Incorporation of [1-14C]-linoleic acid by LLC-WRC256 tumour cells
The incorporation of [14C]‐linoleic acid (LA) into total lipid fractions was higher in LLC‐WRC256 cells from the log phase of growth as compared to those of the plateau phase. LA was mainly incorporated into the phospholipid (PL) fraction of cells during the log phase, whereas in the plateau phase i...
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Veröffentlicht in: | Cell biochemistry and function 2002-12, Vol.20 (4), p.323-325 |
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description | The incorporation of [14C]‐linoleic acid (LA) into total lipid fractions was higher in LLC‐WRC256 cells from the log phase of growth as compared to those of the plateau phase. LA was mainly incorporated into the phospholipid (PL) fraction of cells during the log phase, whereas in the plateau phase it was mostly taken into cholesterol ester. The proportion of radioactivity was higher in phosphatidylserine of cells from the log phase, whereas in the plateau phase it was higher in phosphatidylcholine. This feature of LA incorporation may be an important factor in determining the proliferative capacity of tumour cells. Copyright © 2002 John Wiley & Sons, Ltd. |
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LA was mainly incorporated into the phospholipid (PL) fraction of cells during the log phase, whereas in the plateau phase it was mostly taken into cholesterol ester. The proportion of radioactivity was higher in phosphatidylserine of cells from the log phase, whereas in the plateau phase it was higher in phosphatidylcholine. This feature of LA incorporation may be an important factor in determining the proliferative capacity of tumour cells. 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Funct</addtitle><description>The incorporation of [14C]‐linoleic acid (LA) into total lipid fractions was higher in LLC‐WRC256 cells from the log phase of growth as compared to those of the plateau phase. LA was mainly incorporated into the phospholipid (PL) fraction of cells during the log phase, whereas in the plateau phase it was mostly taken into cholesterol ester. The proportion of radioactivity was higher in phosphatidylserine of cells from the log phase, whereas in the plateau phase it was higher in phosphatidylcholine. This feature of LA incorporation may be an important factor in determining the proliferative capacity of tumour cells. Copyright © 2002 John Wiley & Sons, Ltd.</description><subject>Animals</subject><subject>Carbon Radioisotopes - pharmacology</subject><subject>Cell Division</subject><subject>Cholesterol Esters - metabolism</subject><subject>Chromatography</subject><subject>growth phase</subject><subject>linoleic acid</subject><subject>Linoleic Acid - pharmacology</subject><subject>Phosphatidylserines - metabolism</subject><subject>phospholipids</subject><subject>Phospholipids - metabolism</subject><subject>Rats</subject><subject>Time Factors</subject><subject>Tumor Cells, Cultured</subject><subject>tumour cells</subject><issn>0263-6484</issn><issn>1099-0844</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2002</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp1kMtKxDAUQIMoOj7wD6QrXUj15p0stfiCUUHUEUVCJ02g2pmMyRSdv7fSQVeu7l0cDvcehHYxHGEAcmzH_khLvIIGGLTOQTG2igZABM0FU2wDbab0BgBaUFhHG5gwzLkQA3RyNbUhzkIs53WYZsFnLzjHrHjNm3oaGlfbrLR1lY0X2XBY5KO7gnCRzdtJaGNmXdOkbbTmyya5neXcQg_nZ_fFZT68vbgqToa5pZh2zkqVWjquveJUK-o4s9gr8MRLX7FSEg3AlAQhqWO6EtZTJZklBKzgY0W30H7vncXw0bo0N5M6_VxQTl1ok5FEMAKYd-BBD9oYUorOm1msJ2VcGAzmp5bpapmuVkfuLZXteOKqP26ZpwMOe-CzbtziP48pTs97Xd7TdZq7r1-6jO-me0pyM7q56LaRfHx6vjan9BuwUX31</recordid><startdate>200212</startdate><enddate>200212</enddate><creator>da Costa, Marilena</creator><creator>Vecchia, Marilene G.</creator><creator>Peres, Carmem M.</creator><creator>Curi, Rui</creator><general>John Wiley & Sons, 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>200212</creationdate><title>Incorporation of [1-14C]-linoleic acid by LLC-WRC256 tumour cells</title><author>da Costa, Marilena ; Vecchia, Marilene G. ; Peres, Carmem M. ; Curi, Rui</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3131-1d8a97e59f853983e54c1f80f2f7fd4a729004870673e49d6cf3874c220c65b83</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2002</creationdate><topic>Animals</topic><topic>Carbon Radioisotopes - pharmacology</topic><topic>Cell Division</topic><topic>Cholesterol Esters - metabolism</topic><topic>Chromatography</topic><topic>growth phase</topic><topic>linoleic acid</topic><topic>Linoleic Acid - pharmacology</topic><topic>Phosphatidylserines - metabolism</topic><topic>phospholipids</topic><topic>Phospholipids - metabolism</topic><topic>Rats</topic><topic>Time Factors</topic><topic>Tumor Cells, Cultured</topic><topic>tumour cells</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>da Costa, Marilena</creatorcontrib><creatorcontrib>Vecchia, Marilene G.</creatorcontrib><creatorcontrib>Peres, Carmem M.</creatorcontrib><creatorcontrib>Curi, Rui</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 biochemistry and function</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>da Costa, Marilena</au><au>Vecchia, Marilene G.</au><au>Peres, Carmem M.</au><au>Curi, Rui</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Incorporation of [1-14C]-linoleic acid by LLC-WRC256 tumour cells</atitle><jtitle>Cell biochemistry and function</jtitle><addtitle>Cell Biochem. Funct</addtitle><date>2002-12</date><risdate>2002</risdate><volume>20</volume><issue>4</issue><spage>323</spage><epage>325</epage><pages>323-325</pages><issn>0263-6484</issn><eissn>1099-0844</eissn><abstract>The incorporation of [14C]‐linoleic acid (LA) into total lipid fractions was higher in LLC‐WRC256 cells from the log phase of growth as compared to those of the plateau phase. LA was mainly incorporated into the phospholipid (PL) fraction of cells during the log phase, whereas in the plateau phase it was mostly taken into cholesterol ester. The proportion of radioactivity was higher in phosphatidylserine of cells from the log phase, whereas in the plateau phase it was higher in phosphatidylcholine. This feature of LA incorporation may be an important factor in determining the proliferative capacity of tumour cells. Copyright © 2002 John Wiley & Sons, Ltd.</abstract><cop>Chichester, UK</cop><pub>John Wiley & Sons, Ltd</pub><pmid>12415566</pmid><doi>10.1002/cbf.971</doi><tpages>3</tpages></addata></record> |
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subjects | Animals Carbon Radioisotopes - pharmacology Cell Division Cholesterol Esters - metabolism Chromatography growth phase linoleic acid Linoleic Acid - pharmacology Phosphatidylserines - metabolism phospholipids Phospholipids - metabolism Rats Time Factors Tumor Cells, Cultured tumour cells |
title | Incorporation of [1-14C]-linoleic acid by LLC-WRC256 tumour cells |
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