The Effect of Hydrostatic Pressure on Three-Dimensional Chondroinduction of Human Adipose–Derived Stem Cells
Background: The optimal production of three-dimensional cartilage in vitro requires both inductive factors and specified culture conditions (e.g., hydrostatic pressure [HP], gas concentration, and nutrient supply) to promote cell viability and maintain phenotype. In this study, we optimized the cond...
Gespeichert in:
Veröffentlicht in: | Tissue engineering. Part A 2009-10, Vol.15 (10), p.2937-2945 |
---|---|
Hauptverfasser: | , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 2945 |
---|---|
container_issue | 10 |
container_start_page | 2937 |
container_title | Tissue engineering. Part A |
container_volume | 15 |
creator | Ogawa, Rei Mizuno, Shuichi Murphy, George F. Orgill, Dennis P. |
description | Background:
The optimal production of three-dimensional cartilage
in vitro
requires both inductive factors and specified culture conditions (e.g., hydrostatic pressure [HP], gas concentration, and nutrient supply) to promote cell viability and maintain phenotype. In this study, we optimized the conditions for human cartilage induction using human adipose–derived stem cells (ASCs), collagen scaffolds, and cyclic HP treatment.
Methods:
Human ASCs underwent primary culture and three passages before being seeded into collagen scaffolds. These constructs were incubated for 1 week in an automated bioreactor using cyclic HP at 0–0.5 MPa, 0.5 Hz, and compared to constructs exposed to atmospheric pressure. In both groups, chondrogenic differentiation medium including transforming growth factor-β1 was employed. One, 2, 3, and 4 weeks after incubation, the cell constructs were harvested for histological, immunohistochemical, and gene expression evaluation.
Results:
In histological and immunohistochemical analyzes, pericellular and extracellular metachromatic matrix was observed in both groups and increased over 4 weeks, but accumulated at a higher rate in the HP group. Cell number was maintained in the HP group over 4 weeks but decreased after 2 weeks in the atmospheric pressure group. Chondrogenic-specific gene expression of type II and X collagen, aggrecan, and SRY-box9 was increased in the HP group especially after 2 weeks.
Conclusion:
Our results demonstrate chondrogenic differentiation of ASCs in a three-dimensional collagen scaffolds with treatment of a cyclic HP. Cyclic HP was effective in enhancing accumulation of extracellular matrix and expression of genes indicative of chondrogenic differentiation. |
doi_str_mv | 10.1089/ten.tea.2008.0672 |
format | Article |
fullrecord | <record><control><sourceid>gale_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_2811056</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><galeid>A248094647</galeid><sourcerecordid>A248094647</sourcerecordid><originalsourceid>FETCH-LOGICAL-c608t-2f17f9fc4a3370827e898ee75bd09ae3158ff2bf38b7bec3cce4b2c4c6586efb3</originalsourceid><addsrcrecordid>eNqNksuKFDEUhgtRnIs-gBuJG11Vm1tVUhuh6RkdYUDBFtyFVOpkOkNV0iapgdn5Dr7hPIlpuxkvC5EQEk6-_ycn-avqGcELgmX3OoNfZNALirFc4FbQB9Ux6ZioGWu-PLzfc3JUnaR0jXFbIPG4OiId7bDE_Ljy6w2gc2vBZBQsurgdYkhZZ2fQxwgpzRFQ8Gi9iQD1mZvAJxe8HtFqE3xhnR9mk0vpp3qetEfLwW1Dgrtv388guhsY0KcME1rBOKYn1SOrxwRPD-tp9fnt-Xp1UV9-ePd-tbysTYtlrqklwnbWcM2YwJIKkJ0EEE0_4E4DI420lvaWyV70YJgxwHtquGkb2YLt2Wn1Zu-7nfsJBgM-Rz2qbXSTjrcqaKf-PPFuo67CjaKSENy0xeDVwSCGrzOkrCaXTGlBewhzUoJxLEQjZCFf_pOkhBAuCSvgi7_A6zDH8pZJyY5hSSQvzGLPXOkRlPM2lNuZMgaYnAkerCv1JeUSd7zlogjIXmDKv6UI9r5HgtUuJKqEpEytdiFRu5AUzfPfH-eX4pCKAog9sCtr70cHPcT8H9Y_AMpoz6Q</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>89308184</pqid></control><display><type>article</type><title>The Effect of Hydrostatic Pressure on Three-Dimensional Chondroinduction of Human Adipose–Derived Stem Cells</title><source>Mary Ann Liebert Online Subscription</source><source>MEDLINE</source><source>Alma/SFX Local Collection</source><creator>Ogawa, Rei ; Mizuno, Shuichi ; Murphy, George F. ; Orgill, Dennis P.</creator><creatorcontrib>Ogawa, Rei ; Mizuno, Shuichi ; Murphy, George F. ; Orgill, Dennis P.</creatorcontrib><description>Background:
The optimal production of three-dimensional cartilage
in vitro
requires both inductive factors and specified culture conditions (e.g., hydrostatic pressure [HP], gas concentration, and nutrient supply) to promote cell viability and maintain phenotype. In this study, we optimized the conditions for human cartilage induction using human adipose–derived stem cells (ASCs), collagen scaffolds, and cyclic HP treatment.
