Loading…

Regulation of epidermal homeostasis through P2Y 2 receptors

Previous studies have indicated a role for extracellular ATP in the regulation of epidermal homeostasis. Here we have investigated the expression of P2Y 2 receptors by human keratinocytes, the cells which comprise the epidermis. Reverse transcriptase‐polymerase chain reaction (RT–PCR) revealed expre...

Full description

Saved in:
Bibliographic Details
Published in:British journal of pharmacology 2009-01, Vol.127 (7), p.1680-1686
Main Authors: Dixon, C Jane, Bowler, Wayne B, Littlewood‐Evans, Amanda, Dillon, Jane P, Bilbe, Graeme, Sharpe, Graham R, Gallagher, James A
Format: Article
Language:English
Citations: Items that this one cites
Items that cite this one
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
cited_by cdi_FETCH-LOGICAL-c843-664ddd361b7aeb5b81fcb740b8ad1073f3baa100fe5a056a9c02742c2dbc0f603
cites cdi_FETCH-LOGICAL-c843-664ddd361b7aeb5b81fcb740b8ad1073f3baa100fe5a056a9c02742c2dbc0f603
container_end_page 1686
container_issue 7
container_start_page 1680
container_title British journal of pharmacology
container_volume 127
creator Dixon, C Jane
Bowler, Wayne B
Littlewood‐Evans, Amanda
Dillon, Jane P
Bilbe, Graeme
Sharpe, Graham R
Gallagher, James A
description Previous studies have indicated a role for extracellular ATP in the regulation of epidermal homeostasis. Here we have investigated the expression of P2Y 2 receptors by human keratinocytes, the cells which comprise the epidermis. Reverse transcriptase‐polymerase chain reaction (RT–PCR) revealed expression of mRNA for the G‐protein‐coupled, P2Y 2 receptor in primary cultured human keratinocytes. In situ hybridization studies of skin sections revealed that P2Y 2 receptor transcripts were expressed in the native tissue. These studies demonstrated a striking pattern of localization of P2Y 2 receptor transcripts to the basal layer of the epidermis, the site of cell proliferation. Increases in intracellular free Ca 2+ concentration ([Ca 2+ ] i ) in keratinocytes stimulated with ATP or UTP demonstrated the presence of functional P2Y receptors. In proliferation studies based on the incorporation of bromodeoxyuridine (BrdU), ATP, UTP and ATPγS were found to stimulate the proliferation of keratinocytes. Using a real‐time firefly luciferase and luciferin assay we have shown that under static conditions cultured human keratinocytes release ATP. These findings indicate that P2Y 2 receptors play a major role in epidermal homeostasis, and may provide novel targets for therapy of proliferative disorders of the epidermis, including psoriasis. British Journal of Pharmacology (1999) 127 , 1680–1686; doi: 10.1038/sj.bjp.0702653
doi_str_mv 10.1038/sj.bjp.0702653
format article
fullrecord <record><control><sourceid>crossref</sourceid><recordid>TN_cdi_crossref_primary_10_1038_sj_bjp_0702653</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>10_1038_sj_bjp_0702653</sourcerecordid><originalsourceid>FETCH-LOGICAL-c843-664ddd361b7aeb5b81fcb740b8ad1073f3baa100fe5a056a9c02742c2dbc0f603</originalsourceid><addsrcrecordid>eNotz0tLxDAYheEgCtbRrev8gdYvSXMRVzJ4gwFlmM2sQq7TltaUpLPw3zvirM7ihQMPQvcEGgJMPZShscPcgAQqOLtAFWmlqDlT5BJVACBrQpS6RjelDACnKHmFnrbhcBzN0qdvnCIOc-9DnsyIuzSFVBZT-oKXLqfjocNfdI8pzsGFeUm53KKraMYS7s67QrvXl936vd58vn2snze1Uy2rhWi990wQK02w3CoSnZUtWGU8Ackis8YQgBi4AS7MowMqW-qotw6iALZCzf-ty6mUHKKecz-Z_KMJ6D-5LoM-yfVZzn4ByLxNdA</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype></control><display><type>article</type><title>Regulation of epidermal homeostasis through P2Y 2 receptors</title><source>PubMed Central(OpenAccess)</source><source>Wiley-Blackwell Read &amp; Publish Collection</source><creator>Dixon, C Jane ; Bowler, Wayne B ; Littlewood‐Evans, Amanda ; Dillon, Jane P ; Bilbe, Graeme ; Sharpe, Graham R ; Gallagher, James A</creator><creatorcontrib>Dixon, C Jane ; Bowler, Wayne B ; Littlewood‐Evans, Amanda ; Dillon, Jane P ; Bilbe, Graeme ; Sharpe, Graham R ; Gallagher, James A</creatorcontrib><description>Previous studies have indicated a role for extracellular ATP in the regulation of epidermal homeostasis. Here we have investigated the expression of P2Y 2 receptors by human keratinocytes, the cells which comprise the epidermis. Reverse transcriptase‐polymerase chain reaction (RT–PCR) revealed expression of mRNA for the G‐protein‐coupled, P2Y 2 receptor in primary cultured human keratinocytes. In situ hybridization studies of skin sections revealed that P2Y 2 receptor transcripts were expressed in the native tissue. These studies demonstrated a striking pattern of localization of P2Y 2 receptor transcripts to the basal layer of the epidermis, the site of cell proliferation. Increases in intracellular free Ca 2+ concentration ([Ca 2+ ] i ) in keratinocytes stimulated with ATP or UTP demonstrated the presence of functional P2Y receptors. In proliferation studies based on the incorporation of bromodeoxyuridine (BrdU), ATP, UTP and ATPγS were found to stimulate the proliferation of keratinocytes. Using a real‐time firefly luciferase and luciferin assay we have shown that under static conditions cultured human keratinocytes release ATP. These findings indicate that P2Y 2 receptors play a major role in epidermal homeostasis, and may provide novel targets for therapy of proliferative disorders of the epidermis, including psoriasis. British Journal of Pharmacology (1999) 127 , 1680–1686; doi: 10.1038/sj.bjp.0702653</description><identifier>ISSN: 0007-1188</identifier><identifier>EISSN: 1476-5381</identifier><identifier>DOI: 10.1038/sj.bjp.0702653</identifier><language>eng</language><ispartof>British journal of pharmacology, 2009-01, Vol.127 (7), p.1680-1686</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c843-664ddd361b7aeb5b81fcb740b8ad1073f3baa100fe5a056a9c02742c2dbc0f603</citedby><cites>FETCH-LOGICAL-c843-664ddd361b7aeb5b81fcb740b8ad1073f3baa100fe5a056a9c02742c2dbc0f603</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids></links><search><creatorcontrib>Dixon, C Jane</creatorcontrib><creatorcontrib>Bowler, Wayne B</creatorcontrib><creatorcontrib>Littlewood‐Evans, Amanda</creatorcontrib><creatorcontrib>Dillon, Jane P</creatorcontrib><creatorcontrib>Bilbe, Graeme</creatorcontrib><creatorcontrib>Sharpe, Graham R</creatorcontrib><creatorcontrib>Gallagher, James A</creatorcontrib><title>Regulation of epidermal homeostasis through P2Y 2 receptors</title><title>British journal of pharmacology</title><description>Previous studies have indicated a role for extracellular ATP in the regulation of epidermal homeostasis. Here we have investigated the expression of P2Y 2 receptors by human keratinocytes, the cells which comprise the epidermis. Reverse transcriptase‐polymerase chain reaction (RT–PCR) revealed expression of mRNA for the G‐protein‐coupled, P2Y 2 receptor in primary cultured human keratinocytes. In situ hybridization studies of skin sections revealed that P2Y 2 receptor transcripts were expressed in the native tissue. These studies demonstrated a striking pattern of localization of P2Y 2 receptor transcripts to the basal layer of the epidermis, the site of cell proliferation. Increases in intracellular free Ca 2+ concentration ([Ca 2+ ] i ) in keratinocytes stimulated with ATP or UTP demonstrated the presence of functional P2Y receptors. In proliferation studies based on the incorporation of bromodeoxyuridine (BrdU), ATP, UTP and ATPγS were found to stimulate the proliferation of keratinocytes. Using a real‐time firefly luciferase and luciferin assay we have shown that under static conditions cultured human keratinocytes release ATP. These findings indicate that P2Y 2 receptors play a major role in epidermal homeostasis, and may provide novel targets for therapy of proliferative disorders of the epidermis, including psoriasis. British Journal of Pharmacology (1999) 127 , 1680–1686; doi: 10.1038/sj.bjp.0702653</description><issn>0007-1188</issn><issn>1476-5381</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2009</creationdate><recordtype>article</recordtype><recordid>eNotz0tLxDAYheEgCtbRrev8gdYvSXMRVzJ4gwFlmM2sQq7TltaUpLPw3zvirM7ihQMPQvcEGgJMPZShscPcgAQqOLtAFWmlqDlT5BJVACBrQpS6RjelDACnKHmFnrbhcBzN0qdvnCIOc-9DnsyIuzSFVBZT-oKXLqfjocNfdI8pzsGFeUm53KKraMYS7s67QrvXl936vd58vn2snze1Uy2rhWi990wQK02w3CoSnZUtWGU8Ackis8YQgBi4AS7MowMqW-qotw6iALZCzf-ty6mUHKKecz-Z_KMJ6D-5LoM-yfVZzn4ByLxNdA</recordid><startdate>20090129</startdate><enddate>20090129</enddate><creator>Dixon, C Jane</creator><creator>Bowler, Wayne B</creator><creator>Littlewood‐Evans, Amanda</creator><creator>Dillon, Jane