Loading…
Potential Effect of CD271 on Human Mesenchymal Stromal Cell Proliferation and Differentiation
The Low-Affinity Nerve Growth Factor Receptor (LNGFR), also known as CD271, is a member of the tumor necrosis factor receptor superfamily. The CD271 cell surface marker defines a subset of multipotential mesenchymal stromal cells and may be used to isolate and enrich cells derived from bone marrow a...
Saved in:
Published in: | International journal of molecular sciences 2015-07, Vol.16 (7), p.15609-15624 |
---|---|
Main Authors: | , , , , , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
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-c580t-9f47b205b6f1562b9c7f955ab716fbc268754fa5249c5ee63a667bdec95399743 |
---|---|
cites | cdi_FETCH-LOGICAL-c580t-9f47b205b6f1562b9c7f955ab716fbc268754fa5249c5ee63a667bdec95399743 |
container_end_page | 15624 |
container_issue | 7 |
container_start_page | 15609 |
container_title | International journal of molecular sciences |
container_volume | 16 |
creator | Calabrese, Giovanna Giuffrida, Raffaella Lo Furno, Debora Parrinello, Nunziatina Laura Forte, Stefano Gulino, Rosario Colarossi, Cristina Schinocca, Luciana Rita Giuffrida, Rosario Cardile, Venera Memeo, Lorenzo |
description | The Low-Affinity Nerve Growth Factor Receptor (LNGFR), also known as CD271, is a member of the tumor necrosis factor receptor superfamily. The CD271 cell surface marker defines a subset of multipotential mesenchymal stromal cells and may be used to isolate and enrich cells derived from bone marrow aspirate. In this study, we compare the proliferative and differentiation potentials of CD271+ and CD271- mesenchymal stromal cells. Mesenchymal stromal cells were isolated from bone marrow aspirate and adipose tissue by plastic adherence and positive selection. The proliferation and differentiation potentials of CD271+ and CD271- mesenchymal stromal cells were assessed by inducing osteogenic, adipogenic and chondrogenic in vitro differentiation. Compared to CD271+, CD271- mesenchymal stromal cells showed a lower proliferation rate and a decreased ability to give rise to osteocytes, adipocytes and chondrocytes. Furthermore, we observed that CD271+ mesenchymal stromal cells isolated from adipose tissue displayed a higher efficiency of proliferation and trilineage differentiation compared to CD271+ mesenchymal stromal cells isolated from bone marrow samples, although the CD271 expression levels were comparable. In conclusion, these data show that both the presence of CD271 antigen and the source of mesenchymal stromal cells represent important factors in determining the ability of the cells to proliferate and differentiate. |
doi_str_mv | 10.3390/ijms160715609 |
format | article |
fullrecord | <record><control><sourceid>proquest_doaj_</sourceid><recordid>TN_cdi_doaj_primary_oai_doaj_org_article_d84e1e0002964d9eb8e89867880e49bf</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><doaj_id>oai_doaj_org_article_d84e1e0002964d9eb8e89867880e49bf</doaj_id><sourcerecordid>1698023123</sourcerecordid><originalsourceid>FETCH-LOGICAL-c580t-9f47b205b6f1562b9c7f955ab716fbc268754fa5249c5ee63a667bdec95399743</originalsourceid><addsrcrecordid>eNqFkk1rFTEUhoMotlaXbmXATTdT8_2xEeS2toWKBe2yhEzmpM1lZlKTGaH_3tzeWnrduDrh5OEh581B6D3BR4wZ_Cmux0IkVkRIbF6gfcIpbTGW6uWz8x56U8oaY8qoMK_RHpVEcyLlPrq-TDNMc3RDcxIC-LlJoVkdU0WaNDVny-im5hsUmPzt_VihH3NOm7qCYWgucxpigOzmWGE39c1xrJL8INz03qJXwQ0F3j3WA3T19eTn6qy9-H56vvpy0Xqh8dyawFVHsehkqGPQzngVjBCuU0SGzlOpleDBCcqNFwCSOSlV14M3ghmjODtA51tvn9za3uU4unxvk4v2oZHyjXV5jn4A22sOBHDNwkjeG-g0aKOl0hoDN12ors9b193SjdD7Okx2w45092aKt_Ym_bZcEGOIrILDR0FOvxYosx1j8TUvN0FaiiWaKcY45eT_qDS6fhqhrKIf_0HXaclTTdUShTmTqhor1W4pn1MpGcLTuwm2m32xO_tS-Q_Ph32i_y4I-wNKULoq</addsrcrecordid><sourcetype>Open Website</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1704367424</pqid></control><display><type>article</type><title>Potential Effect of CD271 on