Cytokine-induced prostaglandin E2 production and cyclooxygenase-2 expression in dental pulp cells: downstream calcium signalling via activation of prostaglandin EP receptor

Aim  To determine whether (i) proinflammatory cytokines stimulate prostaglandin E2 (PGE2) production and cyclooxygenase (COX) gene expression in dental pulp cells, and (ii) pulp cells that express different prostaglandin E2 receptor (EP) isoforms and their activation by PGE2 leads to downstream Ca2+...

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Veröffentlicht in:International endodontic journal 2006-10, Vol.39 (10), p.819-826
Hauptverfasser: Chang, M.-C., Chen, Y.-J., Tai, T.-F., Tai, M.-R., Li, M.-Y., Tsai, Y.-L., Lan, W.-H., Wang, Y.-L., Jeng, J.-H.
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container_end_page 826
container_issue 10
container_start_page 819
container_title International endodontic journal
container_volume 39
creator Chang, M.-C.
Chen, Y.-J.
Tai, T.-F.
Tai, M.-R.
Li, M.-Y.
Tsai, Y.-L.
Lan, W.-H.
Wang, Y.-L.
Jeng, J.-H.
description Aim  To determine whether (i) proinflammatory cytokines stimulate prostaglandin E2 (PGE2) production and cyclooxygenase (COX) gene expression in dental pulp cells, and (ii) pulp cells that express different prostaglandin E2 receptor (EP) isoforms and their activation by PGE2 leads to downstream Ca2+ signalling. Methodology  Cultured human dental pulp cells were exposed to interleukin (IL)‐1β and tumour necrotic factor‐alpha (TNF‐α). The expression of COX‐1 and COX‐2 was measured with reverse transcriptase‐polymerase chain reaction (RT‐PCR). The production of PGE2 was measured using an enzyme‐linked immunosorbent assay. Expression of prostaglandin EP receptor isoforms was studied by RT‐PCR, whereas fura‐2 fluorescence was used to measure calcium mobilization. The Kruskal–Wallis test and Wilcoxon sum rank test with Bonferroni correction were used for statistical analysis. Results  Interleukin‐1β and TNF‐α stimulate PGE2 production of human dental pulp cells (P 
doi_str_mv 10.1111/j.1365-2591.2006.01156.x
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Methodology  Cultured human dental pulp cells were exposed to interleukin (IL)‐1β and tumour necrotic factor‐alpha (TNF‐α). The expression of COX‐1 and COX‐2 was measured with reverse transcriptase‐polymerase chain reaction (RT‐PCR). The production of PGE2 was measured using an enzyme‐linked immunosorbent assay. Expression of prostaglandin EP receptor isoforms was studied by RT‐PCR, whereas fura‐2 fluorescence was used to measure calcium mobilization. The Kruskal–Wallis test and Wilcoxon sum rank test with Bonferroni correction were used for statistical analysis. Results  Interleukin‐1β and TNF‐α stimulate PGE2 production of human dental pulp cells (P &lt; 0.05). IL‐1β stimulated the COX‐2 but not COX‐1 mRNA expression. Pulp cells express mainly EP2, EP3 and EP1 receptors as analysed by RT‐PCR. PGE2 (0.25–2 μmol L−1) stimulated the Ca2+ mobilization as indicated by increase in fura‐2 fluorescence. Conclusions  Interleukin‐1β and TNF‐α may stimulate PGE2 production in dental pulp cells. Activation of prostaglandin EP receptors in dental pulp cells by PGE2 may induce Ca2+ signalling to regulate cellular biological activity during inflammation.