P</creator><creator>Bilbe, Graeme</creator><creator>Sharpe, Graham R</creator><creator>Gallagher, James A</creator><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>20090129</creationdate><title>Regulation of epidermal homeostasis through P2Y 2 receptors</title><author>Dixon, C Jane ; Bowler, Wayne B ; Littlewood‐Evans, Amanda ; Dillon, Jane P ; Bilbe, Graeme ; Sharpe, Graham R ; Gallagher, James A</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c843-664ddd361b7aeb5b81fcb740b8ad1073f3baa100fe5a056a9c02742c2dbc0f603</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2009</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Dixon, C Jane</creatorcontrib><creatorcontrib>Bowler, Wayne B</creatorcontrib><creatorcontrib>Littlewood‐Evans, Amanda</creatorcontrib><creatorcontrib>Dillon, Jane P</creatorcontrib><creatorcontrib>Bilbe, Graeme</creatorcontrib><creatorcontrib>Sharpe, Graham R</creatorcontrib><creatorcontrib>Gallagher, James A</creatorcontrib><collection>CrossRef</collection><jtitle>British journal of pharmacology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Dixon, C Jane</au><au>Bowler, Wayne B</au><au>Littlewood‐Evans, Amanda</au><au>Dillon, Jane P</au><au>Bilbe, Graeme</au><au>Sharpe, Graham R</au><au>Gallagher, James A</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Regulation of epidermal homeostasis through P2Y 2 receptors</atitle><jtitle>British journal of pharmacology</jtitle><date>2009-01-29</date><risdate>2009</risdate><volume>127</volume><issue>7</issue><spage>1680</spage><epage>1686</epage><pages>1680-1686</pages><issn>0007-1188</issn><eissn>1476-5381</eissn><abstract>Previous studies have indicated a role for extracellular ATP in the regulation of epidermal homeostasis. Here we have investigated the expression of P2Y 2 receptors by human keratinocytes, the cells which comprise the epidermis. Reverse transcriptase‐polymerase chain reaction (RT–PCR) revealed expression of mRNA for the G‐protein‐coupled, P2Y 2 receptor in primary cultured human keratinocytes. In situ hybridization studies of skin sections revealed that P2Y 2 receptor transcripts were expressed in the native tissue. These studies demonstrated a striking pattern of localization of P2Y 2 receptor transcripts to the basal layer of the epidermis, the site of cell proliferation. Increases in intracellular free Ca 2+ concentration ([Ca 2+ ] i ) in keratinocytes stimulated with ATP or UTP demonstrated the presence of functional P2Y receptors. In proliferation studies based on the incorporation of bromodeoxyuridine (BrdU), ATP, UTP and ATPγS were found to stimulate the proliferation of keratinocytes. Using a real‐time firefly luciferase and luciferin assay we have shown that under static conditions cultured human keratinocytes release ATP. These findings indicate that P2Y 2 receptors play a major role in epidermal homeostasis, and may provide novel targets for therapy of proliferative disorders of the epidermis, including psoriasis. British Journal of Pharmacology (1999) 127 , 1680–1686; doi: 10.1038/sj.bjp.0702653</abstract><doi>10.1038/sj.bjp.0702653</doi><tpages>7</tpages></addata></record>
fulltext fulltext
identifier ISSN: 0007-1188
ispartof British journal of pharmacology, 2009-01, Vol.127 (7), p.1680-1686
issn 0007-1188
1476-5381
language eng
recordid cdi_crossref_primary_10_1038_sj_bjp_0702653
source PubMed Central(OpenAccess); Wiley-Blackwell Read & Publish Collection
title Regulation of epidermal homeostasis through P2Y 2 receptors
url http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-28T05%3A29%3A56IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-crossref&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Regulation%20of%20epidermal%20homeostasis%20through%20P2Y%202%20receptors&rft.jtitle=British%20journal%20of%20pharmacology&rft.au=Dixon,%20C%20Jane&rft.date=2009-01-29&rft.volume=127&rft.issue=7&rft.spage=1680&rft.epage=1686&rft.pages=1680-1686&rft.issn=0007-1188&rft.eissn=1476-5381&rft_id=info:doi/10.1038/sj.bjp.0702653&rft_dat=%3Ccrossref%3E10_1038_sj_bjp_0702653%3C/crossref%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c843-664ddd361b7aeb5b81fcb740b8ad1073f3baa100fe5a056a9c02742c2dbc0f603%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_id=info:pmid/&rfr_iscdi=true