Evaluation of acridine orange, LysoTracker Red, and quinacrine as fluorescent probes for long‐term tracking of acidic vesicles
Acidic vesicles can be imaged and tracked in live cells after staining with several low molecular weight fluorescent probes, or with fluorescently labeled proteins. Three fluorescent dyes, acridine orange, LysoTracker Red DND‐99, and quinacrine, were evaluated as acidic vesicle tracers for confocal...
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Veröffentlicht in: | Cytometry. Part A 2014-08, Vol.85 (8), p.729-737 |
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description | Acidic vesicles can be imaged and tracked in live cells after staining with several low molecular weight fluorescent probes, or with fluorescently labeled proteins. Three fluorescent dyes, acridine orange, LysoTracker Red DND‐99, and quinacrine, were evaluated as acidic vesicle tracers for confocal fluorescence imaging and quantitative analysis. The stability of fluorescent signals, achievable image contrast, and phototoxicity were taken into consideration. The three tested tracers exhibit different advantages and pose different problems in imaging experiments. Acridine orange makes it possible to distinguish acidic vesicles with different internal pH but is fairly phototoxic and can cause spectacular bursts of the dye‐loaded vesicles. LysoTracker Red is less phototoxic but its rapid photobleaching limits the range of useful applications considerably. We demonstrate that quinacrine is most suitable for long‐term imaging when a high number of frames is required. This capacity made it possible to trace acidic vesicles for several hours, during a process of drug‐induced apoptosis. An ability to record the behavior of acidic vesicles over such long periods opens a possibility to study processes like autophagy or long‐term effects of drugs on endocytosis and exocytosis. © 2014 International Society for Advancement of Cytometry |
doi_str_mv | 10.1002/cyto.a.22495 |
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Three fluorescent dyes, acridine orange, LysoTracker Red DND‐99, and quinacrine, were evaluated as acidic vesicle tracers for confocal fluorescence imaging and quantitative analysis. The stability of fluorescent signals, achievable image contrast, and phototoxicity were taken into consideration. The three tested tracers exhibit different advantages and pose different problems in imaging experiments. Acridine orange makes it possible to distinguish acidic vesicles with different internal pH but is fairly phototoxic and can cause spectacular bursts of the dye‐loaded vesicles. LysoTracker Red is less phototoxic but its rapid photobleaching limits the range of useful applications considerably. We demonstrate that quinacrine is most suitable for long‐term imaging when a high number of frames is required. This capacity made it possible to trace acidic vesicles for several hours, during a process of drug‐induced apoptosis. 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Part A</title><addtitle>Cytometry A</addtitle><description>Acidic vesicles can be imaged and tracked in live cells after staining with several low molecular weight fluorescent probes, or with fluorescently labeled proteins. Three fluorescent dyes, acridine orange, LysoTracker Red DND‐99, and quinacrine, were evaluated as acidic vesicle tracers for confocal fluorescence imaging and quantitative analysis. The stability of fluorescent signals, achievable image contrast, and phototoxicity were taken into consideration. The three tested tracers exhibit different advantages and pose different problems in imaging experiments. Acridine orange makes it possible to distinguish acidic vesicles with different internal pH but is fairly phototoxic and can cause spectacular bursts of the dye‐loaded vesicles. LysoTracker Red is less phototoxic but its rapid photobleaching limits the range of useful applications considerably. We demonstrate that quinacrine is most suitable for long‐term imaging when a high number of frames is required. This capacity made it possible to trace acidic vesicles for several hours, during a process of drug‐induced apoptosis. An ability to record the behavior of acidic vesicles over such long periods opens a possibility to study processes like autophagy or long‐term effects of drugs on endocytosis and exocytosis. © 2014 International Society for Advancement of Cytometry</description><subject>acidic organelles</subject><subject>Acids - metabolism</subject><subject>acridine orange</subject><subject>Acridine Orange - metabolism</subject><subject>Amines - metabolism</subject><subject>apoptosis</subject><subject>Apoptosis - drug effects</subject><subject>Biological Transport - drug effects</subject><subject>Camptothecin - pharmacology</subject><subject>Cell Line</subject><subject>Cell Tracking - methods</subject><subject>Cytoplasmic Vesicles - drug effects</subject><subject>Cytoplasmic Vesicles - metabolism</subject><subject>endocytosis</subject><subject>Fluorescence</subject><subject>Fluorescent Dyes - metabolism</subject><subject>Humans</subject><subject>Imaging, Three-Dimensional</subject><subject>lysosomes</subject><subject>LysoTracker Red</subject><subject>quinacrine</subject><subject>Quinacrine - metabolism</subject><subject>Time Factors</subject><subject>vesicular transport</subject><issn>1552-4922</issn><issn>1552-4930</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkbtOwzAUhi0E4lLYmJFHhrY4dpwmI6q4SZWQUBmYLMc-qQyp3doJqBuPwDPyJDgEOiImW9an7_zHP0KnCRknhNALtWncWI4pTQu-gw4TzukoLRjZ3d4pPUBHITwTwjhhdB8ddCxjKTlE71evsm5lY5zFrsJSeaONBey8tAsY4tkmuLmX6gU8fgA9xNJqvG6N7cjIyYCrunUeggLb4JV3JcQn53Ht7OLz_aMBv8RNZzB20Y-IExR-hWBUDeEY7VWyDnDycw7Q4_XVfHo7mt3f3E0vZyPFU8ZHJS11wglolVGax8UmcccimWREMgJpyXihypTIMocMMq4LWWWVLgCqPFE5aDZA5703Rly3EBqxNDFzXUsLrg0iKuOn8DzL_oGmkzyGyiYRHfao8i4ED5VYebOUfiMSIrp6RFePkOK7noif_Zjbcgl6C__2EYG0B95MDZs_ZWL6NL-_7L1f2fye_w</recordid><startdate>201408</startdate><enddate>201408</enddate><creator>Pierzyńska‐Mach, Agnieszka</creator><creator>Janowski, Paweł A.