Mechanism of initial attachment of corneal epithelial cells to polymeric surfaces
The initial attachment of cultured bovine corneal epithelial cells and stromal fibroblasts to two oxygen-containing synthetic polymers was studied. Cultured epithelial cells and stromal fibroblasts were seeded onto two oxygen-containing surfaces: ‘tissue culture’ polystyrene (TCPS) and a polymer fil...
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Veröffentlicht in: | Biomaterials 1997-12, Vol.18 (23), p.1541-1551 |
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description | The initial attachment of cultured bovine corneal epithelial cells and stromal fibroblasts to two oxygen-containing synthetic polymers was studied. Cultured epithelial cells and stromal fibroblasts were seeded onto two oxygen-containing surfaces: ‘tissue culture’ polystyrene (TCPS) and a polymer film deposited by RF plasma deposition using a methylmethacrylate monomer (MMA/FEP). To establish the mechanism of cell attachment, the effect of the selective removal of the vitronectin and fibronectin from the serum used in the culture medium was tested. The attachment of cultured epithelial cells during the first 90 min of culture was reduced by 40% (TCPS)—80% (MMA/FEP) as a result of removing vitronectin from the medium. Attachment of these cells to TCPS was reduced by 85–95% when the serum was depleted of both fibronectin and vitronectin. However, depletion of fibronectin reduced cell attachment to TCPS by 20%, whilst on MMA/FEP cell attachment was equivalent, or higher, than that for intact serum. The attachment of cultured corneal stromal fibroblasts was similarly dependent on vitronectin but less dependent on fibronectin. Therefore, for the attachment of both cultured epithelial cells and fibroblasts to oxygen-containing surfaces in the presence of serum, there is a high requirement for serum vitronectin but a lesser requirement for fibronectin. The effects of the establishment of corneal epithelial cells in culture and the site of origin of the cells, were determined. Primary isolates of epithelial cells isolated from the limbal, central or peripheral regions of the cornea were less dependent on vitronectin for initial attachment to TCPS than were these cells after several passages in culture. Furthermore, the primary isolates were dramatically less responsive to vitronectin than the cultured cells. These results indicate that the mechanism of attachment of corneal epithelial cells to TCPS varies with the culture experience of the cells. Cells that are culture neophytes can employe endogenous mechanisms for the initial attachment to TCPS, whereas cells established in culture are dependent on exogenous vitronectin in order to attach. |
doi_str_mv | 10.1016/S0142-9612(97)80006-3 |
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Cultured epithelial cells and stromal fibroblasts were seeded onto two oxygen-containing surfaces: ‘tissue culture’ polystyrene (TCPS) and a polymer film deposited by RF plasma deposition using a methylmethacrylate monomer (MMA/FEP). To establish the mechanism of cell attachment, the effect of the selective removal of the vitronectin and fibronectin from the serum used in the culture medium was tested. The attachment of cultured epithelial cells during the first 90 min of culture was reduced by 40% (TCPS)—80% (MMA/FEP) as a result of removing vitronectin from the medium. Attachment of these cells to TCPS was reduced by 85–95% when the serum was depleted of both fibronectin and vitronectin. However, depletion of fibronectin reduced cell attachment to TCPS by 20%, whilst on MMA/FEP cell attachment was equivalent, or higher, than that for intact serum. The attachment of cultured corneal stromal fibroblasts was similarly dependent on vitronectin but less dependent on fibronectin. Therefore, for the attachment of both cultured epithelial cells and fibroblasts to oxygen-containing surfaces in the presence of serum, there is a high requirement for serum vitronectin but a lesser requirement for fibronectin. The effects of the establishment of corneal epithelial cells in culture and the site of origin of the cells, were determined. Primary isolates of epithelial cells isolated from the limbal, central or peripheral regions of the cornea were less dependent on vitronectin for initial attachment to TCPS than were these cells after several passages in culture. Furthermore, the primary isolates were dramatically less responsive to vitronectin than the cultured cells. These results indicate that the mechanism of attachment of corneal epithelial cells to TCPS varies with the culture experience of the cells. Cells that are culture neophytes can employe endogenous mechanisms for the initial attachment to TCPS, whereas cells established in culture are dependent on exogenous vitronectin in order to attach.