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Immune Regulation of Protease-Activated Receptor-1 Expression in Murine Small Intestine during Nippostrongylus brasiliensis Infection
Infection with gastrointestinal nematodes exerts profound effects on both immune and physiological responses of the host. Helminth infection induces a hypercontractility of intestinal smooth muscle that is dependent on the Th2 cytokines, IL-4 and IL-13, and may contribute to worm expulsion. Protease...
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Published in: | The Journal of immunology (1950) 2005-08, Vol.175 (4), p.2563-2569 |
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container_title | The Journal of immunology (1950) |
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creator | Zhao, Aiping Morimoto, Motoko Dawson, Harry Elfrey, Justin E Madden, Kathleen B Gause, William C Min, Booki Finkelman, Fred D Urban, Joseph F. Jr Shea-Donohue, Terez |
description | Infection with gastrointestinal nematodes exerts profound effects on both immune and physiological responses of the host. Helminth infection induces a hypercontractility of intestinal smooth muscle that is dependent on the Th2 cytokines, IL-4 and IL-13, and may contribute to worm expulsion. Protease-activated receptors (PARs) are expressed throughout the gut, and activation of PAR-1 was observed in asthma, a Th2-driven pathology. In the current study we investigated the physiologic and immunologic regulation of PAR-1 in the murine small intestine, specifically 1) the effect of PAR-1 agonists on small intestinal smooth muscle contractility, 2) the effects of Nippostrongylus brasiliensis infection on PAR-1 responses, 3) the roles of IL-13 and IL-4 in N. brasiliensis infection-induced alterations in PAR-1 responses, and 4) the STAT6 dependence of these responses. We demonstrate that PAR-1 activation induces contraction of murine intestinal smooth muscle that is enhanced during helminth infection. This hypercontractility is associated with an elevated expression of PAR-1 mRNA and protein. N. brasiliensis-induced changes in PAR-1 function and expression were seen in IL-4-deficient mice, but not in IL-13- or STAT6-deficient mice, indicating the dependence of IL-13 on the STAT6 signaling pathway independent of IL-4. |
doi_str_mv | 10.4049/jimmunol.175.4.2563 |
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Jr ; Shea-Donohue, Terez</creator><creatorcontrib>Zhao, Aiping ; Morimoto, Motoko ; Dawson, Harry ; Elfrey, Justin E ; Madden, Kathleen B ; Gause, William C ; Min, Booki ; Finkelman, Fred D ; Urban, Joseph F. Jr ; Shea-Donohue, Terez</creatorcontrib><description>Infection with gastrointestinal nematodes exerts profound effects on both immune and physiological responses of the host. Helminth infection induces a hypercontractility of intestinal smooth muscle that is dependent on the Th2 cytokines, IL-4 and IL-13, and may contribute to worm expulsion. Protease-activated receptors (PARs) are expressed throughout the gut, and activation of PAR-1 was observed in asthma, a Th2-driven pathology. In the current study we investigated the physiologic and immunologic regulation of PAR-1 in the murine small intestine, specifically 1) the effect of PAR-1 agonists on small intestinal smooth muscle contractility, 2) the effects of Nippostrongylus brasiliensis infection on PAR-1 responses, 3) the roles of IL-13 and IL-4 in N. brasiliensis infection-induced alterations in PAR-1 responses, and 4) the STAT6 dependence of these responses. We demonstrate that PAR-1 activation induces contraction of murine intestinal smooth muscle that is enhanced during helminth infection. This hypercontractility is associated with an elevated expression of PAR-1 mRNA and protein. N. brasiliensis-induced changes in PAR-1 function and expression were seen in IL-4-deficient mice, but not in IL-13- or STAT6-deficient mice, indicating the dependence of IL-13 on the STAT6 signaling pathway independent of IL-4.