Methods:
Human ASCs underwent primary culture and three passages before being seeded into collagen scaffolds. These constructs were incubated for 1 week in an automated bioreactor using cyclic HP at 0–0.5 MPa, 0.5 Hz, and compared to constructs exposed to atmospheric pressure. In both groups, chondrogenic differentiation medium including transforming growth factor-β1 was employed. One, 2, 3, and 4 weeks after incubation, the cell constructs were harvested for histological, immunohistochemical, and gene expression evaluation.
Results:
In histological and immunohistochemical analyzes, pericellular and extracellular metachromatic matrix was observed in both groups and increased over 4 weeks, but accumulated at a higher rate in the HP group. Cell number was maintained in the HP group over 4 weeks but decreased after 2 weeks in the atmospheric pressure group. Chondrogenic-specific gene expression of type II and X collagen, aggrecan, and SRY-box9 was increased in the HP group especially after 2 weeks.
Conclusion:
Our results demonstrate chondrogenic differentiation of ASCs in a three-dimensional collagen scaffolds with treatment of a cyclic HP. Cyclic HP was effective in enhancing accumulation of extracellular matrix and expression of genes indicative of chondrogenic differentiation.</description><identifier>ISSN: 1937-3341</identifier><identifier>EISSN: 1937-335X</identifier><identifier>DOI: 10.1089/ten.tea.2008.0672</identifier><identifier>PMID: 19290804</identifier><language>eng</language><publisher>United States: Mary Ann Liebert, Inc</publisher><subject>Adipocytes - cytology ; Adipocytes - metabolism ; Analysis ; Cartilage ; Cartilage - cytology ; Cartilage - metabolism ; Cell culture ; Cell Differentiation ; Collagen ; Collagen - chemistry ; Collagen - metabolism ; Flow Cytometry ; Gene expression ; Genetic aspects ; Humans ; Hydrostatic Pressure ; Immunohistochemistry ; Optimization ; Original ; Original Articles ; Physiological aspects ; Reverse Transcriptase Polymerase Chain Reaction ; Stem cells ; Stem Cells - cytology ; Stem Cells - metabolism ; Tissue engineering ; Tissue Engineering - methods ; Tissue Scaffolds - chemistry</subject><ispartof>Tissue engineering. Part A, 2009-10, Vol.15 (10), p.2937-2945</ispartof><rights>2009, Mary Ann Liebert, Inc.</rights><rights>COPYRIGHT 2009 Mary Ann Liebert, Inc.</rights><rights>(©) Copyright 2009, Mary Ann Liebert, Inc.</rights><rights>Copyright 2009, Mary Ann Liebert, Inc.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c608t-2f17f9fc4a3370827e898ee75bd09ae3158ff2bf38b7bec3cce4b2c4c6586efb3</citedby><cites>FETCH-LOGICAL-c608t-2f17f9fc4a3370827e898ee75bd09ae3158ff2bf38b7bec3cce4b2c4c6586efb3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.liebertpub.com/doi/epdf/10.1089/ten.tea.2008.0672$$EPDF$$P50$$Gmaryannliebert$$H</linktopdf><linktohtml>$$Uhttps://www.liebertpub.com/doi/full/10.1089/ten.tea.2008.0672$$EHTML$$P50$$Gmaryannliebert$$H</linktohtml><link.rule.ids>230,314,776,780,881,3029,21702,27901,27902,55266,55278</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/19290804$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Ogawa, Rei</creatorcontrib><creatorcontrib>Mizuno, Shuichi</creatorcontrib><creatorcontrib>Murphy, George F.</creatorcontrib><creatorcontrib>Orgill, Dennis P.</creatorcontrib><title>The Effect of Hydrostatic Pressure on Three-Dimensional Chondroinduction of Human Adipose–Derived Stem Cells</title><title>Tissue engineering. Part A</title><addtitle>Tissue Eng Part A</addtitle><description>Background:
The optimal production of three-dimensional cartilage
in vitro
