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Targeting, Capture, and Stabilization of Microtubules at Early Focal Adhesions
By co-injecting fluorescent tubulin and vinculin into fish fibroblasts we have revealed a “cross talk” between microtubules and early sites of substrate contact. This mutuality was first indicated by the targeting of vinculin-rich foci by microtubules during their growth towards the cell periphery....
Autores principales: | , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
The Rockefeller University Press
1998
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2133026/ https://www.ncbi.nlm.nih.gov/pubmed/9660872 |
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author | Kaverina, Irina Rottner, Klemens Small, J. Victor |
author_facet | Kaverina, Irina Rottner, Klemens Small, J. Victor |
author_sort | Kaverina, Irina |
collection | PubMed |
description | By co-injecting fluorescent tubulin and vinculin into fish fibroblasts we have revealed a “cross talk” between microtubules and early sites of substrate contact. This mutuality was first indicated by the targeting of vinculin-rich foci by microtubules during their growth towards the cell periphery. In addition to passing directly over contact sites, the ends of single microtubules could be observed to target several contacts in succession or the same contact repetitively, with intermittent withdrawals. Targeting sometimes involved side-stepping, or the major re-routing of a microtubule, indicative of a guided, rather than a random process. The paths that microtubules followed into contacts were unrelated to the orientation of stress fiber assemblies and targeting occurred also in mouse fibroblasts that lacked a system of intermediate filaments. Further experiments with microtubule inhibitors showed that adhesion foci can: (a) capture microtubules and stabilize them against disassembly by nocodazole; and (b), act as preferred sites of microtubule polymerization, during either early recovery from nocodazole, or brief treatment with taxol. From these and other findings we speculate that microtubules are guided into substrate contact sites and through the motor-dependent delivery of signaling molecules serve to modulate their development. It is further proposed this modulation provides the route whereby microtubules exert their influence on cell shape and polarity. |
format | Text |
id | pubmed-2133026 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 1998 |
publisher | The Rockefeller University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-21330262008-05-01 Targeting, Capture, and Stabilization of Microtubules at Early Focal Adhesions Kaverina, Irina Rottner, Klemens Small, J. Victor J Cell Biol Articles By co-injecting fluorescent tubulin and vinculin into fish fibroblasts we have revealed a “cross talk” between microtubules and early sites of substrate contact. This mutuality was first indicated by the targeting of vinculin-rich foci by microtubules during their growth towards the cell periphery. In addition to passing directly over contact sites, the ends of single microtubules could be observed to target several contacts in succession or the same contact repetitively, with intermittent withdrawals. Targeting sometimes involved side-stepping, or the major re-routing of a microtubule, indicative of a guided, rather than a random process. The paths that microtubules followed into contacts were unrelated to the orientation of stress fiber assemblies and targeting occurred also in mouse fibroblasts that lacked a system of intermediate filaments. Further experiments with microtubule inhibitors showed that adhesion foci can: (a) capture microtubules and stabilize them against disassembly by nocodazole; and (b), act as preferred sites of microtubule polymerization, during either early recovery from nocodazole, or brief treatment with taxol. From these and other findings we speculate that microtubules are guided into substrate contact sites and through the motor-dependent delivery of signaling molecules serve to modulate their development. It is further proposed this modulation provides the route whereby microtubules exert their influence on cell shape and polarity. The Rockefeller University Press 1998-07-13 /pmc/articles/PMC2133026/ /pubmed/9660872 Text en 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 | Articles Kaverina, Irina Rottner, Klemens Small, J. Victor Targeting, Capture, and Stabilization of Microtubules at Early Focal Adhesions |
title | Targeting, Capture, and Stabilization of Microtubules at Early Focal Adhesions |
title_full | Targeting, Capture, and Stabilization of Microtubules at Early Focal Adhesions |
title_fullStr | Targeting, Capture, and Stabilization of Microtubules at Early Focal Adhesions |
title_full_unstemmed | Targeting, Capture, and Stabilization of Microtubules at Early Focal Adhesions |
title_short | Targeting, Capture, and Stabilization of Microtubules at Early Focal Adhesions |
title_sort | targeting, capture, and stabilization of microtubules at early focal adhesions |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2133026/ https://www.ncbi.nlm.nih.gov/pubmed/9660872 |
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