Human Mesenchymal Stromal Cell Proliferation and Differentiation</title><source>Publicly Available Content (ProQuest)</source><source>PubMed Central</source><creator>Calabrese, Giovanna ; Giuffrida, Raffaella ; Lo Furno, Debora ; Parrinello, Nunziatina Laura ; Forte, Stefano ; Gulino, Rosario ; Colarossi, Cristina ; Schinocca, Luciana Rita ; Giuffrida, Rosario ; Cardile, Venera ; Memeo, Lorenzo</creator><creatorcontrib>Calabrese, Giovanna ; Giuffrida, Raffaella ; Lo Furno, Debora ; Parrinello, Nunziatina Laura ; Forte, Stefano ; Gulino, Rosario ; Colarossi, Cristina ; Schinocca, Luciana Rita ; Giuffrida, Rosario ; Cardile, Venera ; Memeo, Lorenzo</creatorcontrib><description>The Low-Affinity Nerve Growth Factor Receptor (LNGFR), also known as CD271, is a member of the tumor necrosis factor receptor superfamily. The CD271 cell surface marker defines a subset of multipotential mesenchymal stromal cells and may be used to isolate and enrich cells derived from bone marrow aspirate. In this study, we compare the proliferative and differentiation potentials of CD271+ and CD271- mesenchymal stromal cells. Mesenchymal stromal cells were isolated from bone marrow aspirate and adipose tissue by plastic adherence and positive selection. The proliferation and differentiation potentials of CD271+ and CD271- mesenchymal stromal cells were assessed by inducing osteogenic, adipogenic and chondrogenic in vitro differentiation. Compared to CD271+, CD271- mesenchymal stromal cells showed a lower proliferation rate and a decreased ability to give rise to osteocytes, adipocytes and chondrocytes. Furthermore, we observed that CD271+ mesenchymal stromal cells isolated from adipose tissue displayed a higher efficiency of proliferation and trilineage differentiation compared to CD271+ mesenchymal stromal cells isolated from bone marrow samples, although the CD271 expression levels were comparable. In conclusion, these data show that both the presence of CD271 antigen and the source of mesenchymal stromal cells represent important factors in determining the ability of the cells to proliferate and differentiate.</description><identifier>ISSN: 1422-0067</identifier><identifier>ISSN: 1661-6596</identifier><identifier>EISSN: 1422-0067</identifier><identifier>DOI: 10.3390/ijms160715609</identifier><identifier>PMID: 26184166</identifier><language>eng</language><publisher>Switzerland: MDPI AG</publisher><subject>Adipogenesis ; adipogenic differentiation ; adipose tissue ; Aged ; Bone marrow ; Bone Marrow Cells - cytology ; Cartilage ; CD271 ; Cell Differentiation ; Cell Proliferation ; Cells, Cultured ; Cellular biology ; Chondrogenesis ; chondrogenic differentiation ; Female ; Humans ; Immunohistochemistry ; Male ; mesenchymal stromal cells ; Mesenchymal Stromal Cells - cytology ; Mesenchymal Stromal Cells - metabolism ; Middle Aged ; Nerve Tissue Proteins - metabolism ; Osteogenesis ; osteogenic differentiation ; Phenotype ; Receptors, Nerve Growth Factor - metabolism</subject><ispartof>International journal of molecular sciences, 2015-07, Vol.16 (7), p.15609-15624</ispartof><rights>Copyright MDPI AG 2015</rights><rights>2015 by the authors; licensee MDPI, Basel, Switzerland. 2015</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c580t-9f47b205b6f1562b9c7f955ab716fbc268754fa5249c5ee63a667bdec95399743</citedby><cites>FETCH-LOGICAL-c580t-9f47b205b6f1562b9c7f955ab716fbc268754fa5249c5ee63a667bdec95399743</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/1704367424/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/1704367424?