Prostaglandin Synthesis by Macrophages Requires a Specific Receptor-Ligand Interaction
The ingestion of particles by macrophages leads to the prompt induction of prostaglandin (PG) synthesis. We have now dissected the endocytic process and examined the requirements of prostaglandin E (PGE) synthesis for particle attachment, membrane interiorization, and phagosome-lysosome fusion. Macr...
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Veröffentlicht in: | Proceedings of the National Academy of Sciences - PNAS 1980-07, Vol.77 (7), p.4279-4282 |
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creator | Rouzer, Carol A. Scott, William A. Kempe, Jennifer Cohn, Zanvil A. |
description | The ingestion of particles by macrophages leads to the prompt induction of prostaglandin (PG) synthesis. We have now dissected the endocytic process and examined the requirements of prostaglandin E (PGE) synthesis for particle attachment, membrane interiorization, and phagosome-lysosome fusion. Macrophages that were loaded with the polyanion dextran sulfate and exhibited a greater than 99% inhibition of phagosome-lysosome fusion produced normal amounts of PGE upon challenge with zymosan. Inhibition of membrane interiorization with cytochalasin D was similarly ineffective in blocking PGE synthesis. The addition of large numbers of unmodified polystyrene latex beads, which were readily ingested by macrophages, failed to stimulate PGE synthesis. However, when macrophages were challenged with latex beads coated with immune complexes, an increased synthesis of PGE resulted. No response occurred if the complex was prepared with the F(ab′)2fragment of IgG. Similar results occurred when nonphagocytizable Sephadex beads coated with immune complexes were employed. We conclude that particle binding to the Fc receptor of the macrophage plasma membrane is a sufficient stimulus for PGE synthesis. |
doi_str_mv | 10.1073/pnas.77.7.4279 |
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We have now dissected the endocytic process and examined the requirements of prostaglandin E (PGE) synthesis for particle attachment, membrane interiorization, and phagosome-lysosome fusion. Macrophages that were loaded with the polyanion dextran sulfate and exhibited a greater than 99% inhibition of phagosome-lysosome fusion produced normal amounts of PGE upon challenge with zymosan. Inhibition of membrane interiorization with cytochalasin D was similarly ineffective in blocking PGE synthesis. The addition of large numbers of unmodified polystyrene latex beads, which were readily ingested by macrophages, failed to stimulate PGE synthesis. However, when macrophages were challenged with latex beads coated with immune complexes, an increased synthesis of PGE resulted. No response occurred if the complex was prepared with the F(ab′)2fragment of IgG. Similar results occurred when nonphagocytizable Sephadex beads coated with immune complexes were employed. We conclude that particle binding to the Fc receptor of the macrophage plasma membrane is a sufficient stimulus for PGE synthesis.</description><identifier>ISSN: 0027-8424</identifier><identifier>EISSN: 1091-6490</identifier><identifier>DOI: 10.1073/pnas.77.7.4279</identifier><identifier>PMID: 6933478</identifier><language>eng</language><publisher>United States: National Academy of Sciences of the United States of America</publisher><subject>Animals ; Antigen-Antibody Complex ; Cell membranes ; Cells, Cultured ; Cultured cells ; Cytochalasins ; Dextrans ; Endocytosis ; Female ; Latex ; Lysosomes - physiology ; Macrophages ; Macrophages - metabolism ; Mice ; Phagocytosis ; Prostaglandins ; Prostaglandins - biosynthesis ; Prostaglandins E - biosynthesis ; Receptors ; Receptors, Drug - metabolism ; Receptors, Fc - metabolism ; Sulfates ; Viability</subject><ispartof>Proceedings of the National Academy of Sciences - PNAS, 1980-07, Vol.77 (7), p.4279-4282</ispartof><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c521t-de8cbe3b9f939df64a0939785be621a088c6ef3c1692cbd0d872dc0f40a2222e3</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Uhttp://www.pnas.org/content/77/7.cover.gif</thumbnail><linktopdf>$$Uhttps://www.jstor.org/stable/pdf/9082$$EPDF$$P50$$Gjstor$$H</linktopdf><linktohtml>$$Uhttps://www.jstor.org/stable/9082$$EHTML$$P50$$Gjstor$$H</linktohtml><link.rule.ids>230,314,727,780,784,803,885,27924,27925,53791,53793,58017,58250</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/6933478$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Rouzer, Carol A.