Expression of Toll-like receptors on human platelets
Introduction: Platelets play a crucial role in arterial thrombosis, which is the main cause of acute coronary syndrome. Some mycobacteriums, such as Chlamydia pneumoniae, were associated with progression of atherosclerosis and they are interacted with Toll-like receptors (TLRs), which have been defi...
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Veröffentlicht in: | Thrombosis research 2004, Vol.113 (6), p.379-385 |
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creator | Shiraki, Rio Inoue, Nobutaka Kawasaki, Satoru Takei, Asumi Kadotani, Makoto Ohnishi, Yoshio Ejiri, Junya Kobayashi, Seiichi Hirata, Ken-ichi Kawashima, Seinosuke Yokoyama, Mitsuhiro |
description | Introduction: Platelets play a crucial role in arterial thrombosis, which is the main cause of acute coronary syndrome. Some mycobacteriums, such as
Chlamydia pneumoniae, were associated with progression of atherosclerosis and they are interacted with Toll-like receptors (TLRs), which have been defined as pathogen-associated molecular pattern recognition molecules in innate immunity. In the present study, we examined whether human platelets express TLRs.
Materials and methods: Human platelets were obtained from healthy volunteers and the mRNA and protein level of TLRs on platelets and Meg-01 cells, megakaryoblastic cell line, were investigated.
Results: Reverse transcription–polymerase chain reaction (RT-PCR) demonstrated that TLR1 and TLR6 mRNA were expressed in platelets and Meg-01 cells. Furthermore, interferon-γ up-regulated their mRNA levels in dose and time dependent manners after stimuli. Both TLR1 and TLR6 proteins in platelets were detected by Western blotting, and their expression of platelets was more than that of Meg-01 cells. Flow cytometry analysis revealed the expression of TLR1 and TLR6 on the cell surface of Meg-01 cells. Furthermore, immunohistochemical analysis using human coronary thrombi obtained from patients with acute coronary syndrome confirmed the expression of TLR1 and TLR6 on platelets.
Conclusion: In summary, we demonstrated that human platelets and Meg-01 cells expressed a family of TLRs for the first time, and our findings indicated that platelets might recognize antigens directly via TLRs. Our findings suggest a possibility that platelets have the ability to recognize the antigens via TLRs and that there are mechanistic relations between infectious inflammation and atherosclerotic vascular diseases. |
doi_str_mv | 10.1016/j.thromres.2004.03.023 |
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Chlamydia pneumoniae, were associated with progression of atherosclerosis and they are interacted with Toll-like receptors (TLRs), which have been defined as pathogen-associated molecular pattern recognition molecules in innate immunity. In the present study, we examined whether human platelets express TLRs.
Materials and methods: Human platelets were obtained from healthy volunteers and the mRNA and protein level of TLRs on platelets and Meg-01 cells, megakaryoblastic cell line, were investigated.
Results: Reverse transcription–polymerase chain reaction (RT-PCR) demonstrated that TLR1 and TLR6 mRNA were expressed in platelets and Meg-01 cells. Furthermore, interferon-γ up-regulated their mRNA levels in dose and time dependent manners after stimuli. Both TLR1 and TLR6 proteins in platelets were detected by Western blotting, and their expression of platelets was more than that of Meg-01 cells. Flow cytometry analysis revealed the expression of TLR1 and TLR6 on the cell surface of Meg-01 cells. Furthermore, immunohistochemical analysis using human coronary thrombi obtained from patients with acute coronary syndrome confirmed the expression of TLR1 and TLR6 on platelets.