</description><identifier>ISSN: 0142-9612</identifier><identifier>EISSN: 1878-5905</identifier><identifier>DOI: 10.1016/S0142-9612(97)80006-3</identifier><identifier>PMID: 9430337</identifier><language>eng</language><publisher>Oxford: Elsevier Ltd</publisher><subject>Adhesion ; Animals ; Biological and medical sciences ; Biomaterials ; Cattle ; cell adhesion ; Cell Adhesion - drug effects ; Cells, Cultured ; Cornea - chemistry ; Cornea - metabolism ; corneal epithelial cells ; Deposition ; Epithelial Cells - chemistry ; Epithelial Cells - metabolism ; fibronectin ; Fibronectins - analysis ; Fibronectins - pharmacology ; Immunoenzyme Techniques ; Medical sciences ; Plasma applications ; Plastic films ; Polymers - chemistry ; Polymers - metabolism ; Polymethyl Methacrylate - chemistry ; Polymethyl methacrylates ; Polystyrenes ; Polystyrenes - chemistry ; Polystyrenes - metabolism ; Radiotherapy. Instrumental treatment. Physiotherapy. Reeducation. Rehabilitation, orthophony, crenotherapy. Diet therapy and various other treatments (general aspects) ; Stromal Cells - chemistry ; Stromal Cells - metabolism ; Technology. Biomaterials. Equipments. Material. Instrumentation ; Tissue culture ; Vitronectin ; Vitronectin - analysis ; Vitronectin - pharmacology</subject><ispartof>Biomaterials, 1997-12, Vol.18 (23), p.1541-1551</ispartof><rights>1997</rights><rights>1998 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c451t-af53965cc78804d9ab09dd8fcd41f668d273a66baab36771aef847d6c555d5fb3</citedby><cites>FETCH-LOGICAL-c451t-af53965cc78804d9ab09dd8fcd41f668d273a66baab36771aef847d6c555d5fb3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/S0142-9612(97)80006-3$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,778,782,3539,27907,27908,45978</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=2085538$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/9430337$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Steele, John G.</creatorcontrib><creatorcontrib>Johnson, Graham</creatorcontrib><creatorcontrib>Griesser, Hans J.</creatorcontrib><creatorcontrib>Underwood, P.Anne</creatorcontrib><title>Mechanism of initial attachment of corneal epithelial cells to polymeric surfaces</title><title>Biomaterials</title><addtitle>Biomaterials</addtitle><description>The initial attachment of cultured bovine corneal epithelial cells and stromal fibroblasts to two oxygen-containing synthetic polymers was studied. Cultured epithelial cells and stromal fibroblasts were seeded onto two oxygen-containing surfaces: ‘tissue culture’ polystyrene (TCPS) and a polymer film deposited by RF plasma deposition using a methylmethacrylate monomer (MMA/FEP). To establish the mechanism of cell attachment, the effect of the selective removal of the vitronectin and fibronectin from the serum used in the culture medium was tested. The attachment of cultured epithelial cells during the first 90 min of culture was reduced by 40% (TCPS)—80% (MMA/FEP) as a result of removing vitronectin from the medium. Attachment of these cells to TCPS was reduced by 85–95% when the serum was depleted of both fibronectin and vitronectin. However, depletion of fibronectin reduced cell attachment to TCPS by 20%, whilst on MMA/FEP cell attachment was equivalent, or higher, than that for intact serum. The attachment of cultured corneal stromal fibroblasts was similarly dependent on vitronectin but less dependent on fibronectin. Therefore, for the attachment of both cultured epithelial cells and fibroblasts to oxygen-containing surfaces in the presence of serum, there is a high requirement for serum vitronectin but a lesser requirement for fibronectin. The effects of the establishment of corneal epithelial cells in culture and the site of origin of the cells, were determined. Primary isolates of epithelial cells isolated from the limbal, central or peripheral regions of the cornea were less dependent on vitronectin for initial attachment to TCPS than were these cells after several passages in culture. Furthermore, the primary isolates were dramatically less responsive to vitronectin than the cultured cells. These results indicate that the mechanism of attachment of corneal epithelial cells to TCPS varies with the culture experience of the cells. Cells that are culture neophytes can employe endogenous mechanisms for the initial attachment to TCPS, whereas cells established in culture are dependent on exogenous vitronectin in order to attach.