Temperature imaging using a cationic linear fluorescent polymeric thermometer and fluorescence lifetime imaging microscopy
Temperature is one of the most important of the physiological parameters that determine the biological status of living organisms. However, intracellular temperature was not imaged at the single-cell level until recently because of the lack of a molecular thermometer that can be applied to living ce...
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Veröffentlicht in: | Nature protocols 2019-04, Vol.14 (4), p.1293-1321 |
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description | Temperature is one of the most important of the physiological parameters that determine the biological status of living organisms. However, intracellular temperature was not imaged at the single-cell level until recently because of the lack of a molecular thermometer that can be applied to living cells. We have recently developed a method for imaging intracellular temperature using a cationic linear fluorescent polymeric thermometer (FPT) and fluorescence lifetime imaging microscopy (FLIM). The cationic linear FPT exhibits cell permeability in various mammalian cell lines and yeast cells, entering live cells within 10 min of incubation. Intracellular thermometry using the cationic linear FPT and FLIM can be used to image temperature with high temperature resolution (0.3–1.29 °C within a temperature range of 25–35 °C). The diffuse intracellular localization of the cationic linear FPT allows a high spatial resolution (i.e., the light microscope’s diffraction limit, 200 nm), enabling the detection of temperature distributions at the subcellular level. This protocol, including the construction of a calibration curve and intracellular temperature imaging, requires ~14 h. Experience in handling cultured mammalian cells and use of a confocal laser-scanning microscope (CLSM) is required.
This protocol describes intracellular temperature imaging with a cationic linear fluorescent polymeric thermometer (FPT). Step-by-step procedures are provided for sensor calibration and imaging by fluorescence lifetime imaging microscopy (FLIM). |
doi_str_mv | 10.1038/s41596-019-0145-7 |
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This protocol describes intracellular temperature imaging with a cationic linear fluorescent polymeric thermometer (FPT). Step-by-step procedures are provided for sensor calibration and imaging by fluorescence lifetime imaging microscopy (FLIM).</description><identifier>ISSN: 1754-2189</identifier><identifier>EISSN: 1750-2799</identifier><identifier>DOI: 10.1038/s41596-019-0145-7</identifier><identifier>PMID: 30903107</identifier><language>eng</language><publisher>London: Nature Publishing Group UK</publisher><subject>Analytical Chemistry ; Animals ; Biological Techniques ; Biomedical and Life Sciences ; Calibration ; Cationic polymerization ; Cell Line ; Cell lines ; Cell permeability ; Cell physiology ; Chlorocebus aethiops ; Computational Biology/Bioinformatics ; COS Cells ; Cytological research ; Design and construction ; Fluorescence ; Fluorescence microscopy ; HEK293 Cells ; HeLa Cells ; High temperature ; Humans ; Image Processing, Computer-Assisted - statistics & numerical data ; Imaging ; Intracellular ; Life Sciences ; Light diffraction ; Localization ; Mammalian cells ; Mammals ; Methods ; Mice ; Microarrays ; Microscopy ; Microscopy, Fluorescence - methods ; Microscopy, Fluorescence - statistics & numerical data ; NIH 3T3 Cells ; Optical Imaging - methods ; Optical Imaging - statistics & numerical data ; Organic Chemistry ; Protocol ; Saccharomyces cerevisiae - ultrastructure ; Spatial discrimination ; Spatial resolution ; T-Lymphocytes - ultrastructure ; Temperature ; Temperature distribution ; Temperature effects ; Temperature measurement ; Temperature requirements ; Thermometers ; Time-Lapse Imaging - methods ; Time-Lapse Imaging - statistics & numerical data ; Yeast ; Yeasts</subject><ispartof>Nature protocols, 2019-04, Vol.14 (4), p.1293-1321</ispartof><rights>The Author(s), under exclusive licence to Springer Nature Limited 2019</rights><rights>COPYRIGHT 2019 Nature Publishing Group</rights><rights>2019© The Author(s), under exclusive