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Targeted fluorescence lifetime probes reveal responsive organelle viscosity and membrane fluidity
The only way to visually observe cellular viscosity, which can greatly influence biological reactions and has been linked to several human diseases, is through viscosity imaging. Imaging cellular viscosity has allowed the mapping of viscosity in cells, and the next frontier is targeted viscosity ima...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6375549/ https://www.ncbi.nlm.nih.gov/pubmed/30763333 http://dx.doi.org/10.1371/journal.pone.0211165 |
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author | Steinmark, Ida Emilie James, Arjuna L. Chung, Pei-Hua Morton, Penny E. Parsons, Maddy Dreiss, Cécile A. Lorenz, Christian D. Yahioglu, Gokhan Suhling, Klaus |
author_facet | Steinmark, Ida Emilie James, Arjuna L. Chung, Pei-Hua Morton, Penny E. Parsons, Maddy Dreiss, Cécile A. Lorenz, Christian D. Yahioglu, Gokhan Suhling, Klaus |
author_sort | Steinmark, Ida Emilie |
collection | PubMed |
description | The only way to visually observe cellular viscosity, which can greatly influence biological reactions and has been linked to several human diseases, is through viscosity imaging. Imaging cellular viscosity has allowed the mapping of viscosity in cells, and the next frontier is targeted viscosity imaging of organelles and their microenvironments. Here we present a fluorescent molecular rotor/FLIM framework to image both organellar viscosity and membrane fluidity, using a combination of chemical targeting and organelle extraction. For demonstration, we image matrix viscosity and membrane fluidity of mitochondria, which have been linked to human diseases, including Alzheimer’s Disease and Leigh’s syndrome. We find that both are highly dynamic and responsive to small environmental and physiological changes, even under non-pathological conditions. This shows that neither viscosity nor fluidity can be assumed to be fixed and underlines the need for single-cell, and now even single-organelle, imaging. |
format | Online Article Text |
id | pubmed-6375549 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-63755492019-03-01 Targeted fluorescence lifetime probes reveal responsive organelle viscosity and membrane fluidity Steinmark, Ida Emilie James, Arjuna L. Chung, Pei-Hua Morton, Penny E. Parsons, Maddy Dreiss, Cécile A. Lorenz, Christian D. Yahioglu, Gokhan Suhling, Klaus PLoS One Research Article The only way to visually observe cellular viscosity, which can greatly influence biological reactions and has been linked to several human diseases, is through viscosity imaging. Imaging cellular viscosity has allowed the mapping of viscosity in cells, and the next frontier is targeted viscosity imaging of organelles and their microenvironments. Here we present a fluorescent molecular rotor/FLIM framework to image both organellar viscosity and membrane fluidity, using a combination of chemical targeting and organelle extraction. For demonstration, we image matrix viscosity and membrane fluidity of mitochondria, which have been linked to human diseases, including Alzheimer’s Disease and Leigh’s syndrome. We find that both are highly dynamic and responsive to small environmental and physiological changes, even under non-pathological conditions. This shows that neither viscosity nor fluidity can be assumed to be fixed and underlines the need for single-cell, and now even single-organelle, imaging. Public Library of Science 2019-02-14 /pmc/articles/PMC6375549/ /pubmed/30763333 http://dx.doi.org/10.1371/journal.pone.0211165 Text en © 2019 Steinmark 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 (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Steinmark, Ida Emilie James, Arjuna L. Chung, Pei-Hua Morton, Penny E. Parsons, Maddy Dreiss, Cécile A. Lorenz, Christian D. Yahioglu, Gokhan Suhling, Klaus Targeted fluorescence lifetime probes reveal responsive organelle viscosity and membrane fluidity |
title | Targeted fluorescence lifetime probes reveal responsive organelle viscosity and membrane fluidity |
title_full | Targeted fluorescence lifetime probes reveal responsive organelle viscosity and membrane fluidity |
title_fullStr | Targeted fluorescence lifetime probes reveal responsive organelle viscosity and membrane fluidity |
title_full_unstemmed | Targeted fluorescence lifetime probes reveal responsive organelle viscosity and membrane fluidity |
title_short | Targeted fluorescence lifetime probes reveal responsive organelle viscosity and membrane fluidity |
title_sort | targeted fluorescence lifetime probes reveal responsive organelle viscosity and membrane fluidity |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6375549/ https://www.ncbi.nlm.nih.gov/pubmed/30763333 http://dx.doi.org/10.1371/journal.pone.0211165 |
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