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Development and pathological characterization of genetically modified macaque monkey with eye disease.

Research Project

Project/Area Number 25670742
Research Category

Grant-in-Aid for Challenging Exploratory Research

Allocation TypeSingle-year Grants
Research Field Ophthalmology
Research Institution独立行政法人国立病院機構(東京医療センター臨床研究センター)

Principal Investigator

IWATA Takeshi  独立行政法人国立病院機構(東京医療センター臨床研究センター), 分子細胞生物学研究部, 部長 (90374157)

Co-Investigator(Kenkyū-buntansha) SHIMOZAWA Nobuhiro  医薬基盤研究所, 霊長類医科学研究センター, 主任研究員 (50300786)
Project Period (FY) 2013-04-01 – 2014-03-31
Project Status Completed (Fiscal Year 2013)
Budget Amount *help
¥3,770,000 (Direct Cost: ¥2,900,000、Indirect Cost: ¥870,000)
Fiscal Year 2013: ¥3,770,000 (Direct Cost: ¥2,900,000、Indirect Cost: ¥870,000)
Keywords霊長類 / ノックアウト / 遺伝子改変 / 疾患モデル動物
Research Abstract

The structural and molecular characteristic of human eye is very unique to primate and different from other species. Development of animal model, which completely mimic the human eye diseases such as glaucoma, age-related macular degeneration and macular dystrophies has been difficult due to technical issues. In this research project we used the zinc finger nuclease (ZFN) technology to develop knockout or knockin macaque monkey. Developed monkeys will be maintained for pathological and visual function examination to understand the progression of the disease.

Report

(2 results)
  • 2013 Annual Research Report   Final Research Report ( PDF )
  • Research Products

    (38 results)

All 2014 2013 Other

All Journal Article (16 results) (of which Peer Reviewed: 11 results) Presentation (16 results) (of which Invited: 1 results) Book (5 results) Remarks (1 results)

  • [Journal Article] Longitudinal clinical course of three Japanese patients with Leber congenital amaurosis/severe early childhood onset retinal dystrophy with RDH12 mutation.2014

    • Author(s)
      Kuniyoshi K, Sakuramoto H, Yoshitake K, Abe K, Ikeo K, Furuno M, Tsunoda K, Kusaka S, Shimomura Y, Iwata T
    • Journal Title

      Documenta Ophthalmologica

      Volume: 印刷中

    • Related Report
      2013 Annual Research Report
    • Peer Reviewed
  • [Journal Article] Autosomal recessive cone-rod dystrophy associated with compound heterozygous mutations in the EYS gene.2014

    • Author(s)
      Katagiri S, Akahori M, Hayashi T, Yoshitake K, Gekka T, Ideo K, Tsuneoka H, Iwata T
    • Journal Title

      Documenta Ophthalmologica

      Volume: 印刷中

    • Related Report
      2013 Annual Research Report
    • Peer Reviewed
  • [Journal Article] What monitor can replace cathode ray tube for visual stimulation to elicit multifocal electroretinograms?2014

    • Author(s)
      Matsumoto CS, Shinoda K, Matsumoto H, Seki K, Nagasaka E, Iwata T, Mizota A
    • Journal Title

      Journal of Vision

      Volume: 印刷中

    • Related Report
      2013 Annual Research Report
    • Peer Reviewed
  • [Journal Article] Plasma Proteome Analysis On Cynomolgus Monkey (Macaca fascicularis) Pedigrees With Early Onset Drusen Formation.2014

    • Author(s)
      Kobayashi H, Okamoto H, Murakami A, Iwata T
    • Journal Title

      Journal of Experimental Animals

      Volume: 印刷中

    • NAID

      130004677825

    • Related Report
      2013 Annual Research Report
    • Peer Reviewed
  • [Journal Article] Retinal angiomatous proliferation associated with risk alleles of ARMS2/HTRA1 gene polymorphisms in Japanese patients.2014

    • Author(s)
      Ohkuma Y, Hayashi T, Sakai T, Watanabe A, Yamada H, Akahori M, Itabashi T, Iwata T, Noda T, Tsuneoka H
    • Journal Title

