Toll-Like Receptor (TLR)2 and TLR4 in Human Peripheral Blood Granulocytes: A Critical Role for Monocytes in Leukocyte Lipopolysaccharide Responses
Leukocyte responsiveness to LPS is dependent upon CD14 and receptors of the Toll-like receptor (TLR) family. Neutrophils respond to LPS, but conflicting data exist regarding LPS responses of eosinophils and basophils, and expression of TLRs at the protein level in these granulocyte lineages has not...
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Veröffentlicht in: | The Journal of immunology (1950) 2002-05, Vol.168 (9), p.4701-4710 |
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description | Leukocyte responsiveness to LPS is dependent upon CD14 and receptors of the Toll-like receptor (TLR) family. Neutrophils respond to LPS, but conflicting data exist regarding LPS responses of eosinophils and basophils, and expression of TLRs at the protein level in these granulocyte lineages has not been fully described. We examined the expression of TLR2, TLR4, and CD14 and found that monocytes expressed relatively high levels of cell surface TLR2, TLR4, and CD14, while neutrophils also expressed all three molecules, but at low levels. In contrast, basophils expressed TLR2 and TLR4 but not CD14, while eosinophils expressed none of these proteins. Tested in a range of functional assays including L-selectin shedding, CD11b up-regulation, IL-8 mRNA generation, and cell survival, neutrophils responded to LPS, but eosinophils and basophils did not. In contrast to previous data, we found, using monocyte depletion by negative magnetic selection, that neutrophil responses to LPS were heavily dependent upon the presence of a very low level of monocytes, and neutrophil survival induced by LPS at 22 h was monocyte dependent. We conclude that LPS has little role in the regulation of peripheral blood eosinophil and basophil function, and that, even in neutrophils, monocytes orchestrate many previously observed leukocyte LPS response patterns. |
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B ; Dower, Steven K</creator><creatorcontrib>Sabroe, Ian ; Jones, Elizabeth C ; Usher, Lynne R ; Whyte, Moira K. B ; Dower, Steven K</creatorcontrib><description>Leukocyte responsiveness to LPS is dependent upon CD14 and receptors of the Toll-like receptor (TLR) family. Neutrophils respond to LPS, but conflicting data exist regarding LPS responses of eosinophils and basophils, and expression of TLRs at the protein level in these granulocyte lineages has not been fully described. We examined the expression of TLR2, TLR4, and CD14 and found that monocytes expressed relatively high levels of cell surface TLR2, TLR4, and CD14, while neutrophils also expressed all three molecules, but at low levels. In contrast, basophils expressed TLR2 and TLR4 but not CD14, while eosinophils expressed none of these proteins. Tested in a range of functional assays including L-selectin shedding, CD11b up-regulation, IL-8 mRNA generation, and cell survival, neutrophils responded to LPS, but eosinophils and basophils did not. In contrast to previous data, we found, using monocyte depletion by negative magnetic selection, that neutrophil responses to LPS were heavily dependent upon the presence of a very low level of monocytes, and neutrophil survival induced by LPS at 22 h was monocyte dependent. We conclude that LPS has little role in the regulation of peripheral blood eosinophil and basophil function, and that, even in neutrophils, monocytes orchestrate many previously observed leukocyte LPS response patterns.</description><identifier>ISSN: 0022-1767</identifier><identifier>EISSN: 1550-6606</identifier><identifier>DOI: 10.4049/jimmunol.168.9.4701</identifier><identifier>PMID: 11971020</identifier><language>eng</language><publisher>United States: Am Assoc Immnol</publisher><subject>Basophils - drug effects ; Basophils - immunology ; Blood - immunology ; CD14 antigen ; Cell Survival - drug effects ; Cells, Cultured ; Dose-Response Relationship, Drug ; Drosophila Proteins ; Eosinophils - drug effects ; Eosinophils - immunology ; Granulocytes - immunology ; Humans ; Interleukin-8 - biosynthesis ; Interleukin-8 - genetics ; L-Selectin - metabolism ; Lipopolysaccharide Receptors - biosynthesis ; Lipopolysaccharide Receptors - genetics ; Lipopolysaccharides - pharmacology ; Macrophage-1 Antigen - biosynthesis ; Membrane Glycoproteins - biosynthesis ; Membrane Glycoproteins - genetics ; Monocytes - immunology ; Neutrophils - drug effects ; Neutrophils - immunology ; Receptors, Cell Surface - biosynthesis ; Receptors, Cell Surface - genetics ; RNA, Messenger - biosynthesis ; TLR2 protein ; TLR4 protein ; Toll-Like Receptor 2 ; Toll-Like Receptor 4 ; Toll-Like