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2014 Fiscal Year Final Research Report

PAMPs, DAMPs regulation by thrombomodulin(TM). Probable role of epithelial TM

Research Project

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Project/Area Number 26670790
Research Category

Grant-in-Aid for Challenging Exploratory Research

Allocation TypeMulti-year Fund
Research Field Emergency medicine
Research InstitutionKagoshima University

Principal Investigator

MARUYAMA Ikuro  鹿児島大学, 医歯(薬)学総合研究科, 特任教授 (20082282)

Co-Investigator(Kenkyū-buntansha) ITO Takashi  鹿児島大学, 大学院医歯学総合研究科, 講師 (20381171)
Co-Investigator(Renkei-kenkyūsha) KAWAHARA Ko-ichi  大阪工業大学, 工学部生命工学科, 特任教授 (10381170)
NAKAHARA Mayumi  鹿児島大学, 大学院医歯学総合研究科, 特任助教 (90707514)
Project Period (FY) 2014-04-01 – 2015-03-31
Keywords感染症 / 細胞・組織 / トロンボモジュリン / PAMPs / DAMP
Outline of Final Research Achievements

We previously cloned thrombomodulin(TM) cDNA and determined its structure. Human TM is composed by five domains, D1 lectin like domain, D2 with 6 EGF-like structures, E1 to E6. Thrombin binds to E4-E6 and fails its procoagulant activity. This thrombin can activate protein C efficientry. Thus TM converts thrombin from a procoagulant to an anticoagulant protease. Moreover we showed that HMGB1, s typical DAMP binds to D1 lectin like domain and loses its proinflammatory activity. After that another group showed that D1 adsorbs LPS. More recently we have showed that TM binds histones, released from necrotic cells. We showed that extracellular histones induce platelets activation.Therefore it will be considered that extracellular histones behave as a DAMP.
We identified that the extracellular histones bind to TM with abolishing the proinflammatory activity. Thus TM acts as a regulator not only thrombin but also DAMPs and PAMP,LPS. This will explain the significant role of epithelilal TM.

Free Research Field

医歯薬学

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Published: 2016-06-03  

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