Loading…
Lipopolysaccharide Regulates Macrophage Fluid Phase Pinocytosis Via CD14-Dependent and CD14-Independent Pathways
Lipopolysaccharide (LPS) is a mediator of inflammation and septic shock during bacterial infection. Although monocytes and macrophages are highly responsive to LPS, the biological effects of LPS in these cell types are only partially understood. We decided, therefore, to investigate the influence of...
Saved in:
Published in: | Blood 1999-06, Vol.93 (11), p.4011-4018 |
---|---|
Main Authors: | , , , , |
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-c293t-c031db85a05470856608f8fa4357b5dd563bf9eca56c7d20cfc88982bd5a56023 |
---|---|
cites | cdi_FETCH-LOGICAL-c293t-c031db85a05470856608f8fa4357b5dd563bf9eca56c7d20cfc88982bd5a56023 |
container_end_page | 4018 |
container_issue | 11 |
container_start_page | 4011 |
container_title | Blood |
container_volume | 93 |
creator | Peppelenbosch, Maikel P. DeSmedt, Marjory ten Hove, Tessa van Deventer, Sander J.H. Grooten, Johan |
description | Lipopolysaccharide (LPS) is a mediator of inflammation and septic shock during bacterial infection. Although monocytes and macrophages are highly responsive to LPS, the biological effects of LPS in these cell types are only partially understood. We decided, therefore, to investigate the influence of LPS on macrophage pinocytosis and Fc receptor–mediated endocytosis, two prominent and related macrophage effector functions. We observed that LPS did not greatly influence endocytosis in either macrophages or monocytes, but did exert a dual action on pinocytosis: at lower concentrations (0.1 to 100 ng/mL), LPS caused a decrease in pinocytosis in both macrophages and monocytes, whereas at higher LPS concentrations, enhanced pinocytosis in macrophages was observed. Detoxified LPS was two orders of magnitude less potent in producing these effects. After inhibition of the LPS receptor CD14, the LPS-induced decrease in pinocytosis was absent, and stimulation of pinocytosis at lower LPS concentrations was unmasked. We conclude that LPS can influence pinocytosis via CD14-dependent and CD14-independent signaling pathways. Furthermore, as addition of LPS to macrophages effected pinocytosis but not Fc receptor–mediated endocytosis, these two processes are independently regulated in macrophages. |
doi_str_mv | 10.1182/blood.V93.11.4011 |
format | article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_69781836</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S0006497120595359</els_id><sourcerecordid>69781836</sourcerecordid><originalsourceid>FETCH-LOGICAL-c293t-c031db85a05470856608f8fa4357b5dd563bf9eca56c7d20cfc88982bd5a56023</originalsourceid><addsrcrecordid>eNp9kMFu1DAQhi0EokvhAbigHBC3LOM4ThxxQlsKlbbqCkGv1sSedI2ycbAT0L49LlnUnjhZ_69vRp6Psdcc1pyr4n3be2_Xt41IcV0C50_YistC5QAFPGUrAKjysqn5GXsR4w8AXopCPmdnHIRoJOcrNm7d6EffHyMas8fgLGVf6W7ucaKYXaMJftzjHWWX_exstttjpGznBm-Ok48uZrcOs80FL_MLGmmwNEwZDnaprlL-V-5w2v_GY3zJnnXYR3p1es_Z98tP3zZf8u3N56vNx21uikZMuQHBbaskgixrULKqQHWqw1LIupXWykq0XUMGZWVqW4DpjFKNKlorUwWFOGfvlr1j8D9nipM-uGio73EgP0ddNbXiSlQJ5AuYTo0xUKfH4A4YjpqDvtes_2rWSXOK-l5zmnlzWj63B7KPJhavCXh7AjAa7LuAg3HxgVOiKLlI2IcFo2Til6Ogo3E0GLIukJm09e4_v_gDbYOazA</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>69781836</pqid></control><display><type>article</type><title>Lipopolysaccharide Regulates Macrophage Fluid Phase Pinocytosis Via CD14-Dependent and CD14-Independent Pathways</title><source>Elsevier ScienceDirect Journals</source><creator>Peppelenbosch, Maikel P. ; DeSmedt, Marjory ; ten Hove, Tessa ; van Deventer, Sander J.H. ; Grooten, Johan</creator><creatorcontrib>Peppelenbosch, Maikel P. ; DeSmedt, Marjory ; ten Hove, Tessa ; van Deventer, Sander J.H. ; Grooten, Johan</creatorcontrib><description>Lipopolysaccharide (LPS) is a mediator of inflammation and septic shock during bacterial infection. Although monocytes and macrophages are highly responsive to LPS, the biological effects of LPS in these cell types are only partially understood. We decided, therefore, to investigate the influence of LPS on macrophage pinocytosis and Fc receptor–mediated endocytosis, two prominent and related macrophage effector functions. We observed that LPS did not greatly influence endocytosis in either macrophages or monocytes, but did exert a dual action on pinocytosis: at lower concentrations (0.1 to 100 ng/mL), LPS caused a decrease in pinocytosis in both macrophages and monocytes, whereas at higher LPS concentrations, enhanced pinocytosis in macrophages was observed. Detoxified LPS was two orders of magnitude less potent in producing these effects. After inhibition of the LPS receptor CD14, the LPS-induced decrease in pinocytosis was absent, and stimulation of pinocytosis at lower LPS concentrations was unmasked. We conclude that LPS can influence pinocytosis via CD14-dependent and CD14-independent signaling pathways. Furthermore, as addition of LPS to macrophages effected pinocytosis but not Fc receptor–mediated endocytosis, these two processes are independently regulated in macrophages.</description><identifier>ISSN: 0006-4971</identifier><identifier>EISSN: 1528-0020</identifier><identifier>DOI: 10.1182/blood.V93.11.4011</identifier><identifier>PMID: 10339511</identifier><language>eng</language><publisher>Washington, DC: Elsevier Inc</publisher><subject>Animals ; Biological and medical sciences ; Cells, Cultured ; Fundamental and applied biological sciences. Psychology ; Fundamental immunology ; Immunobiology ; Lipopolysaccharide Receptors - physiology ; Lipopolysaccharides - pharmacology ; Macrophages - drug effects ; Macrophages - physiology ; Mice ; Myeloid cells: ontogeny, maturation, markers, receptors ; Pinocytosis - drug effects ; Polynuclears ; Signal Transduction - drug effects</subject><ispartof>Blood, 1999-06, Vol.93 (11), p.4011-4018</ispartof><rights>1999 American Society of Hematology</rights><rights>1999 INIST-CNRS</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c293t-c031db85a05470856608f8fa4357b5dd563bf9eca56c7d20cfc88982bd5a56023</citedby><cites>FETCH-LOGICAL-c293t-c031db85a05470856608f8fa4357b5dd563bf9eca56c7d20cfc88982bd5a56023</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0006497120595359$$EHTML$$P50$$Gelsevier$$Hfree_for_read</linktohtml><link.rule.ids>314,776,780,3536,27901,27902,45756</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=1832413$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/10339511$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Peppelenbosch, Maikel P.</creatorcontrib><creatorcontrib>DeSmedt, Marjory</creatorcontrib><creatorcontrib>ten Hove, Tessa</creatorcontrib><creatorcontrib>van Deventer, Sander J.H.</creatorcontrib><creatorcontrib>Grooten, Johan</creatorcontrib><title>Lipopolysaccharide Regulates Macrophage Fluid Phase Pinocytosis Via CD14-Dependent and CD14-Independent Pathways</title><title>Blood</title><addtitle>Blood</addtitle><description>Lipopolysaccharide (LPS) is a mediator of inflammation and septic shock during bacterial infection. Although monocytes and macrophages are highly responsive to LPS, the biological effects of LPS in these cell types are only partially understood. We decided, therefore, to investigate the influence of LPS on macrophage pinocytosis and Fc receptor–mediated endocytosis, two prominent and related macrophage effector functions. We observed that LPS did not greatly influence endocytosis in either macrophages or monocytes, but did exert a dual action on pinocytosis: at lower concentrations (0.1 to 100 ng/mL), LPS caused a decrease in pinocytosis in both macrophages and monocytes, whereas at higher LPS concentrations, enhanced pinocytosis in macrophages was observed. Detoxified LPS was two orders of magnitude less potent in producing these effects. After inhibition of the LPS receptor CD14, the LPS-induced decrease in pinocytosis was absent, and stimulation of pinocytosis at lower LPS concentrations was unmasked. We conclude that LPS can influence pinocytosis via CD14-dependent and CD14-independent signaling pathways. Furthermore, as addition of LPS to macrophages effected pinocytosis but not Fc receptor–mediated endocytosis, these two processes are independently regulated in macrophages.</description><subject>Animals</subject><subject>Biological and medical sciences</subject><subject>Cells, Cultured</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Fundamental immunology</subject><subject>Immunobiology</subject><subject>Lipopolysaccharide Receptors - physiology</subject><subject>Lipopolysaccharides - pharmacology</subject><subject>Macrophages - drug effects</subject><subject>Macrophages - physiology</subject><subject>Mice</subject><subject>Myeloid cells: ontogeny, maturation, markers, receptors</subject><subject>Pinocytosis - drug effects</subject><subject>Polynuclears</subject><subject>Signal Transduction - drug effects</subject><issn>0006-4971</issn><issn>1528-0020</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1999</creationdate><recordtype>article</recordtype><recordid>eNp9kMFu1DAQhi0EokvhAbigHBC3LOM4ThxxQlsKlbbqCkGv1sSedI2ycbAT0L49LlnUnjhZ_69vRp6Psdcc1pyr4n3be2_Xt41IcV0C50_YistC5QAFPGUrAKjysqn5GXsR4w8AXopCPmdnHIRoJOcrNm7d6EffHyMas8fgLGVf6W7ucaKYXaMJftzjHWWX_exstttjpGznBm-Ok48uZrcOs80FL_MLGmmwNEwZDnaprlL-V-5w2v_GY3zJnnXYR3p1es_Z98tP3zZf8u3N56vNx21uikZMuQHBbaskgixrULKqQHWqw1LIupXWykq0XUMGZWVqW4DpjFKNKlorUwWFOGfvlr1j8D9nipM-uGio73EgP0ddNbXiSlQJ5AuYTo0xUKfH4A4YjpqDvtes_2rWSXOK-l5zmnlzWj63B7KPJhavCXh7AjAa7LuAg3HxgVOiKLlI2IcFo2Til6Ogo3E0GLIukJm09e4_v_gDbYOazA</recordid><startdate>19990601</startdate><enddate>19990601</enddate><creator>Peppelenbosch, Maikel P.</creator><creator>DeSmedt, Marjory</creator><creator>ten Hove, Tessa</creator><creator>van Deventer, Sander J.H.</creator><creator>Grooten, Johan</creator><general>Elsevier Inc</general><general>The Americain Society of Hematology</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>7X8</scope></search><sort><creationdate>19990601</creationdate><title>Lipopolysaccharide Regulates Macrophage Fluid Phase Pinocytosis Via CD14-Dependent and CD14-Independent Pathways</title><author>Peppelenbosch, Maikel P. ; DeSmedt, Marjory ; ten Hove, Tessa ; van Deventer, Sander J.H. ; Grooten, Johan</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c293t-c031db85a05470856608f8fa4357b5dd563bf9eca56c7d20cfc88982bd5a56023</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1999</creationdate><topic>Animals</topic><topic>Biological and medical sciences</topic><topic>Cells, Cultured</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Fundamental immunology</topic><topic>Immunobiology</topic><topic>Lipopolysaccharide Receptors - physiology</topic><topic>Lipopolysaccharides - pharmacology</topic><topic>Macrophages - drug effects</topic><topic>Macrophages - physiology</topic><topic>Mice</topic><topic>Myeloid cells: ontogeny, maturation, markers, receptors</topic><topic>Pinocytosis - drug effects</topic><topic>Polynuclears</topic><topic>Signal Transduction - drug effects</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Peppelenbosch, Maikel P.</creatorcontrib><creatorcontrib>DeSmedt, Marjory</creatorcontrib><creatorcontrib>ten Hove, Tessa</creatorcontrib><creatorcontrib>van Deventer, Sander J.H.