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2011 Fiscal Year Final Research Report

Detection of Circulating Endothelial Cells in Severe Sepsis

Research Project

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Project/Area Number 21390482
Research Category

Grant-in-Aid for Scientific Research (B)

Allocation TypeSingle-year Grants
Section一般
Research Field Emergency medicine
Research InstitutionKyoto University

Principal Investigator

KOIKE Kaoru  京都大学, 医学研究科, 教授 (10267164)

Co-Investigator(Kenkyū-buntansha) MATSUDA Naoyuki  名古屋大学, 医学研究科, 教授 (50332466)
Project Period (FY) 2009 – 2011
Keywords敗血症 / 遊離型血管内皮細胞 / CEC / AP-1 / TAK-1 / NF-κB / 播種性血管愛凝固症候群 / DIC
Research Abstract

Sepsis is a severe disorder as systemic inflammation with infection. In this illness, vascular endothelial damage proceeds to induce disseminated intravascular coagulation(DIC). This study revealed that circulating endothelial cell(CEC) was increased and plasma platelet count was decreased in the time dependent manner after sepsis induction by cecal ligation and puncture in male BALB-C mice. Nuclear factor-kappaB decoy oligonucleotides more strongly decreased CEC count than inactivation of FADD, TAK-1, and activator protein-1. The CEC count could be a reliable marker to evaluate DIC and dysfunction of vascular endothelium.

  • Research Products

    (2 results)

All 2010

All Journal Article (2 results)

  • [Journal Article] Up-regulation of histamine H4receptors contributes to splenicapoptosis in septic mice2010

    • Author(s)
      Matsuda N, Teramae H, Futatsugi M, Takano K, Yamamoto S, Tomita K, SuzukiT, Yokoo H, Koike K, Hattori Y
    • Journal Title

      J Pharmacol Exp Ther

      Volume: 332 Pages: 730-7

  • [Journal Article] Increased death receptor pathway of apoptotic signaling in septic mouse aorta2010

    • Author(s)
      Matsuda N, Teramae H, Yamamoto S, Takano K, Takano Y
    • Journal Title

      J Physiol Heart Circ Physiol

      Volume: H92-101 Pages: 298

URL: 

Published: 2013-07-31  

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