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Mitotic cytosol inhibits invagination of coated pits in broken mitotic cells
Receptor-mediated endocytosis is inhibited during mitosis in mammalian cells and earlier work on A431 cells suggested that one of the sites inhibited was the invagination of coated pits (Pypaert, M., J. M. Lucocq, and G. Warren. 1987. Eur. J. Cell Biol. 45: 23-29). To explore this inhibition further...
Formato: | Texto |
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Lenguaje: | English |
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The Rockefeller University Press
1991
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2289130/ https://www.ncbi.nlm.nih.gov/pubmed/1910051 |
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collection | PubMed |
description | Receptor-mediated endocytosis is inhibited during mitosis in mammalian cells and earlier work on A431 cells suggested that one of the sites inhibited was the invagination of coated pits (Pypaert, M., J. M. Lucocq, and G. Warren. 1987. Eur. J. Cell Biol. 45: 23-29). To explore this inhibition further, we have reproduced it in broken HeLa cells. Mitotic or interphase cells were broken by freeze-thawing in liquid nitrogen and warmed in the presence of mitotic or interphase cytosol. Using a morphological assay, we found invagination to be inhibited only when mitotic cells were incubated in mitotic cytosol. This inhibition was reversed by diluting the cytosol during the incubation. Reversal was sensitive to okadaic acid, a potent phosphatase inhibitor, showing that phosphorylation was involved in the inhibition of invagination. This was confirmed using purified cdc2 kinase which alone could partially substitute for mitotic cytosol. |
format | Text |
id | pubmed-2289130 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 1991 |
publisher | The Rockefeller University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-22891302008-05-01 Mitotic cytosol inhibits invagination of coated pits in broken mitotic cells J Cell Biol Articles Receptor-mediated endocytosis is inhibited during mitosis in mammalian cells and earlier work on A431 cells suggested that one of the sites inhibited was the invagination of coated pits (Pypaert, M., J. M. Lucocq, and G. Warren. 1987. Eur. J. Cell Biol. 45: 23-29). To explore this inhibition further, we have reproduced it in broken HeLa cells. Mitotic or interphase cells were broken by freeze-thawing in liquid nitrogen and warmed in the presence of mitotic or interphase cytosol. Using a morphological assay, we found invagination to be inhibited only when mitotic cells were incubated in mitotic cytosol. This inhibition was reversed by diluting the cytosol during the incubation. Reversal was sensitive to okadaic acid, a potent phosphatase inhibitor, showing that phosphorylation was involved in the inhibition of invagination. This was confirmed using purified cdc2 kinase which alone could partially substitute for mitotic cytosol. The Rockefeller University Press 1991-09-02 /pmc/articles/PMC2289130/ /pubmed/1910051 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 Mitotic cytosol inhibits invagination of coated pits in broken mitotic cells |
title | Mitotic cytosol inhibits invagination of coated pits in broken mitotic cells |
title_full | Mitotic cytosol inhibits invagination of coated pits in broken mitotic cells |
title_fullStr | Mitotic cytosol inhibits invagination of coated pits in broken mitotic cells |
title_full_unstemmed | Mitotic cytosol inhibits invagination of coated pits in broken mitotic cells |
title_short | Mitotic cytosol inhibits invagination of coated pits in broken mitotic cells |
title_sort | mitotic cytosol inhibits invagination of coated pits in broken mitotic cells |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2289130/ https://www.ncbi.nlm.nih.gov/pubmed/1910051 |