Interactions between TLR2, TLR4, and mannose receptors with gp43 from Paracoccidioides brasiliensis induce cytokine production by human monocytes
The glycoprotein gp43 is an immunodominant antigen secreted by Paracoccidioides brasiliensis, the agent of paracoccidioidomycosis. The present study evaluated whether gp43 can interact with toll-like (TLR2, TLR4) and mannose (MR) receptors on the surface of human monocytes, and how that affects thei...
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Veröffentlicht in: | Medical mycology (Oxford) 2011-10, Vol.49 (7), p.694-703 |
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creator | Nakaira-Takahagi, Erika Golim, Marjorie A. Bannwart, Camila F. Puccia, Rosana Peraçoli, Maria T. S. |
description | The glycoprotein gp43 is an immunodominant antigen secreted by Paracoccidioides brasiliensis, the agent of paracoccidioidomycosis. The present study evaluated whether gp43 can interact with toll-like (TLR2, TLR4) and mannose (MR) receptors on the surface of human monocytes, and how that affects their expression and cytokine production. Monocytes were incubated with or without monoclonal antibodies anti-TLR2, anti-TLR4, or anti-MR, individually or in combination, prior to the addition of gp43. The gp43 binding to monocyte surface, as well as expression of TLR2, TLR4, and MRs were analyzed by flow cytometry, while production of TNF-α and IL-10 was monitored by ELISA. The results suggested that gp43 binds to TLR2, TLR4, and MR receptors, with TLR2 and MR having the strongest effect. All three receptors influenced the production of IL-10, while TNF-α production was associated with expression of TLR4 and MR. The modulatory effect of gp43 was demonstrated by high levels of TLR4 expression associated with increased production of TNF-α after 4 h of culture. Alternatively, high levels of TLR2 expression, and elevated production of IL-10, were detected after 18 h. We showed that interaction between gp43 and monocytes may affect the innate immune response by modulating the expression of the pattern recognition receptors TLR2, TLR4 and MR, as well as production of pro- and anti-inflammatory cytokines. |
doi_str_mv | 10.3109/13693786.2011.565485 |
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S.</creator><creatorcontrib>Nakaira-Takahagi, Erika ; Golim, Marjorie A. ; Bannwart, Camila F. ; Puccia, Rosana ; Peraçoli, Maria T. S.</creatorcontrib><description>The glycoprotein gp43 is an immunodominant antigen secreted by Paracoccidioides brasiliensis, the agent of paracoccidioidomycosis. The present study evaluated whether gp43 can interact with toll-like (TLR2, TLR4) and mannose (MR) receptors on the surface of human monocytes, and how that affects their expression and cytokine production. Monocytes were incubated with or without monoclonal antibodies anti-TLR2, anti-TLR4, or anti-MR, individually or in combination, prior to the addition of gp43. The gp43 binding to monocyte surface, as well as expression of TLR2, TLR4, and MRs were analyzed by flow cytometry, while production of TNF-α and IL-10 was monitored by ELISA. The results suggested that gp43 binds to TLR2, TLR4, and MR receptors, with TLR2 and MR having the strongest effect. All three receptors influenced the production of IL-10, while TNF-α production was associated with expression of TLR4 and MR. The modulatory effect of gp43 was demonstrated by high levels of TLR4 expression associated with increased production of TNF-α after 4 h of culture. Alternatively, high levels of TLR2 expression, and elevated production of IL-10, were detected after 18 h. We showed that interaction between gp43 and monocytes may affect the innate immune response by modulating the expression of the pattern recognition receptors TLR2, TLR4 and MR, as well as production of pro- and anti-inflammatory cytokines.