia nigra, reactive glial cells in the lesioned area and surrounding the cannula tract showed an increase in the expression of both FGFR1 and FGFR2 mRNAs, whereas no increased expression was found for FGFR3 mRNA. Taken together, these findings showed that these three FGF receptors exist in all subtypes of cells of each brain region. Their apparent cellular specificity suggests that these receptor subtypes can have a differential trophic role in the brain, reflecting the various biological activities shown by the ligands of the FGF family.

Entities:  

Mesh:

Substances:

Year:  1997        PMID: 9050787

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


  37 in total

1.  Fibroblast growth factor-2 promotes axon branching of cortical neurons by influencing morphology and behavior of the primary growth cone.

Authors:  G Szebenyi; E W Dent; J L Callaway; C Seys; H Lueth; K Kalil
Journal:  J Neurosci       Date:  2001-06-01       Impact factor: 6.167

Review 2.  Interactions of interleukin-1 with neurotrophic factors in the central nervous system: beneficial or detrimental?

Authors:  Wilma J Friedman
Journal:  Mol Neurobiol       Date:  2005-10       Impact factor: 5.590

3.  Distinct ontogeny of glucocorticoid and mineralocorticoid receptor and 11beta-hydroxysteroid dehydrogenase types I and II mRNAs in the fetal rat brain suggest a complex control of glucocorticoid actions.

Authors:  R Diaz; R W Brown; J R Seckl
Journal:  J Neurosci       Date:  1998-04-01       Impact factor: 6.167

4.  Basic fibroblast growth factor protects against rotenone-induced dopaminergic cell death through activation of extracellular signal-regulated kinases 1/2 and phosphatidylinositol-3 kinase pathways.

Authors:  Shih-Ling Hsuan; Heather M Klintworth; Zhengui Xia
Journal:  J Neurosci       Date:  2006-04-26       Impact factor: 6.167

Review 5.  Fibroblast growth factor signaling in the developing neuroendocrine hypothalamus.

Authors:  Pei-San Tsai; Leah R Brooks; Johanna R Rochester; Scott I Kavanaugh; Wilson C J Chung
Journal:  Front Neuroendocrinol       Date:  2010-12-01       Impact factor: 8.606

6.  Fgfr1 is required for cortical regeneration and repair after perinatal hypoxia.

Authors:  Devon M Fagel; Yosif Ganat; Elise Cheng; John Silbereis; Yasushi Ohkubo; Laura R Ment; Flora M Vaccarino
Journal:  J Neurosci       Date:  2009-01-28       Impact factor: 6.167

7.  Dysregulation of the fibroblast growth factor system in major depression.

Authors:  S J Evans; P V Choudary; C R Neal; J Z Li; M P Vawter; H Tomita; J F Lopez; R C Thompson; F Meng; J D Stead; D M Walsh; R M Myers; W E Bunney; S J Watson; E G Jones; H Akil
Journal:  Proc Natl Acad Sci U S A       Date:  2004-10-13       Impact factor: 11.205

Review 8.  The FGF-2/FGFRs neurotrophic system promotes neurogenesis in the adult brain.

Authors:  G Mudò; A Bonomo; V Di Liberto; M Frinchi; K Fuxe; Natale Belluardo
Journal:  J Neural Transm (Vienna)       Date:  2009-03-17       Impact factor: 3.575

9.  Control of precerebellar neuron development by Olig3 bHLH transcription factor.

Authors:  Zijing Liu; Hong Li; Xuemei Hu; Ling Yu; Hongbin Liu; Ruifa Han; Rita Colella; George D Mower; Yiping Chen; Mengsheng Qiu
Journal:  J Neurosci       Date:  2008-10-01       Impact factor: 6.167

10.  Fibroblast Growth Factor 2 Modulates Hypothalamic Pituitary Axis Activity and Anxiety Behavior Through Glucocorticoid Receptors.

Authors:  Natalina Salmaso; Hanna E Stevens; Jessica McNeill; Maha ElSayed; Qiuyin Ren; Maria E Maragnoli; Michael L Schwartz; Simone Tomasi; Robert M Sapolsky; Ronald Duman; Flora M Vaccarino
Journal:  Biol Psychiatry       Date:  2016-03-02       Impact factor: 13.382

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.