Literature DB >> 10779704

Interferon-gamma-responsive neuronal sites in the normal rat brain: receptor protein distribution and cell activation revealed by Fos induction.

B Robertson1, G Kong, Z Peng, M Bentivoglio, K Kristensson.   

Abstract

Constitutive expression of the interferon-gamma receptor protein (IFN-gammaR), and the distribution of cells in which Fos, a marker of cell activation, is induced by intracerebroventricular administration of IFN-gamma, were studied in the rat brain by immunohistochemistry. IFN-gammaR immunopositivity was found in neuronal elements, which exhibited a selective distribution being concentrated in the piriform and entorhinal cortex, midline thalamus and medial hypothalamic structures, brainstem nociceptive relays (including the periaqueductal gray, the parabrachial nuclei and the caudal part of the spinal trigeminal nuclei), and circumventricular organs such as the median eminence and area postrema. IFN-gamma-induced Fos expression mostly corresponded to neuronal sites of receptor distribution. Because of its topographical distribution, it is suggested that activation of the IFN-gammaR in neurons may play a role to limit spread of infections in the brain and, in concert with other proinflammatory cytokines, to modulate adaptive responses to an antigen challenge mediated by the central nervous system.

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Year:  2000        PMID: 10779704     DOI: 10.1016/s0361-9230(00)00240-9

Source DB:  PubMed          Journal:  Brain Res Bull        ISSN: 0361-9230            Impact factor:   4.077


  11 in total

1.  Gamma interferon-dependent, noncytolytic clearance of sindbis virus infection from neurons in vitro.

Authors:  Rebeca Burdeinick-Kerr; Diane E Griffin
Journal:  J Virol       Date:  2005-05       Impact factor: 5.103

2.  Measles virus neurovirulence and host immunity.

Authors:  Michael Oglesbee; Stefan Niewiesk
Journal:  Future Virol       Date:  2011-01-01       Impact factor: 1.831

3.  Immune-mediated protection from measles virus-induced central nervous system disease is noncytolytic and gamma interferon dependent.

Authors:  Catherine E Patterson; Diane M P Lawrence; Lisa A Echols; Glenn F Rall
Journal:  J Virol       Date:  2002-05       Impact factor: 5.103

4.  CD8 T cells require gamma interferon to clear borna disease virus from the brain and prevent immune system-mediated neuronal damage.

Authors:  Jürgen Hausmann; Axel Pagenstecher; Karen Baur; Kirsten Richter; Hanns-Joachim Rziha; Peter Staeheli
Journal:  J Virol       Date:  2005-11       Impact factor: 5.103

5.  Toxoplasma gondii infection of neurons induces neuronal cytokine and chemokine production, but gamma interferon- and tumor necrosis factor-stimulated neurons fail to inhibit the invasion and growth of T. gondii.

Authors:  D Schlüter; M Deckert; H Hof; K Frei
Journal:  Infect Immun       Date:  2001-12       Impact factor: 3.441

6.  Noncytolytic clearance of sindbis virus infection from neurons by gamma interferon is dependent on Jak/STAT signaling.

Authors:  Rebeca Burdeinick-Kerr; Dhanasekaran Govindarajan; Diane E Griffin
Journal:  J Virol       Date:  2009-01-28       Impact factor: 5.103

7.  IFN-γ protects from lethal IL-17 mediated viral encephalomyelitis independent of neutrophils.

Authors:  Carine Savarin; Stephen A Stohlman; David R Hinton; Richard M Ransohoff; Daniel J Cua; Cornelia C Bergmann
Journal:  J Neuroinflammation       Date:  2012-05-29       Impact factor: 8.322

Review 8.  Neuronal survival strategies in the face of RNA viral infection.

Authors:  Catherine E Patterson; John K Daley; Glenn F Rall
Journal:  J Infect Dis       Date:  2002-12-01       Impact factor: 5.226

Review 9.  Latent viral infections of the nervous system: role of the host immune response.

Authors:  M Lafon
Journal:  Rev Neurol (Paris)       Date:  2009-12       Impact factor: 2.607

Review 10.  Immune responses to RNA-virus infections of the CNS.

Authors:  Diane E Griffin
Journal:  Nat Rev Immunol       Date:  2003-06       Impact factor: 53.106

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