licence to Springer Nature Limited 2019</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c539t-3b87ec6abce4dde06b42f0d344856d9357b0e171b74485999c4bcce5550c3f453</citedby><cites>FETCH-LOGICAL-c539t-3b87ec6abce4dde06b42f0d344856d9357b0e171b74485999c4bcce5550c3f453</cites><orcidid>0000-0002-5996-2330 ; 0000-0002-9931-4063 ; 0000-0003-4463-1034 ; 0000-0002-1487-7351</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1038/s41596-019-0145-7$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1038/s41596-019-0145-7$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,776,780,27901,27902,41464,42533,51294</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/30903107$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Inada, Noriko</creatorcontrib><creatorcontrib>Fukuda, Nanaho</creatorcontrib><creatorcontrib>Hayashi, Teruyuki</creatorcontrib><creatorcontrib>Uchiyama, Seiichi</creatorcontrib><title>Temperature imaging using a cationic linear fluorescent polymeric thermometer and fluorescence lifetime imaging microscopy</title><title>Nature protocols</title><addtitle>Nat Protoc</addtitle><addtitle>Nat Protoc</addtitle><description>Temperature is one of the most important of the physiological parameters that determine the biological status of living organisms. However, intracellular temperature was not imaged at the single-cell level until recently because of the lack of a molecular thermometer that can be applied to living cells. We have recently developed a method for imaging intracellular temperature using a cationic linear fluorescent polymeric thermometer (FPT) and fluorescence lifetime imaging microscopy (FLIM). The cationic linear FPT exhibits cell permeability in various mammalian cell lines and yeast cells, entering live cells within 10 min of incubation. Intracellular thermometry using the cationic linear FPT and FLIM can be used to image temperature with high temperature resolution (0.3–1.29 °C within a temperature range of 25–35 °C). The diffuse intracellular localization of the cationic linear FPT allows a high spatial resolution (i.e., the light microscope’s diffraction limit, 200 nm), enabling the detection of temperature distributions at the subcellular level. This protocol, including the construction of a calibration curve and intracellular temperature imaging, requires ~14 h. Experience in handling cultured mammalian cells and use of a confocal laser-scanning microscope (CLSM) is required.
This protocol describes intracellular temperature imaging with a cationic linear fluorescent polymeric thermometer (FPT). Step-by-step procedures are provided for sensor calibration and imaging by fluorescence lifetime imaging microscopy (FLIM).</description><subject>Analytical Chemistry</subject><subject>Animals</subject><subject>Biological Techniques</subject><subject>Biomedical and Life Sciences</subject><subject>Calibration</subject><subject>Cationic polymerization</subject><subject>Cell Line</subject><subject>Cell lines</subject><subject>Cell permeability</subject><subject>Cell physiology</subject><subject>Chlorocebus aethiops</subject><subject>Computational Biology/Bioinformatics</subject><subject>COS Cells</subject><subject>Cytological research</subject><subject>Design and construction</subject><subject>Fluorescence</subject><subject>Fluorescence microscopy</subject><subject>HEK293 Cells</subject><subject>HeLa Cells</subject><subject>High temperature</subject><subject>Humans</subject><subject>Image Processing, Computer-Assisted - statistics & numerical data</subject><subject>Imaging</subject><subject>Intracellular</subject><subject>Life Sciences</subject><subject>Light diffraction</subject><subject>Localization</subject><subject>Mammalian cells</subject><subject>Mammals</subject><subject>Methods</subject><subject>Mice</subject><subject>Microarrays</subject><subject>Microscopy</subject><subject>Microscopy, Fluorescence - methods</subject><subject>Microscopy, Fluorescence - statistics & numerical data</subject><subject>NIH 3T3 Cells</subject><subject>Optical Imaging - methods</subject><subject>Optical Imaging - statistics & numerical data</subject><subject>Organic Chemistry</subject><subject>Protocol</subject><subject>Saccharomyces cerevisiae - ultrastructure</subject><subject>Spatial discrimination</subject><subject>Spatial resolution</subject><subject>T-Lymphocytes - ultrastructure</subject><subject>Temperature</subject><subject>Temperature distribution</subject><subject>Temperature effects</subject><subject>Temperature measurement</subject><subject>Temperature requirements</subject><subject>Thermometers</subject><subject>Time-Lapse Imaging - methods</subject><subject>Time-Lapse Imaging - statistics & numerical data</subject><subject>Yeast</subject><subject>Yeasts</subject><issn>1754-2189</issn><issn>1750-2799</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>BENPR</sourceid><recordid>eNp1kt1v1SAYxhujcXP6B3hjmnijF51QoMDlsvixZImJzmtC6dvKUqACTXb866We6fEYDeEj8HuewMtTVc8xOseIiDeJYia7BmFZOmUNf1CdYs5Q03IpH_5c06bFQp5UT1K6RYhy0vHH1QlBEhGM-Gn1_QbcAlHnNUJtnZ6sn-o1baOujc42eGvq2XrQsR7nNURIBnyulzDvHMRymL9CdMFBhlhrP_xBGSjKEbJ1B29nTQzJhGX3tHo06jnBs_v5rPry7u3N5Yfm-uP7q8uL68YwInNDesHBdLo3QIcBUNfTdkQDoVSwbpCE8R4B5rjn246U0tDeGGCMIUNGyshZ9Wrvu8TwbYWUlbPldvOsPYQ1qRbLjrWCCVHQl3-ht2GNvtxuowRjmLfsQE16BmX9GHLUZjNVF0yUj0GMbV7n_6BKG6DUIHgYbdk_Erw-EhQmw12e9JqSuvr86ZjFe3YrZoowqiWWCsedwkht2VD7bKiSDbVlQ_GieXH_uLV3MPxW_ApDAdo9kMqRnyAeXv9_1x_QFcQn</recordid><startdate>20190401</startdate><enddate>20190401</enddate><creator>Inada, Noriko</creator><creator>Fukuda, Nanaho</creator><creator>Hayashi, Teruyuki</creator><creator>Uchiyama, Seiichi</creator><general>Nature Publishing Group UK</general><general>Nature Publishing Group</general><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>ISR</scope><scope>3V.</scope><scope>7QG</scope><scope>7T5</scope><scope>7T7</scope><scope>7TM</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8FD</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AEUYN</scope><scope>AFKRA</scope><scope>ATCPS</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>C1K</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>H94</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M7N</scope><scope>M7P</scope><scope>P64</scope><scope>PATMY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PYCSY</scope><scope>RC3</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0002-5996-2330</orcidid><orcidid>https://orcid.org/0000-0002-9931-4063</orcidid><orcidid>https://orcid.org/0000-0003-4463-1034</orcidid><orcidid>https://orcid.org/0000-0002-1487-7351</orcidid></search><sort><creationdate>20190401</creationdate><title>Temperature imaging using a cationic linear fluorescent polymeric thermometer and fluorescence lifetime imaging microscopy</title><author>Inada, Noriko ; Fukuda, Nanaho ; Hayashi, Teruyuki ; Uchiyama, Seiichi</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c539t-3b87ec6abce4dde06b42f0d344856d9357b0e171b74485999c4bcce5550c3f453</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>Analytical Chemistry</topic><topic>Animals</topic><topic>Biological Techniques</topic><topic>Biomedical and Life Sciences</topic><topic>Calibration</topic><topic>Cationic polymerization</topic><topic>Cell Line</topic><topic>Cell lines</topic><topic>Cell permeability</topic><topic>Cell physiology</topic><topic>Chlorocebus aethiops</topic><topic>Computational Biology/Bioinformatics</topic><topic>COS Cells</topic><topic>Cytological research</topic><topic>Design and construction</topic><topic>Fluorescence</topic><topic>Fluorescence microscopy</topic><topic>HEK293 Cells</topic><topic>HeLa Cells</topic><topic>High temperature</topic><topic>Humans</topic><topic>Image Processing, Computer-Assisted - statistics & numerical data</topic><topic>Imaging</topic><topic>Intracellular</topic><topic>Life Sciences</topic><topic>Light diffraction</topic><topic>Localization</topic><topic>Mammalian cells</topic><topic>Mammals</topic><topic>Methods</topic><topic>Mice</topic><topic>Microarrays</topic><topic>Microscopy</topic><topic>Microscopy, Fluorescence - methods</topic><topic>Microscopy, Fluorescence - statistics & numerical data</topic><topic>NIH 3T3 Cells</topic><topic>Optical Imaging - methods</topic><topic>Optical Imaging - statistics & numerical data</topic><topic>Organic Chemistry</topic><topic>Protocol</topic><topic>Saccharomyces cerevisiae - ultrastructure</topic><topic>Spatial discrimination</topic><topic>Spatial resolution</topic><topic>T-Lymphocytes - ultrastructure</topic><topic>Temperature</topic><topic>Temperature distribution</topic><topic>Temperature effects</topic><topic>Temperature measurement</topic><topic>Temperature requirements</topic><topic>Thermometers</topic><topic>Time-Lapse Imaging - 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Academic</collection><jtitle>Nature protocols</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Inada, Noriko</au><au>Fukuda, Nanaho</au><au>Hayashi, Teruyuki</au><au>Uchiyama, Seiichi</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Temperature imaging using a cationic linear fluorescent polymeric thermometer and fluorescence lifetime imaging microscopy</atitle><jtitle>Nature protocols</jtitle><stitle>Nat Protoc</stitle><addtitle>Nat Protoc</addtitle><date>2019-04-01</date><risdate>2019</risdate><volume>14</volume><issue>4</issue><spage>1293</spage><epage>1321</epage><pages>1293-1321</pages><issn>1754-2189</issn><eissn>1750-2799</eissn><abstract>Temperature is one of the most important of the physiological parameters that determine the biological status of living organisms. However, intracellular temperature was not imaged at the single-cell level until recently because of the lack of a molecular thermometer that can be applied to living cells. We have recently developed a method for imaging intracellular temperature using a cationic linear fluorescent polymeric thermometer (FPT) and fluorescence lifetime imaging microscopy (FLIM). The cationic linear FPT exhibits cell permeability in various mammalian cell lines and yeast cells, entering live cells within 10 min of incubation. Intracellular thermometry using the cationic linear FPT and FLIM can be used to image temperature with high temperature resolution (0.3–1.29 °C within a temperature range of 25–35 °C). The diffuse intracellular localization of the cationic linear FPT allows a high spatial resolution (i.e., the light microscope’s diffraction limit, 200 nm), enabling the detection of temperature distributions at the subcellular level. This protocol, including the construction of a calibration curve and intracellular temperature imaging, requires ~14 h. Experience in handling cultured mammalian cells and use of a confocal laser-scanning microscope (CLSM) is required.
This protocol describes intracellular temperature imaging with a cationic linear fluorescent polymeric thermometer (FPT). Step-by-step procedures are provided for sensor calibration and imaging by fluorescence lifetime imaging microscopy (FLIM).</abstract><cop>London</cop><pub>Nature Publishing Group UK</pub><pmid>30903107</pmid><doi>10.1038/s41596-019-0145-7</doi><tpages>29</tpages><orcidid>https://orcid.org/0000-0002-5996-2330</orcidid><orcidid>https://orcid.org/0000-0002-9931-4063</orcidid><orcidid>https://orcid.org/0000-0003-4463-1034</orcidid><orcidid>https://orcid.org/0000-0002-1487-7351</orcidid></addata></record> |
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subjects | Analytical Chemistry Animals Biological Techniques Biomedical and Life Sciences Calibration Cationic polymerization Cell Line Cell lines Cell permeability Cell physiology Chlorocebus aethiops Computational Biology/Bioinformatics COS Cells Cytological research Design and construction Fluorescence Fluorescence microscopy HEK293 Cells HeLa Cells High temperature Humans Image Processing, Computer-Assisted - statistics & numerical data Imaging Intracellular Life Sciences Light diffraction Localization Mammalian cells Mammals Methods Mice Microarrays Microscopy Microscopy, Fluorescence - methods Microscopy, Fluorescence - statistics & numerical data NIH 3T3 Cells Optical Imaging - methods Optical Imaging - statistics & numerical data Organic Chemistry Protocol Saccharomyces cerevisiae - ultrastructure Spatial discrimination Spatial resolution T-Lymphocytes - ultrastructure Temperature Temperature distribution Temperature effects Temperature measurement Temperature requirements Thermometers Time-Lapse Imaging - methods Time-Lapse Imaging - statistics & numerical data Yeast Yeasts |
title | Temperature imaging using a cationic linear fluorescent polymeric thermometer and fluorescence lifetime imaging microscopy |
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