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
Hauptverfasser: Konger, Raymond L., Brouxhon, Sabine, Partillo, Steven, VanBuskirk, JoAnne, Pentland, Alice P.
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container_end_page 922
container_issue 12
container_start_page 914
container_title Experimental dermatology
container_volume 14
creator Konger, Raymond L.
Brouxhon, Sabine
Partillo, Steven
VanBuskirk, JoAnne
Pentland, Alice P.
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. 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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><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. ; 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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. 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source MEDLINE; Wiley Online Library Journals Frontfile Complete
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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