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Selective deacylation of arachidonate-containing ethanolamine-linked phosphoglycerides in stimulated human neutrophils
The involvement of the ethanolamine-linked phosphoglyceride fraction (PE) in neutrophil signal transduction is suggested by the stimulus-induced release of arachidonic acid from PE (Chilton, F. H., and Connell, T. R. (1988) J. Biol. Chem. 263, 5260-5265) and by the synthesis of acetylated PE species...
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Published in: | The Journal of biological chemistry 1990-12, Vol.265 (34), p.21032-21038 |
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description | The involvement of the ethanolamine-linked phosphoglyceride fraction (PE) in neutrophil signal transduction is suggested by the stimulus-induced release of arachidonic acid from PE (Chilton, F. H., and Connell, T. R. (1988) J. Biol. Chem. 263, 5260-5265) and by the synthesis of acetylated PE species, predominantly 1-O-alk-1‘-enyl-2-acetyl-sn-glycero-3-phosphoethanolamine (alkenylacetyl-GPE; Tessner, T. G., and Wykle, R. L. (1987) J. Biol. Chem. 262, 12660-12664) in stimulated cells. In the studies reported here, we investigated the relationship between arachidonic acid release from PE and generation of the lysophospholipid precursor required in the biosynthesis of alkenylacetyl-GPE. In order to follow these reactions, we prelabeled neutrophils with 1-O-[3H]alk-1‘-enyl-2-arachidonoyl-sn-glycero-3-phosphoethanolamine (alkenyl-acyl-GPE). We also followed the hydrolysis of endogenous PE by analysis as the dinitrophenyl derivative using a high pressure liquid chromatography method we developed. Our results coupled with those of Chilton et al. (Chilton, F. H., Ellis, J. M., Olson, S. C., and Wykle, R. L. (1984) J. Biol. Chem. 259, 12014-12019) indicate that in human neutrophils the metabolism of alkenylacyl-GPE and alkylacyl-sn-glycero-3-phosphocholine (GPC) are strikingly similar with regard to arachidonate metabolism. When added to neutrophils, both 1-O-[3H]alkenyl-2-lyso-GPE and 1-O-[3H]alkyl-2-lyso-GPC are acylated predominantly with arachidonic acid, and the resulting arachidonoyl-containing phospholipids are extensively deacylated upon stimulation. However, hydrolysis of PE in the neutrophil differs from hydrolysis of choline-containing phosphoglycerides in that stimulation leads to a greater accumulation of the ethanolamine-linked lysophospholipid. A comparison of the molecular species of endogenous PE (based on molar concentrations measured as the dinitrophenyl derivative) from resting and stimulated neutrophils indicated that only those species which contain arachidonate are significantly hydrolyzed. |
doi_str_mv | 10.1016/S0021-9258(17)45323-3 |
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H., and Connell, T. R. (1988) J. Biol. Chem. 263, 5260-5265) and by the synthesis of acetylated PE species, predominantly 1-O-alk-1‘-enyl-2-acetyl-sn-glycero-3-phosphoethanolamine (alkenylacetyl-GPE; Tessner, T. G., and Wykle, R. L. (1987) J. Biol. Chem. 262, 12660-12664) in stimulated cells. In the studies reported here, we investigated the relationship between arachidonic acid release from PE and generation of the lysophospholipid precursor required in the biosynthesis of alkenylacetyl-GPE. In order to follow these reactions, we prelabeled neutrophils with 1-O-[3H]alk-1‘-enyl-2-arachidonoyl-sn-glycero-3-phosphoethanolamine (alkenyl-acyl-GPE). We also followed the hydrolysis of endogenous PE by analysis as the dinitrophenyl derivative using a high pressure liquid chromatography method we developed. Our results coupled with those of Chilton et al. (Chilton, F. H., Ellis, J. M., Olson, S. C., and Wykle, R. L. (1984) J. Biol. Chem. 259, 12014-12019) indicate that in human neutrophils the metabolism of alkenylacyl-GPE and alkylacyl-sn-glycero-3-phosphocholine (GPC) are strikingly similar with regard to arachidonate metabolism. When added to neutrophils, both 1-O-[3H]alkenyl-2-lyso-GPE and 1-O-[3H]alkyl-2-lyso-GPC are acylated predominantly with arachidonic acid, and the resulting arachidonoyl-containing phospholipids are extensively deacylated upon stimulation. However, hydrolysis of PE in the neutrophil differs from hydrolysis of choline-containing phosphoglycerides in that stimulation leads to a greater accumulation of the ethanolamine-linked lysophospholipid. 