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Integrin expression by human osteoblasts cultured on degradable polymeric materials applicable for tissue engineered bone
The use of biodegradable polymers in the field of orthopaedic surgery has gained increased popularity, as surgical pins and screws, and as potential biological scaffolds for repairing cartilage and bone defects. One such group of polymers that has gained considerable attention are the polyesters, po...
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Published in: | Journal of orthopaedic research 2002, Vol.20 (1), p.20-28 |
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description | The use of biodegradable polymers in the field of orthopaedic surgery has gained increased popularity, as surgical pins and screws, and as potential biological scaffolds for repairing cartilage and bone defects. One such group of polymers that has gained considerable attention are the polyesters, poly(lactide-co-glycolide) (PLAGA) and polylactic acid (PLA), because of their minimal tissue inflammatory response, favorable biocompatibility and degradation characteristics. The objective of this study was to evaluate human osteoblastic cell adherence and growth on PLAGA and PLA scaffolds by examining integrin receptor (
α
2,
α
3,
α
4,
α
5,
α
6 and
β
1) expression. Primary human osteoblastic cells isolated from trabecular bone adhered efficiently to both PLAGA and PLA, with the rate of adherence on PLAGA comparable to that of control tissue culture polystyrene (TCPS), and significantly higher than on PLA polymers at 3, 6 and 12 h. Human osteoblastic phenotypic expression, alkaline phosphatase (ALP) activity was positive on both degradable matrices, whereas osteocalcin levels were significantly higher on cells grown on PLAGA than on PLA composites. Interestingly, the integrin subunits,
α
2,
α
3,
α
4,
α
5,
α
6 and
β
1 were all expressed at higher levels by osteoblasts cultured on PLAGA than those on PLA as analyzed by westerns blots and by flow cytometry. Among the integrins,
α
2,
α
5 and
β
1 showed the greatest difference in levels between the two surfaces. Thus, both PLA and PLAGA support osteoblastic adhesion and its accompanying engagement of integrin receptor and expression of osteocalcin and ALP. However PLAGA consistently appeared to be a better substrate for osteoblastic cells based on these parameters. This study is one of the first to investigate the ability of primary human osteoblastic cells isolated from trabecular bone to adhere to the biodegradable polymers PLAGA and PLA, and to examine the expression of their key adhesion receptors (integrins) on these substrates. |
doi_str_mv | 10.1016/S0736-0266(01)00062-6 |
format | article |
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α
2,
α
3,
α
4,
α
5,
α
6 and
β
1) expression. Primary human osteoblastic cells isolated from trabecular bone adhered efficiently to both PLAGA and PLA, with the rate of adherence on PLAGA comparable to that of control tissue culture polystyrene (TCPS), and significantly higher than on PLA polymers at 3, 6 and 12 h. Human osteoblastic phenotypic expression, alkaline phosphatase (ALP) activity was positive on both degradable matrices, whereas osteocalcin levels were significantly higher on cells grown on PLAGA than on PLA composites. Interestingly, the integrin subunits,
α
2,
α
3,
α
4,
α
5,
α
6 and
β
1 were all expressed at higher levels by osteoblasts cultured on PLAGA than those on PLA as analyzed by westerns blots and by flow cytometry. Among the integrins,
α
2,
α
5 and
β