</description><identifier>ISSN: 1369-3786</identifier><identifier>EISSN: 1460-2709</identifier><identifier>DOI: 10.3109/13693786.2011.565485</identifier><identifier>PMID: 21417682</identifier><language>eng</language><publisher>UK: Informa Healthcare</publisher><subject>Adult ; Antigens, Fungal - immunology ; Antigens, Fungal - metabolism ; Flow Cytometry ; Fungal Proteins - immunology ; Fungal Proteins - metabolism ; Gene Expression Profiling ; Glycoproteins - immunology ; Glycoproteins - metabolism ; Humans ; Interleukin-10 - secretion ; Lectins, C-Type - immunology ; Lectins, C-Type - metabolism ; Mannose-Binding Lectins - immunology ; Mannose-Binding Lectins - metabolism ; Middle Aged ; Monocytes - immunology ; Monocytes - microbiology ; Paracoccidioides - immunology ; Protein Binding ; Receptors, Cell Surface - immunology ; Receptors, Cell Surface - metabolism ; Toll-Like Receptor 2 - immunology ; Toll-Like Receptor 2 - metabolism ; Toll-Like Receptor 4 - immunology ; Toll-Like Receptor 4 - metabolism ; Tumor Necrosis Factor-alpha - secretion</subject><ispartof>Medical mycology (Oxford), 2011-10, Vol.49 (7), p.694-703</ispartof><rights>2011 ISHAM 2011</rights><rights>2011 International Society for Human and Animal Mycology 2011</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c401t-b7d86cfbf509120205e3818171e1ae0dbc20b15742ebda2bf0934bc7bf22584a3</citedby><cites>FETCH-LOGICAL-c401t-b7d86cfbf509120205e3818171e1ae0dbc20b15742ebda2bf0934bc7bf22584a3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>315,781,785,27929,27930</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/21417682$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Nakaira-Takahagi, Erika</creatorcontrib><creatorcontrib>Golim, Marjorie A.</creatorcontrib><creatorcontrib>Bannwart, Camila F.</creatorcontrib><creatorcontrib>Puccia, Rosana</creatorcontrib><creatorcontrib>Peraçoli, Maria T. S.</creatorcontrib><title>Interactions between TLR2, TLR4, and mannose receptors with gp43 from Paracoccidioides brasiliensis induce cytokine production by human monocytes</title><title>Medical mycology (Oxford)</title><addtitle>Med Mycol</addtitle><description>The glycoprotein gp43 is an immunodominant antigen secreted by Paracoccidioides brasiliensis, the agent of paracoccidioidomycosis. The present study evaluated whether gp43 can interact with toll-like (TLR2, TLR4) and mannose (MR) receptors on the surface of human monocytes, and how that affects their expression and cytokine production. Monocytes were incubated with or without monoclonal antibodies anti-TLR2, anti-TLR4, or anti-MR, individually or in combination, prior to the addition of gp43. The gp43 binding to monocyte surface, as well as expression of TLR2, TLR4, and MRs were analyzed by flow cytometry, while production of TNF-α and IL-10 was monitored by ELISA. The results suggested that gp43 binds to TLR2, TLR4, and MR receptors, with TLR2 and MR having the strongest effect. All three receptors influenced the production of IL-10, while TNF-α production was associated with expression of TLR4 and MR. The modulatory effect of gp43 was demonstrated by high levels of TLR4 expression associated with increased production of TNF-α after 4 h of culture. Alternatively, high levels of TLR2 expression, and elevated production of IL-10, were detected after 18 h. We showed that interaction between gp43 and monocytes may affect the innate immune response by modulating the expression of the pattern recognition receptors TLR2, TLR4 and MR, as well as production of pro- and anti-inflammatory cytokines.