Loading…

P2X and P2Y Receptors in Human Mesenchymal Stem Cell Differentiation

Human adult mesenchymal stem cells (MSCs) derived from adipose tissue possess multiple lineage capacity. Although they have been shown to differentiate into adipocytes and osteoblasts, receptor expressiossion and/or their alteration during these processes is only partly understood. Purinergic 2 (P2)...

Full description

Saved in:
Bibliographic Details
Published in:Tissue engineering. Part A 2009-03, Vol.15 (3), p.698-698
Main Authors: Scholze, N J, Zippel, N, Mueller, CA, Pansky, A, Tobiasch, E
Format: Article
Language:English
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
cited_by
cites
container_end_page 698
container_issue 3
container_start_page 698
container_title Tissue engineering. Part A
container_volume 15
creator Scholze, N J
Zippel, N
Mueller, CA
Pansky, A
Tobiasch, E
description Human adult mesenchymal stem cells (MSCs) derived from adipose tissue possess multiple lineage capacity. Although they have been shown to differentiate into adipocytes and osteoblasts, receptor expressiossion and/or their alteration during these processes is only partly understood. Purinergic 2 (P2) receptors are plasma membrane bound molecules, divided into the ligand-gated ion channels P2X and G-protein coupled P2Y receptors. They are activated by ligand-binding of extracellular nucleotides which triggers intracellular signals affecting various processes including proliferation and differentiation. Here we show that some P2X and P2Y receptors are involved in the differentiation of MSCs towards the osteogenic or the adipogenic lineage. Over a period of four weeks of differentiation several P2 receptors were found to be up-or down-regulated. Further investigations of P2 receptor signalling and their downstream targets are necessary to provide additional insights into the differentiation processes revealing novel options to control stem cell fate.
format article
fullrecord <record><control><sourceid>proquest</sourceid><recordid>TN_cdi_proquest_miscellaneous_20527841</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>20527841</sourcerecordid><originalsourceid>FETCH-proquest_miscellaneous_205278413</originalsourceid><addsrcrecordid>eNqNi7sOgjAUQBujifj4hzu5kUALVGfQsJgQdcCJNHiJNX0gLYN_r4NxdjpnOGdCgnjHeMhYWk9_nsRzsnDuEUVZlHEekKKiNQhzg4pe4YQt9t4ODqSBctTCwBEdmvb-0kLB2aOGHJWCQnYdDmi8FF5asyKzTiiH6y-XZHPYX_Iy7Af7HNH5RkvXfkZh0I6uoVFK-TaJ2d_hGy2fPf4</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>20527841</pqid></control><display><type>article</type><title>P2X and P2Y Receptors in Human Mesenchymal Stem Cell Differentiation</title><source>Mary Ann Liebert Online Subscription</source><creator>Scholze, N J ; Zippel, N ; Mueller, CA ; Pansky, A ; Tobiasch, E</creator><creatorcontrib>Scholze, N J ; Zippel, N ; Mueller, CA ; Pansky, A ; Tobiasch, E</creatorcontrib><description>Human adult mesenchymal stem cells (MSCs) derived from adipose tissue possess multiple lineage capacity. Although they have been shown to differentiate into adipocytes and osteoblasts, receptor expressiossion and/or their alteration during these processes is only partly understood. Purinergic 2 (P2) receptors are plasma membrane bound molecules, divided into the ligand-gated ion channels P2X and G-protein coupled P2Y receptors. They are activated by ligand-binding of extracellular nucleotides which triggers intracellular signals affecting various processes including proliferation and differentiation. Here we show that some P2X and P2Y receptors are involved in the differentiation of MSCs towards the osteogenic or the adipogenic lineage. Over a period of four weeks of differentiation several P2 receptors were found to be up-or down-regulated. Further investigations of P2 receptor signalling and their downstream targets are necessary to provide additional insights into the differentiation processes revealing novel options to control stem cell fate.</description><identifier>ISSN: 1937-3341</identifier><identifier>EISSN: 1937-335X</identifier><language>eng</language><ispartof>Tissue engineering. Part A, 2009-03, Vol.15 (3), p.698-698</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784</link.rule.ids></links><search><creatorcontrib>Scholze, N J</creatorcontrib><creatorcontrib>Zippel, N</creatorcontrib><creatorcontrib>Mueller, CA</creatorcontrib><creatorcontrib>Pansky, A</creatorcontrib><creatorcontrib>Tobiasch, E</creatorcontrib><title>P2X and P2Y Receptors in Human Mesenchymal Stem Cell Differentiation</title><title>Tissue engineering. Part A</title><description>Human adult mesenchymal stem cells (MSCs) derived from adipose tissue possess multiple lineage capacity. Although they have been shown to differentiate into adipocytes and osteoblasts, receptor expressiossion