</creatorcontrib><creatorcontrib>Scott, William A.</creatorcontrib><creatorcontrib>Kempe, Jennifer</creatorcontrib><creatorcontrib>Cohn, Zanvil A.</creatorcontrib><title>Prostaglandin Synthesis by Macrophages Requires a Specific Receptor-Ligand Interaction</title><title>Proceedings of the National Academy of Sciences - PNAS</title><addtitle>Proc Natl Acad Sci U S A</addtitle><description>The ingestion of particles by macrophages leads to the prompt induction of prostaglandin (PG) synthesis. We have now dissected the endocytic process and examined the requirements of prostaglandin E (PGE) synthesis for particle attachment, membrane interiorization, and phagosome-lysosome fusion. Macrophages that were loaded with the polyanion dextran sulfate and exhibited a greater than 99% inhibition of phagosome-lysosome fusion produced normal amounts of PGE upon challenge with zymosan. Inhibition of membrane interiorization with cytochalasin D was similarly ineffective in blocking PGE synthesis. The addition of large numbers of unmodified polystyrene latex beads, which were readily ingested by macrophages, failed to stimulate PGE synthesis. However, when macrophages were challenged with latex beads coated with immune complexes, an increased synthesis of PGE resulted. No response occurred if the complex was prepared with the F(ab′)2fragment of IgG. Similar results occurred when nonphagocytizable Sephadex beads coated with immune complexes were employed. We conclude that particle binding to the Fc receptor of the macrophage plasma membrane is a sufficient stimulus for PGE synthesis.</description><subject>Animals</subject><subject>Antigen-Antibody Complex</subject><subject>Cell membranes</subject><subject>Cells, Cultured</subject><subject>Cultured cells</subject><subject>Cytochalasins</subject><subject>Dextrans</subject><subject>Endocytosis</subject><subject>Female</subject><subject>Latex</subject><subject>Lysosomes - physiology</subject><subject>Macrophages</subject><subject>Macrophages - metabolism</subject><subject>Mice</subject><subject>Phagocytosis</subject><subject>Prostaglandins</subject><subject>Prostaglandins - biosynthesis</subject><subject>Prostaglandins E - biosynthesis</subject><subject>Receptors</subject><subject>Receptors, Drug - metabolism</subject><subject>Receptors, Fc - metabolism</subject><subject>Sulfates</subject><subject>Viability</subject><issn>0027-8424</issn><issn>1091-6490</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1980</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kcFv0zAYxS3ENMrgisQBKafdEj7bSWwfOKCJjUlFQwy4Wo7zpfWUJpntoPW_n6uWqlzwxZ_8fs-23iPkHYWCguAfp8GEQohCFCUT6gVZUFA0r0sFL8kCgIlclqx8RV6H8AAAqpJwTs5rxXkp5IL8_u7HEM2qN0Prhux-O8Q1BheyZpt9M9aP09qsMGQ_8HF2Pg0mu5_Qus7ZdGZxiqPPl26V7NntENEbG904vCFnnekDvj3sF-TX9ZefV1_z5d3N7dXnZW4rRmPeorQN8kZ1iqu2q0sDaRCyarBm1ICUtsaOW1orZpsWWilYa6ErwbC0kF-QT_t7p7nZYGtxiN70evJuY_xWj8bpf5XBrfVq_KN5qSStk__y4Pfj44wh6o0LFvsUB45z0KLiTFQUEljswRRJCB674xsU9K4IvStCC6GF3hWRDB9Of3bED8mf6DvfX_XUf_k_XXdz30d8igl8vwcfQuriSCqQjD8DlcKnhw</recordid><startdate>19800701</startdate><enddate>19800701</enddate><creator>Rouzer, Carol A.</creator><creator>Scott, William A.</creator><creator>Kempe, Jennifer</creator><creator>Cohn, Zanvil A.</creator><general>National Academy of Sciences of the United States of America</general><general>National Acad Sciences</general><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><scope>5PM</scope></search><sort><creationdate>19800701</creationdate><title>Prostaglandin Synthesis by Macrophages Requires a Specific Receptor-Ligand Interaction</title><author>Rouzer, Carol A. ; Scott, William A. ; Kempe, Jennifer ; Cohn, Zanvil A.