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Alpha-actinin-containing aggregates in transformed cells are highly dynamic structures
Normal rat kidney cells infected with a Rous sarcoma virus (strain LA23) were used to study the dynamics of alpha-actinin-containing aggregates in transformed cells. Experiments were performed by microinjecting living cells with iodoacetamidotetramethylrhodamine alpha-actinin and allowing the fluore...
Formato: | Texto |
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Lenguaje: | English |
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The Rockefeller University Press
1987
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2114522/ https://www.ncbi.nlm.nih.gov/pubmed/3034916 |
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collection | PubMed |
description | Normal rat kidney cells infected with a Rous sarcoma virus (strain LA23) were used to study the dynamics of alpha-actinin-containing aggregates in transformed cells. Experiments were performed by microinjecting living cells with iodoacetamidotetramethylrhodamine alpha-actinin and allowing the fluorescent analogue to incorporate into cellular structures. Subsequent time-lapse recording indicated that the alpha-actinin-containing aggregates can undergo rapid formation, movement, and breakdown. In addition, experiments using the photobleaching recovery technique indicated that alpha-actinin molecules associated with the aggregates have a very high rate of exchange, whereas those associated with adhesion plaques in normal cells exchange much more slowly. The dynamic properties of alpha- actinin-containing aggregates may be closely related to the changes in cellular behavior upon oncogenic transformation. |
format | Text |
id | pubmed-2114522 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 1987 |
publisher | The Rockefeller University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-21145222008-05-01 Alpha-actinin-containing aggregates in transformed cells are highly dynamic structures J Cell Biol Articles Normal rat kidney cells infected with a Rous sarcoma virus (strain LA23) were used to study the dynamics of alpha-actinin-containing aggregates in transformed cells. Experiments were performed by microinjecting living cells with iodoacetamidotetramethylrhodamine alpha-actinin and allowing the fluorescent analogue to incorporate into cellular structures. Subsequent time-lapse recording indicated that the alpha-actinin-containing aggregates can undergo rapid formation, movement, and breakdown. In addition, experiments using the photobleaching recovery technique indicated that alpha-actinin molecules associated with the aggregates have a very high rate of exchange, whereas those associated with adhesion plaques in normal cells exchange much more slowly. The dynamic properties of alpha- actinin-containing aggregates may be closely related to the changes in cellular behavior upon oncogenic transformation. The Rockefeller University Press 1987-06-01 /pmc/articles/PMC2114522/ /pubmed/3034916 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 Alpha-actinin-containing aggregates in transformed cells are highly dynamic structures |
title | Alpha-actinin-containing aggregates in transformed cells are highly dynamic structures |
title_full | Alpha-actinin-containing aggregates in transformed cells are highly dynamic structures |
title_fullStr | Alpha-actinin-containing aggregates in transformed cells are highly dynamic structures |
title_full_unstemmed | Alpha-actinin-containing aggregates in transformed cells are highly dynamic structures |
title_short | Alpha-actinin-containing aggregates in transformed cells are highly dynamic structures |
title_sort | alpha-actinin-containing aggregates in transformed cells are highly dynamic structures |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2114522/ https://www.ncbi.nlm.nih.gov/pubmed/3034916 |