1 showed the greatest difference in levels between the two surfaces. Thus, both PLA and PLAGA support osteoblastic adhesion and its accompanying engagement of integrin receptor and expression of osteocalcin and ALP. However PLAGA consistently appeared to be a better substrate for osteoblastic cells based on these parameters. This study is one of the first to investigate the ability of primary human osteoblastic cells isolated from trabecular bone to adhere to the biodegradable polymers PLAGA and PLA, and to examine the expression of their key adhesion receptors (integrins) on these substrates.</description><identifier>ISSN: 0736-0266</identifier><identifier>EISSN: 1554-527X</identifier><identifier>DOI: 10.1016/S0736-0266(01)00062-6</identifier><identifier>PMID: 11853086</identifier><language>eng</language><publisher>Hoboken: Elsevier Ltd</publisher><subject>Absorbable Implants ; Blotting, Western ; Bone Regeneration ; Cell Adhesion ; Cell-polymer interaction ; Cells, Cultured ; Flow Cytometry ; Human osteoblast ; Humans ; Integrins ; Integrins - analysis ; Integrins - biosynthesis ; Microscopy, Electron, Scanning ; Osteoblasts - chemistry ; Osteoblasts - cytology ; Osteoblasts - metabolism ; polyesters ; polylactic acid ; Polymers ; Tissue Engineering</subject><ispartof>Journal of orthopaedic research, 2002, Vol.20 (1), p.20-28</ispartof><rights>2002 Elsevier Science Ltd</rights><rights>Copyright © 2002 Orthopaedic Research Society</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c5345-68cab25bd96e3d9767a1b2efe4bf78cf8ffeffd431debfa4ff0ab6fb77229e303</citedby><cites>FETCH-LOGICAL-c5345-68cab25bd96e3d9767a1b2efe4bf78cf8ffeffd431debfa4ff0ab6fb77229e303</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0736026601000626$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,780,784,3549,4024,27923,27924,27925,45780</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/11853086$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>El-Amin, Saadiq F</creatorcontrib><creatorcontrib>Attawia, Mohamed</creatorcontrib><creatorcontrib>Lu, Helen H</creatorcontrib><creatorcontrib>Shah, Asist K</creatorcontrib><creatorcontrib>Chang, Richard</creatorcontrib><creatorcontrib>Hickok, Noreen J</creatorcontrib><creatorcontrib>Tuan, Rocky S</creatorcontrib><creatorcontrib>Laurencin, Cato T</creatorcontrib><title>Integrin expression by human osteoblasts cultured on degradable polymeric materials applicable for tissue engineered bone</title><title>Journal of orthopaedic research</title><addtitle>J. Orthop. Res</addtitle><description>The use of biodegradable polymers in the field of orthopaedic surgery has gained increased popularity, as surgical pins and screws, and as potential biological scaffolds for repairing cartilage and bone defects. One such group of polymers that has gained considerable attention are the polyesters, poly(lactide-co-glycolide) (PLAGA) and polylactic acid (PLA), because of their minimal tissue inflammatory response, favorable biocompatibility and degradation characteristics. The objective of this study was to evaluate human osteoblastic cell adherence and growth on PLAGA and PLA scaffolds by examining integrin receptor (
α
2,
α
3,
α
4,
α
5,
α
6 and
β
1) expression. Primary human osteoblastic cells isolated from trabecular bone adhered efficiently to both PLAGA and PLA, with the rate of adherence on PLAGA comparable to that of control tissue culture polystyrene (TCPS), and significantly higher than on PLA polymers at 3, 6 and 12 h. Human osteoblastic phenotypic expression, alkaline phosphatase (ALP) activity was positive on both degradable matrices, whereas osteocalcin levels were significantly higher on cells grown on PLAGA than on PLA composites. Interestingly, the integrin subunits,
α
2,
α
3,
α
4,
α
5,
α
6 and
β
1 were all expressed at higher levels by osteoblasts cultured on PLAGA than those on PLA as analyzed by westerns blots and by flow cytometry. Among the integrins,
α
2,
α
5 and
β