Conclusion: In summary, we demonstrated that human platelets and Meg-01 cells expressed a family of TLRs for the first time, and our findings indicated that platelets might recognize antigens directly via TLRs. Our findings suggest a possibility that platelets have the ability to recognize the antigens via TLRs and that there are mechanistic relations between infectious inflammation and atherosclerotic vascular diseases.</description><identifier>ISSN: 0049-3848</identifier><identifier>EISSN: 1879-2472</identifier><identifier>DOI: 10.1016/j.thromres.2004.03.023</identifier><identifier>PMID: 15226092</identifier><identifier>CODEN: THBRAA</identifier><language>eng</language><publisher>New York, NY: Elsevier Ltd</publisher><subject>Biological and medical sciences ; Biomarkers - metabolism ; Blood and lymphatic vessels ; Blood coagulation. Blood cells ; Blood Platelets - metabolism ; Blood vessels and receptors ; Cardiology. Vascular system ; Cell Line, Tumor ; Cells, Cultured ; Coronary artery disease ; Coronary Thrombosis - metabolism ; Coronary Thrombosis - pathology ; Diseases of the peripheral vessels. Diseases of the vena cava. Miscellaneous ; Fundamental and applied biological sciences. Psychology ; Humans ; Infection ; Inflammation ; Leukemia, Megakaryoblastic, Acute - metabolism ; Medical sciences ; Membrane Glycoproteins - metabolism ; Molecular and cellular biology ; Monocytes - metabolism ; Platelet ; Receptors, Cell Surface - metabolism ; Thrombosis ; Toll-Like Receptor 1 ; Toll-Like Receptor 6 ; Toll-Like Receptors ; Vertebrates: cardiovascular system</subject><ispartof>Thrombosis research, 2004, Vol.113 (6), p.379-385</ispartof><rights>2004 Elsevier Ltd</rights><rights>2004 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c513t-d4f50b653f7263d5c2e6f9c0ddb3018e9b8bd62a0c793b04f9fff3860f5e15533</citedby><cites>FETCH-LOGICAL-c513t-d4f50b653f7263d5c2e6f9c0ddb3018e9b8bd62a0c793b04f9fff3860f5e15533</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.thromres.2004.03.023$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>315,781,785,3551,4025,27927,27928,27929,45999</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=15936754$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/15226092$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Shiraki, Rio</creatorcontrib><creatorcontrib>Inoue, Nobutaka</creatorcontrib><creatorcontrib>Kawasaki, Satoru</creatorcontrib><creatorcontrib>Takei, Asumi</creatorcontrib><creatorcontrib>Kadotani, Makoto</creatorcontrib><creatorcontrib>Ohnishi, Yoshio</creatorcontrib><creatorcontrib>Ejiri, Junya</creatorcontrib><creatorcontrib>Kobayashi, Seiichi</creatorcontrib><creatorcontrib>Hirata, Ken-ichi</creatorcontrib><creatorcontrib>Kawashima, Seinosuke</creatorcontrib><creatorcontrib>Yokoyama, Mitsuhiro</creatorcontrib><title>Expression of Toll-like receptors on human platelets</title><title>Thrombosis research</title><addtitle>Thromb Res</addtitle><description>Introduction: Platelets play a crucial role in arterial thrombosis, which is the main cause of acute coronary syndrome. Some mycobacteriums, such as
Chlamydia pneumoniae, were associated with progression of atherosclerosis and they are interacted with Toll-like receptors (TLRs), which have been defined as pathogen-associated molecular pattern recognition molecules in innate immunity. In the present study, we examined whether human platelets express TLRs.
Materials and methods: Human platelets were obtained from healthy volunteers and the mRNA and protein level of TLRs on platelets and Meg-01 cells, megakaryoblastic cell line, were investigated.
Results: Reverse transcription–polymerase chain reaction (RT-PCR) demonstrated that TLR1 and TLR6 mRNA were expressed in platelets and Meg-01 cells. Furthermore, interferon-γ up-regulated their mRNA levels in dose and time dependent manners after stimuli. Both TLR1 and TLR6 proteins in platelets were detected by Western blotting, and their expression of platelets was more than that of Meg-01 cells. Flow cytometry analysis revealed the expression of TLR1 and TLR6 on the cell surface of Meg-01 cells. Furthermore, immunohistochemical analysis using human coronary thrombi obtained from patients with acute coronary syndrome confirmed the expression of TLR1 and TLR6 on platelets.