and/or their alteration during these processes is only partly understood. Purinergic 2 (P2) receptors are plasma membrane bound molecules, divided into the ligand-gated ion channels P2X and G-protein coupled P2Y receptors. They are activated by ligand-binding of extracellular nucleotides which triggers intracellular signals affecting various processes including proliferation and differentiation. Here we show that some P2X and P2Y receptors are involved in the differentiation of MSCs towards the osteogenic or the adipogenic lineage. Over a period of four weeks of differentiation several P2 receptors were found to be up-or down-regulated. Further investigations of P2 receptor signalling and their downstream targets are necessary to provide additional insights into the differentiation processes revealing novel options to control stem cell fate.</description><issn>1937-3341</issn><issn>1937-335X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2009</creationdate><recordtype>article</recordtype><recordid>eNqNi7sOgjAUQBujifj4hzu5kUALVGfQsJgQdcCJNHiJNX0gLYN_r4NxdjpnOGdCgnjHeMhYWk9_nsRzsnDuEUVZlHEekKKiNQhzg4pe4YQt9t4ODqSBctTCwBEdmvb-0kLB2aOGHJWCQnYdDmi8FF5asyKzTiiH6y-XZHPYX_Iy7Af7HNH5RkvXfkZh0I6uoVFK-TaJ2d_hGy2fPf4</recordid><startdate>20090301</startdate><enddate>20090301</enddate><creator>Scholze, N J</creator><creator>Zippel, N</creator><creator>Mueller, CA</creator><creator>Pansky, A</creator><creator>Tobiasch, E</creator><scope>7QO</scope><scope>8FD</scope><scope>FR3</scope><scope>P64</scope></search><sort><creationdate>20090301</creationdate><title>P2X and P2Y Receptors in Human Mesenchymal Stem Cell Differentiation</title><author>Scholze, N J ; Zippel, N ; Mueller, CA ; Pansky, A ; Tobiasch, E</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-proquest_miscellaneous_205278413</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2009</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Scholze, N J</creatorcontrib><creatorcontrib>Zippel, N</creatorcontrib><creatorcontrib>Mueller, CA</creatorcontrib><creatorcontrib>Pansky, A</creatorcontrib><creatorcontrib>Tobiasch, E</creatorcontrib><collection>Biotechnology Research Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><jtitle>Tissue engineering. Part A</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Scholze, N J</au><au>Zippel, N</au><au>Mueller, CA</au><au>Pansky, A</au><au>Tobiasch, E</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>P2X and P2Y Receptors in Human Mesenchymal Stem Cell Differentiation</atitle><jtitle>Tissue engineering. Part A</jtitle><date>2009-03-01</date><risdate>2009</risdate><volume>15</volume><issue>3</issue><spage>698</spage><epage>698</epage><pages>698-698</pages><issn>1937-3341</issn><eissn>1937-335X</eissn><abstract>Human adult mesenchymal stem cells (MSCs) derived from adipose tissue possess multiple lineage capacity. Although they have been shown to differentiate into adipocytes and osteoblasts, receptor expressiossion and/or their alteration during these processes is only partly understood. Purinergic 2 (P2) receptors are plasma membrane bound molecules, divided into the ligand-gated ion channels P2X and G-protein coupled P2Y receptors. They are activated by ligand-binding of extracellular nucleotides which triggers intracellular signals affecting various processes including proliferation and differentiation. Here we show that some P2X and P2Y receptors are involved in the differentiation of MSCs towards the osteogenic or the adipogenic lineage. Over a period of four weeks of differentiation several P2 receptors were found to be up-or down-regulated. Further investigations of P2 receptor signalling and their downstream targets are necessary to provide additional insights into the differentiation processes revealing novel options to control stem cell fate.</abstract></addata></record>
fulltext fulltext
identifier ISSN: 1937-3341
ispartof Tissue engineering. Part A, 2009-03, Vol.15 (3), p.698-698
issn 1937-3341
1937-335X
language eng
recordid cdi_proquest_miscellaneous_20527841
source Mary Ann Liebert Online Subscription
title P2X and P2Y Receptors in Human Mesenchymal Stem Cell Differentiation
url http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-21T02%3A56%3A21IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=P2X%20and%20P2Y%20Receptors%20in%20Human%20Mesenchymal%20Stem%20Cell%20Differentiation&rft.jtitle=Tissue%20engineering.%20Part%20A&rft.au=Scholze,%20N%20J&rft.date=2009-03-01&rft.volume=15&rft.issue=3&rft.spage=698&rft.epage=698&rft.pages=698-698&rft.issn=1937-3341&rft.eissn=1937-335X&rft_id=info:doi/&rft_dat=%3Cproquest%3E20527841%3C/proquest%3E%3Cgrp_id%3Ecdi_FETCH-proquest_miscellaneous_205278413%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=20527841&rft_id=info:pmid/&rfr_iscdi=true