4.5 Article

Dissecting Regional Variations in Stress Fiber Mechanics in Living Cells with Laser Nanosurgery

Journal

BIOPHYSICAL JOURNAL
Volume 99, Issue 9, Pages 2775-2783

Publisher

CELL PRESS
DOI: 10.1016/j.bpj.2010.08.071

Keywords

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Categories

Funding

  1. National Science Foundation [CMMI0727420]
  2. NIH Physical Science-Oncology Center [IU54CA143836]
  3. Arnold and Mabel Beckman Young Investigator Award
  4. NIH [IDP2OD004213]
  5. U.S. Department of Defense Breast Cancer [W81XWH-09-1-0666]
  6. California Breast Cancer Research Program [14GB-0007]
  7. U.S. Department of Energy, Office of Biological and Environmental Research
  8. Low Dose Radiation Program [DE-AC02-05CH1123]
  9. National Cancer Institute [R37CA064786, U54CA126552, R01CA057621, U54CA112970, U01CA143233, NCI U54CA143836-Bay]
  10. U.S. Department of Defense [W81XWH0810736]

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The ability of a cell to distribute contractile stresses across the extracellular matrix in a spatially heterogeneous fashion underlies many cellular behaviors, including motility and tissue assembly. Here we investigate the biophysical basis of this phenomenon by using femtosecond laser nanosurgery to measure the viscoelastic recoil and cell-shape contributions of contractile stress fibers (SFs) located in specific compartments of living cells. Upon photodisruption and recoil, myosin light chain kinase-dependent SFs located along the cell periphery display much lower effective elasticities and higher plateau retraction distances than Rho-associated kinase-dependent SFs located in the cell center, with severing of peripheral fibers uniquely triggering a dramatic contraction of the entire cell within minutes of fiber irradiation. Image correlation spectroscopy reveals that when one population of SFs is pharmacologically dissipated, actin density flows toward the other population. Furthermore, dissipation of peripheral fibers reduces the elasticity and increases the plateau retraction distance of central fibers, and severing central fibers under these conditions triggers cellular contraction. Together, these findings show that SFs regulated by different myosin activators exhibit different mechanical properties and cell shape contributions. They also suggest that some fibers can absorb components and assume mechanical roles of other fibers to stabilize cell shape.

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