      Journal of Clinical Ophthalmology

      Volume: 8 Pages: 143-148

    • Related Report
      2013 Annual Research Report
    • Peer Reviewed
  • [Journal Article] Whole-exome sequencing identifies a novel ALMS1 mutation (p.Q2051X) in two Japanese brothers with Alstrom Syndrome2013

    • Author(s)
      Katagiri S, Yoshitake K, Akahori M, Hayashi T, Furuno M, Nishino J, Ikeo K, Tsuneoka H, Iwata T
    • Journal Title

      Molecular Vision

      Volume: 19 Pages: 2393-406

    • Related Report
      2013 Final Research Report
  • [Journal Article] Two siblings with late-onset cone-rod dystrophy and no visible macular degeneration2013

    • Author(s)
      Sakuramoto H, Kuniyoshi K, Tsunoda K, Akahori M, Iwata T, Shimomura Y
    • Journal Title

      Journal of Clinical Ophthalmology

      Volume: 7 Pages: 1703-11

    • Related Report
      2013 Final Research Report
  • [Journal Article] Long-term observation over ten years of four cases of cone dystrophy with supernormal rod electroretinogram2013

    • Author(s)
      Nakamura N, Tsunoda K, Fujinami K, Shinoda K, Tomita K, Hatase T, Usui T, Akahori M, Iwata T, Miyake Y
    • Journal Title

      Nihon Ganka Gakkai Zasshi

      Volume: 117 Pages: 629-40

    • NAID

      10031189436

    • Related Report
      2013 Final Research Report
  • [Journal Article] Molecular characteristics of four Japanese cases with KCNV2 retinopathy : report of novel disease-causing variants2013

    • Author(s)
      Fujinami K, Tsunoda K, Nakamura N, Kato Y, Noda T, Shinoda K, Tomita K, Hatase T, Usui T, Akahori M, Itabashi T, Iwata T, Ozawa Y, Tsubota K, Miyake Y.
    • Journal Title

      Molecular Vision

      Volume: 19 Pages: 1580-90

    • Related Report
      2013 Final Research Report
  • [Journal Article] Enhanced optineurin E50K-TBK1 interaction evokes protein insolubility and initiates familial primary open-angle glaucoma2013

    • Author(s)
      Minegishi Y, Iejima D, Kobayashi H, Chi Z-L, Kawase K, Yamamoto T, Seki T, Yuasa S, Fukuda K, Iwata T
    • Journal Title

      Human Molecular Genetics

      Volume: 22 Pages: 3559-67

    • Related Report
      2013 Final Research Report
  • [Journal Article] Whole-exome sequencing identifies a novel ALMS1 mutation (p.Q2051X) in two Japanese brothers with Alstrom Syndrome.2013

    • Author(s)
      Katagiri S, Yoshitake K, Akahori M, Hayashi T, Furuno M, Nishino J, Ikeo K, Tsuneoka H, Iwata T
    • Journal Title

      Molecular Vision

      Volume: 19 Pages: 2393-2406

    • Related Report
      2013 Annual Research Report
    • Peer Reviewed
  • [Journal Article] Two siblings with late-onset cone-rod dystrophy and no visible macular degeneration.2013

    • Author(s)
      Sakuramoto H, Kuniyoshi K, Tsunoda K, Akahori M, Iwata T, Shimomura Y
    • Journal Title

      Journal of Clinical Ophthalmology

      Volume: 7 Pages: 1703-1711

    • Related Report
      2013 Annual Research Report
    • Peer Reviewed
  • [Journal Article] [Long-term observation over ten years of four cases of cone dystrophy with supernormal rod electroretinogram].2013

    • Author(s)
      Nakamura N, Tsunoda K, Fujinami K, Shinoda K, Tomita K, Hatase T, Usui T, Akahori M, Iwata T, Miyake Y
    • Journal Title

      Nihon Ganka Gakkai Zasshi

      Volume: 117 Pages: 629-640

    • NAID

      10031189436

    • Related Report
      2013 Annual Research Report
    • Peer Reviewed
  • [Journal Article] Molecular characteristics of four Japanese cases with KCNV2 retinopathy: report of novel disease-causing variants.2013

    • Author(s)
      Fujinami K, Tsunoda K, Nakamura N, Kato Y, Noda T, Shinoda K, Tomita K, Hatase T, Usui T, Akahori M, Itabashi T, Iwata T, Ozawa Y, Tsubota K, Miyake Y
    • Journal Title