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Psychology ; Humans ; In Vitro Techniques ; Kinetics ; Molecular and cellular biology ; Neutrophils - drug effects ; Neutrophils - physiology ; Phospholipids - blood ; Phospholipids - isolation & purification ; Plasmalogens - blood ; Signal Transduction ; Time Factors ; Tritium</subject><ispartof>The Journal of biological chemistry, 1990-12, Vol.265 (34), p.21032-21038</ispartof><rights>1990 © 1990 ASBMB. 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H., and Connell, T. R. (1988) J. Biol. Chem. 263, 5260-5265) and by the synthesis of acetylated PE species, predominantly 1-O-alk-1‘-enyl-2-acetyl-sn-glycero-3-phosphoethanolamine (alkenylacetyl-GPE; Tessner, T. G., and Wykle, R. L. (1987) J. Biol. Chem. 262, 12660-12664) in stimulated cells. In the studies reported here, we investigated the relationship between arachidonic acid release from PE and generation of the lysophospholipid precursor required in the biosynthesis of alkenylacetyl-GPE. In order to follow these reactions, we prelabeled neutrophils with 1-O-[3H]alk-1‘-enyl-2-arachidonoyl-sn-glycero-3-phosphoethanolamine (alkenyl-acyl-GPE). We also followed the hydrolysis of endogenous PE by analysis as the dinitrophenyl derivative using a high pressure liquid chromatography method we developed. Our results coupled with those of Chilton et al. (Chilton, F. H., Ellis, J. M., Olson, S. C., and Wykle, R. L. (1984) J. Biol. Chem. 259, 12014-12019) indicate that in human neutrophils the metabolism of alkenylacyl-GPE and alkylacyl-sn-glycero-3-phosphocholine (GPC) are strikingly similar with regard to arachidonate metabolism. When added to neutrophils, both 1-O-[3H]alkenyl-2-lyso-GPE and 1-O-[3H]alkyl-2-lyso-GPC are acylated predominantly with arachidonic acid, and the resulting arachidonoyl-containing phospholipids are extensively deacylated upon stimulation. However, hydrolysis of PE in the neutrophil differs from hydrolysis of choline-containing phosphoglycerides in that stimulation leads to a greater accumulation of the ethanolamine-linked lysophospholipid. A comparison of the molecular species of endogenous PE (based on molar concentrations measured as the dinitrophenyl derivative) from resting and stimulated neutrophils indicated that only those species which contain arachidonate are significantly hydrolyzed.</description><subject>arachidonic acid</subject><subject>Arachidonic Acids - blood</subject><subject>Biological and medical sciences</subject><subject>Calcimycin - pharmacology</subject><subject>Cell physiology</subject><subject>Chromatography, High Pressure Liquid</subject><subject>ethanolamine</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Humans</subject><subject>In Vitro Techniques</subject><subject>Kinetics</subject><subject>Molecular and cellular biology</subject><subject>Neutrophils - drug effects</subject><subject>Neutrophils - physiology</subject><subject>Phospholipids - blood</subject><subject>Phospholipids - isolation & purification</subject><subject>Plasmalogens - blood</subject><subject>Signal Transduction</subject><subject>Time Factors</subject><subject>Tritium</subject><issn>0021-9258</issn><issn>1083-351X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1990</creationdate><recordtype>article</recordtype><recordid>eNqFUctq3DAUFaUhnU77CQEv2tIu3OrqYVurUEIfgUAXaaE7IcvXY7W2NJXsKfP30WSGZBmB0IXzEvcQcgH0I1CoPt1SyqBUTDbvof4gJGe85M_ICmiTBwm_n5PVA-UFeZnSH5qPUHBOzhmTeVYrsrvFEe3sdlh0aOx-NLMLvgh9YaKxg-uCNzOWNvjZOO_8psB5MD6MZnIey9H5v9gV2yGkfDfj3mJ0HabC-SLNblqyX8aHZTK-8LjMMWwHN6ZX5Kw3Y8LXp3dNfn398vPqe3nz49v11eeb0gpVz2XbK2aFrRm3plGVaZvKYo9MQtuD4BXlFfTcVqaWTdW2TFZguOqEpahqgJqvybuj7zaGfwumWU8uWRxH4zEsSTcUREOZepIIshFKMMhEeSTaGFKK2OttdJOJew1UH4rR98Xow9Y11Pq-GM2z7uIUsLQTdg-qUxMZf3vCTbJm7KPx1qVHcyWUBHXIf3PkDW4z_HcRdeuCHXDSrJKaC82A5sQ1uTzSMG935zDqZB16i12W2Fl3wT3x4TtvfLin</recordid><startdate>19901205</startdate><enddate>19901205</enddate><creator>Tessner, T G</creator><creator>Greene, D G</creator><creator>Wykle, R L</creator><general>Elsevier Inc</general><general>American Society for Biochemistry and Molecular Biology</general><scope>6I.