Increased FITC fluorescence on LPS stimulated neutrophils cultured in whole blood
Recently, it has been observed that Annexin V labelling of phosphatidylserine (PS) on non-apoptotic cells can vary in different leukocyte populations and with the activation of cells, due to differences in the absolute level of exposed PS. We have also observed changes in the absolute level of Annex...
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Veröffentlicht in: | Cell biology international 2006-04, Vol.30 (4), p.394-399 |
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description | Recently, it has been observed that Annexin V labelling of phosphatidylserine (PS) on non-apoptotic cells can vary in different leukocyte populations and with the activation of cells, due to differences in the absolute level of exposed PS. We have also observed changes in the absolute level of Annexin V-FITC intensity, but under conditions where absolute PS expression did not change. In the present study, we have explored the effect of neutrophil cell activation on Annexin V-FITC fluorescence intensity by comparing alternatively labelled matched antibodies against Annexin V. Human venous whole blood was cultured with and without stimulation with lipopolysaccharide (LPS). Apoptosis in the neutrophil and lymphocyte populations was analyzed by flow cytometry and the intensity of FITC labelling was compared to matched fluorochromes conjugated to the same cell surface markers. There was an increase in the intensity of Annexin V-FITC in non-apoptotic neutrophils when stimulated with LPS, which did not correlate with increased apoptosis. Furthermore, CD65-FITC intensity also increased on activated neutrophils. Activated neutrophils exhibited higher amounts of FITC fluorescence that were not associated with changes in extracellular PS expression. This effect appears to be fluorochrome related, likely due to an increase in the pH surrounding activated neutrophils. |
doi_str_mv | 10.1016/j.cellbi.2005.12.006 |
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We have also observed changes in the absolute level of Annexin V-FITC intensity, but under conditions where absolute PS expression did not change. In the present study, we have explored the effect of neutrophil cell activation on Annexin V-FITC fluorescence intensity by comparing alternatively labelled matched antibodies against Annexin V. Human venous whole blood was cultured with and without stimulation with lipopolysaccharide (LPS). Apoptosis in the neutrophil and lymphocyte populations was analyzed by flow cytometry and the intensity of FITC labelling was compared to matched fluorochromes conjugated to the same cell surface markers. There was an increase in the intensity of Annexin V-FITC in non-apoptotic neutrophils when stimulated with LPS, which did not correlate with increased apoptosis. Furthermore, CD65-FITC intensity also increased on activated neutrophils. Activated neutrophils exhibited higher amounts of FITC fluorescence that were not associated with changes in extracellular PS expression. This effect appears to be fluorochrome related, likely due to an increase in the pH surrounding activated neutrophils.</description><identifier>ISSN: 1065-6995</identifier><identifier>EISSN: 1095-8355</identifier><identifier>DOI: 10.1016/j.cellbi.2005.12.006</identifier><identifier>PMID: 16503408</identifier><language>eng</language><publisher>Oxford, UK: Elsevier Ltd</publisher><subject>Adult ; Annexin A5 - metabolism ; Apoptosis ; Blood ; Carbocyanines - pharmacology ; Cell Culture Techniques - methods ; Cells, Cultured ; Fluorescein-5-isothiocyanate - analysis ; Fluorescein-5-isothiocyanate - chemistry ; Fluorescence ; Human ; Humans ; Lipopolysaccharides - pharmacology ; Lymphocytes - immunology ; Neutrophil ; Neutrophils - cytology ; Neutrophils - drug effects ; Neutrophils - metabolism ; Propidium - pharmacology</subject><ispartof>Cell biology international, 2006-04, Vol.30 (4), p.394-399</ispartof><rights>2006</rights><rights>The Author(s) Journal compilation © 2006 International Federation for