</description><identifier>ISSN: 0143-2885</identifier><identifier>EISSN: 1365-2591</identifier><identifier>DOI: 10.1111/j.1365-2591.2006.01156.x</identifier><identifier>PMID: 16948668</identifier><language>eng</language><publisher>Oxford, UK: Blackwell Publishing Ltd</publisher><subject>calcium mobilization ; Calcium Signaling - physiology ; Cells, Cultured ; Cyclooxygenase 2 - biosynthesis ; Cyclooxygenase 2 - genetics ; Cytokines - physiology ; Dental Pulp - cytology ; Dental Pulp - metabolism ; Dentistry ; Dinoprostone - biosynthesis ; Dinoprostone - genetics ; Dinoprostone - physiology ; Enzyme Activation ; Enzyme-Linked Immunosorbent Assay ; Fluorescent Dyes ; Fura-2 - analogs &amp; derivatives ; Gene Expression Regulation ; Humans ; inflammation ; Interleukin-1 - physiology ; prostaglandin ; prostaglandin receptor ; Protein Isoforms ; pulp cells ; Pulpitis - metabolism ; Receptors, Prostaglandin E - physiology ; Reverse Transcriptase Polymerase Chain Reaction ; Statistics, Nonparametric ; Tumor Necrosis Factor-alpha - physiology</subject><ispartof>International endodontic journal, 2006-10, Vol.39 (10), p.819-826</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1111%2Fj.1365-2591.2006.01156.x$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2Fj.1365-2591.2006.01156.x$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,776,780,1411,27903,27904,45553,45554</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/16948668$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Chang, M.-C.</creatorcontrib><creatorcontrib>Chen, Y.-J.</creatorcontrib><creatorcontrib>Tai, T.-F.</creatorcontrib><creatorcontrib>Tai, M.-R.</creatorcontrib><creatorcontrib>Li, M.-Y.</creatorcontrib><creatorcontrib>Tsai, Y.-L.</creatorcontrib><creatorcontrib>Lan, W.-H.</creatorcontrib><creatorcontrib>Wang, Y.-L.</creatorcontrib><creatorcontrib>Jeng, J.-H.</creatorcontrib><title>Cytokine-induced prostaglandin E2 production and cyclooxygenase-2 expression in dental pulp cells: downstream calcium signalling via activation of prostaglandin EP receptor</title><title>International endodontic journal</title><addtitle>Int Endod J</addtitle><description>Aim  To determine whether (i) proinflammatory cytokines stimulate prostaglandin E2 (PGE2) production and cyclooxygenase (COX) gene expression in dental pulp cells, and (ii) pulp cells that express different prostaglandin E2 receptor (EP) isoforms and their activation by PGE2 leads to downstream Ca2+ signalling. Methodology  Cultured human dental pulp cells were exposed to interleukin (IL)‐1β and tumour necrotic factor‐alpha (TNF‐α). The expression of COX‐1 and COX‐2 was measured with reverse transcriptase‐polymerase chain reaction (RT‐PCR). The production of PGE2 was measured using an enzyme‐linked immunosorbent assay. Expression of prostaglandin EP receptor isoforms was studied by RT‐PCR, whereas fura‐2 fluorescence was used to measure calcium mobilization. The Kruskal–Wallis test and Wilcoxon sum rank test with Bonferroni correction were used for statistical analysis. Results  Interleukin‐1β and TNF‐α stimulate PGE2 production of human dental pulp cells (P &lt; 0.05). IL‐1β stimulated the COX‐2 but not COX‐1 mRNA expression. Pulp cells express mainly EP2, EP3 and EP1 receptors as analysed by RT‐PCR. PGE2 (0.25–2 μmol L−1) stimulated the Ca2+ mobilization as indicated by increase in fura‐2 fluorescence. Conclusions  Interleukin‐1β and TNF‐α may stimulate PGE2 production in dental pulp cells. Activation of prostaglandin EP receptors in dental pulp cells by PGE2 may induce Ca2+ signalling to regulate cellular biological activity during inflammation.</description><subject>calcium mobilization</subject><subject>Calcium Signaling - physiology</subject><subject>Cells, Cultured</subject><subject>Cyclooxygenase 2 - biosynthesis</subject><subject>Cyclooxygenase 2 - genetics</subject><subject>Cytokines - physiology</subject><subject>Dental Pulp - cytology</subject><subject>Dental Pulp - metabolism</subject><subject>Dentistry</subject><subject>Dinoprostone - biosynthesis</subject><subject>Dinoprostone - genetics</subject><subject>Dinoprostone - physiology</subject><subject>Enzyme Activation</subject><subject>Enzyme-Linked