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2000 Fiscal Year Final Research Report Summary

Down-regulation of murine tissue factor pathway inhibitor mRNA by endotoxin and tumor neerosis factor-alpha In vitro and In vivo.

Research Project

Project/Area Number 11470209
Research Category

Grant-in-Aid for Scientific Research (B).

Allocation TypeSingle-year Grants
Section一般
Research Field Hematology
Research InstitutionNagoya University

Principal Investigator

SAITO Hidehiko  School of Medicine, Nagoya University, Professor, 医学部, 教授 (20153819)

Co-Investigator(Kenkyū-buntansha) YAMAMOTO Koji  School of Medicine, Nagoya University, Medical Staff, 医学部, 医員
KOJIMA Tetsuhito  School of Medicine, Nagoya University, Professor, 医学部, 教授 (40161913)
Project Period (FY) 1999 – 2000
KeywordsThrombosis / Sepsis / TFPI / TNF-alpha / IL-1 / Gene Expression / Fibrin deposition
Research Abstract

Tissue factor pathway inhibitor (TFPI) is the protease inhibitor that regulates the extrinsic coagulation pathway initiated by the factor VIIa/TF complex. In this study, we first investigated tissue distribution of TFPI mRNA in the mouse and found that TFPI mRNA expression level was by far the highest in the lung, followed by the heart, adrenal, and adipose tissue. Since little has been known concerning the regulation of TFPI gene expression in vivo, we further analyzed the changes in the TFPI mRNA level in murine tissues after intraperitoneal injection of lipopolysaccharide (LPS), tumor necrosis factor-alpha (TNF-alpha), and interleukin-1 (IL-1). LPS and TNF-alpha dramatically decreased TFPI mRNA expression in four tissues examined (e.g., lung, heart, kidney, and adipose tissue, in which fibrin deposition were observed), whereas the suppressive effect of IL-1 on TFPI mRNA was limited. The down-regulation of TFPI mRNA expression by LPS and TNF-alpha was also observed in cultured mouse endothelial cells and in cardiomyocyte cell lines. The decreased TFPI gene expression by LPS and TNF-alpha in tissues and in the specific cell types may contribute to an increase in the local procoagulant potential, resulting in the thrombotic tendency under septic and/or inflammatory conditions.

  • Research Products

    (12 results)

All Other

All Publications (12 results)

  • [Publications] Kida M.,Souri M., Saito.H., et al.: "Transcriptional Regulation of Cell Type-specific Expression of the TATA-less A Subunit Gene for Human Coagulation Factor XIII."J.Biol Chem. 274. 6138-6147 (1999)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] Nichols,W.C.,Terry,V.H.,Saito.H., et al.: "ERGIC-53 Gene Structure and Mutation Analysis in 19 Combined Factors V and VIII Deficiency Families."Blood. 93. 2261-2266 (1999)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] Yamamoto,K.,Shimokawa,T.,Saito.H., et al.: "Regulation of murine protein C gene expression in vivo : effect of tumor necrosis factor-α, inteleukin-1, and transforming growth factor-β."Thromb Haemost. 82. 1297-1301 (1999)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] Ishiguro,K.,Kadomatsu,K.,Saito.H., et al.: "Syndecan-4 deficiency impairs focal adhesion formation only under restricted conditions."J.Biol.Chem.. 275. 5249-5252 (2000)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] Ishiguro,K.,Kojima,T.Saito.H., et al.: "Complete antithrombin deficiency in mice results in embryonic lethality."J.Clin.Invest.. 106. 873-878 (2000)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] Shimokawa T,Yamamoto K,Saito.H., et al.: "Down-regulation of murine tissue factor pathway inhibitor mRNA by endotoxin and tumor necrosis factor-alpha In vitro and In vivo."Thromb.Res.. 100. 211-221 (2000)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] Kida, M., Souri, M., Saito, H., et al.: "Transcriptional Regulation of Cell Type-specific Expression of the TATA-less A Subunit Gene for Human Coagulation Factor XIII."J.Biol Chem. 274. 6138-6147 (1999)

    • Description
      「研究成果報告書概要(欧文)」より
  • [Publications] Nichols, W.C., Terry, V.H., Saito, H., et al.: "ERGIC-53 Gene Structure and Mutation Analysis in 19 Combined Factors V and VIII Deficiency Families."Blood. 93. 2261-2266 (1999)

    • Description
      「研究成果報告書概要(欧文)」より
  • [Publications] Yamamoto, K., Shimokawa, T., Saito, H., et al.: "Regulation of Murine Protein C Gene Expression in Vivo : Effects of Tumor Necrosis Factor-α, Interleukin-1, and Transforming Growth Factor-β."Thromb Haemost. 82. 1297-1301 (1999)

    • Description
      「研究成果報告書概要(欧文)」より
  • [Publications] Ishiguro, K., Kadomatsu, K., Saito, H., et al.: "Syndecan-4 deficiency impairs focal adhesion formation only under restricted conditions."J Biol Chem. 275. 5249-5252 (2000)

    • Description
      「研究成果報告書概要(欧文)」より
  • [Publications] Ishiguro, K., Kojima, T., Saito, H., et al.: "Complete antithrombin deficiency in mice results in embryonic lethality."J Clin Invest. 106. 873-878 (2000)

    • Description
      「研究成果報告書概要(欧文)」より
  • [Publications] Shimokawa T, Yamamoto K, Saito, H., et al.: "Down-regulation of murine tissue factor pathway inhibitor mRNA by endotoxin and tumor necrosis factor-alpha In vitro and In vivo."Thromb Res. 100. 211-221 (2000)

    • Description
      「研究成果報告書概要(欧文)」より

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Published: 2002-03-26  

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