Cell Biology</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4786-e460dae7f05b6409743d09b2128b5703c381c0c7eb87c0a9ad87e2b98f9457a93</citedby><cites>FETCH-LOGICAL-c4786-e460dae7f05b6409743d09b2128b5703c381c0c7eb87c0a9ad87e2b98f9457a93</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1016%2Fj.cellbi.2005.12.006$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1016%2Fj.cellbi.2005.12.006$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,780,784,1417,27924,27925,45574,45575</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/16503408$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Wilkins, R.C.</creatorcontrib><creatorcontrib>Bellier, P.V.</creatorcontrib><creatorcontrib>Kutzner, B.C.</creatorcontrib><creatorcontrib>McNamee, J.P.</creatorcontrib><title>Increased FITC fluorescence on LPS stimulated neutrophils cultured in whole blood</title><title>Cell biology international</title><addtitle>Cell Biol Int</addtitle><description>Recently, it has been observed that Annexin V labelling of phosphatidylserine (PS) on non-apoptotic cells can vary in different leukocyte populations and with the activation of cells, due to differences in the absolute level of exposed PS. We have also observed changes in the absolute level of Annexin V-FITC intensity, but under conditions where absolute PS expression did not change. In the present study, we have explored the effect of neutrophil cell activation on Annexin V-FITC fluorescence intensity by comparing alternatively labelled matched antibodies against Annexin V. Human venous whole blood was cultured with and without stimulation with lipopolysaccharide (LPS). Apoptosis in the neutrophil and lymphocyte populations was analyzed by flow cytometry and the intensity of FITC labelling was compared to matched fluorochromes conjugated to the same cell surface markers. There was an increase in the intensity of Annexin V-FITC in non-apoptotic neutrophils when stimulated with LPS, which did not correlate with increased apoptosis. Furthermore, CD65-FITC intensity also increased on activated neutrophils. Activated neutrophils exhibited higher amounts of FITC fluorescence that were not associated with changes in extracellular PS expression. This effect appears to be fluorochrome related, likely due to an increase in the pH surrounding activated neutrophils.</description><subject>Adult</subject><subject>Annexin A5 - metabolism</subject><subject>Apoptosis</subject><subject>Blood</subject><subject>Carbocyanines - pharmacology</subject><subject>Cell Culture Techniques - methods</subject><subject>Cells, Cultured</subject><subject>Fluorescein-5-isothiocyanate - analysis</subject><subject>Fluorescein-5-isothiocyanate - chemistry</subject><subject>Fluorescence</subject><subject>Human</subject><subject>Humans</subject><subject>Lipopolysaccharides - pharmacology</subject><subject>Lymphocytes - immunology</subject><subject>Neutrophil</subject><subject>Neutrophils - cytology</subject><subject>Neutrophils - drug effects</subject><subject>Neutrophils - metabolism</subject><subject>Propidium - pharmacology</subject><issn>1065-6995</issn><issn>1095-8355</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2006</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkc1u1DAURi0EoqXwBghlxS7hOon_WCDRKVMGjUoRRSwtx7lRPXjiqZ1Q-vYkygh2iJUt63yfr48JeUmhoED5m11h0fvGFSUAK2hZAPBH5JSCYrmsGHs87znLuVLshDxLaQdAaS35U3JCOYOqBnlKvmx6G9EkbLP15maVdX4MEZPF3mIW-mx7_TVLg9uP3gwT0-M4xHC4dT5ldvTDGKdD12f3t8Fj1vgQ2ufkSWd8whfH9Yx8W3-4WX3Mt58vN6v329zWQvIcaw6tQdEBa3gNStRVC6opaSkbJqCylaQWrMBGCgtGmVYKLBslO1UzYVR1Rl4vvYcY7kZMg967NCsxPYYxaS4k41DCBNYLaGNIKWKnD9HtTXzQFPSsUu_0olLPKjUt9aRyir069o_NHtu_oaO7CXi7APfO48N_lerV-eaKCja350vYpQF__Qmb-GMavBJMf7-61Befttfna36h58veLTxOSn86jDpZN39S6yLaQbfB_fs5vwGmPqds</recordid><startdate>200604</startdate><enddate>200604</enddate><creator>Wilkins, R.C.</creator><creator>Bellier, P.V.</creator><creator>Kutzner, B.C.</creator><creator>McNamee, J.P.