In order to elucidate the mechanotransduction mechanism of adherent cells, it is crucial to clarify how forces applied to cells are transmitted through intracellular components. Actin stress fibers (SFs) play important roles in various cellular events including cell proliferation [1], differentiation [2] and gene expression [3]. SFs generate internal forces and contribute to physical interactions between cells and extracellular matrices [4]. It has recently been suggested that cytoskeletons have the potential to interact with nuclei via certain nuclear membrane proteins [5, 6]. However, it remains unclear at this stage whether SFs are involved in a mechanical interaction with the cell nucleus and their internal forces are transmitted directly to the nucleus.
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ASME 2011 Summer Bioengineering Conference
June 22–25, 2011
Farmington, Pennsylvania, USA
Conference Sponsors:
- Bioengineering Division
ISBN:
978-0-7918-5458-7
PROCEEDINGS PAPER
In Situ Observation of Nuclear Behavior During Laser Nano-Dissection of Actin Stress Fibers: Mechanical Interaction Between Actin Stress Fibers and Nucleus
Kazuaki Nagayama,
Kazuaki Nagayama
Nagoya Institute of Technology, Nagoya, Aichi, Japan
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Yuki Yahiro,
Yuki Yahiro
Nagoya Institute of Technology, Nagoya, Aichi, Japan
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Takeo Matsumoto
Takeo Matsumoto
Nagoya Institute of Technology, Nagoya, Aichi, Japan
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Kazuaki Nagayama
Nagoya Institute of Technology, Nagoya, Aichi, Japan
Yuki Yahiro
Nagoya Institute of Technology, Nagoya, Aichi, Japan
Takeo Matsumoto
Nagoya Institute of Technology, Nagoya, Aichi, Japan
Paper No:
SBC2011-53264, pp. 319-320; 2 pages
Published Online:
July 17, 2013
Citation
Nagayama, K, Yahiro, Y, & Matsumoto, T. "In Situ Observation of Nuclear Behavior During Laser Nano-Dissection of Actin Stress Fibers: Mechanical Interaction Between Actin Stress Fibers and Nucleus." Proceedings of the ASME 2011 Summer Bioengineering Conference. ASME 2011 Summer Bioengineering Conference, Parts A and B. Farmington, Pennsylvania, USA. June 22–25, 2011. pp. 319-320. ASME. https://doi.org/10.1115/SBC2011-53264
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