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Force Mapping during the Formation and Maturation of Cell Adhesion Sites with Multiple Optical Tweezers
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 inv...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3556026/ https://www.ncbi.nlm.nih.gov/pubmed/23372781 http://dx.doi.org/10.1371/journal.pone.0054850 |
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author | Schwingel, Melanie Bastmeyer, Martin |
author_facet | Schwingel, Melanie Bastmeyer, Martin |
author_sort | Schwingel, Melanie |
collection | PubMed |
description | 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 µm, 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. |
format | Online Article Text |
id | pubmed-3556026 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-35560262013-01-31 Force Mapping during the Formation and Maturation of Cell Adhesion Sites with Multiple Optical Tweezers Schwingel, Melanie Bastmeyer, Martin PLoS One Research Article 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 µm, 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. Public Library of Science 2013-01-25 /pmc/articles/PMC3556026/ /pubmed/23372781 http://dx.doi.org/10.1371/journal.pone.0054850 Text en © 2013 Schwingel, Bastmeyer http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Schwingel, Melanie Bastmeyer, Martin Force Mapping during the Formation and Maturation of Cell Adhesion Sites with Multiple Optical Tweezers |
title | Force Mapping during the Formation and Maturation of Cell Adhesion Sites with Multiple Optical Tweezers |
title_full | Force Mapping during the Formation and Maturation of Cell Adhesion Sites with Multiple Optical Tweezers |
title_fullStr | Force Mapping during the Formation and Maturation of Cell Adhesion Sites with Multiple Optical Tweezers |
title_full_unstemmed | Force Mapping during the Formation and Maturation of Cell Adhesion Sites with Multiple Optical Tweezers |
title_short | Force Mapping during the Formation and Maturation of Cell Adhesion Sites with Multiple Optical Tweezers |
title_sort | force mapping during the formation and maturation of cell adhesion sites with multiple optical tweezers |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3556026/ https://www.ncbi.nlm.nih.gov/pubmed/23372781 http://dx.doi.org/10.1371/journal.pone.0054850 |
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