requires both inductive factors and specified culture conditions (e.g., hydrostatic pressure [HP], gas concentration, and nutrient supply) to promote cell viability and maintain phenotype. In this study, we optimized the conditions for human cartilage induction using human adipose–derived stem cells (ASCs), collagen scaffolds, and cyclic HP treatment.
Methods:
Human ASCs underwent primary culture and three passages before being seeded into collagen scaffolds. These constructs were incubated for 1 week in an automated bioreactor using cyclic HP at 0–0.5 MPa, 0.5 Hz, and compared to constructs exposed to atmospheric pressure. In both groups, chondrogenic differentiation medium including transforming growth factor-β1 was employed. One, 2, 3, and 4 weeks after incubation, the cell constructs were harvested for histological, immunohistochemical, and gene expression evaluation.
Results:
In histological and immunohistochemical analyzes, pericellular and extracellular metachromatic matrix was observed in both groups and increased over 4 weeks, but accumulated at a higher rate in the HP group. Cell number was maintained in the HP group over 4 weeks but decreased after 2 weeks in the atmospheric pressure group. Chondrogenic-specific gene expression of type II and X collagen, aggrecan, and SRY-box9 was increased in the HP group especially after 2 weeks.
Conclusion:
Our results demonstrate chondrogenic differentiation of ASCs in a three-dimensional collagen scaffolds with treatment of a cyclic HP. Cyclic HP was effective in enhancing accumulation of extracellular matrix and expression of genes indicative of chondrogenic differentiation.</description><subject>Adipocytes - cytology</subject><subject>Adipocytes - metabolism</subject><subject>Analysis</subject><subject>Cartilage</subject><subject>Cartilage - cytology</subject><subject>Cartilage - metabolism</subject><subject>Cell culture</subject><subject>Cell Differentiation</subject><subject>Collagen</subject><subject>Collagen - chemistry</subject><subject>Collagen - metabolism</subject><subject>Flow Cytometry</subject><subject>Gene expression</subject><subject>Genetic aspects</subject><subject>Humans</subject><subject>Hydrostatic Pressure</subject><subject>Immunohistochemistry</subject><subject>Optimization</subject><subject>Original</subject><subject>Original Articles</subject><subject>Physiological aspects</subject><subject>Reverse Transcriptase Polymerase Chain Reaction</subject><subject>Stem cells</subject><subject>Stem Cells - cytology</subject><subject>Stem Cells - metabolism</subject><subject>Tissue engineering</subject><subject>Tissue Engineering - methods</subject><subject>Tissue Scaffolds - chemistry</subject><issn>1937-3341</issn><issn>1937-335X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2009</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>BENPR</sourceid><recordid>eNqNksuKFDEUhgtRnIs-gBuJG11Vm1tVUhuh6RkdYUDBFtyFVOpkOkNV0iapgdn5Dr7hPIlpuxkvC5EQEk6-_ycn-avqGcELgmX3OoNfZNALirFc4FbQB9Ux6ZioGWu-PLzfc3JUnaR0jXFbIPG4OiId7bDE_Ljy6w2gc2vBZBQsurgdYkhZZ2fQxwgpzRFQ8Gi9iQD1mZvAJxe8HtFqE3xhnR9mk0vpp3qetEfLwW1Dgrtv388guhsY0KcME1rBOKYn1SOrxwRPD-tp9fnt-Xp1UV9-ePd-tbysTYtlrqklwnbWcM2YwJIKkJ0EEE0_4E4DI420lvaWyV70YJgxwHtquGkb2YLt2Wn1Zu-7nfsJBgM-Rz2qbXSTjrcqaKf-PPFuo67CjaKSENy0xeDVwSCGrzOkrCaXTGlBewhzUoJxLEQjZCFf_pOkhBAuCSvgi7_A6zDH8pZJyY5hSSQvzGLPXOkRlPM2lNuZMgaYnAkerCv1JeUSd7zlogjIXmDKv6UI9r5HgtUuJKqEpEytdiFRu5AUzfPfH-eX4pCKAog9sCtr70cHPcT8H9Y_AMpoz6Q</recordid><startdate>20091001</startdate><enddate>20091001</enddate><creator>Ogawa, Rei</creator><creator>Mizuno, Shuichi</creator><creator>Murphy, George F.</creator><creator>Orgill, Dennis P.