Contribution of intermediate filaments to cell stiffness, stiffening, and growth

被引:219
作者
Wang, N
Stamenovic, D
机构
[1] Harvard Univ, Sch Publ Hlth, Dept Environm Hlth, Physiol Program, Boston, MA 02115 USA
[2] Boston Univ, Dept Biomed Engn, Boston, MA 02215 USA
来源
AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY | 2000年 / 279卷 / 01期
关键词
vimentin; cytoskeleton; cellular mechanics; magnetic twisting cytometry; deoxyribonucleic acid synthesis;
D O I
10.1152/ajpcell.2000.279.1.C188
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
It has been shown previously that intermediate filament (IF) gels in vitro exhibit stiffening at high-applied stress, and it was suggested that this stiffening property of IFs might be important for maintaining cell integrity at large deformations (Janmey PA, Evtenever V, Traub P, and Schliwa M, J Cell Biol 113: 155-160, 1991). In this study, the contribution of IFs to cell mechanical behavior was investigated by measuring cell stiffness in response to applied stress in adherent wild-type and vimentin-deficient fibroblasts using magnetic twisting cytometry. It was found that vimentin-deficient cells were less stiff and exhibited less stiffening than wild-type cells, except at the lowest applied stress (10 dyn/cm(2)) where the difference in the stiffness was not significant. Similar results were obtained from measurements on wild-type fibroblasts and endothelial cells after vimentin IFs were disrupted by acrylamide. If, however, cells were plated over an extended period of time (16 h), they exhibited a significantly greater stiffness before than after acrylamide, even at the lowest applied stress. A possible reason could be that the initially slack IFs became fully extended due to a high degree of cell spreading and thus contributed to the transmission of mechanical stress across the cell. Taken together, these findings were consistent with the notion that IFs play important roles in the mechanical properties of the cell during large deformation. The experimental data also showed that depleting or disrupting IFs reduced, but did not entirely abolish, cell stiffening. This residual stiffening might be attributed to the effect of geometrical realignment of cytoskeletal filaments in the direction of applied load. It was also found that vimentin-deficient cells exhibited a slower rate of proliferation and DNA synthesis than wild-type cells. This could be a direct consequence of the absence of the intracellular IFs that may be necessary for efficient mediation of mechanical signals within the cell. Taken together, results of this study suggest that IFs play important roles in the mechanical properties of cells and in cell growth.
引用
收藏
页码:C188 / C194
页数:7
相关论文
共 26 条
[1]  
Amos LA, 1991, MOL CYTOSKELETON
[2]   Regulation of cytoskeletal mechanics and cell growth by myosin light chain phosphorylation [J].
Cai, S ;
Pestic-Dragovich, L ;
O'Donnell, ME ;
Wang, N ;
Ingber, D ;
Elson, E ;
De Lanerolle, P .
AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY, 1998, 275 (05) :C1349-C1356
[3]   A tensegrity structure with buckling compression elements: Application to cell mechanics [J].
Coughlin, MF ;
Stamenovic, D .
JOURNAL OF APPLIED MECHANICS-TRANSACTIONS OF THE ASME, 1997, 64 (03) :480-486
[4]  
COUGHLIN MF, 1998, ASME, V120, P770
[5]  
Eckes B, 1998, J CELL SCI, V111, P1897
[6]   CHROMATIN MOTION IN NEURONAL INTERPHASE NUCLEI - CHANGES INDUCED BY DISRUPTION OF INTERMEDIATE FILAMENTS [J].
HAY, M ;
DEBONI, U .
CELL MOTILITY AND THE CYTOSKELETON, 1991, 18 (01) :63-75
[7]   Control of cyclin D1, p27Kip1, and cell cycle progression in human capillary endothelial cells by cell shape and cytoskeletal tension [J].
Huang, S ;
Chen, CS ;
Ingber, DE .
MOLECULAR BIOLOGY OF THE CELL, 1998, 9 (11) :3179-3193
[8]   The architecture of life [J].
Ingber, DE .
SCIENTIFIC AMERICAN, 1998, 278 (01) :48-57
[9]   VISCOELASTIC PROPERTIES OF VIMENTIN COMPARED WITH OTHER FILAMENTOUS BIOPOLYMER NETWORKS [J].
JANMEY, PA ;
EUTENEUER, U ;
TRAUB, P ;
SCHLIWA, M .
JOURNAL OF CELL BIOLOGY, 1991, 113 (01) :155-160
[10]   Cytoskeletal plasticity in cells expressing neuronal microtubule-associated proteins [J].
Kaech, S ;
Ludin, B ;
Matus, A .
NEURON, 1996, 17 (06) :1189-1199