      Molecular Vision

      Volume: 19 Pages: 1580-1590

    • Related Report
      2013 Annual Research Report
    • Peer Reviewed
  • [Journal Article] Enhanced optineurin E50K-TBK1 interaction evokes protein insolubility and initiates familial primary open-angle glaucoma.2013

    • Author(s)
      Minegishi Y, Iejima D, Kobayashi H, Chi Z-L, Kawase K, Yamamoto T, Seki T, Yuasa S, Fukuda K, Iwata T
    • Journal Title

      Human Molecular Genetics

      Volume: 22 Pages: 3559-3567

    • Related Report
      2013 Annual Research Report
    • Peer Reviewed
  • [Journal Article] 日米の眼研究の架け橋 Jin H. Kinoshita先生を偲んで (編集:堀田喜裕)2013

    • Author(s)
      岩田岳 (編集:堀田喜裕)
    • Journal Title

      あたらしい眼科

      Volume: 30 Pages: 1417-1418

    • Related Report
      2013 Annual Research Report
    • Peer Reviewed
  • [Presentation] 滲出型加齢黄斑変性感受性遺伝子 ARMS2-HtrA1のプロモーターの解析2014

    • Author(s)
      家島大輔,板橋剛,川村雄一,野田徹,湯浅慎介,岡千緒,福田恵一,岩田岳
    • Organizer
      Retina Research Meeting (RRM)東京
    • Related Report
      2013 Final Research Report
  • [Presentation] 加齢黄斑変性感受性遺伝子HtrA1のトランスジェニックマウスの病態と習慣因子(喫煙)の影響2014

    • Author(s)
      中山真央 、家島大輔 、亀井淳三 、岩田岳
    • Organizer
      Retina Research Meeting (RRM)
    • Place of Presentation
      東京
    • Related Report
      2013 Final Research Report
  • [Presentation]2013

    • Organizer
      第17回眼科分子生物学研究会主催(会長:岩田岳、開催準備 : 分子細胞生物学研究部)
    • Place of Presentation
      静岡県焼津市
    • Related Report
      2013 Final Research Report
  • [Presentation]2013

    • Author(s)
      Iwata T.
    • Organizer
      National Eye Institute Audacious GoalMeeting
    • Place of Presentation
      Potomac, Maryland, USA
    • Related Report
      2013 Final Research Report
  • [Presentation] Enhanced optineurin E50K-TBK1 interaction evokes protein insolubility and initiates familial primary open angle glaucoma2013

    • Author(s)
      Iwata T.
    • Organizer
      ISER Sarasota Symposium
    • Place of Presentation
      Sarasota, Florida, USA( University of Florida Gainesville, Department of Ophthalmology )
    • Related Report
      2013 Final Research Report
    • Invited
  • [Presentation] Animal models for glaucoma and age-related macular degeneration2013

    • Author(s)
      Iwata T.
    • Place of Presentation
      Gainesville, Florida, USA
    • Related Report
      2013 Final Research Report
  • [Presentation] Molecular mechanism of POAG by optineurin E50K mutation2013

    • Author(s)
      Iwata T.
    • Organizer
      Asia ARVO 2013
    • Place of Presentation
      New Delhi,India
    • Related Report
      2013 Final Research Report
  • [Presentation] Characterization of early-onset drusen forming cynomolgus monkeys2013

    • Author(s)
      Iwata T.
    • Organizer
      Asia ARVO 2013
    • Place of Presentation
      New Delhi,India(2013年10月第6回Retina Research Meeting (RRM)主催(世話人:村上晶、岩田岳、溝田淳、渡辺すみ子)JPタワー東京)
    • Related Report
      2013 Final Research Report
  • [Presentation] 緑内障原因遺伝子オプチニューリンと E50K変異によるタンパクの不溶化と病態発症との関連2013

    • Author(s)
      峯岸ゆり子、家島大輔、小林宏明、池在龍、川瀬和秀、山本哲也、関倫久、湯浅慎介、福田恵一、岩田岳
    • Organizer
      第17回眼科分子生物学研究会
    • Place of Presentation
      静岡
    • Related Report
      2013 Final Research Report
  • [Presentation] Overexpression of HtrA1 and Smoking Evokes Choroidal Neovascularization and Retinal Deposit in Aged Mice2013

