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Characterization of alternatively spliced isoforms of the type I interleukin-1 receptor on iNOS induction in rat hepatocytes.

Characterization of alternatively spliced isoforms of the type I interleukin-1 receptor on iNOS induction in rat hepatocytes. Research Abstract Details 

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  • Characterization of alternatively spliced isoforms of the type I interleukin-1 receptor on iNOS induction in rat hepatocytes. Abstract Text:

    masanori yamadaMasanori Yamada,mikio nishizawaMikio Nishizawa,richi nakatakeRichi Nakatake,kozo habaraKozo Habara,hideyuki yoshidaHideyuki Yoshida,takashi ozakiTakashi Ozaki,kosuke matsuiKosuke Matsui,yoshinori hamadaYoshinori Hamada,yasuo kamiyamaYasuo Kamiyama,seiji itoSeiji Ito,tadayoshi okumuraTadayoshi Okumura,

    In animal models of liver injury, proinflammatory cytokines are implicated in inducing iNOS, which is followed by the production of NO in hepatocytes. Previously we have reported that the up-regulation of type I IL-1 receptor (IL-1RI) is required for the transcriptional activation of iNOS gene, in concert with the activation of transcription factor NF-kappaB. In this study, we found three alternatively spliced isoforms of IL-1RI in primary cultured rat hepatocytes: two (long and short) membrane-bound and one soluble IL-1RI. Interleukin (IL)-1beta markedly augmented the mRNA levels of long and short IL-1RI with time, but was less effective for soluble IL-1RI. Two membrane-bound IL-1RI were localized in the intracellular fraction, whereas soluble IL-1RI was released into the culture medium. Cotransfection experiments with iNOS promoter-luciferase constructs revealed that the overexpression of long and short IL-1RI, but not soluble IL-1RI, significantly increased the transactivation of iNOS promoter and the stabilization of its mRNA. In contrast, the addition of conditioned medium containing soluble IL-1RI reduced the induction of iNOS and NO production stimulated by IL-1beta. These results further suggest that the enhancement of IL-1RI isoforms may contribute to the regulation of iNOS induction in hepatocytes.

    Characterization of alternatively spliced isoforms of the type I interleukin-1 receptor on iNOS induction in rat hepatocytes. Publishing Authors By Initials

    m yamadaM Yamada,m nishizawaM Nishizawa,r nakatakeR Nakatake,k habaraK Habara,h yoshidaH Yoshida,t ozakiT Ozaki,k matsuiK Matsui,y hamadaY Hamada,y kamiyamaY Kamiyama,s itoS Ito,t okumuraT Okumura,

    For similar genetic processes: gene expression regulation: trans-activation (genetics) research abstracts see: genetic processes: gene expression regulation: trans-activation (genetics) research

    PUBMED ID PMID:

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    Characterization of alternatively spliced isoforms of the type I interleukin-1 receptor on iNOS induction in rat hepatocytes. Journal Published:

    PUBLICATION TYPE: Research Support, Non-U.S. Gov

    Journal: Nitric oxide : biology and chemistry / official jo

    VOLUME: 17

    Page Numbers: 98-105

    Journal Abbreviation: Nitric Oxide

    ISSN: 1089-8603

    DAY: 1

    MONTH: 07

    YEAR: 2007

    Characterization of alternatively spliced isoforms of the type I interleukin-1 receptor on iNOS induction in rat hepatocytes. Information

    Number of References:

    LANGUAGE: eng

    NlmUniqueID: 9709307

    Characterization of alternatively spliced isoforms of the type I interleukin-1 receptor on iNOS induction in rat hepatocytes. Keywords Mesh Terms:

    KEYWORDS: Trans-Activation (Genetics)

    MESH TERMS: physiology

    Chemical & Substance for Abstract: Characterization of alternatively spliced isoforms of the type I interleukin-1 receptor on iNOS induction in rat hepatocytes. Information

    Substance Name: Nitric Oxide Synthase Type II

    Registry Number: EC 1.14.13.39

    Grant and Affiliation Information for Characterization of alternatively spliced isoforms of the type I interleukin-1 receptor on iNOS induction in rat hepatocytes.

    AFFILIATION: Department of Surgery, Kansai Medical University, Moriguchi, Osaka 570-8506, Japan.

    Country: United States

    United States Research PublicationUnited States Research Publication

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    MEDLINETA: Nitric Oxide

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