</description><subject>Adult</subject><subject>Antigens, Fungal - immunology</subject><subject>Antigens, Fungal - metabolism</subject><subject>Flow Cytometry</subject><subject>Fungal Proteins - immunology</subject><subject>Fungal Proteins - metabolism</subject><subject>Gene Expression Profiling</subject><subject>Glycoproteins - immunology</subject><subject>Glycoproteins - metabolism</subject><subject>Humans</subject><subject>Interleukin-10 - secretion</subject><subject>Lectins, C-Type - immunology</subject><subject>Lectins, C-Type - metabolism</subject><subject>Mannose-Binding Lectins - immunology</subject><subject>Mannose-Binding Lectins - metabolism</subject><subject>Middle Aged</subject><subject>Monocytes - immunology</subject><subject>Monocytes - microbiology</subject><subject>Paracoccidioides - immunology</subject><subject>Protein Binding</subject><subject>Receptors, Cell Surface - immunology</subject><subject>Receptors, Cell Surface - metabolism</subject><subject>Toll-Like Receptor 2 - immunology</subject><subject>Toll-Like Receptor 2 - metabolism</subject><subject>Toll-Like Receptor 4 - immunology</subject><subject>Toll-Like Receptor 4 - metabolism</subject><subject>Tumor Necrosis Factor-alpha - secretion</subject><issn>1369-3786</issn><issn>1460-2709</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2011</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkctu1TAQhi0Eohd4A4S8Y9Oc-pbY2SChCkqlI1FVZW3ZzoTjktjBTlSdx-CNcZSWJWJjW9Y334zmR-gdJTtOSXtJedNyqZodI5Tu6qYWqn6BTqloSMUkaV-Wd0GqlTlBZzk_EEJly_hrdMKooLJR7BT9vgkzJONmH0PGFuZHgIDv93fsYj3FBTahw6MJIWbACRxMc0wZP_r5gH9MguM-xRHfmuKIzvnOR99BMSWT_eAhZJ-xD93iALvjHH_6AHhKsXysLbE94sNS9HiMIRYA8hv0qjdDhrdP9zn6_uXz_dXXav_t-ubq075ygtC5srJTjettX5OWMsJIDVxRRSUFaoB01jFiaS0FA9sZZnvScmGdtD1jtRKGn6MPm7dM82uBPOvRZwfDYALEJWulZCuEILyQYiNdijkn6PWU_GjSUVOi1yz0cxZ6zUJvWZSy908NFjtC97foefkFuNyAuEz_q_y4VfjQxzSaA5hhPjiTQD_EJYWyr38L_gDG2afb</recordid><startdate>20111001</startdate><enddate>20111001</enddate><creator>Nakaira-Takahagi, Erika</creator><creator>Golim, Marjorie A.</creator><creator>Bannwart, Camila F.</creator><creator>Puccia, Rosana</creator><creator>Peraçoli, Maria T. S.</creator><general>Informa Healthcare</general><general>Informa UK Ltd</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></search><sort><creationdate>20111001</creationdate><title>Interactions between TLR2, TLR4, and mannose receptors with gp43 from Paracoccidioides brasiliensis induce cytokine production by human monocytes</title><author>Nakaira-Takahagi, Erika ; Golim, Marjorie A. ; Bannwart, Camila F. ; Puccia, Rosana ; Peraçoli, Maria T. S.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c401t-b7d86cfbf509120205e3818171e1ae0dbc20b15742ebda2bf0934bc7bf22584a3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2011</creationdate><topic>Adult</topic><topic>Antigens, Fungal - immunology</topic><topic>Antigens, Fungal - metabolism</topic><topic>Flow Cytometry</topic><topic>Fungal Proteins - immunology</topic><topic>Fungal Proteins - metabolism</topic><topic>Gene Expression Profiling</topic><topic>Glycoproteins - immunology</topic><topic>Glycoproteins - metabolism</topic><topic>Humans</topic><topic>Interleukin-10 - secretion</topic><topic>Lectins, C-Type - immunology</topic><topic>Lectins, C-Type - metabolism</topic><topic>Mannose-Binding Lectins - immunology</topic><topic>Mannose-Binding Lectins - metabolism</topic><topic>Middle Aged</topic><topic>Monocytes - immunology</topic><topic>Monocytes - microbiology</topic><topic>Paracoccidioides - immunology</topic><topic>Protein Binding</topic><topic>Receptors, Cell Surface - immunology</topic><topic>Receptors, Cell Surface - metabolism</topic><topic>Toll-Like Receptor 2 - immunology</topic><topic>Toll-Like Receptor 2 - metabolism</topic><topic>Toll-Like Receptor 4 - immunology</topic><topic>Toll-Like Receptor 4 - metabolism</topic><topic>Tumor Necrosis Factor-alpha - secretion</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Nakaira-Takahagi, Erika</creatorcontrib><creatorcontrib>Golim, Marjorie A.