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2015 Fiscal Year Final Research Report

The presence and its significance of non-canonical action of decoy receptors

Research Project

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Project/Area Number 26670808
Research Category

Grant-in-Aid for Challenging Exploratory Research

Allocation TypeMulti-year Fund
Research Field Functional basic dentistry
Research InstitutionOkayama University

Principal Investigator

TAKIGAWA MASAHARU  岡山大学, 医歯(薬)学総合研究科, 教授 (20112063)

Co-Investigator(Kenkyū-buntansha) KUBOTA SATOSHI  岡山大学, 大学院医歯薬学総合研究科, 教授 (90221936)
AOYAMA ERIKO  岡山大学, 大学院医歯薬学総合研究科, 助教 (10432650)
NISHIDA TAKASHI  岡山大学, 大学院医歯薬学総合研究科, 准教授 (30322233)
HATTORI TAKAKO  岡山大学, 大学院医歯薬学総合研究科, 助教 (00228488)
Co-Investigator(Renkei-kenkyūsha) TAKAESU KAZUMI (河田 かずみ)  岡山大学, 大学院医歯薬学総合研究科, 助教 (10457228)
Project Period (FY) 2014-04-01 – 2016-03-31
Keywordsdecoy receptor / osteoprotegerin (OPG) / PDGFRL / CCN family / CCN2 / signaling / osteoclasts / chondrocytes
Outline of Final Research Achievements

In this study, we proposed a new concept showing the presence and its significance of non-canonical action of decoy receptor (-like) molecules by demonstrating 2 examples. 1) Osteoprotegerin (OPG) bound to CCN family protein 2 (CCN2), which binds to RANK and positively regulates RALK signaling, thereby inhibiting osteoclastogenesis via RANK signaling. 2) Platelet-derived growth factor receptor-like (PDGFRL) did not bind to PDGF which is the ligand for PDGF. Instead, PDGFRL did bind to CCN2 which plays important roles in chondrogenesis and endochondral ossification and another member of CCN family CCN3. These findings suggest that PDGFRL plays an important role in the cartilage biology, possibly by regulating the molecular behavior of CCN2. 3) We also found that c-type lectin receptor CD302 bound to CCN2, suggesting possible discovery of another example which supports our new concept.

Free Research Field

機能系基礎歯科学

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Published: 2017-05-10  

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