Loading…

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...

Full description

Saved in:
Bibliographic Details
Published in:The Journal of biological chemistry 1990-12, Vol.265 (34), p.21032-21038
Main Authors: Tessner, T G, Greene, D G, Wykle, R L
Format: Article
Language:English
Subjects:
Citations: Items that this one cites
Items that cite this one
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
cited_by cdi_FETCH-LOGICAL-c497t-bf92c4c723ca896ab86cefe251bf14360361f3c6a7586bb2561a39d4c0e971173
cites cdi_FETCH-LOGICAL-c497t-bf92c4c723ca896ab86cefe251bf14360361f3c6a7586bb2561a39d4c0e971173
container_end_page 21038
container_issue 34
container_start_page 21032
container_title The Journal of biological chemistry
container_volume 265
creator Tessner, T G
Greene, D G
Wykle, R L
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
format article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_80148029</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S0021925817453233</els_id><sourcerecordid>15849421</sourcerecordid><originalsourceid>FETCH-LOGICAL-c497t-bf92c4c723ca896ab86cefe251bf14360361f3c6a7586bb2561a39d4c0e971173</originalsourceid><addsrcrecordid>eNqFUctq3DAUFaUhnU77CQEv2tIu3OrqYVurUEIfgUAXaaE7IcvXY7W2NJXsKfP30WSGZBmB0IXzEvcQcgH0I1CoPt1SyqBUTDbvof4gJGe85M_ICmiTBwm_n5PVA-UFeZnSH5qPUHBOzhmTeVYrsrvFEe3sdlh0aOx-NLMLvgh9YaKxg-uCNzOWNvjZOO_8psB5MD6MZnIey9H5v9gV2yGkfDfj3mJ0HabC-SLNblqyX8aHZTK-8LjMMWwHN6ZX5Kw3Y8LXp3dNfn398vPqe3nz49v11eeb0gpVz2XbK2aFrRm3plGVaZvKYo9MQtuD4BXlFfTcVqaWTdW2TFZguOqEpahqgJqvybuj7zaGfwumWU8uWRxH4zEsSTcUREOZepIIshFKMMhEeSTaGFKK2OttdJOJew1UH4rR98Xow9Y11Pq-GM2z7uIUsLQTdg-qUxMZf3vCTbJm7KPx1qVHcyWUBHXIf3PkDW4z_HcRdeuCHXDSrJKaC82A5sQ1uTzSMG935zDqZB16i12W2Fl3wT3x4TtvfLin</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>15849421</pqid></control><display><type>article</type><title>Selective deacylation of arachidonate-containing ethanolamine-linked phosphoglycerides in stimulated human neutrophils</title><source>ScienceDirect Journals</source><creator>Tessner, T G ; Greene, D G ; Wykle, R L</creator><creatorcontrib>Tessner, T G ; Greene, D G ; Wykle, R L</creatorcontrib><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.</description><identifier>ISSN: 0021-9258</identifier><identifier>EISSN: 1083-351X</identifier><identifier>DOI: 10.1016/S0021-9258(17)45323-3</identifier><identifier>PMID: 2250009</identifier><identifier>CODEN: JBCHA3</identifier><language>eng</language><publisher>Bethesda, MD: Elsevier Inc</publisher><subject>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 &amp; 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. Currently published by Elsevier Inc; originally published by American Society for Biochemistry and Molecular Biology.</rights><rights>1991 INIST-CNRS</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c497t-bf92c4c723ca896ab86cefe251bf14360361f3c6a7586bb2561a39d4c0e971173</citedby><cites>FETCH-LOGICAL-c497t-bf92c4c723ca896ab86cefe251bf14360361f3c6a7586bb2561a39d4c0e971173</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0021925817453233$$EHTML$$P50$$Gelsevier$$Hfree_for_read</linktohtml><link.rule.ids>314,780,784,3549,27924,27925,45780</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=19495191$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/2250009$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Tessner, T G</creatorcontrib><creatorcontrib>Greene, D G</creatorcontrib><creatorcontrib>Wykle, R L</creatorcontrib><title>Selective deacylation of arachidonate-containing ethanolamine-linked phosphoglycerides in stimulated human neutrophils</title><title>The Journal of biological chemistry</title><addtitle>J Biol Chem</addtitle><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.</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 &amp; 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 &amp; 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>
fulltext fulltext
identifier ISSN: 0021-9258
ispartof The Journal of biological chemistry, 1990-12, Vol.265 (34), p.21032-21038
issn 0021-9258
1083-351X
language eng
recordid cdi_proquest_miscellaneous_80148029
source ScienceDirect Journals
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
url http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-27T03%3A30%3A22IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Selective%20deacylation%20of%20arachidonate-containing%20ethanolamine-linked%20phosphoglycerides%20in%20stimulated%20human%20neutrophils&rft.jtitle=The%20Journal%20of%20biological%20chemistry&rft.au=Tessner,%20T%20G&rft.date=1990-12-05&rft.volume=265&rft.issue=34&rft.spage=21032&rft.epage=21038&rft.pages=21032-21038&rft.issn=0021-9258&rft.eissn=1083-351X&rft.coden=JBCHA3&rft_id=info:doi/10.1016/S0021-9258(17)45323-3&rft_dat=%3Cproquest_cross%3E15849421%3C/proquest_cross%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c497t-bf92c4c723ca896ab86cefe251bf14360361f3c6a7586bb2561a39d4c0e971173%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=15849421&rft_id=info:pmid/2250009&rfr_iscdi=true