1 showed the greatest difference in levels between the two surfaces. Thus, both PLA and PLAGA support osteoblastic adhesion and its accompanying engagement of integrin receptor and expression of osteocalcin and ALP. However PLAGA consistently appeared to be a better substrate for osteoblastic cells based on these parameters. This study is one of the first to investigate the ability of primary human osteoblastic cells isolated from trabecular bone to adhere to the biodegradable polymers PLAGA and PLA, and to examine the expression of their key adhesion receptors (integrins) on these substrates.</description><subject>Absorbable Implants</subject><subject>Blotting, Western</subject><subject>Bone Regeneration</subject><subject>Cell Adhesion</subject><subject>Cell-polymer interaction</subject><subject>Cells, Cultured</subject><subject>Flow Cytometry</subject><subject>Human osteoblast</subject><subject>Humans</subject><subject>Integrins</subject><subject>Integrins - analysis</subject><subject>Integrins - biosynthesis</subject><subject>Microscopy, Electron, Scanning</subject><subject>Osteoblasts - chemistry</subject><subject>Osteoblasts - cytology</subject><subject>Osteoblasts - metabolism</subject><subject>polyesters</subject><subject>polylactic acid</subject><subject>Polymers</subject><subject>Tissue Engineering</subject><issn>0736-0266</issn><issn>1554-527X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2002</creationdate><recordtype>article</recordtype><recordid>eNqNkcFu1DAURS0EokPhE0BeIVgEbCe2MyuKKmiLRq0ERczOsp3nYkjiYCfQ_D2eyagsy-ot3rnH8rsIPafkDSVUvP1CZCkKwoR4RehrQohghXiAVpTzquBMbh-i1R1yhJ6k9CNDkrL6MTqitOYlqcUKzRf9CDfR9xhuhwgp-dBjM-PvU6d7HNIIwbQ6jQnbqR2nCA3OQJMjutGmBTyEdu4geos7Peap24T1MLTe7tcuRDz6lCbA0N_4HmCnMKGHp-iRyzA8O8xj9PXjh-vT82JzdXZx-n5TWF5WvBB1FjFumrWAsllLITU1DBxUxsnauto5cK6pStqAcbpyjmgjnJGSsTWUpDxGLxfvEMOvCdKoOp8stK3uIUxJSVoJwcT6XjDfTDLBZQb5AtoYUorg1BB9p-OsKFG7ctS-HLW7vCJU7ctRIudeHB6YTAfNv9ShjQycLMAf38L8f1b16eozpYQwQijhWVEsCp-ru71T6PhTCVlKrr5dnqnza7a53G6zNvPvFh5yBb89RJWsh95C4yPYUTXB3_Orv41ixEk</recordid><startdate>2002</startdate><enddate>2002</enddate><creator>El-Amin, Saadiq F</creator><creator>Attawia, Mohamed</creator><creator>Lu, Helen H</creator><creator>Shah, Asist K</creator><creator>Chang, Richard</creator><creator>Hickok, Noreen J</creator><creator>Tuan, Rocky S</creator><creator>Laurencin, Cato T</creator><general>Elsevier Ltd</general><general>Wiley Subscription Services, Inc., A Wiley Company</general><scope>BSCLL</scope><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>7QO</scope><scope>7QP</scope><scope>8FD</scope><scope>FR3</scope><scope>P64</scope><scope>7X8</scope></search><sort><creationdate>2002</creationdate><title>Integrin expression by human osteoblasts cultured on degradable polymeric materials applicable for tissue engineered bone</title><author>El-Amin, Saadiq F ; Attawia, Mohamed ; Lu, Helen H ; Shah, Asist K ; Chang, Richard ; Hickok, Noreen J ; Tuan, Rocky S ; Laurencin, Cato T</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c5345-68cab25bd96e3d9767a1b2efe4bf78cf8ffeffd431debfa4ff0ab6fb77229e303</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2002</creationdate><topic>Absorbable Implants</topic><topic>Blotting, Western</topic><topic>Bone Regeneration</topic><topic>Cell Adhesion</topic><topic>Cell-polymer interaction</topic><topic>Cells, Cultured</topic><topic>Flow Cytometry</topic><topic>Human osteoblast</topic><topic>Humans</topic><topic>Integrins</topic><topic>Integrins - analysis</topic><topic>Integrins - biosynthesis</topic><topic>Microscopy, Electron, Scanning</topic><topic>Osteoblasts - chemistry</topic><topic>Osteoblasts - cytology</topic><topic>Osteoblasts - metabolism</topic><topic>polyesters</topic><topic>polylactic acid</topic><topic>Polymers</topic><topic>Tissue Engineering</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>El-Amin, Saadiq F</creatorcontrib><creatorcontrib>Attawia, Mohamed</creatorcontrib><creatorcontrib>Lu, Helen