An optimized procedure for quantitative analysis of mitophagy with the mtKeima system using flow cytometry

Mitophagy is the process by which mitochondria are selectively targeted and removed via autophagic machinery to maintain mitochondrial homeostasis in the cell. Recently, flow cytometry-based assays that utilize the fluorescent mtKeima reporter system have allowed for quantitative assessment of mitop...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:BioTechniques 2020-10, Vol.69 (4), p.249-256
Hauptverfasser: Winsor, Nathaniel J., Killackey, Samuel A., Philpott, Dana J., Girardin, Stephen E.
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 256
container_issue 4
container_start_page 249
container_title BioTechniques
container_volume 69
creator Winsor, Nathaniel J.
Killackey, Samuel A.
Philpott, Dana J.
Girardin, Stephen E.
description Mitophagy is the process by which mitochondria are selectively targeted and removed via autophagic machinery to maintain mitochondrial homeostasis in the cell. Recently, flow cytometry-based assays that utilize the fluorescent mtKeima reporter system have allowed for quantitative assessment of mitophagy at a single-cell level. However, clear guidelines for appropriate flow cytometry workflow and downstream analysis are lacking and studies using flow cytometry in mtKeima-expressing cells often display incorrect and arbitrary binary mitophagic or nonmitophagic cutoffs that prevent proper quantitative analyses. In this paper we propose a novel method of mtKeima data analysis that preserves subtle differences present within flow cytometry data in a manner that ensures reproducibility. In this report we propose an outline for the transfection of mtKeima into a cell monolayer, cell preparation and downstream analysis using flow cytometry and associated software, with emphasis on a novel data processing technique.
doi_str_mv 10.2144/btn-2020-0071
format Article
fullrecord <record><control><sourceid>proquest_futur</sourceid><recordid>TN_cdi_futurescience_futuremedicine_10_2144_btn_2020_0071</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><doaj_id>oai_doaj_org_article_e22e909199ca4fd4a0f1d086eeefbedc</doaj_id><sourcerecordid>2435187011</sourcerecordid><originalsourceid>FETCH-LOGICAL-c425t-be6cb92a514b46ab0fff3841065238cf875315d52dae193d261a9c9f1f1931163</originalsourceid><addsrcrecordid>eNqNkUFv1DAQRiNERZe2R-4-IqHA2LGT-FitKFRU4kLPluOMd71K7G3ssAq_Hm8DvSFxssd638zIryjeUfjIKOefuuRLBgxKgIa-KjZUcihlS9vXxQaaqi5rBuKyeBvjATLWNPJNcVmxFmrJ5aY43HoSjsmN7hf25DgFg_08IbFhIk-z9sklndxPJNrrYYkukmDJ6FI47vVuISeX9iTtkYzpG7pRk7jEhCOZo_M7YodwImZJYcQ0LdfFhdVDxJs_51XxePf5x_Zr-fD9y_329qE0nIlUdlibTjItKO94rTuw1lYtp1ALVrXGto2oqOgF6zVSWfWsploaaanNFaV1dVXcr337oA_qOOW1pkUF7dTzQ5h2Sk_JmQEVMoYSJJXSaG57rsHSHtoaEW2Hvcm93q-98s88zRiTGl00OAzaY5ijYrwStG2A0oyWK2qmEOOE9mU0BXVWpbIqdValzqoy_2HlT9gFG41Db_AlAwCiZkIAzzc40-3_09tnacFvw-xTjso1aueU1f7NrtWIvTPO4z-W_A0B3LuV</addsrcrecordid><sourcetype>Open Website</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2435187011</pqid></control><display><type>article</type><title>An optimized procedure for quantitative analysis of mitophagy with the mtKeima system using flow cytometry</title><source>DOAJ Directory of Open Access Journals</source><source>Web of Science - Science Citation Index Expanded - 2020&lt;img src="https://exlibris-pub.s3.amazonaws.com/fromwos-v2.jpg" /&gt;</source><source>Access via Taylor &amp; Francis (Open Access Collection)</source><source>EZB-FREE-00999 freely available EZB journals</source><creator>Winsor, Nathaniel J. ; Killackey, Samuel A. ; Philpott, Dana J. ; Girardin, Stephen E.</creator><creatorcontrib>Winsor, Nathaniel J. ; Killackey, Samuel A. ; Philpott, Dana J. ; Girardin, Stephen E.</creatorcontrib><description>Mitophagy is the process by which mitochondria are selectively targeted and removed via autophagic machinery to maintain mitochondrial homeostasis in the cell. Recently, flow cytometry-based assays that utilize the fluorescent mtKeima reporter system have allowed for quantitative assessment of mitophagy at a single-cell level. However, clear guidelines for appropriate flow cytometry workflow and downstream analysis are lacking and studies using flow cytometry in mtKeima-expressing cells often display incorrect and arbitrary binary mitophagic or nonmitophagic cutoffs that prevent proper quantitative analyses. In this paper we propose a novel method of mtKeima data analysis that preserves subtle differences present within flow cytometry data in a manner that ensures reproducibility. In this report we propose an outline for the transfection of mtKeima into a cell monolayer, cell preparation and downstream analysis using flow cytometry and associated software, with emphasis on a novel data processing technique.