Receptors</subject><ispartof>The Journal of immunology (1950), 2002-05, Vol.168 (9), p.4701-4710</ispartof><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c475t-ccc7291e1ee0f0eabefe3d1264bb48ba18eb84cac7de451fd350182fe2fc9f193</citedby><cites>FETCH-LOGICAL-c475t-ccc7291e1ee0f0eabefe3d1264bb48ba18eb84cac7de451fd350182fe2fc9f193</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27903,27904</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/11971020$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Sabroe, Ian</creatorcontrib><creatorcontrib>Jones, Elizabeth C</creatorcontrib><creatorcontrib>Usher, Lynne R</creatorcontrib><creatorcontrib>Whyte, Moira K. B</creatorcontrib><creatorcontrib>Dower, Steven K</creatorcontrib><title>Toll-Like Receptor (TLR)2 and TLR4 in Human Peripheral Blood Granulocytes: A Critical Role for Monocytes in Leukocyte Lipopolysaccharide Responses</title><title>The Journal of immunology (1950)</title><addtitle>J Immunol</addtitle><description>Leukocyte responsiveness to LPS is dependent upon CD14 and receptors of the Toll-like receptor (TLR) family. Neutrophils respond to LPS, but conflicting data exist regarding LPS responses of eosinophils and basophils, and expression of TLRs at the protein level in these granulocyte lineages has not been fully described. We examined the expression of TLR2, TLR4, and CD14 and found that monocytes expressed relatively high levels of cell surface TLR2, TLR4, and CD14, while neutrophils also expressed all three molecules, but at low levels. In contrast, basophils expressed TLR2 and TLR4 but not CD14, while eosinophils expressed none of these proteins. Tested in a range of functional assays including L-selectin shedding, CD11b up-regulation, IL-8 mRNA generation, and cell survival, neutrophils responded to LPS, but eosinophils and basophils did not. In contrast to previous data, we found, using monocyte depletion by negative magnetic selection, that neutrophil responses to LPS were heavily dependent upon the presence of a very low level of monocytes, and neutrophil survival induced by LPS at 22 h was monocyte dependent. We conclude that LPS has little role in the regulation of peripheral blood eosinophil and basophil function, and that, even in neutrophils, monocytes orchestrate many previously observed leukocyte LPS response patterns.</description><subject>Basophils - drug effects</subject><subject>Basophils - immunology</subject><subject>Blood - immunology</subject><subject>CD14 antigen</subject><subject>Cell Survival - drug effects</subject><subject>Cells, Cultured</subject><subject>Dose-Response Relationship, Drug</subject><subject>Drosophila Proteins</subject><subject>Eosinophils - drug effects</subject><subject>Eosinophils - immunology</subject><subject>Granulocytes - immunology</subject><subject>Humans</subject><subject>Interleukin-8 - biosynthesis</subject><subject>Interleukin-8 - genetics</subject><subject>L-Selectin - metabolism</subject><subject>Lipopolysaccharide Receptors - biosynthesis</subject><subject>Lipopolysaccharide Receptors - genetics</subject><subject>Lipopolysaccharides - pharmacology</subject><subject>Macrophage-1 Antigen - biosynthesis</subject><subject>Membrane Glycoproteins - biosynthesis</subject><subject>Membrane Glycoproteins - genetics</subject><subject>Monocytes - immunology</subject><subject>Neutrophils - drug effects</subject><subject>Neutrophils - immunology</subject><subject>Receptors, Cell Surface - biosynthesis</subject><subject>Receptors, Cell Surface - genetics</subject><subject>RNA, Messenger - biosynthesis</subject><subject>TLR2 protein</subject><subject>TLR4 protein</subject><subject>Toll-Like Receptor 2</subject><subject>Toll-Like Receptor 4</subject><subject>Toll-Like Receptors</subject><issn>0022-1767</issn><issn>1550-6606</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2002</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkctu1DAUQC0EokPhC5CQVxQWGXwd52F27ai0SEGg0bC2HOeGcevEwU40mt_oF5PpTAU7VrZ1zz1eHELeAlsKJuSnO9t1U-_dEvJyKZeiYPCMLCDLWJLnLH9OFoxxnkCRF2fkVYx3jLGccfGSnAHIAhhnC_Kw8c4llb1HukaDw-gD_bCp1h851X1D55ugtqe3U6d7-gODHbYYtKNXzvuG3gTdT86b_YjxM72kq2BHa-bx2juk7ez65vvj-GCpcLp_fNHKDn7wbh-1MVsdbHP4Pg6-jxhfkxetdhHfnM5z8vPL9WZ1m1Tfb76uLqvEiCIbE2NMwSUgILKWoa6xxbQBnou6FmWtocS6FEabokGRQdukGYOSt8hbI1uQ6Tl5f_QOwf-eMI6qs9Ggc7pHP0VVQM65LMV_QShTKCVLZzA9gib4GAO2agi202GvgKlDM_XUTM3NlFSHZvPWu5N-qjts_u6cIs3AxRHY2l_bnQ2oYqedm3FQu93uH9UfIPWkjw</recordid><startdate>20020501</startdate><enddate>20020501</enddate><creator>Sabroe, Ian</creator><creator>Jones, Elizabeth C</creator><creator>Usher, Lynne R</creator><creator>Whyte, Moira K. 