</description><subject>Adhesion</subject><subject>Animals</subject><subject>Biological and medical sciences</subject><subject>Biomaterials</subject><subject>Cattle</subject><subject>cell adhesion</subject><subject>Cell Adhesion - drug effects</subject><subject>Cells, Cultured</subject><subject>Cornea - chemistry</subject><subject>Cornea - metabolism</subject><subject>corneal epithelial cells</subject><subject>Deposition</subject><subject>Epithelial Cells - chemistry</subject><subject>Epithelial Cells - metabolism</subject><subject>fibronectin</subject><subject>Fibronectins - analysis</subject><subject>Fibronectins - pharmacology</subject><subject>Immunoenzyme Techniques</subject><subject>Medical sciences</subject><subject>Plasma applications</subject><subject>Plastic films</subject><subject>Polymers - chemistry</subject><subject>Polymers - metabolism</subject><subject>Polymethyl Methacrylate - chemistry</subject><subject>Polymethyl methacrylates</subject><subject>Polystyrenes</subject><subject>Polystyrenes - chemistry</subject><subject>Polystyrenes - metabolism</subject><subject>Radiotherapy. Instrumental treatment. Physiotherapy. Reeducation. Rehabilitation, orthophony, crenotherapy. Diet therapy and various other treatments (general aspects)</subject><subject>Stromal Cells - chemistry</subject><subject>Stromal Cells - metabolism</subject><subject>Technology. Biomaterials. Equipments. Material. Instrumentation</subject><subject>Tissue culture</subject><subject>Vitronectin</subject><subject>Vitronectin - analysis</subject><subject>Vitronectin - pharmacology</subject><issn>0142-9612</issn><issn>1878-5905</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1997</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkclqHDEQhoWJcSZOHsHQhxCcQ9tSq7WdTDDOAg7BODmLaqnEyPQyljQBv727PcNc51RU_V8t1E_IBaNXjDJ5_UhZ29RGsubSqK-aUiprfkJWTCtdC0PFO7I6IO_Jh5yf6JzTtjkjZ6bllHO1Ig-_0a1hjHmoplDFMZYIfQWlgFsPOJal6qY04lzFTSxr7BfAYd_nqkzVZupfBkzRVXmbAjjMH8lpgD7jp308J_--3_29_Vnf__nx6_bbfe1awUoNQXAjhXNKa9p6Ax013uvgfMuClNo3ioOUHUDHpVIMMOhWeemEEF6Ejp-TL7u5mzQ9bzEXO8S83AUjTttslRFUS9UcBRsptOSaHQcZp4ZyNYNiB7o05Zww2E2KA6QXy6hdzLFv5tjl89Yo-2aO5XPfxX7BthvQH7r2bsz6570O2UEfEowu5gPWUC0E1zN2s8Nwfu__iMlmF3F06GNCV6yf4pFDXgHQdKuM</recordid><startdate>19971201</startdate><enddate>19971201</enddate><creator>Steele, John G.</creator><creator>Johnson, Graham</creator><creator>Griesser, Hans J.</creator><creator>Underwood, P.Anne</creator><general>Elsevier Ltd</general><general>Elsevier Science</general><scope>IQODW</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>7SR</scope><scope>8FD</scope><scope>JG9</scope><scope>7X8</scope></search><sort><creationdate>19971201</creationdate><title>Mechanism of initial attachment of corneal epithelial cells to polymeric surfaces</title><author>Steele, John G. ; Johnson, Graham ; Griesser, Hans J. ; Underwood, P.Anne</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c451t-af53965cc78804d9ab09dd8fcd41f668d273a66baab36771aef847d6c555d5fb3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1997</creationdate><topic>Adhesion</topic><topic>Animals</topic><topic>Biological and medical sciences</topic><topic>Biomaterials</topic><topic>Cattle</topic><topic>cell adhesion</topic><topic>Cell Adhesion - drug effects</topic><topic>Cells, Cultured</topic><topic>Cornea - chemistry</topic><topic>Cornea - metabolism</topic><topic>corneal epithelial cells</topic><topic>Deposition</topic><topic>Epithelial Cells - chemistry</topic><topic>Epithelial Cells - metabolism</topic><topic>fibronectin</topic><topic>Fibronectins - analysis</topic><topic>Fibronectins - pharmacology</topic><topic>Immunoenzyme Techniques</topic><topic>Medical sciences</topic><topic>Plasma applications</topic><topic>Plastic films</topic><topic>Polymers - chemistry</topic><topic>Polymers - metabolism</topic><topic>Polymethyl Methacrylate - chemistry</topic><topic>Polymethyl methacrylates</topic><topic>Polystyrenes</topic><topic>Polystyrenes - chemistry</topic><topic>Polystyrenes - metabolism</topic><topic>Radiotherapy. Instrumental treatment. Physiotherapy. Reeducation. Rehabilitation, orthophony, crenotherapy. Diet therapy and various other treatments (general aspects)</topic><topic>Stromal Cells - chemistry</topic><topic>Stromal Cells - metabolism</topic><topic>Technology. Biomaterials. Equipments. Material. Instrumentation</topic><topic>Tissue culture</topic><topic>Vitronectin</topic><topic>Vitronectin - analysis</topic><topic>Vitronectin - pharmacology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Steele, John G.