The EP3 receptor stimulates ceramide and diacylglycerol release and inhibits growth of primary keratinocytes
: Primary human keratinocytes (PHKs) are known to express the EP3 subtype of prostaglandin E2 receptor. To better understand the role of EP3 receptors in regulating epidermal function, we characterized their expression, localization, and signaling effects in human skin. Three different splice varia...
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Veröffentlicht in: | Experimental dermatology 2005-12, Vol.14 (12), p.914-922 |
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description | : Primary human keratinocytes (PHKs) are known to express the EP3 subtype of prostaglandin E2 receptor. To better understand the role of EP3 receptors in regulating epidermal function, we characterized their expression, localization, and signaling effects in human skin. Three different splice variants of the EP3 receptor (EP3A1, EP3C, and EP3D) were found to be expressed. Immunohistochemical analysis of human skin demonstrated that EP3 receptors were most prominently expressed in the basal and lower spinous layers of the epidermis. The EP3 receptor agonist sulprostone was then used to examine EP3 receptor‐dependent keratinocyte signaling pathways and functional effects. We observed that sulprostone inhibits keratinocyte growth at doses between 0.02 and 2 nM and induces sn‐1,2‐diacylglycerol (DAG) and ceramide production. Concurrent expression of the cell‐cycle inhibitory protein p21WAF1 also occurred. These data suggest that EP3 receptors produce epidermal growth inhibition through the action of DAG and ceramide second messengers. |
doi_str_mv | 10.1111/j.1600-0625.2005.00381.x |
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To better understand the role of EP3 receptors in regulating epidermal function, we characterized their expression, localization, and signaling effects in human skin. Three different splice variants of the EP3 receptor (EP3A1, EP3C, and EP3D) were found to be expressed. Immunohistochemical analysis of human skin demonstrated that EP3 receptors were most prominently expressed in the basal and lower spinous layers of the epidermis. The EP3 receptor agonist sulprostone was then used to examine EP3 receptor‐dependent keratinocyte signaling pathways and functional effects. We observed that sulprostone inhibits keratinocyte growth at doses between 0.02 and 2 nM and induces sn‐1,2‐diacylglycerol (DAG) and ceramide production. Concurrent expression of the cell‐cycle inhibitory protein p21WAF1 also occurred. These data suggest that EP3 receptors produce epidermal growth inhibition through the action of DAG and ceramide second messengers.</description><identifier>ISSN: 0906-6705</identifier><identifier>EISSN: 1600-0625</identifier><identifier>DOI: 10.1111/j.1600-0625.2005.00381.x</identifier><identifier>PMID: 16274459</identifier><language>eng</language><publisher>Oxford, UK; Malden, USA: Munksgaard International Publishers</publisher><subject>Biological and medical sciences ; Blotting, Western ; Cell Proliferation ; Cells, Cultured ; ceramide ; Ceramides - metabolism ; Cyclin-Dependent Kinase Inhibitor p21 - metabolism ; Dermatology ; diacylglycerol ; Diglycerides - metabolism ; DNA, Recombinant ; EP3 receptors ; Epidermis - metabolism ; growth inhibition ; Humans ; Immunohistochemistry ; immunolocalization ; Keratinocytes - cytology ; Keratinocytes - metabolism ; Medical sciences ; Receptors, Prostaglandin E - genetics ; Receptors, Prostaglandin E - physiology ; Receptors, Prostaglandin E, EP3 Subtype ; Tissue Distribution</subject><ispartof>Experimental dermatology, 2005-12, Vol.14 (12), p.914-922</ispartof><rights>2005 INIST-CNRS</rights><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.1600-0625.2005.00381.x$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2Fj.1600-0625.2005.00381.x$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,776,780,1411,27901,27902,45550,45551</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=17243841$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/16274459$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Konger, Raymond L.