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2012 Fiscal Year Final Research Report

Role of GRK in engulfment of apoptotic cells

Research Project

  • PDF
Project/Area Number 23659043
Research Category

Grant-in-Aid for Challenging Exploratory Research

Allocation TypeMulti-year Fund
Research Field Biological pharmacy
Research InstitutionKyushu University

Principal Investigator

KUROSE Hitoshi  九州大学, 薬学研究院, 教授 (10183039)

Project Period (FY) 2011 – 2012
KeywordsG タンパク質共役型受容体キナーゼ / 細胞内シグナル伝達 / アポトーシス / 自己免疫疾患 / 貪食 / マクロファージ
Research Abstract

In the body, apoptotic cells are rapidly removed by the cells such as macrophages and dendritic cells. Otherwise, inefficient removal of apoptotic cells results in transition of apoptotic cells to late necrotic cells and leakage of their own intracellular contents. This leakage causes appearance of autoantibody and induction of inflammation, leading to collapse of the body’ s homeostasis. The removal of apoptotic cells is called as engulfment. So far, there are three engulfment pathways: Abl/Abi, ELMO/DOCK180, and ABC/MFGF10/GULF/dynamin signaling pathways. In this study, we revealed that G protein-coupled receptor (GPCR) kinase 6 (GRK6), which is believed to regulate GPCR function, was involved in engulfment. This pathway was independent of three known pathways. GRK6 bound Ezrin/Radixin/Moesin (ERM) and ultimately activated Rac1 that is indispensable for engulfment. GRK6-mediated engulfment was also observed in endogenous macrophages. In GRK6 knockout (GRK6-KO) mice, systemic lupus erythematosus (SLE), one of autoimmune diseases, -like symptoms such as increased anti-double strand DNA antibody in the plasma and deposition of immunocomplex in the kidney were observed. Furthermore, we observed abnormalities in the spleen. In white pulp of the spleen that removes apoptotic B cells, the number of ungulfed apoptotic cells in GRK6-KO mice was higher than that in wild type mice. In red pulp of the spleen that removes aged red blood cells, we observed the increased iron deposition due to impaired removal of aged red blood cells. These results suggest that GRK6 is a mediator of engulf apoptotic cells, and impaired function of GRK6 results in autoimmune disease and affects recycling of red blood cells. This study reveals that GRK has a new role in the cells andbody, although GRK is generally accepted as a mediator of GPCR regulation.

  • Research Products

    (5 results)

All 2013 2012 Other

All Journal Article (2 results) Presentation (2 results) Remarks (1 results)

  • [Journal Article] GRK6-deficiency in mice causes autoimmune disease due to impaired apoptotic cell clearance2013

    • Author(s)
      Nakaya M, Tajima M, Kosako H, Nakaya N, Hashimoto A, Watari K, Nishihara H, Ohba M, Komiya S, TaniN, Nishida M, Taniguchi H, Sato Y, Matsumoto M, Tsuda M, Kuroda M, Inoue K, Kurose H
    • Journal Title

      Nature Communications

      Volume: 4 Pages: 1532

    • DOI

      DOI:10.1038/ncomms2540.

  • [Journal Article] Induction of cardiac fibrosis by ・-blocker in G protein-independent and GRK5/・-arrestin2-dependent signaling pathways2012

    • Author(s)
      Nakaya M, Chikura S, Watari K, Mizuno N, Mochinaga K, Mangmool S, Koyanagi S, Ohdo S, Sato Y, Ide T, Nishida M, Kurose H
    • Journal Title

      Journal of Biological Chemistry

      Volume: 287 (42) Pages: 35669-35677

    • DOI

      DOI:10.1074/jbc.M112.357871.

  • [Presentation] G タンパク質共役型受容体の G タンパク質依存性と非依存性の細胞応答(シンポジウム 55「心臓・循環生理の新たな調節機構-三量体G 蛋白質シグナルの新コンセプト-」)2013

    • Author(s)
      黒瀬等
    • Organizer
      第90回日本生理学会大会
    • Place of Presentation
      タワーホール船堀
    • Year and Date
      2013-03-29
  • [Presentation] G タンパク質共役型受容体の活性を調節する分子群の疾患での役割 シンポジウム2S-04「G蛋白質共役型受容体(GPCR)およびGPCRキナーゼの機能不全によって引き起こされる疾患」2012

    • Author(s)
      黒瀬等、仲矢道雄
    • Organizer
      第85回資本生化学会大会
    • Place of Presentation
      福岡国際会議場
    • Year and Date
      2012-12-15
  • [Remarks]

    • URL

      http://chudoku.phar.kyushu-u.ac.jp/

URL: 

Published: 2014-09-25   Modified: 2015-11-26  

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