    • Author(s)
      Nakayama M, Iejima D, Akahori M, Kamei J, Iwata T.
    • Organizer
      ARVO Annual Meeting 2013
    • Place of Presentation
      Seattle, WA, USA.
    • Related Report
      2013 Final Research Report
  • [Presentation] Characterization of HtrA1 Promoter in Patients with Exudative Age-Related Macular Degeneration2013

    • Author(s)
      Iejima D, Noda T, Mizota A, Iwata T.
    • Organizer
      ARVO Annual Meeting 2013
    • Place of Presentation
      Seattle, WA, USA
    • Related Report
      2013 Final Research Report
  • [Presentation] 網膜疾患におけるExome解析2013

    • Author(s)
      赤堀正和、岩田岳
    • Organizer
      NGS現場の会(第三回)
    • Place of Presentation
      大阪
    • Related Report
      2013 Final Research Report
  • [Presentation] 慢性甲状腺炎に発症した片眼性の急性後部多発性斑状色素上皮症の1例2013

    • Author(s)
      片桐聡,林孝彰,月花環,青柳蘭子,伊藤直子,大熊康弘,常岡寛
    • Organizer
      第30回日本眼循環学会
    • Place of Presentation
      東京
    • Related Report
      2013 Final Research Report
  • [Presentation] Alstrom症候群の兄弟例2013

    • Author(s)
      片桐聡,林孝彰,月花環,伊藤直子,岩田岳,常岡寛
    • Organizer
      第61回日本臨床視覚電気生理学会
    • Place of Presentation
      大阪
    • Related Report
      2013 Final Research Report
  • [Presentation] H A novel CYP4V2 mutation (S121Y) in choroideremia like phenotype2013

    • Author(s)
      Katagiri S, Hayashi T, Gekka T, Yamada H, Iwata T, Tsuneoka
    • Organizer
      The 8th APVRS Congress &第52回日本網膜硝子体学会総会
    • Place of Presentation
      名古屋
    • Related Report
      2013 Final Research Report
  • [Presentation]

    • Organizer
      International Society for Eye Research (ISER) Sarasota Symposium
    • Place of Presentation
      (主催(世話人: Ernst Tamm, MD -Program Chair, Tailoi Chan-Ling, PhD, Mike Fautsch, PhD, Takeshi Iwata, PhD, Rob Nickells, PhD, Dan Stamer, PhD))
    • Related Report
      2013 Final Research Report
  • [Book] RETINA Medicine2014

    • Author(s)
      赤堀正和、岩田岳
    • Total Pages
      5
    • Publisher
      先端医学社
    • Related Report
      2013 Annual Research Report
  • [Book] Animal Models for Eye Diseases, Handbook of Laboratory Animal Science III2014

    • Author(s)
      Iwata T, (Editor: Hau J and Schapiro SJ)
    • Total Pages
      23
    • Publisher
      CRC Press
    • Related Report
      2013 Annual Research Report
  • [Book] 全エクソーム解析による遺伝性網脈絡膜疾患の原因遺伝子探索、エクソーム解析‐成果と将来-(編集 : 松本直道)、医学のあゆみ2013

    • Author(s)
      岩田岳、古野正朗、池尾一穂
    • Total Pages
      245
    • Publisher
      医歯薬出版株式会社
    • Related Report
      2013 Final Research Report
  • [Book] Optineurinと正常眼圧緑内障、Digestシリーズ(編集 : 本庶佑)、Medical Science Digest2013

    • Author(s)
      岩田岳
    • Total Pages
      39
    • Publisher
      ニューサイエンス社
    • Related Report
      2013 Final Research Report
  • [Book] 緑内障の遺伝子とその機能解析、緑内障の病態と疫学、高齢者の視覚障害とそのケア2013

    • Author(s)
      岩田岳(編集:小口芳久)
    • Publisher
      公益財団法人長寿科学振興財団
    • Related Report
      2013 Final Research Report
  • [Remarks]

    • URL

      http://www.eye.go.jp

    • Related Report
      2013 Final Research Report

URL: 

Published: 2014-07-25   Modified: 2016-11-25  

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