</creatorcontrib><creatorcontrib>Brouxhon, Sabine</creatorcontrib><creatorcontrib>Partillo, Steven</creatorcontrib><creatorcontrib>VanBuskirk, JoAnne</creatorcontrib><creatorcontrib>Pentland, Alice P.</creatorcontrib><title>The EP3 receptor stimulates ceramide and diacylglycerol release and inhibits growth of primary keratinocytes</title><title>Experimental dermatology</title><addtitle>Exp Dermatol</addtitle><description>: Primary human keratinocytes (PHKs) are known to express the EP3 subtype of prostaglandin E2 receptor. To better understand the role of EP3 receptors in regulating epidermal function, we characterized their expression, localization, and signaling effects in human skin. Three different splice variants of the EP3 receptor (EP3A1, EP3C, and EP3D) were found to be expressed. Immunohistochemical analysis of human skin demonstrated that EP3 receptors were most prominently expressed in the basal and lower spinous layers of the epidermis. The EP3 receptor agonist sulprostone was then used to examine EP3 receptor‐dependent keratinocyte signaling pathways and functional effects. We observed that sulprostone inhibits keratinocyte growth at doses between 0.02 and 2 nM and induces sn‐1,2‐diacylglycerol (DAG) and ceramide production. Concurrent expression of the cell‐cycle inhibitory protein p21WAF1 also occurred. These data suggest that EP3 receptors produce epidermal growth inhibition through the action of DAG and ceramide second messengers.</description><subject>Biological and medical sciences</subject><subject>Blotting, Western</subject><subject>Cell Proliferation</subject><subject>Cells, Cultured</subject><subject>ceramide</subject><subject>Ceramides - metabolism</subject><subject>Cyclin-Dependent Kinase Inhibitor p21 - metabolism</subject><subject>Dermatology</subject><subject>diacylglycerol</subject><subject>Diglycerides - metabolism</subject><subject>DNA, Recombinant</subject><subject>EP3 receptors</subject><subject>Epidermis - metabolism</subject><subject>growth inhibition</subject><subject>Humans</subject><subject>Immunohistochemistry</subject><subject>immunolocalization</subject><subject>Keratinocytes - cytology</subject><subject>Keratinocytes - metabolism</subject><subject>Medical sciences</subject><subject>Receptors, Prostaglandin E - genetics</subject><subject>Receptors, Prostaglandin E - physiology</subject><subject>Receptors, Prostaglandin E, EP3 Subtype</subject><subject>Tissue Distribution</subject><issn>0906-6705</issn><issn>1600-0625</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2005</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpFkV1v2yAYhdG0ac26_YWJm-3OLhgMWNrN1GVdpaofUqbtDmH8uiHFdgqOGv_74SVtuYGX85wjxEEIU5LTtM42ORWEZEQUZV4QUuaEMEXz_Ru0eBHeogWpiMiEJOUJ-hDjhhAqmSzfoxMqCsl5WS2QX60BL28ZDmBhOw4Bx9F1O29GiNhCMJ1rAJu-wY0zdvL3fkq3g0-8BxMPkuvXrnZjxPdheBrXeGjxNrjOhAk_pIjR9YOdUuBH9K41PsKn436Kfv9crs5_ZVc3F5fn368yxypBM65AVYbySgjVQlEz0bQCaMtpQWtopOKGqpZCrRpeM2IYr2jTFqq2VFpBK3aKvh5yt2F43EEcdeeiBe9ND8MuaqGkolXBEvj5CO7qDhp9fLV-_p8EfDkCJlrj22B66-IrJwvOFKeJ-3bgnpyH6VUneu5Lb_Rci55r0XNf-n9feq-Xf3-kQ7JnB7uLI-xf7CY8aDFXpv9cX-i7VSm5SsMd-wdcGphZ</recordid><startdate>200512</startdate><enddate>200512</enddate><creator>Konger, Raymond L.</creator><creator>Brouxhon, Sabine</creator><creator>Partillo, Steven</creator><creator>VanBuskirk, JoAnne</creator><creator>Pentland, Alice P.</creator><general>Munksgaard International Publishers</general><general>Blackwell</general><scope>BSCLL</scope><scope>IQODW</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>200512</creationdate><title>The EP3 receptor stimulates ceramide and diacylglycerol release and inhibits growth of primary keratinocytes</title><author>Konger, Raymond L. ; Brouxhon, Sabine ; Partillo, Steven ; VanBuskirk, JoAnne ; Pentland, Alice P.