</creatorcontrib><creatorcontrib>Grooten, Johan</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>MEDLINE - Academic</collection><jtitle>Blood</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Peppelenbosch, Maikel P.</au><au>DeSmedt, Marjory</au><au>ten Hove, Tessa</au><au>van Deventer, Sander J.H.</au><au>Grooten, Johan</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Lipopolysaccharide Regulates Macrophage Fluid Phase Pinocytosis Via CD14-Dependent and CD14-Independent Pathways</atitle><jtitle>Blood</jtitle><addtitle>Blood</addtitle><date>1999-06-01</date><risdate>1999</risdate><volume>93</volume><issue>11</issue><spage>4011</spage><epage>4018</epage><pages>4011-4018</pages><issn>0006-4971</issn><eissn>1528-0020</eissn><abstract>Lipopolysaccharide (LPS) is a mediator of inflammation and septic shock during bacterial infection. Although monocytes and macrophages are highly responsive to LPS, the biological effects of LPS in these cell types are only partially understood. We decided, therefore, to investigate the influence of LPS on macrophage pinocytosis and Fc receptor–mediated endocytosis, two prominent and related macrophage effector functions. We observed that LPS did not greatly influence endocytosis in either macrophages or monocytes, but did exert a dual action on pinocytosis: at lower concentrations (0.1 to 100 ng/mL), LPS caused a decrease in pinocytosis in both macrophages and monocytes, whereas at higher LPS concentrations, enhanced pinocytosis in macrophages was observed. Detoxified LPS was two orders of magnitude less potent in producing these effects. After inhibition of the LPS receptor CD14, the LPS-induced decrease in pinocytosis was absent, and stimulation of pinocytosis at lower LPS concentrations was unmasked. We conclude that LPS can influence pinocytosis via CD14-dependent and CD14-independent signaling pathways. Furthermore, as addition of LPS to macrophages effected pinocytosis but not Fc receptor–mediated endocytosis, these two processes are independently regulated in macrophages.</abstract><cop>Washington, DC</cop><pub>Elsevier Inc</pub><pmid>10339511</pmid><doi>10.1182/blood.V93.11.4011</doi><tpages>8</tpages><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0006-4971 |
ispartof | Blood, 1999-06, Vol.93 (11), p.4011-4018 |
issn | 0006-4971 1528-0020 |
language | eng |
recordid | cdi_proquest_miscellaneous_69781836 |
source | Elsevier ScienceDirect Journals |
subjects | Animals Biological and medical sciences Cells, Cultured Fundamental and applied biological sciences. Psychology Fundamental immunology Immunobiology Lipopolysaccharide Receptors - physiology Lipopolysaccharides - pharmacology Macrophages - drug effects Macrophages - physiology Mice Myeloid cells: ontogeny, maturation, markers, receptors Pinocytosis - drug effects Polynuclears Signal Transduction - drug effects |
title | Lipopolysaccharide Regulates Macrophage Fluid Phase Pinocytosis Via CD14-Dependent and CD14-Independent Pathways |
url | http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-23T10%3A23%3A46IST&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=Lipopolysaccharide%20Regulates%20Macrophage%20Fluid%20Phase%20Pinocytosis%20Via%20CD14-Dependent%20and%20CD14-Independent%20Pathways&rft.jtitle=Blood&rft.au=Peppelenbosch,%20Maikel%20P.&rft.date=1999-06-01&rft.volume=93&rft.issue=11&rft.spage=4011&rft.epage=4018&rft.pages=4011-4018&rft.issn=0006-4971&rft.eissn=1528-0020&rft_id=info:doi/10.1182/blood.V93.11.4011&rft_dat=%3Cproquest_cross%3E69781836%3C/proquest_cross%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c293t-c031db85a05470856608f8fa4357b5dd563bf9eca56c7d20cfc88982bd5a56023%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=69781836&rft_id=info:pmid/10339511&rfr_iscdi=true |