</description><identifier>ISSN: 0736-6205</identifier><identifier>EISSN: 1940-9818</identifier><identifier>DOI: 10.2144/btn-2020-0071</identifier><identifier>PMID: 32806949</identifier><language>eng</language><publisher>LONDON: Future Science Ltd</publisher><subject>Biochemical Research Methods ; Biochemistry &amp; Molecular Biology ; flow cytometry assays ; gating strategies ; Life Sciences &amp; Biomedicine ; mitophagy ; mtKeima ; ratio gating ; Science &amp; Technology</subject><ispartof>BioTechniques, 2020-10, Vol.69 (4), p.249-256</ispartof><rights>2020 Stephen E Girardin</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>true</woscitedreferencessubscribed><woscitedreferencescount>3</woscitedreferencescount><woscitedreferencesoriginalsourcerecordid>wos000562550400001</woscitedreferencesoriginalsourcerecordid><citedby>FETCH-LOGICAL-c425t-be6cb92a514b46ab0fff3841065238cf875315d52dae193d261a9c9f1f1931163</citedby><cites>FETCH-LOGICAL-c425t-be6cb92a514b46ab0fff3841065238cf875315d52dae193d261a9c9f1f1931163</cites><orcidid>0000-0002-4984-3012</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>315,781,785,865,2103,2115,27929,27930,28253</link.rule.ids></links><search><creatorcontrib>Winsor, Nathaniel J.</creatorcontrib><creatorcontrib>Killackey, Samuel A.</creatorcontrib><creatorcontrib>Philpott, Dana J.</creatorcontrib><creatorcontrib>Girardin, Stephen E.</creatorcontrib><title>An optimized procedure for quantitative analysis of mitophagy with the mtKeima system using flow cytometry</title><title>BioTechniques</title><addtitle>BIOTECHNIQUES</addtitle><description>Mitophagy is the process by which mitochondria are selectively targeted and removed via autophagic machinery to maintain mitochondrial homeostasis in the cell. Recently, flow cytometry-based assays that utilize the fluorescent mtKeima reporter system have allowed for quantitative assessment of mitophagy at a single-cell level. However, clear guidelines for appropriate flow cytometry workflow and downstream analysis are lacking and studies using flow cytometry in mtKeima-expressing cells often display incorrect and arbitrary binary mitophagic or nonmitophagic cutoffs that prevent proper quantitative analyses. In this paper we propose a novel method of mtKeima data analysis that preserves subtle differences present within flow cytometry data in a manner that ensures reproducibility. In this report we propose an outline for the transfection of mtKeima into a cell monolayer, cell preparation and downstream analysis using flow cytometry and associated software, with emphasis on a novel data processing technique.</description><subject>Biochemical Research Methods</subject><subject>Biochemistry &amp; Molecular Biology</subject><subject>flow cytometry assays</subject><subject>gating strategies</subject><subject>Life Sciences &amp; Biomedicine</subject><subject>mitophagy</subject><subject>mtKeima</subject><subject>ratio gating</subject><subject>Science &amp; Technology</subject><issn>0736-6205</issn><issn>1940-9818</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><sourceid>AOWDO</sourceid><sourceid>DOA</sourceid><recordid>eNqNkUFv1DAQRiNERZe2R-4-IqHA2LGT-FitKFRU4kLPluOMd71K7G3ssAq_Hm8DvSFxssd638zIryjeUfjIKOefuuRLBgxKgIa-KjZUcihlS9vXxQaaqi5rBuKyeBvjATLWNPJNcVmxFmrJ5aY43HoSjsmN7hf25DgFg_08IbFhIk-z9sklndxPJNrrYYkukmDJ6FI47vVuISeX9iTtkYzpG7pRk7jEhCOZo_M7YodwImZJYcQ0LdfFhdVDxJs_51XxePf5x_Zr-fD9y_329qE0nIlUdlibTjItKO94rTuw1lYtp1ALVrXGto2oqOgF6zVSWfWsploaaanNFaV1dVXcr337oA_qOOW1pkUF7dTzQ5h2Sk_JmQEVMoYSJJXSaG57rsHSHtoaEW2Hvcm93q-98s88zRiTGl00OAzaY5ijYrwStG2A0oyWK2qmEOOE9mU0BXVWpbIqdValzqoy_2HlT9gFG41Db_AlAwCiZkIAzzc40-3_09tnacFvw-xTjso1aueU1f7NrtWIvTPO4z-W_A0B3LuV</recordid><startdate>20201001</startdate><enddate>20201001</enddate><creator>Winsor, Nathaniel J.</creator><creator>Killackey, Samuel A.</creator><creator>Philpott, Dana J.</creator><creator>Girardin, Stephen E.</creator><general>Future Science Ltd</general><general>Future Sci Ltd</general><general>Taylor &amp; Francis Group</general><scope>FUSOA</scope><scope>AOWDO</scope><scope>BLEPL</scope><scope>DTL</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>DOA</scope><orcidid>https://orcid.org/0000-0002-4984-3012</orcidid></search><sort><creationdate>20201001</creationdate><title>An optimized procedure for quantitative analysis of mitophagy with the mtKeima system using flow cytometry</title><author>Winsor, Nathaniel J. ; Killackey, Samuel A. ; Philpott, Dana J. ; Girardin, Stephen E.