</description><identifier>ISSN: 1550-6606</identifier><identifier>ISSN: 0022-1767</identifier><identifier>EISSN: 1550-6606</identifier><identifier>DOI: 10.4049/jimmunol.175.4.2563</identifier><identifier>PMID: 16081830</identifier><language>eng</language><publisher>United States: Am Assoc Immnol</publisher><subject>Animals ; Dose-Response Relationship, Drug ; Female ; gene expression ; immune response ; Interleukin-13 - administration & dosage ; Interleukin-13 - deficiency ; Interleukin-13 - physiology ; Interleukin-4 - deficiency ; Interleukin-4 - genetics ; Interleukin-4 - physiology ; Jejunum - drug effects ; Jejunum - immunology ; Jejunum - metabolism ; Jejunum - parasitology ; messenger RNA ; Mice ; Mice, Inbred BALB C ; Mice, Knockout ; muscle contraction ; Muscle Contraction - drug effects ; Muscle, Smooth - drug effects ; Muscle, Smooth - physiology ; Nematoda ; nematode infections ; Nippostrongylus - immunology ; Nippostrongylus brasiliensis ; Oligopeptides - pharmacology ; protease-activated receptor-1 ; proteinases ; Receptor, PAR-1 - agonists ; Receptor, PAR-1 - biosynthesis ; Receptor, PAR-1 - metabolism ; receptors ; small intestine ; smooth muscle ; STAT6 Transcription Factor - deficiency ; STAT6 Transcription Factor - genetics ; STAT6 Transcription Factor - physiology ; Strongylida Infections - immunology ; Strongylida Infections - metabolism ; Up-Regulation - immunology</subject><ispartof>The Journal of immunology (1950), 2005-08, Vol.175 (4), p.2563-2569</ispartof><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c459t-e53f431f91de86c588d21f883bb6019929bd8e2b51afa55b514ed70788d0686e3</citedby><cites>FETCH-LOGICAL-c459t-e53f431f91de86c588d21f883bb6019929bd8e2b51afa55b514ed70788d0686e3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,780,784,885,27923,27924</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/16081830$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Zhao, Aiping</creatorcontrib><creatorcontrib>Morimoto, Motoko</creatorcontrib><creatorcontrib>Dawson, Harry</creatorcontrib><creatorcontrib>Elfrey, Justin E</creatorcontrib><creatorcontrib>Madden, Kathleen B</creatorcontrib><creatorcontrib>Gause, William C</creatorcontrib><creatorcontrib>Min, Booki</creatorcontrib><creatorcontrib>Finkelman, Fred D</creatorcontrib><creatorcontrib>Urban, Joseph F. Jr</creatorcontrib><creatorcontrib>Shea-Donohue, Terez</creatorcontrib><title>Immune Regulation of Protease-Activated Receptor-1 Expression in Murine Small Intestine during Nippostrongylus brasiliensis Infection</title><title>The Journal of immunology (1950)</title><addtitle>J Immunol</addtitle><description>Infection with gastrointestinal nematodes exerts profound effects on both immune and physiological responses of the host. Helminth infection induces a hypercontractility of intestinal smooth muscle that is dependent on the Th2 cytokines, IL-4 and IL-13, and may contribute to worm expulsion. Protease-activated receptors (PARs) are expressed throughout the gut, and activation of PAR-1 was observed in asthma, a Th2-driven pathology. In the current study we investigated the physiologic and immunologic regulation of PAR-1 in the murine small intestine, specifically 1) the effect of PAR-1 agonists on small intestinal smooth muscle contractility, 2) the effects of Nippostrongylus brasiliensis infection on PAR-1 responses, 3) the roles of IL-13 and IL-4 in N. brasiliensis infection-induced alterations in PAR-1 responses, and 4) the STAT6 dependence of these responses. We demonstrate that PAR-1 activation induces contraction of murine intestinal smooth muscle that is enhanced during helminth infection. This hypercontractility is associated with an elevated expression of PAR-1 mRNA and protein. N. brasiliensis-induced changes in PAR-1 function and expression were seen in IL-4-deficient mice, but not in IL-13- or STAT6-deficient mice, indicating the dependence of IL-13 on the STAT6 signaling pathway independent of IL-4.</description><subject>Animals</subject><subject>Dose-Response Relationship, Drug</subject><subject>Female</subject><subject>gene expression</subject><subject>immune response</subject><subject>Interleukin-13 - administration & dosage</subject><subject>Interleukin-13 - deficiency</subject><subject>Interleukin-13 - physiology</subject><subject>Interleukin-4 - deficiency</subject><subject>Interleukin-4 - genetics</subject><subject>Interleukin-4 - physiology</subject><subject>Jejunum - drug effects</subject><subject>Jejunum - immunology</subject><subject>Jejunum - metabolism</subject><subject>Jejunum - parasitology</subject><subject>messenger RNA</subject><subject>Mice</subject><subject>Mice, Inbred BALB C</subject><subject>Mice, Knockout</subject><subject>muscle contraction</subject><subject>Muscle Contraction - drug effects</subject><subject>Muscle, Smooth - drug effects</subject><subject>Muscle, Smooth - physiology</subject><subject>Nematoda</subject><subject>nematode infections</subject><subject>Nippostrongylus - immunology</subject><subject>Nippostrongylus brasiliensis</subject><subject>Oligopeptides - pharmacology</subject><subject>protease-activated receptor-1</subject><subject>proteinases</subject><subject>Receptor, PAR-1 - agonists</subject><subject>Receptor, PAR-1 - biosynthesis</subject><subject>Receptor, PAR-1 - metabolism</subject><subject>receptors</subject><subject>small intestine</subject><subject>smooth muscle</subject><subject>STAT6 Transcription Factor - deficiency</subject><subject>STAT6 Transcription Factor - genetics</subject><subject>STAT6 Transcription Factor - physiology</subject><subject>Strongylida Infections - immunology</subject><subject>Strongylida Infections - metabolism</subject><subject>Up-Regulation - immunology</subject><issn>1550-6606</issn><issn>0022-1767</issn><issn>1550-6606</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2005</creationdate><recordtype>article</recordtype><recordid>eNpVkdtu1DAQhi0EomXhCZAgV3CVxY4P69wgVVWBlcpBlF5bTjLJunLiYDtd-gC8N7Z2gdY347G_-ceeH6GXBK8ZZvW7GzOOy-Tsmmz4mq0rLugjdEo4x6UQWDy-tz9Bz0K4wRgLXLGn6IQILImk-BT93mYRKL7DsFgdjZsK1xffvIugA5RnbTS3OkKXgBbm6HxJiotfs4cQMmum4vPiTRK4GrW1xXaKEGLOu3w8FF_MPLsQvZuGO7uEovE6GGtgCiYkuoc293yOnvTaBnhxjCt0_eHix_mn8vLrx-352WXZMl7HEjjtGSV9TTqQouVSdhXppaRNIzCp66puOglVw4nuNecpMug2eJM4LKQAukLvD7rz0ozQtTBFr62avRm1v1NOG_XwZjI7NbhbVaXZ0bRW6M1RwLufS_qqGk1owVo9gVuCSlbUjBGeQHoAW-9C8ND_a0Kwyvapv_blGsVUti9Vvbr_vv81R78S8PYA7Myw2xsPKuS5J5yo_X7_QOr1gey1U3rwJqjrqwoTiomsNrgW9A9PQbPT</recordid><startdate>20050815</startdate><enddate>20050815</enddate><creator>Zhao, Aiping</creator><creator>Morimoto, Motoko</creator><creator>Dawson, Harry</creator><creator>Elfrey, Justin E</creator><creator>Madden, Kathleen B</creator><creator>Gause, William C</creator><creator>Min, Booki</creator><creator>Finkelman, Fred D</creator><creator>Urban, Joseph F. 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In the current study we investigated the physiologic and immunologic regulation of PAR-1 in the murine small intestine, specifically 1) the effect of PAR-1 agonists on small intestinal smooth muscle contractility, 2) the effects of Nippostrongylus brasiliensis infection on PAR-1 responses, 3) the roles of IL-13 and IL-4 in N. brasiliensis infection-induced alterations in PAR-1 responses, and 4) the STAT6 dependence of these responses. We demonstrate that PAR-1 activation induces contraction of murine intestinal smooth muscle that is enhanced during helminth infection. This hypercontractility is associated with an elevated expression of PAR-1 mRNA and protein. N. brasiliensis-induced changes in PAR-1 function and expression were seen in IL-4-deficient mice, but not in IL-13- or STAT6-deficient mice, indicating the dependence of IL-13 on the STAT6 signaling pathway independent of IL-4.</abstract><cop>United States</cop><pub>Am Assoc Immnol</pub><pmid>16081830</pmid><doi>10.4049/jimmunol.175.4.2563</doi><tpages>7</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Animals Dose-Response Relationship, Drug Female gene expression immune response Interleukin-13 - administration & dosage Interleukin-13 - deficiency Interleukin-13 - physiology Interleukin-4 - deficiency Interleukin-4 - genetics Interleukin-4 - physiology Jejunum - drug effects Jejunum - immunology Jejunum - metabolism Jejunum - parasitology messenger RNA Mice Mice, Inbred BALB C Mice, Knockout muscle contraction Muscle Contraction - drug effects Muscle, Smooth - drug effects Muscle, Smooth - physiology Nematoda nematode infections Nippostrongylus - immunology Nippostrongylus brasiliensis Oligopeptides - pharmacology protease-activated receptor-1 proteinases Receptor, PAR-1 - agonists Receptor, PAR-1 - biosynthesis Receptor, PAR-1 - metabolism receptors small intestine smooth muscle STAT6 Transcription Factor - deficiency STAT6 Transcription Factor - genetics STAT6 Transcription Factor - physiology Strongylida Infections - immunology Strongylida Infections - metabolism Up-Regulation - immunology |
title | Immune Regulation of Protease-Activated Receptor-1 Expression in Murine Small Intestine during Nippostrongylus brasiliensis Infection |
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