</scope><scope>AAFTH</scope><scope>IQODW</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>8FD</scope><scope>FR3</scope><scope>M7Z</scope><scope>P64</scope><scope>7X8</scope></search><sort><creationdate>19901205</creationdate><title>Selective deacylation of arachidonate-containing ethanolamine-linked phosphoglycerides in stimulated human neutrophils</title><author>Tessner, T G ; Greene, D G ; Wykle, R L</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c497t-bf92c4c723ca896ab86cefe251bf14360361f3c6a7586bb2561a39d4c0e971173</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1990</creationdate><topic>arachidonic acid</topic><topic>Arachidonic Acids - blood</topic><topic>Biological and medical sciences</topic><topic>Calcimycin - pharmacology</topic><topic>Cell physiology</topic><topic>Chromatography, High Pressure Liquid</topic><topic>ethanolamine</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Humans</topic><topic>In Vitro Techniques</topic><topic>Kinetics</topic><topic>Molecular and cellular biology</topic><topic>Neutrophils - drug effects</topic><topic>Neutrophils - physiology</topic><topic>Phospholipids - blood</topic><topic>Phospholipids - isolation & purification</topic><topic>Plasmalogens - blood</topic><topic>Signal Transduction</topic><topic>Time Factors</topic><topic>Tritium</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Tessner, T G</creatorcontrib><creatorcontrib>Greene, D G</creatorcontrib><creatorcontrib>Wykle, R L</creatorcontrib><collection>ScienceDirect Open Access Titles</collection><collection>Elsevier:ScienceDirect:Open Access</collection><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Biochemistry Abstracts 1</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>The Journal of biological chemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Tessner, T G</au><au>Greene, D G</au><au>Wykle, R L</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Selective deacylation of arachidonate-containing ethanolamine-linked phosphoglycerides in stimulated human neutrophils</atitle><jtitle>The Journal of biological chemistry</jtitle><addtitle>J Biol Chem</addtitle><date>1990-12-05</date><risdate>1990</risdate><volume>265</volume><issue>34</issue><spage>21032</spage><epage>21038</epage><pages>21032-21038</pages><issn>0021-9258</issn><eissn>1083-351X</eissn><coden>JBCHA3</coden><abstract>The involvement of the ethanolamine-linked phosphoglyceride fraction (PE) in neutrophil signal transduction is suggested by the stimulus-induced release of arachidonic acid from PE (Chilton, F. H., and Connell, T. R. (1988) J. Biol. Chem. 263, 5260-5265) and by the synthesis of acetylated PE species, predominantly 1-O-alk-1‘-enyl-2-acetyl-sn-glycero-3-phosphoethanolamine (alkenylacetyl-GPE; Tessner, T. G., and Wykle, R. L. (1987) J. Biol. Chem. 262, 12660-12664) in stimulated cells. In the studies reported here, we investigated the relationship between arachidonic acid release from PE and generation of the lysophospholipid precursor required in the biosynthesis of alkenylacetyl-GPE. In order to follow these reactions, we prelabeled neutrophils with 1-O-[3H]alk-1‘-enyl-2-arachidonoyl-sn-glycero-3-phosphoethanolamine (alkenyl-acyl-GPE). We also followed the hydrolysis of endogenous PE by analysis as the dinitrophenyl derivative using a high pressure liquid chromatography method we developed. Our results coupled with those of Chilton et al. (Chilton, F. H., Ellis, J. M., Olson, S. C., and Wykle, R. L. (1984) J. Biol. Chem. 259, 12014-12019) indicate that in human neutrophils the metabolism of alkenylacyl-GPE and alkylacyl-sn-glycero-3-phosphocholine (GPC) are strikingly similar with regard to arachidonate metabolism. When added to neutrophils, both 1-O-[3H]alkenyl-2-lyso-GPE and 1-O-[3H]alkyl-2-lyso-GPC are acylated predominantly with arachidonic acid, and the resulting arachidonoyl-containing phospholipids are extensively deacylated upon stimulation. However, hydrolysis of PE in the neutrophil differs from hydrolysis of choline-containing phosphoglycerides in that stimulation leads to a greater accumulation of the ethanolamine-linked lysophospholipid. A comparison of the molecular species of endogenous PE (based on molar concentrations measured as the dinitrophenyl derivative) from resting and stimulated neutrophils indicated that only those species which contain arachidonate are significantly hydrolyzed.</abstract><cop>Bethesda, MD</cop><pub>Elsevier Inc</pub><pmid>2250009</pmid><doi>10.1016/S0021-9258(17)45323-3</doi><tpages>7</tpages><oa>free_for_read</oa></addata></record> |
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subjects | arachidonic acid Arachidonic Acids - blood Biological and medical sciences Calcimycin - pharmacology Cell physiology Chromatography, High Pressure Liquid ethanolamine Fundamental and applied biological sciences. Psychology Humans In Vitro Techniques Kinetics Molecular and cellular biology Neutrophils - drug effects Neutrophils - physiology Phospholipids - blood Phospholipids - isolation & purification Plasmalogens - blood Signal Transduction Time Factors Tritium |
title | Selective deacylation of arachidonate-containing ethanolamine-linked phosphoglycerides in stimulated human neutrophils |
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