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A lipidomics investigation of the induced hypoxia stress on HeLa cells by using MS and NMR techniques
Induced hypoxia stress on cervical cancer derived cells (HeLa cells) leads to significant changes in their membrane lipid profiles. The lipidome of HeLa cells was characterized by a joint approach wherein liquid chromatography-mass spectrometry (LC-MS) analysis was followed by high resolution NMR me...
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Published in: | Molecular bioSystems 2014-01, Vol.1 (4), p.878-89 |
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creator | Yu, Yang Vidalino, Laura Anesi, Andrea Macchi, Paolo Guella, Graziano |
description | Induced hypoxia stress on cervical cancer derived cells (HeLa cells) leads to significant changes in their membrane lipid profiles. The lipidome of HeLa cells was characterized by a joint approach wherein liquid chromatography-mass spectrometry (LC-MS) analysis was followed by high resolution NMR measurements. Multivariate data analysis showed apparent separation between control and hypoxia-treated HeLa cells and thus demonstrated hypoxia effects on lipid metabolism. The most striking finding was that hypoxia stimulation significantly reduced the total amount of cellular phosphoinositols (PI) but caused a prominent increase in the amount of lyso phosphocholines (lyso-PC) and lyso phosphoethanolamines (lyso-PE). The observed decrease of PI amount under hypoxic conditions is probably due to the accumulation of cellular myo-inositol, which is known to play a critical role in
de novo
synthesis of PI. Moreover, our study suggests that polyunsaturated phospholipid species are stronger biomarkers for discriminating the effect of hypoxia treatment. The evaluation of changes in the average unsaturation index (UI) of the membrane lipids acyl chains reveals that UI slightly increases in several lipid classes, thus affecting membrane fluidity and further membrane-dependent functions. The plausible mechanisms by which HeLa cells adapt to hypoxia conditions are also briefly reported.
Induced hypoxia stress on cervical cancer derived cells (HeLa cells) leads to significant changes in their membrane lipid profiles. |
doi_str_mv | 10.1039/c3mb70540d |
format | article |
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de novo
synthesis of PI. Moreover, our study suggests that polyunsaturated phospholipid species are stronger biomarkers for discriminating the effect of hypoxia treatment. The evaluation of changes in the average unsaturation index (UI) of the membrane lipids acyl chains reveals that UI slightly increases in several lipid classes, thus affecting membrane fluidity and further membrane-dependent functions. The plausible mechanisms by which HeLa cells adapt to hypoxia conditions are also briefly reported.
Induced hypoxia stress on cervical cancer derived cells (HeLa cells) leads to significant changes in their membrane lipid profiles.</description><identifier>ISSN: 1742-206X</identifier><identifier>EISSN: 1742-2051</identifier><identifier>DOI: 10.1039/c3mb70540d</identifier><identifier>PMID: 24496110</identifier><language>eng</language><publisher>England</publisher><subject>Biomarkers ; Cell Hypoxia - physiology ; Cell Line, Tumor ; Chromatography, Liquid - methods ; Cobalt - chemistry ; HeLa Cells ; Humans ; Lipid Metabolism ; Lysophosphatidylcholines - metabolism ; Lysophospholipids - metabolism ; Magnetic Resonance Imaging - methods ; Mass Spectrometry - methods ; Membrane Lipids - chemistry ; Phosphatidylinositols - metabolism ; Stress, Physiological - physiology</subject><ispartof>Molecular bioSystems, 2014-01, Vol.1 (4), p.878-89</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c401t-d2b9717c0e099c59473a921de12aa7834b2bad12b3608299529f2d06032f43243</citedby><cites>FETCH-LOGICAL-c401t-d2b9717c0e099c59473a921de12aa7834b2bad12b3608299529f2d06032f43243</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/24496110$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Yu, Yang</creatorcontrib><creatorcontrib>Vidalino, Laura</creatorcontrib><creatorcontrib>Anesi, Andrea</creatorcontrib><creatorcontrib>Macchi, Paolo</creatorcontrib><creatorcontrib>Guella, Graziano</creatorcontrib><title>A lipidomics investigation of the induced hypoxia stress on HeLa cells by using MS and NMR techniques</title><title>Molecular bioSystems</title><addtitle>Mol Biosyst</addtitle><description>Induced hypoxia stress on cervical cancer derived cells (HeLa cells) leads to significant changes in their membrane lipid profiles. The lipidome of HeLa cells was characterized by a joint approach wherein liquid chromatography-mass spectrometry (LC-MS) analysis was followed by high resolution NMR measurements. Multivariate data analysis showed apparent separation between control and hypoxia-treated HeLa cells and thus demonstrated hypoxia effects on lipid metabolism. The most striking finding was that hypoxia stimulation significantly reduced the total amount of cellular phosphoinositols (PI) but caused a prominent increase in the amount of lyso phosphocholines (lyso-PC) and lyso phosphoethanolamines (lyso-PE). The observed decrease of PI amount under hypoxic conditions is probably due to the accumulation of cellular myo-inositol, which is known to play a critical role in
de novo
synthesis of PI. Moreover, our study suggests that polyunsaturated phospholipid species are stronger biomarkers for discriminating the effect of hypoxia treatment. The evaluation of changes in the average unsaturation index (UI) of the membrane lipids acyl chains reveals that UI slightly increases in several lipid classes, thus affecting membrane fluidity and further membrane-dependent functions. The plausible mechanisms by which HeLa cells adapt to hypoxia conditions are also briefly reported.
Induced hypoxia stress on cervical cancer derived cells (HeLa cells) leads to significant changes in their membrane lipid profiles.</description><subject>Biomarkers</subject><subject>Cell Hypoxia - physiology</subject><subject>Cell Line, Tumor</subject><subject>Chromatography, Liquid - methods</subject><subject>Cobalt - chemistry</subject><subject>HeLa Cells</subject><subject>Humans</subject><subject>Lipid Metabolism</subject><subject>Lysophosphatidylcholines - metabolism</subject><subject>Lysophospholipids - metabolism</subject><subject>Magnetic Resonance Imaging - methods</subject><subject>Mass Spectrometry - methods</subject><subject>Membrane Lipids - chemistry</subject><subject>Phosphatidylinositols - metabolism</subject><subject>Stress, Physiological - physiology</subject><issn>1742-206X</issn><issn>1742-2051</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><recordid>eNp9kUlPwzAQhS0EolC4cAeZG0IKjJfE9bGUpUgtSCwSt8ixndYoG3GC6L8npaXcOM1o3qc3ozcIHRG4IMDkpWZ5IiDkYLbQHhGcBhRCsr3po7ce2vf-HYANOIFd1KOcy4gQ2EN2iDNXOVPmTnvsik_rGzdTjSsLXKa4mdtuaFptDZ4vqvLLKeyb2nqPO2BsJwprm2UeJwvcelfM8PQZq8Lgh-kTbqyeF-6jtf4A7aQq8_ZwXfvo9fbmZTQOJo9396PhJNAcSBMYmkhBhAYLUupQcsGUpMRYQpUSA8YTmihDaMIiGFApQypTaiACRlPOKGd9dLbyrepyubeJc-eXB6rClq2PSQhccCKk6NDzFarr0vvapnFVu1zVi5hAvIw1HrHp1U-s1x18svZtk9yaDfqbYwccr4Da643695dOP_1PjyuTsm8VKYZi</recordid><startdate>20140101</startdate><enddate>20140101</enddate><creator>Yu, Yang</creator><creator>Vidalino, Laura</creator><creator>Anesi, Andrea</creator><creator>Macchi, Paolo</creator><creator>Guella, Graziano</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></search><sort><creationdate>20140101</creationdate><title>A lipidomics investigation of the induced hypoxia stress on HeLa cells by using MS and NMR techniques</title><author>Yu, Yang ; Vidalino, Laura ; Anesi, Andrea ; Macchi, Paolo ; Guella, Graziano</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c401t-d2b9717c0e099c59473a921de12aa7834b2bad12b3608299529f2d06032f43243</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><topic>Biomarkers</topic><topic>Cell Hypoxia - physiology</topic><topic>Cell Line, Tumor</topic><topic>Chromatography, Liquid - methods</topic><topic>Cobalt - chemistry</topic><topic>HeLa Cells</topic><topic>Humans</topic><topic>Lipid Metabolism</topic><topic>Lysophosphatidylcholines - metabolism</topic><topic>Lysophospholipids - metabolism</topic><topic>Magnetic Resonance Imaging - methods</topic><topic>Mass Spectrometry - methods</topic><topic>Membrane Lipids - chemistry</topic><topic>Phosphatidylinositols - metabolism</topic><topic>Stress, Physiological - physiology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Yu, Yang</creatorcontrib><creatorcontrib>Vidalino, Laura</creatorcontrib><creatorcontrib>Anesi, Andrea</creatorcontrib><creatorcontrib>Macchi, Paolo</creatorcontrib><creatorcontrib>Guella, Graziano</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><jtitle>Molecular bioSystems</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Yu, Yang</au><au>Vidalino, Laura</au><au>Anesi, Andrea</au><au>Macchi, Paolo</au><au>Guella, Graziano</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>A lipidomics investigation of the induced hypoxia stress on HeLa cells by using MS and NMR techniques</atitle><jtitle>Molecular bioSystems</jtitle><addtitle>Mol Biosyst</addtitle><date>2014-01-01</date><risdate>2014</risdate><volume>1</volume><issue>4</issue><spage>878</spage><epage>89</epage><pages>878-89</pages><issn>1742-206X</issn><eissn>1742-2051</eissn><abstract>Induced hypoxia stress on cervical cancer derived cells (HeLa cells) leads to significant changes in their membrane lipid profiles. The lipidome of HeLa cells was characterized by a joint approach wherein liquid chromatography-mass spectrometry (LC-MS) analysis was followed by high resolution NMR measurements. Multivariate data analysis showed apparent separation between control and hypoxia-treated HeLa cells and thus demonstrated hypoxia effects on lipid metabolism. The most striking finding was that hypoxia stimulation significantly reduced the total amount of cellular phosphoinositols (PI) but caused a prominent increase in the amount of lyso phosphocholines (lyso-PC) and lyso phosphoethanolamines (lyso-PE). The observed decrease of PI amount under hypoxic conditions is probably due to the accumulation of cellular myo-inositol, which is known to play a critical role in
de novo
synthesis of PI. Moreover, our study suggests that polyunsaturated phospholipid species are stronger biomarkers for discriminating the effect of hypoxia treatment. The evaluation of changes in the average unsaturation index (UI) of the membrane lipids acyl chains reveals that UI slightly increases in several lipid classes, thus affecting membrane fluidity and further membrane-dependent functions. The plausible mechanisms by which HeLa cells adapt to hypoxia conditions are also briefly reported.
Induced hypoxia stress on cervical cancer derived cells (HeLa cells) leads to significant changes in their membrane lipid profiles.</abstract><cop>England</cop><pmid>24496110</pmid><doi>10.1039/c3mb70540d</doi><tpages>13</tpages></addata></record> |
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subjects | Biomarkers Cell Hypoxia - physiology Cell Line, Tumor Chromatography, Liquid - methods Cobalt - chemistry HeLa Cells Humans Lipid Metabolism Lysophosphatidylcholines - metabolism Lysophospholipids - metabolism Magnetic Resonance Imaging - methods Mass Spectrometry - methods Membrane Lipids - chemistry Phosphatidylinositols - metabolism Stress, Physiological - physiology |
title | A lipidomics investigation of the induced hypoxia stress on HeLa cells by using MS and NMR techniques |
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