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Nuclear transport in 3T3 fibroblasts: effects of growth factors, transformation, and cell shape
Nucleocytoplasmic transport of fluorescent-labeled macromolecules was investigated in transformed and nontransformed 3T3 fibroblasts. Insulin and epidermal growth factor enhanced transport three-fold after 1-2-h incubation with nontransformed adhering fibroblasts; no enhancement of transport was obs...
Formato: | Texto |
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Lenguaje: | English |
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The Rockefeller University Press
1988
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2114954/ https://www.ncbi.nlm.nih.gov/pubmed/2448310 |
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collection | PubMed |
description | Nucleocytoplasmic transport of fluorescent-labeled macromolecules was investigated in transformed and nontransformed 3T3 fibroblasts. Insulin and epidermal growth factor enhanced transport three-fold after 1-2-h incubation with nontransformed adhering fibroblasts; no enhancement of transport was observed for spherical unattached fibroblasts. The concentration of growth factor for maximal enhancement was 3-10 nM. Nuclear transport for Kirsten murine sarcoma virus-transformed BALB/c 3T3 fibroblasts, however, was maximally enhanced before addition of growth factors; addition of insulin or epidermal growth factor causes no additional transport enhancement. Transformation also minimizes cell shape effects on macromolecular nuclear transport. These results provide evidence that protein growth factors and oncogenic transformation may use a similar mechanism for activation of nuclear transport. |
format | Text |
id | pubmed-2114954 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 1988 |
publisher | The Rockefeller University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-21149542008-05-01 Nuclear transport in 3T3 fibroblasts: effects of growth factors, transformation, and cell shape J Cell Biol Articles Nucleocytoplasmic transport of fluorescent-labeled macromolecules was investigated in transformed and nontransformed 3T3 fibroblasts. Insulin and epidermal growth factor enhanced transport three-fold after 1-2-h incubation with nontransformed adhering fibroblasts; no enhancement of transport was observed for spherical unattached fibroblasts. The concentration of growth factor for maximal enhancement was 3-10 nM. Nuclear transport for Kirsten murine sarcoma virus-transformed BALB/c 3T3 fibroblasts, however, was maximally enhanced before addition of growth factors; addition of insulin or epidermal growth factor causes no additional transport enhancement. Transformation also minimizes cell shape effects on macromolecular nuclear transport. These results provide evidence that protein growth factors and oncogenic transformation may use a similar mechanism for activation of nuclear transport. The Rockefeller University Press 1988-01-01 /pmc/articles/PMC2114954/ /pubmed/2448310 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 Nuclear transport in 3T3 fibroblasts: effects of growth factors, transformation, and cell shape |
title | Nuclear transport in 3T3 fibroblasts: effects of growth factors, transformation, and cell shape |
title_full | Nuclear transport in 3T3 fibroblasts: effects of growth factors, transformation, and cell shape |
title_fullStr | Nuclear transport in 3T3 fibroblasts: effects of growth factors, transformation, and cell shape |
title_full_unstemmed | Nuclear transport in 3T3 fibroblasts: effects of growth factors, transformation, and cell shape |
title_short | Nuclear transport in 3T3 fibroblasts: effects of growth factors, transformation, and cell shape |
title_sort | nuclear transport in 3t3 fibroblasts: effects of growth factors, transformation, and cell shape |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2114954/ https://www.ncbi.nlm.nih.gov/pubmed/2448310 |