Conclusion: In summary, we demonstrated that human platelets and Meg-01 cells expressed a family of TLRs for the first time, and our findings indicated that platelets might recognize antigens directly via TLRs. Our findings suggest a possibility that platelets have the ability to recognize the antigens via TLRs and that there are mechanistic relations between infectious inflammation and atherosclerotic vascular diseases.</description><subject>Biological and medical sciences</subject><subject>Biomarkers - metabolism</subject><subject>Blood and lymphatic vessels</subject><subject>Blood coagulation. Blood cells</subject><subject>Blood Platelets - metabolism</subject><subject>Blood vessels and receptors</subject><subject>Cardiology. Vascular system</subject><subject>Cell Line, Tumor</subject><subject>Cells, Cultured</subject><subject>Coronary artery disease</subject><subject>Coronary Thrombosis - metabolism</subject><subject>Coronary Thrombosis - pathology</subject><subject>Diseases of the peripheral vessels. Diseases of the vena cava. Miscellaneous</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Humans</subject><subject>Infection</subject><subject>Inflammation</subject><subject>Leukemia, Megakaryoblastic, Acute - metabolism</subject><subject>Medical sciences</subject><subject>Membrane Glycoproteins - metabolism</subject><subject>Molecular and cellular biology</subject><subject>Monocytes - metabolism</subject><subject>Platelet</subject><subject>Receptors, Cell Surface - metabolism</subject><subject>Thrombosis</subject><subject>Toll-Like Receptor 1</subject><subject>Toll-Like Receptor 6</subject><subject>Toll-Like Receptors</subject><subject>Vertebrates: cardiovascular system</subject><issn>0049-3848</issn><issn>1879-2472</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2004</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkE1P3DAQhq0KVJaPv4ByaW9Jx3bsxLciBKUSUi9wthxnLLw4cbCzVfvvMdpF7Y25zGGed2b0EHJJoaFA5bdtsz6lOCXMDQNoG-ANMP6JbGjfqZq1HTsimzJQNe_b_oSc5rwFoB1V4jM5oYIxCYptSHvzZylLso9zFV31EEOog3_GKqHFZY0pV2XytJvMXC3BrBhwzefk2JmQ8eLQz8jj7c3D9V19_-vHz-ur-9oKytd6bJ2AQQruOib5KCxD6ZSFcRw40B7V0A-jZAZsp_gArVPOOd5LcAKpEJyfka_7vUuKLzvMq558thiCmTHuspalhFCqgHIP2hRzTuj0kvxk0l9NQb_50lv97ku_-dLAdfFVgpeHC7thwvFf7CCoAF8OgMnWBJfMbH3-j1NcdqIt3Pc9h8XHb49JZ-txtjj6YnLVY_Qf_fIKwoyMXg</recordid><startdate>2004</startdate><enddate>2004</enddate><creator>Shiraki, Rio</creator><creator>Inoue, Nobutaka</creator><creator>Kawasaki, Satoru</creator><creator>Takei, Asumi</creator><creator>Kadotani, Makoto</creator><creator>Ohnishi, Yoshio</creator><creator>Ejiri, Junya</creator><creator>Kobayashi, Seiichi</creator><creator>Hirata, Ken-ichi</creator><creator>Kawashima, Seinosuke</creator><creator>Yokoyama, Mitsuhiro</creator><general>Elsevier Ltd</general><general>Elsevier Science</general><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>2004</creationdate><title>Expression of Toll-like receptors on human platelets</title><author>Shiraki, Rio ; Inoue, Nobutaka ; Kawasaki, Satoru ; Takei, Asumi ; Kadotani, Makoto ; Ohnishi, Yoshio ; Ejiri, Junya ; Kobayashi, Seiichi ; Hirata, Ken-ichi ; Kawashima, Seinosuke ; Yokoyama, Mitsuhiro</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c513t-d4f50b653f7263d5c2e6f9c0ddb3018e9b8bd62a0c793b04f9fff3860f5e15533</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2004</creationdate><topic>Biological and medical sciences</topic><topic>Biomarkers - metabolism</topic><topic>Blood and lymphatic vessels</topic><topic>Blood coagulation. Blood cells</topic><topic>Blood Platelets - metabolism</topic><topic>Blood vessels and receptors</topic><topic>Cardiology. Vascular system</topic><topic>Cell Line, Tumor</topic><topic>Cells, Cultured</topic><topic>Coronary artery disease</topic><topic>Coronary Thrombosis - metabolism</topic><topic>Coronary Thrombosis - pathology</topic><topic>Diseases of the peripheral vessels. Diseases of the vena cava. Miscellaneous</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Humans</topic><topic>Infection</topic><topic>Inflammation</topic><topic>Leukemia, Megakaryoblastic, Acute - metabolism</topic><topic>Medical sciences</topic><topic>Membrane Glycoproteins - metabolism</topic><topic>Molecular and cellular biology</topic><topic>Monocytes - metabolism</topic><topic>Platelet</topic><topic>Receptors, Cell Surface - metabolism</topic><topic>Thrombosis</topic><topic>Toll-Like