</creator><creator>Dobrucki, Jurek W.</creator><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>7QO</scope><scope>8FD</scope><scope>FR3</scope><scope>P64</scope></search><sort><creationdate>201408</creationdate><title>Evaluation of acridine orange, LysoTracker Red, and quinacrine as fluorescent probes for long‐term tracking of acidic vesicles</title><author>Pierzyńska‐Mach, Agnieszka ; Janowski, Paweł A. ; Dobrucki, Jurek W.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c5435-b2bd150edc6228155749391760a30e4b359cb40ab8e6e65d9af6fd9eef81c8ed3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><topic>acidic organelles</topic><topic>Acids - metabolism</topic><topic>acridine orange</topic><topic>Acridine Orange - metabolism</topic><topic>Amines - metabolism</topic><topic>apoptosis</topic><topic>Apoptosis - drug effects</topic><topic>Biological Transport - drug effects</topic><topic>Camptothecin - pharmacology</topic><topic>Cell Line</topic><topic>Cell Tracking - methods</topic><topic>Cytoplasmic Vesicles - drug effects</topic><topic>Cytoplasmic Vesicles - metabolism</topic><topic>endocytosis</topic><topic>Fluorescence</topic><topic>Fluorescent Dyes - metabolism</topic><topic>Humans</topic><topic>Imaging, Three-Dimensional</topic><topic>lysosomes</topic><topic>LysoTracker Red</topic><topic>quinacrine</topic><topic>Quinacrine - metabolism</topic><topic>Time Factors</topic><topic>vesicular transport</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Pierzyńska‐Mach, Agnieszka</creatorcontrib><creatorcontrib>Janowski, Paweł A.</creatorcontrib><creatorcontrib>Dobrucki, Jurek W.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>Biotechnology Research Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><jtitle>Cytometry. Part A</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Pierzyńska‐Mach, Agnieszka</au><au>Janowski, Paweł A.</au><au>Dobrucki, Jurek W.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Evaluation of acridine orange, LysoTracker Red, and quinacrine as fluorescent probes for long‐term tracking of acidic vesicles</atitle><jtitle>Cytometry. Part A</jtitle><addtitle>Cytometry A</addtitle><date>2014-08</date><risdate>2014</risdate><volume>85</volume><issue>8</issue><spage>729</spage><epage>737</epage><pages>729-737</pages><issn>1552-4922</issn><eissn>1552-4930</eissn><abstract>Acidic vesicles can be imaged and tracked in live cells after staining with several low molecular weight fluorescent probes, or with fluorescently labeled proteins. Three fluorescent dyes, acridine orange, LysoTracker Red DND‐99, and quinacrine, were evaluated as acidic vesicle tracers for confocal fluorescence imaging and quantitative analysis. The stability of fluorescent signals, achievable image contrast, and phototoxicity were taken into consideration. The three tested tracers exhibit different advantages and pose different problems in imaging experiments. Acridine orange makes it possible to distinguish acidic vesicles with different internal pH but is fairly phototoxic and can cause spectacular bursts of the dye‐loaded vesicles. LysoTracker Red is less phototoxic but its rapid photobleaching limits the range of useful applications considerably. We demonstrate that quinacrine is most suitable for long‐term imaging when a high number of frames is required. This capacity made it possible to trace acidic vesicles for several hours, during a process of drug‐induced apoptosis. An ability to record the behavior of acidic vesicles over such long periods opens a possibility to study processes like autophagy or long‐term effects of drugs on endocytosis and exocytosis. © 2014 International Society for Advancement of Cytometry</abstract><cop>United States</cop><pmid>24953340</pmid><doi>10.1002/cyto.a.22495</doi><tpages>9</tpages><oa>free_for_read</oa></addata></record> |
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subjects | acidic organelles Acids - metabolism acridine orange Acridine Orange - metabolism Amines - metabolism apoptosis Apoptosis - drug effects Biological Transport - drug effects Camptothecin - pharmacology Cell Line Cell Tracking - methods Cytoplasmic Vesicles - drug effects Cytoplasmic Vesicles - metabolism endocytosis Fluorescence Fluorescent Dyes - metabolism Humans Imaging, Three-Dimensional lysosomes LysoTracker Red quinacrine Quinacrine - metabolism Time Factors vesicular transport |
title | Evaluation of acridine orange, LysoTracker Red, and quinacrine as fluorescent probes for long‐term tracking of acidic vesicles |
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