Immunosorbent Assay</subject><subject>Fluorescent Dyes</subject><subject>Fura-2 - analogs &amp; derivatives</subject><subject>Gene Expression Regulation</subject><subject>Humans</subject><subject>inflammation</subject><subject>Interleukin-1 - physiology</subject><subject>prostaglandin</subject><subject>prostaglandin receptor</subject><subject>Protein Isoforms</subject><subject>pulp cells</subject><subject>Pulpitis - metabolism</subject><subject>Receptors, Prostaglandin E - physiology</subject><subject>Reverse Transcriptase Polymerase Chain Reaction</subject><subject>Statistics, Nonparametric</subject><subject>Tumor Necrosis Factor-alpha - physiology</subject><issn>0143-2885</issn><issn>1365-2591</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2006</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpdkc1u1DAUhS0EokPhFZBX7BL8EzsJEgsYTX-GqnQBYml57JuRp44T4qRN3omHJOm0RcIbW_ecc33tDyFMSUrn9fGQUi5FwkRJU0aITAmlQqbjC7R6Fl6iFaEZT1hRiBP0JsYDIUQQTl-jEyrLrJCyWKE_66lvbl2AxAU7GLC47ZrY673XwbqAN2wpzErvmoDnGjaT8U0zTnsIOkLCMIxtBzEu-hywEHrtcTv4FhvwPn7CtrkPse9A19hob9xQ4-j2QXvvwh7fOY313P5OP1zRVP9PcIM7MND2TfcWvaq0j_DucT9FP882P9YXydX388v1l6vEMSploiGDHatyrrWpKqN5zkVWGqEzJmyZW82MqTJe0HJnSbHLLFCSZ8byzBgpKeOn6MOx7zzJ7wFir2oXl8foAM0QlSwKRvNCzMb3j8ZhV4NVbedq3U3q6X9nw-ej4d55mP7pRC0c1UEtuNSCSy0c1QNHNarLzXY5zfnkmHexh_E5r7tbJXOeC_Xr-lyJb9fbrzfbtTrjfwHR7aV7</recordid><startdate>200610</startdate><enddate>200610</enddate><creator>Chang, M.-C.</creator><creator>Chen, Y.-J.</creator><creator>Tai, T.-F.</creator><creator>Tai, M.-R.</creator><creator>Li, M.-Y.</creator><creator>Tsai, Y.-L.</creator><creator>Lan, W.-H.</creator><creator>Wang, Y.-L.</creator><creator>Jeng, J.-H.</creator><general>Blackwell Publishing Ltd</general><scope>BSCLL</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>7X8</scope></search><sort><creationdate>200610</creationdate><title>Cytokine-induced prostaglandin E2 production and cyclooxygenase-2 expression in dental pulp cells: downstream calcium signalling via activation of prostaglandin EP receptor</title><author>Chang, M.-C. ; Chen, Y.-J. ; Tai, T.-F. ; Tai, M.-R. ; Li, M.-Y. ; Tsai, Y.-L. ; Lan, W.-H. ; Wang, Y.-L. ; Jeng, J.-H.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-i2166-ae4eb2f73aacffca373549c5a425d97da2ccf43819bd08b4de1074cd34cc66123</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2006</creationdate><topic>calcium mobilization</topic><topic>Calcium Signaling - physiology</topic><topic>Cells, Cultured</topic><topic>Cyclooxygenase 2 - biosynthesis</topic><topic>Cyclooxygenase 2 - genetics</topic><topic>Cytokines - physiology</topic><topic>Dental Pulp - cytology</topic><topic>Dental Pulp - metabolism</topic><topic>Dentistry</topic><topic>Dinoprostone - biosynthesis</topic><topic>Dinoprostone - genetics</topic><topic>Dinoprostone - physiology</topic><topic>Enzyme Activation</topic><topic>Enzyme-Linked Immunosorbent Assay</topic><topic>Fluorescent Dyes</topic><topic>Fura-2 - analogs &amp; derivatives</topic><topic>Gene Expression Regulation</topic><topic>Humans</topic><topic>inflammation</topic><topic>Interleukin-1 - physiology</topic><topic>prostaglandin</topic><topic>prostaglandin receptor</topic><topic>Protein Isoforms</topic><topic>pulp cells</topic><topic>Pulpitis - metabolism</topic><topic>Receptors, Prostaglandin E - physiology</topic><topic>Reverse Transcriptase Polymerase Chain Reaction</topic><topic>Statistics, Nonparametric</topic><topic>Tumor Necrosis Factor-alpha - physiology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Chang, M.-C.</creatorcontrib><creatorcontrib>Chen, Y.-J.</creatorcontrib><creatorcontrib>Tai, T.-F.</creatorcontrib><creatorcontrib>Tai, M.-R.</creatorcontrib><creatorcontrib>Li, M.-Y.</creatorcontrib><creatorcontrib>Tsai, Y.