</creatorcontrib><creatorcontrib>Bannwart, Camila F.</creatorcontrib><creatorcontrib>Puccia, Rosana</creatorcontrib><creatorcontrib>Peraçoli, Maria T. S.</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><jtitle>Medical mycology (Oxford)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Nakaira-Takahagi, Erika</au><au>Golim, Marjorie A.</au><au>Bannwart, Camila F.</au><au>Puccia, Rosana</au><au>Peraçoli, Maria T. S.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Interactions between TLR2, TLR4, and mannose receptors with gp43 from Paracoccidioides brasiliensis induce cytokine production by human monocytes</atitle><jtitle>Medical mycology (Oxford)</jtitle><addtitle>Med Mycol</addtitle><date>2011-10-01</date><risdate>2011</risdate><volume>49</volume><issue>7</issue><spage>694</spage><epage>703</epage><pages>694-703</pages><issn>1369-3786</issn><eissn>1460-2709</eissn><abstract>The glycoprotein gp43 is an immunodominant antigen secreted by Paracoccidioides brasiliensis, the agent of paracoccidioidomycosis. The present study evaluated whether gp43 can interact with toll-like (TLR2, TLR4) and mannose (MR) receptors on the surface of human monocytes, and how that affects their expression and cytokine production. Monocytes were incubated with or without monoclonal antibodies anti-TLR2, anti-TLR4, or anti-MR, individually or in combination, prior to the addition of gp43. The gp43 binding to monocyte surface, as well as expression of TLR2, TLR4, and MRs were analyzed by flow cytometry, while production of TNF-α and IL-10 was monitored by ELISA. The results suggested that gp43 binds to TLR2, TLR4, and MR receptors, with TLR2 and MR having the strongest effect. All three receptors influenced the production of IL-10, while TNF-α production was associated with expression of TLR4 and MR. The modulatory effect of gp43 was demonstrated by high levels of TLR4 expression associated with increased production of TNF-α after 4 h of culture. Alternatively, high levels of TLR2 expression, and elevated production of IL-10, were detected after 18 h. We showed that interaction between gp43 and monocytes may affect the innate immune response by modulating the expression of the pattern recognition receptors TLR2, TLR4 and MR, as well as production of pro- and anti-inflammatory cytokines.</abstract><cop>UK</cop><pub>Informa Healthcare</pub><pmid>21417682</pmid><doi>10.3109/13693786.2011.565485</doi><tpages>10</tpages></addata></record> |
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source | MEDLINE; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; Oxford University Press Journals All Titles (1996-Current) |
subjects | Adult Antigens, Fungal - immunology Antigens, Fungal - metabolism Flow Cytometry Fungal Proteins - immunology Fungal Proteins - metabolism Gene Expression Profiling Glycoproteins - immunology Glycoproteins - metabolism Humans Interleukin-10 - secretion Lectins, C-Type - immunology Lectins, C-Type - metabolism Mannose-Binding Lectins - immunology Mannose-Binding Lectins - metabolism Middle Aged Monocytes - immunology Monocytes - microbiology Paracoccidioides - immunology Protein Binding Receptors, Cell Surface - immunology Receptors, Cell Surface - metabolism Toll-Like Receptor 2 - immunology Toll-Like Receptor 2 - metabolism Toll-Like Receptor 4 - immunology Toll-Like Receptor 4 - metabolism Tumor Necrosis Factor-alpha - secretion |
title | Interactions between TLR2, TLR4, and mannose receptors with gp43 from Paracoccidioides brasiliensis induce cytokine production by human monocytes |
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