Force Mapping during the Formation and Maturation of Cell Adhesion Sites with Multiple Optical Tweezers

被引:29
|
作者
Schwingel, Melanie [1 ,2 ]
Bastmeyer, Martin [1 ,2 ]
机构
[1] KIT, Inst Zool, Karlsruhe, Germany
[2] KIT, DFG Ctr Funct Nanostruct CFN, Karlsruhe, Germany
来源
PLOS ONE | 2013年 / 8卷 / 01期
关键词
SINGLE KINESIN MOLECULES; F-ACTIN FLOW; FLUORESCENT SPECKLE MICROSCOPY; NEURONAL GROWTH CONES; FOCAL ADHESIONS; EXTRACELLULAR-MATRIX; RETROGRADE FLOW; MIGRATING CELLS; IN-VIVO; MECHANICAL-PROPERTIES;
D O I
10.1371/journal.pone.0054850
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Focal contacts act as mechanosensors allowing cells to respond to their biomechanical environment. Force transmission through newly formed contact sites is a highly dynamic process requiring a stable link between the intracellular cytoskeleton and the extracellular environment. To simultaneously investigate cellular traction forces in several individual maturing adhesion sites within the same cell, we established a custom-built multiple trap optical tweezers setup. Beads functionalized with fibronectin or RGD-peptides were placed onto the apical surface of a cell and trapped with a maximum force of 160 pN. Cells form adhesion contacts around the beads as demonstrated by vinculin accumulation and start to apply traction forces after 30 seconds. Force transmission was found to strongly depend on bead size, surface density of integrin ligands and bead location on the cell surface. Highest traction forces were measured for beads positioned on the leading edge. For mouse embryonic fibroblasts, traction forces acting on single beads are in the range of 80 pN after 5 minutes. If two beads were positioned parallel to the leading edge and with a center-to-center distance less than 10 mm, traction forces acting on single beads were reduced by 40%. This indicates a spatial and temporal coordination of force development in closely related adhesion sites. We also used our setup to compare traction forces, retrograde transport velocities, and migration velocities between two cell lines (mouse melanoma and fibroblasts) and primary chick fibroblasts. We find that maximal force development differs considerably between the three cell types with the primary cells being the strongest. In addition, we observe a linear relation between force and retrograde transport velocity: a high retrograde transport velocity is associated with strong cellular traction forces. In contrast, migration velocity is inversely related to traction forces and retrograde transport velocity.
引用
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页数:12
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