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Nanometer targeting of microtubules to focal adhesions
Although cell movement is driven by actin, polarization and directional locomotion require an intact microtubule cytoskeleton that influences polarization by modulating substrate adhesion via specific targeting interactions with adhesion complexes. The fidelity of adhesion site targeting is precise;...
Autores principales: | , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
The Rockefeller University Press
2003
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2172972/ https://www.ncbi.nlm.nih.gov/pubmed/12782685 http://dx.doi.org/10.1083/jcb.200301102 |
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author | Krylyshkina, Olga Anderson, Kurt I. Kaverina, Irina Upmann, Irene Manstein, Dietmar J. Small, J. Victor Toomre, Derek K. |
author_facet | Krylyshkina, Olga Anderson, Kurt I. Kaverina, Irina Upmann, Irene Manstein, Dietmar J. Small, J. Victor Toomre, Derek K. |
author_sort | Krylyshkina, Olga |
collection | PubMed |
description | Although cell movement is driven by actin, polarization and directional locomotion require an intact microtubule cytoskeleton that influences polarization by modulating substrate adhesion via specific targeting interactions with adhesion complexes. The fidelity of adhesion site targeting is precise; using total internal reflection fluorescence microscopy (TIRFM), we now show microtubule ends (visualized by incorporation of GFP tubulin) are within 50 nm of the substrate when polymerizing toward the cell periphery, but not when shrinking from it. Multiple microtubules sometimes followed similar tracks, suggesting guidance along a common cytoskeletal element. Use of TIRFM with GFP- or DsRed-zyxin in combination with either GFP-tubulin or GFP–CLIP-170 further revealed that the polymerizing microtubule plus ends that tracked close to the dorsal surface consistently targeted substrate adhesion complexes. This supports a central role for the microtubule tip complex in the guidance of microtubules into adhesion foci, and provides evidence for an intimate cross-talk between microtubule tips and substrate adhesions in the range of molecular dimensions. |
format | Text |
id | pubmed-2172972 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2003 |
publisher | The Rockefeller University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-21729722008-05-01 Nanometer targeting of microtubules to focal adhesions Krylyshkina, Olga Anderson, Kurt I. Kaverina, Irina Upmann, Irene Manstein, Dietmar J. Small, J. Victor Toomre, Derek K. J Cell Biol Report Although cell movement is driven by actin, polarization and directional locomotion require an intact microtubule cytoskeleton that influences polarization by modulating substrate adhesion via specific targeting interactions with adhesion complexes. The fidelity of adhesion site targeting is precise; using total internal reflection fluorescence microscopy (TIRFM), we now show microtubule ends (visualized by incorporation of GFP tubulin) are within 50 nm of the substrate when polymerizing toward the cell periphery, but not when shrinking from it. Multiple microtubules sometimes followed similar tracks, suggesting guidance along a common cytoskeletal element. Use of TIRFM with GFP- or DsRed-zyxin in combination with either GFP-tubulin or GFP–CLIP-170 further revealed that the polymerizing microtubule plus ends that tracked close to the dorsal surface consistently targeted substrate adhesion complexes. This supports a central role for the microtubule tip complex in the guidance of microtubules into adhesion foci, and provides evidence for an intimate cross-talk between microtubule tips and substrate adhesions in the range of molecular dimensions. The Rockefeller University Press 2003-06-09 /pmc/articles/PMC2172972/ /pubmed/12782685 http://dx.doi.org/10.1083/jcb.200301102 Text en Copyright © 2003, The Rockefeller University Press This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 4.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/4.0/). |
spellingShingle | Report Krylyshkina, Olga Anderson, Kurt I. Kaverina, Irina Upmann, Irene Manstein, Dietmar J. Small, J. Victor Toomre, Derek K. Nanometer targeting of microtubules to focal adhesions |
title | Nanometer targeting of microtubules to focal adhesions |
title_full | Nanometer targeting of microtubules to focal adhesions |
title_fullStr | Nanometer targeting of microtubules to focal adhesions |
title_full_unstemmed | Nanometer targeting of microtubules to focal adhesions |
title_short | Nanometer targeting of microtubules to focal adhesions |
title_sort | nanometer targeting of microtubules to focal adhesions |
topic | Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2172972/ https://www.ncbi.nlm.nih.gov/pubmed/12782685 http://dx.doi.org/10.1083/jcb.200301102 |
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