H</creatorcontrib><creatorcontrib>Shah, Asist K</creatorcontrib><creatorcontrib>Chang, Richard</creatorcontrib><creatorcontrib>Hickok, Noreen J</creatorcontrib><creatorcontrib>Tuan, Rocky S</creatorcontrib><creatorcontrib>Laurencin, Cato T</creatorcontrib><collection>Istex</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Biotechnology Research Abstracts</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of orthopaedic research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>El-Amin, Saadiq F</au><au>Attawia, Mohamed</au><au>Lu, Helen H</au><au>Shah, Asist K</au><au>Chang, Richard</au><au>Hickok, Noreen J</au><au>Tuan, Rocky S</au><au>Laurencin, Cato T</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Integrin expression by human osteoblasts cultured on degradable polymeric materials applicable for tissue engineered bone</atitle><jtitle>Journal of orthopaedic research</jtitle><addtitle>J. Orthop. Res</addtitle><date>2002</date><risdate>2002</risdate><volume>20</volume><issue>1</issue><spage>20</spage><epage>28</epage><pages>20-28</pages><issn>0736-0266</issn><eissn>1554-527X</eissn><abstract>The use of biodegradable polymers in the field of orthopaedic surgery has gained increased popularity, as surgical pins and screws, and as potential biological scaffolds for repairing cartilage and bone defects. One such group of polymers that has gained considerable attention are the polyesters, poly(lactide-co-glycolide) (PLAGA) and polylactic acid (PLA), because of their minimal tissue inflammatory response, favorable biocompatibility and degradation characteristics. The objective of this study was to evaluate human osteoblastic cell adherence and growth on PLAGA and PLA scaffolds by examining integrin receptor (
α
2,
α
3,
α
4,
α
5,
α
6 and
β
1) expression. Primary human osteoblastic cells isolated from trabecular bone adhered efficiently to both PLAGA and PLA, with the rate of adherence on PLAGA comparable to that of control tissue culture polystyrene (TCPS), and significantly higher than on PLA polymers at 3, 6 and 12 h. Human osteoblastic phenotypic expression, alkaline phosphatase (ALP) activity was positive on both degradable matrices, whereas osteocalcin levels were significantly higher on cells grown on PLAGA than on PLA composites. Interestingly, the integrin subunits,
α
2,
α
3,
α
4,
α
5,
α
6 and
β
1 were all expressed at higher levels by osteoblasts cultured on PLAGA than those on PLA as analyzed by westerns blots and by flow cytometry. Among the integrins,
α
2,
α
5 and
β
1 showed the greatest difference in levels between the two surfaces. Thus, both PLA and PLAGA support osteoblastic adhesion and its accompanying engagement of integrin receptor and expression of osteocalcin and ALP. However PLAGA consistently appeared to be a better substrate for osteoblastic cells based on these parameters. This study is one of the first to investigate the ability of primary human osteoblastic cells isolated from trabecular bone to adhere to the biodegradable polymers PLAGA and PLA, and to examine the expression of their key adhesion receptors (integrins) on these substrates.</abstract><cop>Hoboken</cop><pub>Elsevier Ltd</pub><pmid>11853086</pmid><doi>10.1016/S0736-0266(01)00062-6</doi><tpages>9</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Absorbable Implants Blotting, Western Bone Regeneration Cell Adhesion Cell-polymer interaction Cells, Cultured Flow Cytometry Human osteoblast Humans Integrins Integrins - analysis Integrins - biosynthesis Microscopy, Electron, Scanning Osteoblasts - chemistry Osteoblasts - cytology Osteoblasts - metabolism polyesters polylactic acid Polymers Tissue Engineering |
title | Integrin expression by human osteoblasts cultured on degradable polymeric materials applicable for tissue engineered bone |
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