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An Improved Chamber for Direct Visualisation of Chemotaxis

There has been a growing appreciation over the last decade that chemotaxis plays an important role in cancer migration, invasion and metastasis. Research into the field of cancer cell chemotaxis is still in its infancy and traditional investigative tools have been developed with other cell types and...

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Detalles Bibliográficos
Autores principales: Muinonen-Martin, Andrew J., Veltman, Douwe M., Kalna, Gabriela, Insall, Robert H.
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3001854/
https://www.ncbi.nlm.nih.gov/pubmed/21179457
http://dx.doi.org/10.1371/journal.pone.0015309
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author Muinonen-Martin, Andrew J.
Veltman, Douwe M.
Kalna, Gabriela
Insall, Robert H.
author_facet Muinonen-Martin, Andrew J.
Veltman, Douwe M.
Kalna, Gabriela
Insall, Robert H.
author_sort Muinonen-Martin, Andrew J.
collection PubMed
description There has been a growing appreciation over the last decade that chemotaxis plays an important role in cancer migration, invasion and metastasis. Research into the field of cancer cell chemotaxis is still in its infancy and traditional investigative tools have been developed with other cell types and purposes in mind. Direct visualisation chambers are considered the gold standard for investigating the behaviour of cells migrating in a chemotactic gradient. We therefore drew up a list of key attributes that a chemotaxis chamber should have for investigating cancer cell chemotaxis. These include (1) compatibility with thin cover slips for optimal optical properties and to allow use of high numerical aperture (NA) oil immersion objectives; (2) gradients that are relatively stable for at least 24 hours due to the slow migration of cancer cells; (3) gradients of different steepnesses in a single experiment, with defined, consistent directions to avoid the need for complicated analysis; and (4) simple handling and disposability for use with medical samples. Here we describe and characterise the Insall chamber, a novel direct visualisation chamber. We use it to show GFP-lifeact transfected MV3 melanoma cells chemotaxing using a 60x high NA oil immersion objective, which cannot usually be done with other chemotaxis chambers. Linear gradients gave very efficient chemotaxis, contradicting earlier results suggesting that only polynomial gradients were effective. In conclusion, the chamber satisfies our design criteria, most importantly allowing high NA oil immersion microscopy to track chemotaxing cancer cells in detail over 24 hours.
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spelling pubmed-30018542010-12-21 An Improved Chamber for Direct Visualisation of Chemotaxis Muinonen-Martin, Andrew J. Veltman, Douwe M. Kalna, Gabriela Insall, Robert H. PLoS One Research Article There has been a growing appreciation over the last decade that chemotaxis plays an important role in cancer migration, invasion and metastasis. Research into the field of cancer cell chemotaxis is still in its infancy and traditional investigative tools have been developed with other cell types and purposes in mind. Direct visualisation chambers are considered the gold standard for investigating the behaviour of cells migrating in a chemotactic gradient. We therefore drew up a list of key attributes that a chemotaxis chamber should have for investigating cancer cell chemotaxis. These include (1) compatibility with thin cover slips for optimal optical properties and to allow use of high numerical aperture (NA) oil immersion objectives; (2) gradients that are relatively stable for at least 24 hours due to the slow migration of cancer cells; (3) gradients of different steepnesses in a single experiment, with defined, consistent directions to avoid the need for complicated analysis; and (4) simple handling and disposability for use with medical samples. Here we describe and characterise the Insall chamber, a novel direct visualisation chamber. We use it to show GFP-lifeact transfected MV3 melanoma cells chemotaxing using a 60x high NA oil immersion objective, which cannot usually be done with other chemotaxis chambers. Linear gradients gave very efficient chemotaxis, contradicting earlier results suggesting that only polynomial gradients were effective. In conclusion, the chamber satisfies our design criteria, most importantly allowing high NA oil immersion microscopy to track chemotaxing cancer cells in detail over 24 hours. Public Library of Science 2010-12-14 /pmc/articles/PMC3001854/ /pubmed/21179457 http://dx.doi.org/10.1371/journal.pone.0015309 Text en Muinonen-Martin et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Muinonen-Martin, Andrew J.
Veltman, Douwe M.
Kalna, Gabriela
Insall, Robert H.
An Improved Chamber for Direct Visualisation of Chemotaxis
title An Improved Chamber for Direct Visualisation of Chemotaxis
title_full An Improved Chamber for Direct Visualisation of Chemotaxis
title_fullStr An Improved Chamber for Direct Visualisation of Chemotaxis
title_full_unstemmed An Improved Chamber for Direct Visualisation of Chemotaxis
title_short An Improved Chamber for Direct Visualisation of Chemotaxis
title_sort improved chamber for direct visualisation of chemotaxis
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3001854/
https://www.ncbi.nlm.nih.gov/pubmed/21179457
http://dx.doi.org/10.1371/journal.pone.0015309
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