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Study of physiological importance of extracellular microenvironment on neovascularization through a development of multi dimentional co-culture system.

Research Project

Project/Area Number 26670144
Research Category

Grant-in-Aid for Challenging Exploratory Research

Allocation TypeMulti-year Fund
Research Field General medical chemistry
Research InstitutionOkazaki Research Facilities, National Institutes of Natural Sciences

Principal Investigator

Numaga-Tomita Takuro  大学共同利用機関法人自然科学研究機構(岡崎共通研究施設), 岡崎統合バイオサイエンスセンター, 助教 (60705060)

Project Period (FY) 2014-04-01 – 2016-03-31
Project Status Completed (Fiscal Year 2015)
Budget Amount *help
¥3,640,000 (Direct Cost: ¥2,800,000、Indirect Cost: ¥840,000)
Fiscal Year 2015: ¥1,820,000 (Direct Cost: ¥1,400,000、Indirect Cost: ¥420,000)
Fiscal Year 2014: ¥1,820,000 (Direct Cost: ¥1,400,000、Indirect Cost: ¥420,000)
Keywordsメカノバイオロジー / 心血管細胞 / 血管成熟 / 細胞外マトリクス
Outline of Final Research Achievements

Cardiovascular tissue is physically dynamic. Therefore, most of cardiovascular cells maintain their homeostasis by adopting to physical changes of extracellular environment.However underlying mechanisms remain elusive. In this study, we focused on microenvironmental stiffness surrounding cardiovascular cells and studied how the cells respond and adapt to the changes of extracellular stiffness. At first we hod tried to utilize hydrogel which change their elasticity in response to light stimulation. However, the hydrogel was instable and difficult to manipulate. Therefore, we developed the culture system based on PDMS with different stiffness and revealed a possibility that the stiffness close to healthy tissue was critical to supported stress reduction by secretion.

Report

(3 results)
  • 2015 Annual Research Report   Final Research Report ( PDF )
  • 2014 Research-status Report
  • Research Products

    (5 results)

All 2016 2015 2014

All Journal Article (2 results) (of which Int'l Joint Research: 2 results,  Peer Reviewed: 2 results,  Open Access: 2 results,  Acknowledgement Compliant: 1 results) Presentation (3 results) (of which Invited: 1 results)

  • [Journal Article] The purinergic P2Y6 receptor heterodimerizes with the angiotensin AT1 receptor to promote angiotensin II-induced hypertension2016

    • Author(s)
      A. Nishimura, C. Sunggip, H. Tozaki-Saitoh, T. Shimauchi, T. Numaga-Tomita, K. Hirano, T. Ide, J-M. Boeynaems, H. Kurose, M. Tsuda, B. Robaye, K. Inoue and M. Nishida
    • Journal Title

      Science Signaling

      Volume: Jan 19;9(411) Issue: 411

    • DOI

      10.1126/scisignal.aac9187

    • Related Report
      2015 Annual Research Report
    • Peer Reviewed / Open Access / Int'l Joint Research / Acknowledgement Compliant
  • [Journal Article] TRPC3 amplifies B cell receptor-induced ERK signaling via protein kinase D-dependent Rap1 activation2016

    • Author(s)
      T. Numaga-Tomita, M. Nishida, J.W. Jr. Putney and Y. Mori
    • Journal Title

      Biochem J

      Volume: 473(2) Issue: 2 Pages: 201-210

    • DOI

      10.1042/bj20150596

    • Related Report
      2015 Annual Research Report
    • Peer Reviewed / Open Access / Int'l Joint Research
  • [Presentation] B細胞受容体刺激に惹起されるERK活性化におけるTRPC3を介したシグナル伝達機構の解明2016

    • Author(s)
      冨田(沼賀)拓郎、西田基宏、James W, Putney, Jr.、森泰生
    • Organizer
      第93回日本生理学会大会
    • Place of Presentation
      北海道、札幌市、札幌コンベンションセンター
    • Year and Date
      2016-03-22
    • Related Report
      2015 Annual Research Report
  • [Presentation] 下肢虚血後の運動機能障害におけるTRPC6チャネル欠損の効果2015

    • Author(s)
      冨田拓郎
    • Organizer
      日本薬理学会年会
    • Place of Presentation
      名古屋国際会議場 愛知県名古屋市
    • Year and Date
      2015-03-18 – 2015-03-20
    • Related Report
      2014 Research-status Report
  • [Presentation] TRPCチャネルによる末梢循環調節とその治療応用2014

    • Author(s)
      冨田拓郎
    • Organizer
      日本平滑筋学会
    • Place of Presentation
      新横浜プリンスホテル 神奈川県横浜市
    • Year and Date
      2014-08-07 – 2014-08-08
    • Related Report
      2014 Research-status Report
    • Invited

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Published: 2014-04-04   Modified: 2017-05-10  

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