</creator><general>Elsevier Ltd</general><general>Blackwell Publishing Ltd</general><scope>BSCLL</scope><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></search><sort><creationdate>200604</creationdate><title>Increased FITC fluorescence on LPS stimulated neutrophils cultured in whole blood</title><author>Wilkins, R.C. ; Bellier, P.V. ; Kutzner, B.C. ; McNamee, J.P.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4786-e460dae7f05b6409743d09b2128b5703c381c0c7eb87c0a9ad87e2b98f9457a93</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2006</creationdate><topic>Adult</topic><topic>Annexin A5 - metabolism</topic><topic>Apoptosis</topic><topic>Blood</topic><topic>Carbocyanines - pharmacology</topic><topic>Cell Culture Techniques - methods</topic><topic>Cells, Cultured</topic><topic>Fluorescein-5-isothiocyanate - analysis</topic><topic>Fluorescein-5-isothiocyanate - chemistry</topic><topic>Fluorescence</topic><topic>Human</topic><topic>Humans</topic><topic>Lipopolysaccharides - pharmacology</topic><topic>Lymphocytes - immunology</topic><topic>Neutrophil</topic><topic>Neutrophils - cytology</topic><topic>Neutrophils - drug effects</topic><topic>Neutrophils - metabolism</topic><topic>Propidium - pharmacology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Wilkins, R.C.</creatorcontrib><creatorcontrib>Bellier, P.V.</creatorcontrib><creatorcontrib>Kutzner, B.C.</creatorcontrib><creatorcontrib>McNamee, J.P.</creatorcontrib><collection>Istex</collection><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><jtitle>Cell biology international</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Wilkins, R.C.</au><au>Bellier, P.V.</au><au>Kutzner, B.C.</au><au>McNamee, J.P.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Increased FITC fluorescence on LPS stimulated neutrophils cultured in whole blood</atitle><jtitle>Cell biology international</jtitle><addtitle>Cell Biol Int</addtitle><date>2006-04</date><risdate>2006</risdate><volume>30</volume><issue>4</issue><spage>394</spage><epage>399</epage><pages>394-399</pages><issn>1065-6995</issn><eissn>1095-8355</eissn><abstract>Recently, it has been observed that Annexin V labelling of phosphatidylserine (PS) on non-apoptotic cells can vary in different leukocyte populations and with the activation of cells, due to differences in the absolute level of exposed PS. We have also observed changes in the absolute level of Annexin V-FITC intensity, but under conditions where absolute PS expression did not change. In the present study, we have explored the effect of neutrophil cell activation on Annexin V-FITC fluorescence intensity by comparing alternatively labelled matched antibodies against Annexin V. Human venous whole blood was cultured with and without stimulation with lipopolysaccharide (LPS). Apoptosis in the neutrophil and lymphocyte populations was analyzed by flow cytometry and the intensity of FITC labelling was compared to matched fluorochromes conjugated to the same cell surface markers. There was an increase in the intensity of Annexin V-FITC in non-apoptotic neutrophils when stimulated with LPS, which did not correlate with increased apoptosis. Furthermore, CD65-FITC intensity also increased on activated neutrophils. Activated neutrophils exhibited higher amounts of FITC fluorescence that were not associated with changes in extracellular PS expression. This effect appears to be fluorochrome related, likely due to an increase in the pH surrounding activated neutrophils.</abstract><cop>Oxford, UK</cop><pub>Elsevier Ltd</pub><pmid>16503408</pmid><doi>10.1016/j.cellbi.2005.12.006</doi><tpages>6</tpages></addata></record> |
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subjects | Adult Annexin A5 - metabolism Apoptosis Blood Carbocyanines - pharmacology Cell Culture Techniques - methods Cells, Cultured Fluorescein-5-isothiocyanate - analysis Fluorescein-5-isothiocyanate - chemistry Fluorescence Human Humans Lipopolysaccharides - pharmacology Lymphocytes - immunology Neutrophil Neutrophils - cytology Neutrophils - drug effects Neutrophils - metabolism Propidium - pharmacology |
title | Increased FITC fluorescence on LPS stimulated neutrophils cultured in whole blood |
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