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,25753,27924,27925,37012,37013,44590,53791,53793,74998</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/26184166$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Calabrese, Giovanna</creatorcontrib><creatorcontrib>Giuffrida, Raffaella</creatorcontrib><creatorcontrib>Lo Furno, Debora</creatorcontrib><creatorcontrib>Parrinello, Nunziatina Laura</creatorcontrib><creatorcontrib>Forte, Stefano</creatorcontrib><creatorcontrib>Gulino, Rosario</creatorcontrib><creatorcontrib>Colarossi, Cristina</creatorcontrib><creatorcontrib>Schinocca, Luciana Rita</creatorcontrib><creatorcontrib>Giuffrida, Rosario</creatorcontrib><creatorcontrib>Cardile, Venera</creatorcontrib><creatorcontrib>Memeo, Lorenzo</creatorcontrib><title>Potential Effect of CD271 on Human Mesenchymal Stromal Cell Proliferation and Differentiation</title><title>International journal of molecular sciences</title><addtitle>Int J Mol Sci</addtitle><description>The Low-Affinity Nerve Growth Factor Receptor (LNGFR), also known as CD271, is a member of the tumor necrosis factor receptor superfamily. The CD271 cell surface marker defines a subset of multipotential mesenchymal stromal cells and may be used to isolate and enrich cells derived from bone marrow aspirate. In this study, we compare the proliferative and differentiation potentials of CD271+ and CD271- mesenchymal stromal cells. Mesenchymal stromal cells were isolated from bone marrow aspirate and adipose tissue by plastic adherence and positive selection. The proliferation and differentiation potentials of CD271+ and CD271- mesenchymal stromal cells were assessed by inducing osteogenic, adipogenic and chondrogenic in vitro differentiation. Compared to CD271+, CD271- mesenchymal stromal cells showed a lower proliferation rate and a decreased ability to give rise to osteocytes, adipocytes and chondrocytes. Furthermore, we observed that CD271+ mesenchymal stromal cells isolated from adipose tissue displayed a higher efficiency of proliferation and trilineage differentiation compared to CD271+ mesenchymal stromal cells isolated from bone marrow samples, although the CD271 expression levels were comparable. In conclusion, these data show that both the presence of CD271 antigen and the source of mesenchymal stromal cells represent important factors in determining the ability of the cells to proliferate and differentiate.</description><subject>Adipogenesis</subject><subject>adipogenic differentiation</subject><subject>adipose tissue</subject><subject>Aged</subject><subject>Bone marrow</subject><subject>Bone Marrow Cells - cytology</subject><subject>Cartilage</subject><subject>CD271</subject><subject>Cell Differentiation</subject><subject>Cell Proliferation</subject><subject>Cells, Cultured</subject><subject>Cellular biology</subject><subject>Chondrogenesis</subject><subject>chondrogenic differentiation</subject><subject>Female</subject><subject>Humans</subject><subject>Immunohistochemistry</subject><subject>Male</subject><subject>mesenchymal stromal cells</subject><subject>Mesenchymal Stromal Cells - cytology</subject><subject>Mesenchymal Stromal Cells - metabolism</subject><subject>Middle Aged</subject><subject>Nerve Tissue Proteins - metabolism</subject><subject>Osteogenesis</subject><subject>osteogenic differentiation</subject><subject>Phenotype</subject><subject>Receptors, Nerve Growth Factor - metabolism</subject><issn>1422-0067</issn><issn>1661-6596</issn><issn>1422-0067</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNqFkk1rFTEUhoMotlaXbmXATTdT8_2xEeS2toWKBe2yhEzmpM1lZlKTGaH_3tzeWnrduDrh5OEh581B6D3BR4wZ_Cmux0IkVkRIbF6gfcIpbTGW6uWz8x56U8oaY8qoMK_RHpVEcyLlPrq-TDNMc3RDcxIC-LlJoVkdU0WaNDVny-im5hsUmPzt_VihH3NOm7qCYWgucxpigOzmWGE39c1xrJL8INz03qJXwQ0F3j3WA3T19eTn6qy9-H56vvpy0Xqh8dyawFVHsehkqGPQzngVjBCuU0SGzlOpleDBCcqNFwCSOSlV14M3ghmjODtA51tvn9za3uU4unxvk4v2oZHyjXV5jn4A22sOBHDNwkjeG-g0aKOl0hoDN12ors9b193SjdD7Okx2w45092aKt_Ym_bZcEGOIrILDR0FOvxYosx1j8TUvN0FaiiWaKcY45eT_qDS6fhqhrKIf_0HXaclTTdUShTmTqhor1W4pn1MpGcLTuwm2m32xO_tS-Q_Ph32i_y4I-wNKULoq</recordid><startdate>20150709</startdate><enddate>20150709</enddate><creator>Calabrese, Giovanna</creator><creator>Giuffrida, Raffaella</creator><creator>Lo Furno, Debora</creator><creator>Parrinello, Nunziatina