TY - JOUR
T1 - Cellular dynamics of bovine aortic smooth muscle cells measured using MEMS force sensors
AU - Tsukagoshi, Takuya
AU - Nguyen, Thanh Vinh
AU - Shoji, Kayoko Hirayama
AU - Takahashi, Hidetoshi
AU - Matsumoto, Kiyoshi
AU - Shimoyama, Isao
N1 - Funding Information:
The authors thank Ms Reiko Terada and Ms Chie Fukazawa for their technical assistance. This study was supported by JSPS KAKENHI Grant Number 25000010 and a Grant-in-Aid for JSPS Fellows. The EB photo mask fabrication was performed using the EB lithography apparatus at the VLSI Design and Education Center (VDEC) at the University of Tokyo.
Publisher Copyright:
© 2018 IOP Publishing Ltd.
PY - 2018/3/12
Y1 - 2018/3/12
N2 - Adhesive cells perceive the mechanical properties of the substrates to which they adhere, adjusting their cellular mechanical forces according to their biological characteristics. This mechanical interaction subsequently affects the growth, locomotion, and differentiation of the cell. However, little is known about the detailed mechanism that underlies this interaction between adherent cells and substrates because dynamically measuring mechanical phenomena is difficult. Here, we utilize microelectromechamical systems force sensors that can measure cellular traction forces with high temporal resolution (∼2.5 μs) over long periods (∼3 h). We found that the cellular dynamics reflected physical phenomena with time scales from milliseconds to hours, which contradicts the idea that cellular motion is slow. A single focal adhesion (FA) generates an average force of 7 nN, which disappears in ms via the action of trypsin-ethylenediaminetetraacetic acid. The force-changing rate obtained from our measurements suggests that the time required for an FA to decompose was nearly proportional to the force acting on the FA.
AB - Adhesive cells perceive the mechanical properties of the substrates to which they adhere, adjusting their cellular mechanical forces according to their biological characteristics. This mechanical interaction subsequently affects the growth, locomotion, and differentiation of the cell. However, little is known about the detailed mechanism that underlies this interaction between adherent cells and substrates because dynamically measuring mechanical phenomena is difficult. Here, we utilize microelectromechamical systems force sensors that can measure cellular traction forces with high temporal resolution (∼2.5 μs) over long periods (∼3 h). We found that the cellular dynamics reflected physical phenomena with time scales from milliseconds to hours, which contradicts the idea that cellular motion is slow. A single focal adhesion (FA) generates an average force of 7 nN, which disappears in ms via the action of trypsin-ethylenediaminetetraacetic acid. The force-changing rate obtained from our measurements suggests that the time required for an FA to decompose was nearly proportional to the force acting on the FA.
KW - cellular dynamics
KW - focal adhesion
KW - piezoresistive cantilever
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U2 - 10.1088/1361-6463/aab146
DO - 10.1088/1361-6463/aab146
M3 - Article
AN - SCOPUS:85044958247
SN - 0022-3727
VL - 51
JO - Journal of Physics D: Applied Physics
JF - Journal of Physics D: Applied Physics
IS - 14
M1 - 145401
ER -