</creator><general>Mary Ann Liebert, Inc</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>7QP</scope><scope>7T5</scope><scope>7TK</scope><scope>7TM</scope><scope>7TO</scope><scope>7X7</scope><scope>7XB</scope><scope>88A</scope><scope>88E</scope><scope>88I</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>H94</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M2P</scope><scope>M7P</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>Q9U</scope><scope>7QO</scope><scope>8FD</scope><scope>FR3</scope><scope>P64</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20091001</creationdate><title>The Effect of Hydrostatic Pressure on Three-Dimensional Chondroinduction of Human Adipose–Derived Stem Cells</title><author>Ogawa, Rei ; Mizuno, Shuichi ; Murphy, George F. ; Orgill, Dennis P.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c608t-2f17f9fc4a3370827e898ee75bd09ae3158ff2bf38b7bec3cce4b2c4c6586efb3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2009</creationdate><topic>Adipocytes - cytology</topic><topic>Adipocytes - metabolism</topic><topic>Analysis</topic><topic>Cartilage</topic><topic>Cartilage - cytology</topic><topic>Cartilage - metabolism</topic><topic>Cell culture</topic><topic>Cell Differentiation</topic><topic>Collagen</topic><topic>Collagen - chemistry</topic><topic>Collagen - metabolism</topic><topic>Flow Cytometry</topic><topic>Gene expression</topic><topic>Genetic aspects</topic><topic>Humans</topic><topic>Hydrostatic Pressure</topic><topic>Immunohistochemistry</topic><topic>Optimization</topic><topic>Original</topic><topic>Original Articles</topic><topic>Physiological aspects</topic><topic>Reverse Transcriptase Polymerase Chain Reaction</topic><topic>Stem cells</topic><topic>Stem Cells - cytology</topic><topic>Stem Cells - metabolism</topic><topic>Tissue engineering</topic><topic>Tissue Engineering - methods</topic><topic>Tissue Scaffolds - chemistry</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Ogawa, Rei</creatorcontrib><creatorcontrib>Mizuno, Shuichi</creatorcontrib><creatorcontrib>Murphy, George F.</creatorcontrib><creatorcontrib>Orgill, Dennis P.</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>Calcium & Calcified Tissue Abstracts</collection><collection>Immunology Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Oncogenes and Growth Factors Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Biology Database (Alumni Edition)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Science Database (Alumni Edition)</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Science Database</collection><collection>Biological Science Database</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>Biotechnology Research Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Tissue engineering. Part A</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Ogawa, Rei</au><au>Mizuno, Shuichi</au><au>Murphy, George F.</au><au>Orgill, Dennis P.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The Effect of Hydrostatic Pressure on Three-Dimensional Chondroinduction of Human Adipose–Derived Stem Cells</atitle><jtitle>Tissue engineering. Part A</jtitle><addtitle>Tissue Eng Part A</addtitle><date>2009-10-01</date><risdate>2009</risdate><volume>15</volume><issue>10</issue><spage>2937</spage><epage>2945</epage><pages>2937-2945</pages><issn>1937-3341</issn><eissn>1937-335X</eissn><abstract>Background:
The optimal production of three-dimensional cartilage
in vitro
requires both inductive factors and specified culture conditions (e.g., hydrostatic pressure [HP], gas concentration, and nutrient supply) to promote cell viability and maintain phenotype. In this study, we optimized the conditions for human cartilage induction using human adipose–derived stem cells (ASCs), collagen scaffolds, and cyclic HP treatment.