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B ; Dower, Steven K</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c475t-ccc7291e1ee0f0eabefe3d1264bb48ba18eb84cac7de451fd350182fe2fc9f193</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2002</creationdate><topic>Basophils - drug effects</topic><topic>Basophils - immunology</topic><topic>Blood - immunology</topic><topic>CD14 antigen</topic><topic>Cell Survival - drug effects</topic><topic>Cells, Cultured</topic><topic>Dose-Response Relationship, Drug</topic><topic>Drosophila Proteins</topic><topic>Eosinophils - drug effects</topic><topic>Eosinophils - immunology</topic><topic>Granulocytes - immunology</topic><topic>Humans</topic><topic>Interleukin-8 - biosynthesis</topic><topic>Interleukin-8 - genetics</topic><topic>L-Selectin - metabolism</topic><topic>Lipopolysaccharide Receptors - biosynthesis</topic><topic>Lipopolysaccharide Receptors - genetics</topic><topic>Lipopolysaccharides - pharmacology</topic><topic>Macrophage-1 Antigen - biosynthesis</topic><topic>Membrane Glycoproteins - biosynthesis</topic><topic>Membrane Glycoproteins - genetics</topic><topic>Monocytes - immunology</topic><topic>Neutrophils - drug effects</topic><topic>Neutrophils - immunology</topic><topic>Receptors, Cell Surface - biosynthesis</topic><topic>Receptors, Cell Surface - genetics</topic><topic>RNA, Messenger - biosynthesis</topic><topic>TLR2 protein</topic><topic>TLR4 protein</topic><topic>Toll-Like Receptor 2</topic><topic>Toll-Like Receptor 4</topic><topic>Toll-Like Receptors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Sabroe, Ian</creatorcontrib><creatorcontrib>Jones, Elizabeth C</creatorcontrib><creatorcontrib>Usher, Lynne R</creatorcontrib><creatorcontrib>Whyte, Moira K. 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B</au><au>Dower, Steven K</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Toll-Like Receptor (TLR)2 and TLR4 in Human Peripheral Blood Granulocytes: A Critical Role for Monocytes in Leukocyte Lipopolysaccharide Responses</atitle><jtitle>The Journal of immunology (1950)</jtitle><addtitle>J Immunol</addtitle><date>2002-05-01</date><risdate>2002</risdate><volume>168</volume><issue>9</issue><spage>4701</spage><epage>4710</epage><pages>4701-4710</pages><issn>0022-1767</issn><eissn>1550-6606</eissn><abstract>Leukocyte responsiveness to LPS is dependent upon CD14 and receptors of the Toll-like receptor (TLR) family. Neutrophils respond to LPS, but conflicting data exist regarding LPS responses of eosinophils and basophils, and expression of TLRs at the protein level in these granulocyte lineages has not been fully described. We examined the expression of TLR2, TLR4, and CD14 and found that monocytes expressed relatively high levels of cell surface TLR2, TLR4, and CD14, while neutrophils also expressed all three molecules, but at low levels. In contrast, basophils expressed TLR2 and TLR4 but not CD14, while eosinophils expressed none of these proteins. Tested in a range of functional assays including L-selectin shedding, CD11b up-regulation, IL-8 mRNA generation, and cell survival, neutrophils responded to LPS, but eosinophils and basophils did not. In contrast to previous data, we found, using monocyte depletion by negative magnetic selection, that neutrophil responses to LPS were heavily dependent upon the presence of a very low level of monocytes, and neutrophil survival induced by LPS at 22 h was monocyte dependent. We conclude that LPS has little role in the regulation of peripheral blood eosinophil and basophil function, and that, even in neutrophils, monocytes orchestrate many previously observed leukocyte LPS response patterns.</abstract><cop>United States</cop><pub>Am Assoc Immnol</pub><pmid>11971020</pmid><doi>10.4049/jimmunol.168.9.4701</doi><tpages>10</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Basophils - drug effects Basophils - immunology Blood - immunology CD14 antigen Cell Survival - drug effects Cells, Cultured Dose-Response Relationship, Drug Drosophila Proteins Eosinophils - drug effects Eosinophils - immunology Granulocytes - immunology Humans Interleukin-8 - biosynthesis Interleukin-8 - genetics L-Selectin - metabolism Lipopolysaccharide Receptors - biosynthesis Lipopolysaccharide Receptors - genetics Lipopolysaccharides - pharmacology Macrophage-1 Antigen - biosynthesis Membrane Glycoproteins - biosynthesis Membrane Glycoproteins - genetics Monocytes - immunology Neutrophils - drug effects Neutrophils - immunology Receptors, Cell Surface - biosynthesis Receptors, Cell Surface - genetics RNA, Messenger - biosynthesis TLR2 protein TLR4 protein Toll-Like Receptor 2 Toll-Like Receptor 4 Toll-Like Receptors |
title | Toll-Like Receptor (TLR)2 and TLR4 in Human Peripheral Blood Granulocytes: A Critical Role for Monocytes in Leukocyte Lipopolysaccharide Responses |
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