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c521t-de8cbe3b9f939df64a0939785be621a088c6ef3c1692cbd0d872dc0f40a2222e3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1980</creationdate><topic>Animals</topic><topic>Antigen-Antibody Complex</topic><topic>Cell membranes</topic><topic>Cells, Cultured</topic><topic>Cultured cells</topic><topic>Cytochalasins</topic><topic>Dextrans</topic><topic>Endocytosis</topic><topic>Female</topic><topic>Latex</topic><topic>Lysosomes - physiology</topic><topic>Macrophages</topic><topic>Macrophages - metabolism</topic><topic>Mice</topic><topic>Phagocytosis</topic><topic>Prostaglandins</topic><topic>Prostaglandins - biosynthesis</topic><topic>Prostaglandins E - biosynthesis</topic><topic>Receptors</topic><topic>Receptors, Drug - metabolism</topic><topic>Receptors, Fc - metabolism</topic><topic>Sulfates</topic><topic>Viability</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Rouzer, Carol A.</creatorcontrib><creatorcontrib>Scott, William A.</creatorcontrib><creatorcontrib>Kempe, Jennifer</creatorcontrib><creatorcontrib>Cohn, Zanvil A.</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><collection>PubMed Central (Full Participant titles)</collection><jtitle>Proceedings of the National Academy of Sciences - PNAS</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Rouzer, Carol A.</au><au>Scott, William A.</au><au>Kempe, Jennifer</au><au>Cohn, Zanvil A.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Prostaglandin Synthesis by Macrophages Requires a Specific Receptor-Ligand Interaction</atitle><jtitle>Proceedings of the National Academy of Sciences - PNAS</jtitle><addtitle>Proc Natl Acad Sci U S A</addtitle><date>1980-07-01</date><risdate>1980</risdate><volume>77</volume><issue>7</issue><spage>4279</spage><epage>4282</epage><pages>4279-4282</pages><issn>0027-8424</issn><eissn>1091-6490</eissn><abstract>The ingestion of particles by macrophages leads to the prompt induction of prostaglandin (PG) synthesis. We have now dissected the endocytic process and examined the requirements of prostaglandin E (PGE) synthesis for particle attachment, membrane interiorization, and phagosome-lysosome fusion. Macrophages that were loaded with the polyanion dextran sulfate and exhibited a greater than 99% inhibition of phagosome-lysosome fusion produced normal amounts of PGE upon challenge with zymosan. Inhibition of membrane interiorization with cytochalasin D was similarly ineffective in blocking PGE synthesis. The addition of large numbers of unmodified polystyrene latex beads, which were readily ingested by macrophages, failed to stimulate PGE synthesis. However, when macrophages were challenged with latex beads coated with immune complexes, an increased synthesis of PGE resulted. No response occurred if the complex was prepared with the F(ab′)2fragment of IgG. Similar results occurred when nonphagocytizable Sephadex beads coated with immune complexes were employed. We conclude that particle binding to the Fc receptor of the macrophage plasma membrane is a sufficient stimulus for PGE synthesis.</abstract><cop>United States</cop><pub>National Academy of Sciences of the United States of America</pub><pmid>6933478</pmid><doi>10.1073/pnas.77.7.4279</doi><tpages>4</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Animals Antigen-Antibody Complex Cell membranes Cells, Cultured Cultured cells Cytochalasins Dextrans Endocytosis Female Latex Lysosomes - physiology Macrophages Macrophages - metabolism Mice Phagocytosis Prostaglandins Prostaglandins - biosynthesis Prostaglandins E - biosynthesis Receptors Receptors, Drug - metabolism Receptors, Fc - metabolism Sulfates Viability |
title | Prostaglandin Synthesis by Macrophages Requires a Specific Receptor-Ligand Interaction |
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