Methods:
Human ASCs underwent primary culture and three passages before being seeded into collagen scaffolds. These constructs were incubated for 1 week in an automated bioreactor using cyclic HP at 0–0.5 MPa, 0.5 Hz, and compared to constructs exposed to atmospheric pressure. In both groups, chondrogenic differentiation medium including transforming growth factor-β1 was employed. One, 2, 3, and 4 weeks after incubation, the cell constructs were harvested for histological, immunohistochemical, and gene expression evaluation.
Results:
In histological and immunohistochemical analyzes, pericellular and extracellular metachromatic matrix was observed in both groups and increased over 4 weeks, but accumulated at a higher rate in the HP group. Cell number was maintained in the HP group over 4 weeks but decreased after 2 weeks in the atmospheric pressure group. Chondrogenic-specific gene expression of type II and X collagen, aggrecan, and SRY-box9 was increased in the HP group especially after 2 weeks.
Conclusion:
Our results demonstrate chondrogenic differentiation of ASCs in a three-dimensional collagen scaffolds with treatment of a cyclic HP. Cyclic HP was effective in enhancing accumulation of extracellular matrix and expression of genes indicative of chondrogenic differentiation.</abstract><cop>United States</cop><pub>Mary Ann Liebert, Inc</pub><pmid>19290804</pmid><doi>10.1089/ten.tea.2008.0672</doi><tpages>9</tpages><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 1937-3341 |
ispartof | Tissue engineering. Part A, 2009-10, Vol.15 (10), p.2937-2945 |
issn | 1937-3341 1937-335X |
language | eng |
recordid | cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_2811056 |
source | Mary Ann Liebert Online Subscription; MEDLINE; Alma/SFX Local Collection |
subjects | Adipocytes - cytology Adipocytes - metabolism Analysis Cartilage Cartilage - cytology Cartilage - metabolism Cell culture Cell Differentiation Collagen Collagen - chemistry Collagen - metabolism Flow Cytometry Gene expression Genetic aspects Humans Hydrostatic Pressure Immunohistochemistry Optimization Original Original Articles Physiological aspects Reverse Transcriptase Polymerase Chain Reaction Stem cells Stem Cells - cytology Stem Cells - metabolism Tissue engineering Tissue Engineering - methods Tissue Scaffolds - chemistry |
title | The Effect of Hydrostatic Pressure on Three-Dimensional Chondroinduction of Human Adipose–Derived Stem Cells |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-08T10%3A52%3A04IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-gale_pubme&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=The%20Effect%20of%20Hydrostatic%20Pressure%20on%20Three-Dimensional%20Chondroinduction%20of%20Human%20Adipose%E2%80%93Derived%20Stem%20Cells&rft.jtitle=Tissue%20engineering.%20Part%20A&rft.au=Ogawa,%20Rei&rft.date=2009-10-01&rft.volume=15&rft.issue=10&rft.spage=2937&rft.epage=2945&rft.pages=2937-2945&rft.issn=1937-3341&rft.eissn=1937-335X&rft_id=info:doi/10.1089/ten.tea.2008.0672&rft_dat=%3Cgale_pubme%3EA248094647%3C/gale_pubme%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=89308184&rft_id=info:pmid/19290804&rft_galeid=A248094647&rfr_iscdi=true |