Laura</creator><creator>Forte, Stefano</creator><creator>Gulino, Rosario</creator><creator>Colarossi, Cristina</creator><creator>Schinocca, Luciana Rita</creator><creator>Giuffrida, Rosario</creator><creator>Cardile, Venera</creator><creator>Memeo, Lorenzo</creator><general>MDPI AG</general><general>MDPI</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>8G5</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>GUQSH</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>M2O</scope><scope>MBDVC</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>Q9U</scope><scope>7X8</scope><scope>7TK</scope><scope>5PM</scope><scope>DOA</scope></search><sort><creationdate>20150709</creationdate><title>Potential Effect of CD271 on Human Mesenchymal Stromal Cell Proliferation and Differentiation</title><author>Calabrese, Giovanna ; Giuffrida, Raffaella ; Lo Furno, Debora ; Parrinello, Nunziatina Laura ; Forte, Stefano ; Gulino, Rosario ; Colarossi, Cristina ; Schinocca, Luciana Rita ; Giuffrida, Rosario ; Cardile, Venera ; Memeo, Lorenzo</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c580t-9f47b205b6f1562b9c7f955ab716fbc268754fa5249c5ee63a667bdec95399743</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>Adipogenesis</topic><topic>adipogenic differentiation</topic><topic>adipose tissue</topic><topic>Aged</topic><topic>Bone marrow</topic><topic>Bone Marrow Cells - cytology</topic><topic>Cartilage</topic><topic>CD271</topic><topic>Cell Differentiation</topic><topic>Cell Proliferation</topic><topic>Cells, Cultured</topic><topic>Cellular biology</topic><topic>Chondrogenesis</topic><topic>chondrogenic differentiation</topic><topic>Female</topic><topic>Humans</topic><topic>Immunohistochemistry</topic><topic>Male</topic><topic>mesenchymal stromal cells</topic><topic>Mesenchymal Stromal Cells - cytology</topic><topic>Mesenchymal Stromal Cells - metabolism</topic><topic>Middle Aged</topic><topic>Nerve Tissue Proteins - metabolism</topic><topic>Osteogenesis</topic><topic>osteogenic differentiation</topic><topic>Phenotype</topic><topic>Receptors, Nerve Growth Factor - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Calabrese, Giovanna</creatorcontrib><creatorcontrib>Giuffrida, Raffaella</creatorcontrib><creatorcontrib>Lo Furno, Debora</creatorcontrib><creatorcontrib>Parrinello, Nunziatina Laura</creatorcontrib><creatorcontrib>Forte, Stefano</creatorcontrib><creatorcontrib>Gulino, Rosario</creatorcontrib><creatorcontrib>Colarossi, Cristina</creatorcontrib><creatorcontrib>Schinocca, Luciana Rita</creatorcontrib><creatorcontrib>Giuffrida, Rosario</creatorcontrib><creatorcontrib>Cardile, Venera</creatorcontrib><creatorcontrib>Memeo, Lorenzo</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>ProQuest Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>Research Library (Alumni Edition)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>ProQuest Central Essentials</collection><collection>AUTh Library subscriptions: ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>Research Library Prep</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>ProQuest research library</collection><collection>Research Library (Corporate)</collection><collection>Publicly Available Content (ProQuest)</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>ProQuest Central Basic</collection><collection>MEDLINE - Academic</collection><collection>Neurosciences Abstracts</collection><collection>PubMed Central (Full Participant titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>International journal of molecular sciences</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Calabrese, Giovanna</au><au>Giuffrida, Raffaella</au><au>Lo Furno, Debora</au><au>Parrinello, Nunziatina Laura</au><au>Forte, Stefano</au><au>Gulino, Rosario</au><au>Colarossi, Cristina</au><au>Schinocca, Luciana