2023-10-20 マサチューセッツ工科大学(MIT)
◆研究によれば、定期的な力学的運動により筋繊維が成長し、同じ方向に整列します。この新しいデバイスを使用して、強力で機能的な筋肉をパターン化し、ソフトロボットや疾患組織の修復に使用できる可能性があります。研究者は、このデバイスを使って、筋肉の再成長を促進する方法や加齢の影響を軽減する方法を研究し、医学分野での応用を模索する予定です。
<関連情報>
- https://news.mit.edu/2023/wobbly-gel-mat-trains-muscle-cells-work-together-1020
- https://www.cell.com/device/fulltext/S2666-9986(23)00149-7
作動する細胞外マトリックスで人工筋肉の異方性を機械的にプログラミングする Mechanically programming anisotropy in engineered muscle with actuating extracellular matrices
Brandon Rios,Angel Bu,Tara Sheehan,Hiba Kobeissi,Sonika Kohli,Karina Shah,Emma Lejeune,Ritu Raman
Device Published:October 20, 2023
DOI:https://doi.org/10.1016/j.device.2023.100097
Highlights
•Magnetic microparticles are embedded in an extracellular-matrix-mimicking gel
•Controlled movement of a permanent magnet drives gel actuation
•Magnetic matrix actuation (MagMA) programs alignment of skeletal muscle fibers
•MagMA-aligned muscle tissues generate synchronous contractile twitch
The bigger picture
Cells within tissues communicate with each other, and with their surrounding matrix, thorough biochemical, electrical, and mechanical signals. While there are a range of techniques for mapping and controlling electrical and biochemical communication within multicellular systems, there is a significant need for tools that measure and modulate mechanical stimuli in a similar manner. A platform for dynamically patterning forces within tissues would enable mechanically programming morphology and function of various adaptive mechanobiological processes.
Summary
The hierarchical design and adaptive functionalities of biological tissues are driven by dynamic biochemical, electrical, and mechanical signaling between cells and their extracellular matrices. While existing tools enable monitoring and controlling biochemical and electrical signaling in multicellular systems, there is a significant need for techniques that enable mapping and modulating intercellular mechanical signaling. We have developed a magnetically actuated extracellular matrix that serves as a mechanically active substrate for cells and can program morphological and functional anisotropy in tissues such as skeletal muscle. This method improves the ease and efficiency of programming muscle force directionality and synchronicity for applications ranging from medicine to robotics. Additionally, we present an open-source computational framework enabling quantitative analyses of muscle contractility. Our actuating matrices and accompanying tools are broadly applicable across cell types and hydrogel chemistries, and they can drive fundamental studies in mechanobiology as well as translational applications of engineered tissues in medicine and machines.