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-i3961-48e89a149668fe2b36df6e1f4121bed784a18f1eb8d4b30a3491df28bc17c6193</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2005</creationdate><topic>Biological and medical sciences</topic><topic>Blotting, Western</topic><topic>Cell Proliferation</topic><topic>Cells, Cultured</topic><topic>ceramide</topic><topic>Ceramides - metabolism</topic><topic>Cyclin-Dependent Kinase Inhibitor p21 - metabolism</topic><topic>Dermatology</topic><topic>diacylglycerol</topic><topic>Diglycerides - metabolism</topic><topic>DNA, Recombinant</topic><topic>EP3 receptors</topic><topic>Epidermis - metabolism</topic><topic>growth inhibition</topic><topic>Humans</topic><topic>Immunohistochemistry</topic><topic>immunolocalization</topic><topic>Keratinocytes - cytology</topic><topic>Keratinocytes - metabolism</topic><topic>Medical sciences</topic><topic>Receptors, Prostaglandin E - genetics</topic><topic>Receptors, Prostaglandin E - physiology</topic><topic>Receptors, Prostaglandin E, EP3 Subtype</topic><topic>Tissue Distribution</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Konger, Raymond L.</creatorcontrib><creatorcontrib>Brouxhon, Sabine</creatorcontrib><creatorcontrib>Partillo, Steven</creatorcontrib><creatorcontrib>VanBuskirk, JoAnne</creatorcontrib><creatorcontrib>Pentland, Alice P.</creatorcontrib><collection>Istex</collection><collection>Pascal-Francis</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>Experimental dermatology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Konger, Raymond L.</au><au>Brouxhon, Sabine</au><au>Partillo, Steven</au><au>VanBuskirk, JoAnne</au><au>Pentland, Alice P.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The EP3 receptor stimulates ceramide and diacylglycerol release and inhibits growth of primary keratinocytes</atitle><jtitle>Experimental dermatology</jtitle><addtitle>Exp Dermatol</addtitle><date>2005-12</date><risdate>2005</risdate><volume>14</volume><issue>12</issue><spage>914</spage><epage>922</epage><pages>914-922</pages><issn>0906-6705</issn><eissn>1600-0625</eissn><abstract>: Primary human keratinocytes (PHKs) are known to express the EP3 subtype of prostaglandin E2 receptor. To better understand the role of EP3 receptors in regulating epidermal function, we characterized their expression, localization, and signaling effects in human skin. Three different splice variants of the EP3 receptor (EP3A1, EP3C, and EP3D) were found to be expressed. Immunohistochemical analysis of human skin demonstrated that EP3 receptors were most prominently expressed in the basal and lower spinous layers of the epidermis. The EP3 receptor agonist sulprostone was then used to examine EP3 receptor‐dependent keratinocyte signaling pathways and functional effects. We observed that sulprostone inhibits keratinocyte growth at doses between 0.02 and 2 nM and induces sn‐1,2‐diacylglycerol (DAG) and ceramide production. Concurrent expression of the cell‐cycle inhibitory protein p21WAF1 also occurred. These data suggest that EP3 receptors produce epidermal growth inhibition through the action of DAG and ceramide second messengers.</abstract><cop>Oxford, UK; Malden, USA</cop><pub>Munksgaard International Publishers</pub><pmid>16274459</pmid><doi>10.1111/j.1600-0625.2005.00381.x</doi><tpages>9</tpages></addata></record> |
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subjects | Biological and medical sciences Blotting, Western Cell Proliferation Cells, Cultured ceramide Ceramides - metabolism Cyclin-Dependent Kinase Inhibitor p21 - metabolism Dermatology diacylglycerol Diglycerides - metabolism DNA, Recombinant EP3 receptors Epidermis - metabolism growth inhibition Humans Immunohistochemistry immunolocalization Keratinocytes - cytology Keratinocytes - metabolism Medical sciences Receptors, Prostaglandin E - genetics Receptors, Prostaglandin E - physiology Receptors, Prostaglandin E, EP3 Subtype Tissue Distribution |
title | The EP3 receptor stimulates ceramide and diacylglycerol release and inhibits growth of primary keratinocytes |
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