Rita</au><au>Giuffrida, Rosario</au><au>Cardile, Venera</au><au>Memeo, Lorenzo</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Potential Effect of CD271 on Human Mesenchymal Stromal Cell Proliferation and Differentiation</atitle><jtitle>International journal of molecular sciences</jtitle><addtitle>Int J Mol Sci</addtitle><date>2015-07-09</date><risdate>2015</risdate><volume>16</volume><issue>7</issue><spage>15609</spage><epage>15624</epage><pages>15609-15624</pages><issn>1422-0067</issn><issn>1661-6596</issn><eissn>1422-0067</eissn><abstract>The Low-Affinity Nerve Growth Factor Receptor (LNGFR), also known as CD271, is a member of the tumor necrosis factor receptor superfamily. The CD271 cell surface marker defines a subset of multipotential mesenchymal stromal cells and may be used to isolate and enrich cells derived from bone marrow aspirate. In this study, we compare the proliferative and differentiation potentials of CD271+ and CD271- mesenchymal stromal cells. Mesenchymal stromal cells were isolated from bone marrow aspirate and adipose tissue by plastic adherence and positive selection. The proliferation and differentiation potentials of CD271+ and CD271- mesenchymal stromal cells were assessed by inducing osteogenic, adipogenic and chondrogenic in vitro differentiation. Compared to CD271+, CD271- mesenchymal stromal cells showed a lower proliferation rate and a decreased ability to give rise to osteocytes, adipocytes and chondrocytes. Furthermore, we observed that CD271+ mesenchymal stromal cells isolated from adipose tissue displayed a higher efficiency of proliferation and trilineage differentiation compared to CD271+ mesenchymal stromal cells isolated from bone marrow samples, although the CD271 expression levels were comparable. In conclusion, these data show that both the presence of CD271 antigen and the source of mesenchymal stromal cells represent important factors in determining the ability of the cells to proliferate and differentiate.</abstract><cop>Switzerland</cop><pub>MDPI AG</pub><pmid>26184166</pmid><doi>10.3390/ijms160715609</doi><tpages>16</tpages><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 1422-0067 |
ispartof | International journal of molecular sciences, 2015-07, Vol.16 (7), p.15609-15624 |
issn | 1422-0067 1661-6596 1422-0067 |
language | eng |
recordid | cdi_doaj_primary_oai_doaj_org_article_d84e1e0002964d9eb8e89867880e49bf |
source | Publicly Available Content (ProQuest); PubMed Central |
subjects | Adipogenesis adipogenic differentiation adipose tissue Aged Bone marrow Bone Marrow Cells - cytology Cartilage CD271 Cell Differentiation Cell Proliferation Cells, Cultured Cellular biology Chondrogenesis chondrogenic differentiation Female Humans Immunohistochemistry Male mesenchymal stromal cells Mesenchymal Stromal Cells - cytology Mesenchymal Stromal Cells - metabolism Middle Aged Nerve Tissue Proteins - metabolism Osteogenesis osteogenic differentiation Phenotype Receptors, Nerve Growth Factor - metabolism |
title | Potential Effect of CD271 on Human Mesenchymal Stromal Cell Proliferation and Differentiation |
url | http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-08T00%3A23%3A17IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_doaj_&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Potential%20Effect%20of%20CD271%20on%20Human%20Mesenchymal%20Stromal%20Cell%20Proliferation%20and%20Differentiation&rft.jtitle=International%20journal%20of%20molecular%20sciences&rft.au=Calabrese,%20Giovanna&rft.date=2015-07-09&rft.volume=16&rft.issue=7&rft.spage=15609&rft.epage=15624&rft.pages=15609-15624&rft.issn=1422-0067&rft.eissn=1422-0067&rft_id=info:doi/10.3390/ijms160715609&rft_dat=%3Cproquest_doaj_%3E1698023123%3C/proquest_doaj_%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c580t-9f47b205b6f1562b9c7f955ab716fbc268754fa5249c5ee63a667bdec95399743%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=1704367424&rft_id=info:pmid/26184166&rfr_iscdi=true |