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2021 Fiscal Year Annual Research Report

Utilization of viscoelastic substrates to study actin/MTs coordination and subsequent mechanobiological functionalities

Research Project

Project/Area Number 21J40229
Allocation TypeSingle-year Grants
Research InstitutionNational Institute for Materials Science

Principal Investigator

Abdelaleem Shimaa  国立研究開発法人物質・材料研究機構, 機能性材料研究拠点, 特別研究員(RPD)

Project Period (FY) 2021-04-28 – 2024-03-31
KeywordsMechanobiology / Viscoelastic material / EMT / Actomyosin / ECM concentration
Outline of Annual Research Achievements

Human cells are impeded in complex polymeric network of proteins called extracellular matrix (ECM). The utilization of biomaterials with certain mechanical and biochemical cues is done to deeply understand the underlaying cytoskeletal systems (actomyosin and MTs) interplays and cell-matrix interactions.
Firstly, in joint research; the viscoelastic materials on which elasticity and stress relaxation could be varied independently were used to study the early EMT like behavior that alter the E/N cadherin expression. Within our system, E-cadherin changes with changes in the interfacial elasticity, whereas N-cadherin is regulated by both elasticity and relaxation. (published Langmuir 2022). While still the interactions with the cytoskeletal systems are under investigations.
Furthermore, I focused on the ECM concentrations as a chemical cue and to what extent the actomyosin activity would be manipulated during the TGF-b induced EMT. Substrates with different cRGD concentrations were used. Low cRGD concentration as a chemical cue have synergistically weakened the cell-cell cohesion during TGF-b induced EMT, the acquisition of mesenchymal phenotype by TGF-b is associated with different cytoskeleton arrangements based on the cRGD concentration (Preliminary results was presented in conference). Further investigation would be conducted.

Current Status of Research Progress
Current Status of Research Progress

2: Research has progressed on the whole more than it was originally planned.

Reason

My aim is to simplify the complexity of natural ECM to understand in depth various cellular responses in relation to mechanical and biochemical cues. This purpose is achieved by the synthesized of established biomaterials with specific mechanical and chemical cues.
The study of biological interactions as the cytoskeletal system interactions with such material characteristics is performed in a reasonable basis, there are some interruptions happened based on the Corona situation. But other than that, research results are obtained within a reasonable time frame.

Strategy for Future Research Activity

Now I use these unique mechanical and chemical cues to deeply understand the details about on several biological functionalities as cytoskeletal system interactions, EMT transition, and migratory behavior. I focus on the mechanical feedback between ECM characteristics and cellular responses in general and cytoskeletal system in special. In another word identify the role of mechanical and biochemical cues by tracking several cellular responses such as 1) MTs biochemical status 2). MTs dynamics and the actin polymerization. 3) Formation of different actomyosin structures. 4) the real time mechanisms of actin/MTs crosstalk.

  • Research Products

    (2 results)

All 2022 2021

All Journal Article (1 results) Presentation (1 results) (of which Int'l Joint Research: 1 results)

  • [Journal Article] Precise Tuning and Characterization of Viscoelastic Interfaces for the Study of Early Epithelial Mesenchymal Transition Behaviors2022

    • Author(s)
      Chang Alice Chinghsuan、Uto Koichiro、Abdellatef Shimaa A.、Nakanishi Jun
    • Journal Title

      Langmuir

      Volume: 38 Pages: 5307~5314

    • DOI

      10.1021/acs.langmuir.1c03048

  • [Presentation] Impact of extracellular matrix ligand densities on TGF-β-induced EMT.2021

    • Author(s)
      S. A. Abdellatef and Jun Nakanishi,
    • Organizer
      Virtual TERMIS workshop, Online (June 2021).
    • Int'l Joint Research

URL: 

Published: 2022-12-28   Modified: 2023-08-01  

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