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Cloning of gene involved in facial pain

Research Project

Project/Area Number 07457501
Research Category

Grant-in-Aid for Scientific Research (B)

Allocation TypeSingle-year Grants
Section一般
Research Field Surgical dentistry
Research InstitutionOsaka Dental University

Principal Investigator

UEDA Yutaka  Osaka Dental University, Faculty of Dentistry, Professor, 歯学部, 教授 (10067001)

Co-Investigator(Kenkyū-buntansha) MOMOTA Yoshihiro  Osaka Dental University, Faculty of Dentistry, Assistant, 歯学部, 助手 (60247880)
Project Period (FY) 1995 – 1996
Project Status Completed (Fiscal Year 1996)
Budget Amount *help
¥4,800,000 (Direct Cost: ¥4,800,000)
Fiscal Year 1996: ¥1,500,000 (Direct Cost: ¥1,500,000)
Fiscal Year 1995: ¥3,300,000 (Direct Cost: ¥3,300,000)
KeywordsNociception / Cloning / Differential display / STAT family / Cytokine signaling / JAK family / Trigeminal ganglion / Cytokine receptor / Pain / Inflammation / Primary Sensory Neuron / Trigeminal spinal nucleus Caudalis / pain / chronic constristion injury / cloning / Differential display / Rat
Research Abstract

This research aimed at analizing of pain sensory system. We examined cloning of genes involved in nociception by differential display method. We got a lot of distinctive bands. But we have not got distinctive genes yet. The localization of some cytokine receptors and their downstream intracellular signaling molecules was examined in the rat trigeminal ganglion. Amongcytokine receptor components, we examined signal transduction subchain, gp130, IL-2Rgamma and IL-5Rbeta, which are common to respective groups of cytokine receptors. Most of the sensory ganglion neurons expressed gp130, but not IL-2Rgamma nor IL-5beta. We further examined the localization of Janus kinase family members which were reported to be associated with various kind of cytokine receptors and are thought to be implicated in majorcytokine receptor-signaling pathways. While JAK1 and Tyk 2 were expressed in all type of neurons, JAK2 was predominantly expressed in the small neurons. In addition, JAK3 immunoreactivity was only found in satellite cells. The present results indicate that most of neurons express gp130, and that the localization of JAK family members differs with the cell type. This also suggests that the cytokine receptor-signaling pathway may be different in neuronal and glial cells.

Report

(3 results)
  • 1996 Annual Research Report   Final Research Report Summary
  • 1995 Annual Research Report
  • Research Products

    (3 results)

All Other

All Publications (3 results)

  • [Publications] Makoto MIZUNO, et al.: "Localization of molecules involved in cytokine receptor signaling in the rat trigeminal ganglion" Molecular Brain Research. 44. 163-166 (1997)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      1996 Final Research Report Summary
  • [Publications] Makoto Mizuno, et al.: "Localization of molecules involved in cytokine receptor signaling in the rat trigeminal ganglion" Molecular Brain Research. 44. 163-166 (1997)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      1996 Final Research Report Summary
  • [Publications] Makoto Mizuno,et al.,: "Localization of molecules involved in cytokine receptor signaling in tha rat Trigeminal ganglion" Molecular Brain Research. 44. 163-166 (1997)

    • Related Report
      1996 Annual Research Report

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Published: 1995-04-01   Modified: 2016-04-21  

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