Receptor 1</topic><topic>Toll-Like Receptor 6</topic><topic>Toll-Like Receptors</topic><topic>Vertebrates: cardiovascular system</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Shiraki, Rio</creatorcontrib><creatorcontrib>Inoue, Nobutaka</creatorcontrib><creatorcontrib>Kawasaki, Satoru</creatorcontrib><creatorcontrib>Takei, Asumi</creatorcontrib><creatorcontrib>Kadotani, Makoto</creatorcontrib><creatorcontrib>Ohnishi, Yoshio</creatorcontrib><creatorcontrib>Ejiri, Junya</creatorcontrib><creatorcontrib>Kobayashi, Seiichi</creatorcontrib><creatorcontrib>Hirata, Ken-ichi</creatorcontrib><creatorcontrib>Kawashima, Seinosuke</creatorcontrib><creatorcontrib>Yokoyama, Mitsuhiro</creatorcontrib><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>Thrombosis research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Shiraki, Rio</au><au>Inoue, Nobutaka</au><au>Kawasaki, Satoru</au><au>Takei, Asumi</au><au>Kadotani, Makoto</au><au>Ohnishi, Yoshio</au><au>Ejiri, Junya</au><au>Kobayashi, Seiichi</au><au>Hirata, Ken-ichi</au><au>Kawashima, Seinosuke</au><au>Yokoyama, Mitsuhiro</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Expression of Toll-like receptors on human platelets</atitle><jtitle>Thrombosis research</jtitle><addtitle>Thromb Res</addtitle><date>2004</date><risdate>2004</risdate><volume>113</volume><issue>6</issue><spage>379</spage><epage>385</epage><pages>379-385</pages><issn>0049-3848</issn><eissn>1879-2472</eissn><coden>THBRAA</coden><abstract>Introduction: Platelets play a crucial role in arterial thrombosis, which is the main cause of acute coronary syndrome. Some mycobacteriums, such as
Chlamydia pneumoniae, were associated with progression of atherosclerosis and they are interacted with Toll-like receptors (TLRs), which have been defined as pathogen-associated molecular pattern recognition molecules in innate immunity. In the present study, we examined whether human platelets express TLRs.
Materials and methods: Human platelets were obtained from healthy volunteers and the mRNA and protein level of TLRs on platelets and Meg-01 cells, megakaryoblastic cell line, were investigated.
Results: Reverse transcription–polymerase chain reaction (RT-PCR) demonstrated that TLR1 and TLR6 mRNA were expressed in platelets and Meg-01 cells. Furthermore, interferon-γ up-regulated their mRNA levels in dose and time dependent manners after stimuli. Both TLR1 and TLR6 proteins in platelets were detected by Western blotting, and their expression of platelets was more than that of Meg-01 cells. Flow cytometry analysis revealed the expression of TLR1 and TLR6 on the cell surface of Meg-01 cells. Furthermore, immunohistochemical analysis using human coronary thrombi obtained from patients with acute coronary syndrome confirmed the expression of TLR1 and TLR6 on platelets.
Conclusion: In summary, we demonstrated that human platelets and Meg-01 cells expressed a family of TLRs for the first time, and our findings indicated that platelets might recognize antigens directly via TLRs. Our findings suggest a possibility that platelets have the ability to recognize the antigens via TLRs and that there are mechanistic relations between infectious inflammation and atherosclerotic vascular diseases.</abstract><cop>New York, NY</cop><pub>Elsevier Ltd</pub><pmid>15226092</pmid><doi>10.1016/j.thromres.2004.03.023</doi><tpages>7</tpages></addata></record> |
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subjects | Biological and medical sciences Biomarkers - metabolism Blood and lymphatic vessels Blood coagulation. Blood cells Blood Platelets - metabolism Blood vessels and receptors Cardiology. Vascular system Cell Line, Tumor Cells, Cultured Coronary artery disease Coronary Thrombosis - metabolism Coronary Thrombosis - pathology Diseases of the peripheral vessels. Diseases of the vena cava. Miscellaneous Fundamental and applied biological sciences. Psychology Humans Infection Inflammation Leukemia, Megakaryoblastic, Acute - metabolism Medical sciences Membrane Glycoproteins - metabolism Molecular and cellular biology Monocytes - metabolism Platelet Receptors, Cell Surface - metabolism Thrombosis Toll-Like Receptor 1 Toll-Like Receptor 6 Toll-Like Receptors Vertebrates: cardiovascular system |
title | Expression of Toll-like receptors on human platelets |
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