TY - JOUR
T1 - High extensibility of stress fibers revealed by in vitro micromanipulation with fluorescence imaging
AU - Matsui, Tsubasa S.
AU - Sato, Masaaki
AU - Deguchi, Shinji
N1 - Funding Information:
This work was supported in part by the JSPS KAKENHI Grants ( 11J07552 to T.S.M., 20001007 to M.S., and 24680049 to S.D.). Author contributions: T.S.M. performed the majority of the experiments and analyzed the data; M.S. contributed reagents/materials/analysis tools; S.D. performed the experiments and wrote the paper with feedback from co-authors.
Publisher Copyright:
© 2013 Elsevier Inc. All rights reserved.
PY - 2013/5/10
Y1 - 2013/5/10
N2 - Stress fibers (SFs), subcellular bundles of actin and myosin filaments, are physically connected at their ends to cell adhesions. The intracellular force transmitted via SFs plays an essential role in cell adhesion regulation and downstream signaling. However, biophysical properties intrinsic to individual SFs remain poorly understood partly because SFs are surrounded by other cytoplasmic components that restrict the deformation of the embedded materials. To characterize their inherent properties independent of other structural components, we isolated SFs from vascular smooth muscle cells and mechanically stretched them by in vitro manipulation while visualizing strain with fluorescent quantum dots attached along their length. SFs were elongated along their entire length, with the length being approximately 4-fold of the stress-free length. This surprisingly high extensibility was beyond that explained by the tandem connection of actin filaments and myosin II bipolar filaments present in SFs, thus suggesting the involvement of other structural components in their passive biophysical properties.
AB - Stress fibers (SFs), subcellular bundles of actin and myosin filaments, are physically connected at their ends to cell adhesions. The intracellular force transmitted via SFs plays an essential role in cell adhesion regulation and downstream signaling. However, biophysical properties intrinsic to individual SFs remain poorly understood partly because SFs are surrounded by other cytoplasmic components that restrict the deformation of the embedded materials. To characterize their inherent properties independent of other structural components, we isolated SFs from vascular smooth muscle cells and mechanically stretched them by in vitro manipulation while visualizing strain with fluorescent quantum dots attached along their length. SFs were elongated along their entire length, with the length being approximately 4-fold of the stress-free length. This surprisingly high extensibility was beyond that explained by the tandem connection of actin filaments and myosin II bipolar filaments present in SFs, thus suggesting the involvement of other structural components in their passive biophysical properties.
KW - Cell biophysics
KW - Intracellular force transmission
KW - Smooth muscle cells
KW - Stress fibers
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U2 - 10.1016/j.bbrc.2013.03.093
DO - 10.1016/j.bbrc.2013.03.093
M3 - Article
C2 - 23583399
AN - SCOPUS:84880455315
SN - 0006-291X
VL - 434
SP - 444
EP - 448
JO - Biochemical and Biophysical Research Communications
JF - Biochemical and Biophysical Research Communications
IS - 3
ER -