</creatorcontrib><creatorcontrib>Johnson, Graham</creatorcontrib><creatorcontrib>Griesser, Hans J.</creatorcontrib><creatorcontrib>Underwood, P.Anne</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Engineered Materials Abstracts</collection><collection>Technology Research Database</collection><collection>Materials Research Database</collection><collection>MEDLINE - Academic</collection><jtitle>Biomaterials</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Steele, John G.</au><au>Johnson, Graham</au><au>Griesser, Hans J.</au><au>Underwood, P.Anne</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Mechanism of initial attachment of corneal epithelial cells to polymeric surfaces</atitle><jtitle>Biomaterials</jtitle><addtitle>Biomaterials</addtitle><date>1997-12-01</date><risdate>1997</risdate><volume>18</volume><issue>23</issue><spage>1541</spage><epage>1551</epage><pages>1541-1551</pages><issn>0142-9612</issn><eissn>1878-5905</eissn><abstract>The initial attachment of cultured bovine corneal epithelial cells and stromal fibroblasts to two oxygen-containing synthetic polymers was studied. Cultured epithelial cells and stromal fibroblasts were seeded onto two oxygen-containing surfaces: ‘tissue culture’ polystyrene (TCPS) and a polymer film deposited by RF plasma deposition using a methylmethacrylate monomer (MMA/FEP). To establish the mechanism of cell attachment, the effect of the selective removal of the vitronectin and fibronectin from the serum used in the culture medium was tested. The attachment of cultured epithelial cells during the first 90 min of culture was reduced by 40% (TCPS)—80% (MMA/FEP) as a result of removing vitronectin from the medium. Attachment of these cells to TCPS was reduced by 85–95% when the serum was depleted of both fibronectin and vitronectin. However, depletion of fibronectin reduced cell attachment to TCPS by 20%, whilst on MMA/FEP cell attachment was equivalent, or higher, than that for intact serum. The attachment of cultured corneal stromal fibroblasts was similarly dependent on vitronectin but less dependent on fibronectin. Therefore, for the attachment of both cultured epithelial cells and fibroblasts to oxygen-containing surfaces in the presence of serum, there is a high requirement for serum vitronectin but a lesser requirement for fibronectin. The effects of the establishment of corneal epithelial cells in culture and the site of origin of the cells, were determined. Primary isolates of epithelial cells isolated from the limbal, central or peripheral regions of the cornea were less dependent on vitronectin for initial attachment to TCPS than were these cells after several passages in culture. Furthermore, the primary isolates were dramatically less responsive to vitronectin than the cultured cells. These results indicate that the mechanism of attachment of corneal epithelial cells to TCPS varies with the culture experience of the cells. Cells that are culture neophytes can employe endogenous mechanisms for the initial attachment to TCPS, whereas cells established in culture are dependent on exogenous vitronectin in order to attach.</abstract><cop>Oxford</cop><pub>Elsevier Ltd</pub><pmid>9430337</pmid><doi>10.1016/S0142-9612(97)80006-3</doi><tpages>11</tpages></addata></record> |
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subjects | Adhesion Animals Biological and medical sciences Biomaterials Cattle cell adhesion Cell Adhesion - drug effects Cells, Cultured Cornea - chemistry Cornea - metabolism corneal epithelial cells Deposition Epithelial Cells - chemistry Epithelial Cells - metabolism fibronectin Fibronectins - analysis Fibronectins - pharmacology Immunoenzyme Techniques Medical sciences Plasma applications Plastic films Polymers - chemistry Polymers - metabolism Polymethyl Methacrylate - chemistry Polymethyl methacrylates Polystyrenes Polystyrenes - chemistry Polystyrenes - metabolism Radiotherapy. Instrumental treatment. Physiotherapy. Reeducation. Rehabilitation, orthophony, crenotherapy. Diet therapy and various other treatments (general aspects) Stromal Cells - chemistry Stromal Cells - metabolism Technology. Biomaterials. Equipments. Material. Instrumentation Tissue culture Vitronectin Vitronectin - analysis Vitronectin - pharmacology |
title | Mechanism of initial attachment of corneal epithelial cells to polymeric surfaces |
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