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c425t-be6cb92a514b46ab0fff3841065238cf875315d52dae193d261a9c9f1f1931163</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>Biochemical Research Methods</topic><topic>Biochemistry &amp; Molecular Biology</topic><topic>flow cytometry assays</topic><topic>gating strategies</topic><topic>Life Sciences &amp; Biomedicine</topic><topic>mitophagy</topic><topic>mtKeima</topic><topic>ratio gating</topic><topic>Science &amp; Technology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Winsor, Nathaniel J.</creatorcontrib><creatorcontrib>Killackey, Samuel A.</creatorcontrib><creatorcontrib>Philpott, Dana J.</creatorcontrib><creatorcontrib>Girardin, Stephen E.</creatorcontrib><collection>Future Science (Open Access)</collection><collection>Web of Science - Science Citation Index Expanded - 2020</collection><collection>Web of Science Core Collection</collection><collection>Science Citation Index Expanded</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>BioTechniques</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Winsor, Nathaniel J.</au><au>Killackey, Samuel A.</au><au>Philpott, Dana J.</au><au>Girardin, Stephen E.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>An optimized procedure for quantitative analysis of mitophagy with the mtKeima system using flow cytometry</atitle><jtitle>BioTechniques</jtitle><stitle>BIOTECHNIQUES</stitle><date>2020-10-01</date><risdate>2020</risdate><volume>69</volume><issue>4</issue><spage>249</spage><epage>256</epage><pages>249-256</pages><issn>0736-6205</issn><eissn>1940-9818</eissn><abstract>Mitophagy is the process by which mitochondria are selectively targeted and removed via autophagic machinery to maintain mitochondrial homeostasis in the cell. Recently, flow cytometry-based assays that utilize the fluorescent mtKeima reporter system have allowed for quantitative assessment of mitophagy at a single-cell level. However, clear guidelines for appropriate flow cytometry workflow and downstream analysis are lacking and studies using flow cytometry in mtKeima-expressing cells often display incorrect and arbitrary binary mitophagic or nonmitophagic cutoffs that prevent proper quantitative analyses. In this paper we propose a novel method of mtKeima data analysis that preserves subtle differences present within flow cytometry data in a manner that ensures reproducibility. In this report we propose an outline for the transfection of mtKeima into a cell monolayer, cell preparation and downstream analysis using flow cytometry and associated software, with emphasis on a novel data processing technique.</abstract><cop>LONDON</cop><pub>Future Science Ltd</pub><pmid>32806949</pmid><doi>10.2144/btn-2020-0071</doi><tpages>8</tpages><orcidid>https://orcid.org/0000-0002-4984-3012</orcidid><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 0736-6205
ispartof BioTechniques, 2020-10, Vol.69 (4), p.249-256
issn 0736-6205
1940-9818
language eng
recordid cdi_futurescience_futuremedicine_10_2144_btn_2020_0071
source DOAJ Directory of Open Access Journals; Web of Science - Science Citation Index Expanded - 2020<img src="https://exlibris-pub.s3.amazonaws.com/fromwos-v2.jpg" />; Access via Taylor & Francis (Open Access Collection); EZB-FREE-00999 freely available EZB journals
subjects Biochemical Research Methods
Biochemistry & Molecular Biology
flow cytometry assays
gating strategies
Life Sciences & Biomedicine
mitophagy
mtKeima
ratio gating
Science & Technology
title An optimized procedure for quantitative analysis of mitophagy with the mtKeima system using flow cytometry
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-12T05%3A12%3A03IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_futur&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=An%20optimized%20procedure%20for%20quantitative%20analysis%20of%20mitophagy%20with%20the%20mtKeima%20system%20using%20flow%20cytometry&rft.jtitle=BioTechniques&rft.au=Winsor,%20Nathaniel%20J.&rft.date=2020-10-01&rft.volume=69&rft.issue=4&rft.spage=249&rft.epage=256&rft.pages=249-256&rft.issn=0736-6205&rft.eissn=1940-9818&rft_id=info:doi/10.2144/btn-2020-0071&rft_dat=%3Cproquest_futur%3E2435187011%3C/proquest_futur%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=2435187011&rft_id=info:pmid/32806949&rft_doaj_id=oai_doaj_org_article_e22e909199ca4fd4a0f1d086eeefbedc&rfr_iscdi=true