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Computerized detection of morphological changes to glioma cells during estramustine and ion-channel blocker perifusion.
A perifusion technique for microscopy with computerized detection of early changes in cell morphology during continuous perifusion was used to show that the geometry of cultured glioma cells (MG-251) changes rapidly when they are exposed to estramustine phosphate (EMP). When the cells were exposed t...
Autores principales: | , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
1997
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2224065/ https://www.ncbi.nlm.nih.gov/pubmed/9252198 |
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author | Behnam-Motlagh, P. Jonsson, O. Engström, K. G. Henriksson, R. Grankvist, K. |
author_facet | Behnam-Motlagh, P. Jonsson, O. Engström, K. G. Henriksson, R. Grankvist, K. |
author_sort | Behnam-Motlagh, P. |
collection | PubMed |
description | A perifusion technique for microscopy with computerized detection of early changes in cell morphology during continuous perifusion was used to show that the geometry of cultured glioma cells (MG-251) changes rapidly when they are exposed to estramustine phosphate (EMP). When the cells were exposed to 20 or 40 mg l(-1) EMP, cell volume projected cell area (PCA) rapidly increased. When the Na+,K+-ATPase blocker ouabain (100 micromol l(-1)) was added to the EMP (40 mg l(-1)) perifusion, the acute EMP response was eradicated. When the PCA curve for ouabain alone was subtracted from the curve of combined ouabain and EMP perifusion, the resulting curve showed that ouabain completely blocked the EMP-induced increase in PCA. When the Na+, K+, Cl- co-transport inhibitors bumetanide (10 micromol l(-1)), or furosemide (100 micromol l(-1)), were added to EMP (40 mg l(-1)), the acute increase in PCA seen for EMP alone was also completely blocked. This study shows that inhibitors of ion transmembrane transport can modify EMP-induced cell volume increases. This may be of particular importance since the blockers have been found to interfere also with the cytotoxic function of EMP during cell culture. Thus, it is possible that cell volume changes could serve as a rapid technique for predicting the cytotoxic activity of antineoplastic drugs. |
format | Text |
id | pubmed-2224065 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 1997 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-22240652009-09-10 Computerized detection of morphological changes to glioma cells during estramustine and ion-channel blocker perifusion. Behnam-Motlagh, P. Jonsson, O. Engström, K. G. Henriksson, R. Grankvist, K. Br J Cancer Research Article A perifusion technique for microscopy with computerized detection of early changes in cell morphology during continuous perifusion was used to show that the geometry of cultured glioma cells (MG-251) changes rapidly when they are exposed to estramustine phosphate (EMP). When the cells were exposed to 20 or 40 mg l(-1) EMP, cell volume projected cell area (PCA) rapidly increased. When the Na+,K+-ATPase blocker ouabain (100 micromol l(-1)) was added to the EMP (40 mg l(-1)) perifusion, the acute EMP response was eradicated. When the PCA curve for ouabain alone was subtracted from the curve of combined ouabain and EMP perifusion, the resulting curve showed that ouabain completely blocked the EMP-induced increase in PCA. When the Na+, K+, Cl- co-transport inhibitors bumetanide (10 micromol l(-1)), or furosemide (100 micromol l(-1)), were added to EMP (40 mg l(-1)), the acute increase in PCA seen for EMP alone was also completely blocked. This study shows that inhibitors of ion transmembrane transport can modify EMP-induced cell volume increases. This may be of particular importance since the blockers have been found to interfere also with the cytotoxic function of EMP during cell culture. Thus, it is possible that cell volume changes could serve as a rapid technique for predicting the cytotoxic activity of antineoplastic drugs. Nature Publishing Group 1997 /pmc/articles/PMC2224065/ /pubmed/9252198 Text en https://creativecommons.org/licenses/by/4.0/This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit https://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Research Article Behnam-Motlagh, P. Jonsson, O. Engström, K. G. Henriksson, R. Grankvist, K. Computerized detection of morphological changes to glioma cells during estramustine and ion-channel blocker perifusion. |
title | Computerized detection of morphological changes to glioma cells during estramustine and ion-channel blocker perifusion. |
title_full | Computerized detection of morphological changes to glioma cells during estramustine and ion-channel blocker perifusion. |
title_fullStr | Computerized detection of morphological changes to glioma cells during estramustine and ion-channel blocker perifusion. |
title_full_unstemmed | Computerized detection of morphological changes to glioma cells during estramustine and ion-channel blocker perifusion. |
title_short | Computerized detection of morphological changes to glioma cells during estramustine and ion-channel blocker perifusion. |
title_sort | computerized detection of morphological changes to glioma cells during estramustine and ion-channel blocker perifusion. |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2224065/ https://www.ncbi.nlm.nih.gov/pubmed/9252198 |
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