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2017 Fiscal Year Final Research Report

The role of PPP1r18, an actin binding protein, in osteoclastic bone resorption

Research Project

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Project/Area Number 16K20423
Research Category

Grant-in-Aid for Young Scientists (B)

Allocation TypeMulti-year Fund
Research Field Functional basic dentistry
Research InstitutionKyushu Dental College

Principal Investigator

Matsubara Takuma  九州歯科大学, 歯学部, 助教 (00423137)

Co-Investigator(Renkei-kenkyūsha) JIMI Eijiro  九州歯科大学, 分子情報生化学分野, 教授 (40276598)
KOKABU Shoichiro  九州歯科大学, 分子情報生化学分野, 准教授 (30448899)
Research Collaborator NAKATOMI Chihiro  
URATA MARIKO  
TOYAMA Kenya  
KOBAYAKAWA Miki  
YAGINUMA Tatsuki  
Project Period (FY) 2016-04-01 – 2018-03-31
Keywords破骨細胞 / 骨吸収
Outline of Final Research Achievements

Osteoclasts in tyrosine kinase Src deficient mice that show osteopetrosis hardly resorb bone matrix because of disable to attachment to bone matrix. Src organizes actin accumulation and regulates actin ring formation for attachment. However molecular mechanisms how Src regulates actin ring formation in osteoclasts are not fully understood. We identified an actin binding protein PPP1r18 as Src binding protein by mass spectrum analysis. PPP1r18 was expressed and localized in actin ring with Src of osteoclasts. These results suggest that PPP1r18 bind to Src and involved in actin ring formation. Downregulation of PPP1r18 expression promoted actin ring formation. On the other hand, overexpression of PPP1r18 inhibited actin ring formation and bone resorption. Mutation of protein phosphatase 1 binding domain of PPP1r18 canceled inhibition of actin ring formation by PPP1r18. These results suggest that PPP1r18 negatively regulates actin ring formation and bone resorption.

Free Research Field

機能系基礎歯科学

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Published: 2019-03-29  

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