TY - JOUR
T1 - Spatial distribution of filament elasticity determines the migratory behaviors of a cell
AU - Harn, Hans I.Chen
AU - Hsu, Chao Kai
AU - Wang, Yang Kao
AU - Huang, Yi Wei
AU - Chiu, Wen Tai
AU - Lin, Hsi Hui
AU - Cheng, Chao Min
AU - Tang, Ming Jer
N1 - Publisher Copyright:
© 2016 The Author(s). Published with license by Taylor & Francis Group, LLC © 2016 Hans I-Chen Harn, Chao-Kai Hsu, Yang-Kao Wang, Yi-Wei Huang, Wen-Tai Chiu, Hsi-Hui Lin, Chao-Min Cheng, and Ming-Jer Tang.
PY - 2016/7/3
Y1 - 2016/7/3
N2 - Any cellular response leading to morphological changes is highly tuned to balance the force generated from structural reorganization, provided by actin cytoskeleton. Actin filaments serve as the backbone of intracellular force, and transduce external mechanical signal via focal adhesion complex into the cell. During migration, cells not only undergo molecular changes but also rapid mechanical modulation. Here we focus on determining, the role of spatial distribution of mechanical changes of actin filaments in epithelial, mesenchymal, fibrotic and cancer cells with non-migration, directional migration, and non-directional migration behaviors using the atomic force microscopy. We found 1) non-migratory cells only generated one type of filament elasticity, 2) cells generating spatially distributed two types of filament elasticity showed directional migration, and 3) pathologic cells that autonomously generated two types of filament elasticity without spatial distribution were actively migrating non-directionally. The demonstration of spatial regulation of filament elasticity of different cell types at the nano-scale highlights the coupling of cytoskeletal function with physical characters at the sub-cellular level, and provides new research directions for migration related disease.
AB - Any cellular response leading to morphological changes is highly tuned to balance the force generated from structural reorganization, provided by actin cytoskeleton. Actin filaments serve as the backbone of intracellular force, and transduce external mechanical signal via focal adhesion complex into the cell. During migration, cells not only undergo molecular changes but also rapid mechanical modulation. Here we focus on determining, the role of spatial distribution of mechanical changes of actin filaments in epithelial, mesenchymal, fibrotic and cancer cells with non-migration, directional migration, and non-directional migration behaviors using the atomic force microscopy. We found 1) non-migratory cells only generated one type of filament elasticity, 2) cells generating spatially distributed two types of filament elasticity showed directional migration, and 3) pathologic cells that autonomously generated two types of filament elasticity without spatial distribution were actively migrating non-directionally. The demonstration of spatial regulation of filament elasticity of different cell types at the nano-scale highlights the coupling of cytoskeletal function with physical characters at the sub-cellular level, and provides new research directions for migration related disease.
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U2 - 10.1080/19336918.2016.1156825
DO - 10.1080/19336918.2016.1156825
M3 - Article
C2 - 26919488
AN - SCOPUS:84965055070
SN - 1933-6918
VL - 10
SP - 368
EP - 377
JO - Cell Adhesion and Migration
JF - Cell Adhesion and Migration
IS - 4
ER -