-L.</creatorcontrib><creatorcontrib>Lan, W.-H.</creatorcontrib><creatorcontrib>Wang, Y.-L.</creatorcontrib><creatorcontrib>Jeng, J.-H.</creatorcontrib><collection>Istex</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>MEDLINE - Academic</collection><jtitle>International endodontic journal</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Chang, M.-C.</au><au>Chen, Y.-J.</au><au>Tai, T.-F.</au><au>Tai, M.-R.</au><au>Li, M.-Y.</au><au>Tsai, Y.-L.</au><au>Lan, W.-H.</au><au>Wang, Y.-L.</au><au>Jeng, J.-H.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Cytokine-induced prostaglandin E2 production and cyclooxygenase-2 expression in dental pulp cells: downstream calcium signalling via activation of prostaglandin EP receptor</atitle><jtitle>International endodontic journal</jtitle><addtitle>Int Endod J</addtitle><date>2006-10</date><risdate>2006</risdate><volume>39</volume><issue>10</issue><spage>819</spage><epage>826</epage><pages>819-826</pages><issn>0143-2885</issn><eissn>1365-2591</eissn><abstract>Aim  To determine whether (i) proinflammatory cytokines stimulate prostaglandin E2 (PGE2) production and cyclooxygenase (COX) gene expression in dental pulp cells, and (ii) pulp cells that express different prostaglandin E2 receptor (EP) isoforms and their activation by PGE2 leads to downstream Ca2+ signalling. Methodology  Cultured human dental pulp cells were exposed to interleukin (IL)‐1β and tumour necrotic factor‐alpha (TNF‐α). The expression of COX‐1 and COX‐2 was measured with reverse transcriptase‐polymerase chain reaction (RT‐PCR). The production of PGE2 was measured using an enzyme‐linked immunosorbent assay. Expression of prostaglandin EP receptor isoforms was studied by RT‐PCR, whereas fura‐2 fluorescence was used to measure calcium mobilization. The Kruskal–Wallis test and Wilcoxon sum rank test with Bonferroni correction were used for statistical analysis. Results  Interleukin‐1β and TNF‐α stimulate PGE2 production of human dental pulp cells (P &lt; 0.05). IL‐1β stimulated the COX‐2 but not COX‐1 mRNA expression. Pulp cells express mainly EP2, EP3 and EP1 receptors as analysed by RT‐PCR. PGE2 (0.25–2 μmol L−1) stimulated the Ca2+ mobilization as indicated by increase in fura‐2 fluorescence. Conclusions  Interleukin‐1β and TNF‐α may stimulate PGE2 production in dental pulp cells. Activation of prostaglandin EP receptors in dental pulp cells by PGE2 may induce Ca2+ signalling to regulate cellular biological activity during inflammation.</abstract><cop>Oxford, UK</cop><pub>Blackwell Publishing Ltd</pub><pmid>16948668</pmid><doi>10.1111/j.1365-2591.2006.01156.x</doi><tpages>8</tpages></addata></record>
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source MEDLINE; Wiley Online Library Journals Frontfile Complete
subjects calcium mobilization
Calcium Signaling - physiology
Cells, Cultured
Cyclooxygenase 2 - biosynthesis
Cyclooxygenase 2 - genetics
Cytokines - physiology
Dental Pulp - cytology
Dental Pulp - metabolism
Dentistry
Dinoprostone - biosynthesis
Dinoprostone - genetics
Dinoprostone - physiology
Enzyme Activation
Enzyme-Linked Immunosorbent Assay
Fluorescent Dyes
Fura-2 - analogs & derivatives
Gene Expression Regulation
Humans
inflammation
Interleukin-1 - physiology
prostaglandin
prostaglandin receptor
Protein Isoforms
pulp cells
Pulpitis - metabolism
Receptors, Prostaglandin E - physiology
Reverse Transcriptase Polymerase Chain Reaction
Statistics, Nonparametric
Tumor Necrosis Factor-alpha - physiology
title Cytokine-induced prostaglandin E2 production and cyclooxygenase-2 expression in dental pulp cells: downstream calcium signalling via activation of prostaglandin EP receptor
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