In vitro cytokeratin expression profiling of human oral mucosa substitutes developed by tissue engineering
In this work we performed a study of cytokeratin (CK) expression profiling on human artificial oral mucosa developed in vitro by tissue engineering at different stages of maturation (from immature to well-developed stages) at the protein and mRNA levels. Human artificial oral mucosa was generated in...
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Veröffentlicht in: | International journal of artificial organs 2009-10, Vol.32 (10), p.711-719 |
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container_title | International journal of artificial organs |
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creator | Garzon, Ingrid Serrato, Deyanira Roda, Olga Del Carmen Sanchez-Quevedo, Maria Gonzales-Jaranay, Maximino Moreu, Gerardo Nieto-Aguilar, Renato Alaminos, Miguel Campos, Antonio |
description | In this work we performed a study of cytokeratin (CK) expression profiling on human artificial oral mucosa developed in vitro by tissue engineering at different stages of maturation (from immature to well-developed stages) at the protein and mRNA levels. Human artificial oral mucosa was generated in the laboratory using fibrin-agarose biomaterials. As controls, we used human native normal oral mucosa and embryonic oral tissues. Our results demonstrated that human embryonic oral tissues tended to express CK8 and CK19. In contrast, monolayered bioengineered oral mucosa did not show any CK expression by immunohistochemistry, whereas bilayered and multilayered artificial oral mucosa showed several markers of stratified epithelia, but did not express CK10. These results suggest that the CK expression pattern is strongly dependent on the maturation state of the artificial tissues and that the CK expression profile of our model of artificial oral mucosa was partially similar to that of the non-keratinized human adult oral mucosa. However, the expression of CK8 by the artificial oral mucosa suggests that these samples correspond to an early stage of development while kept in vitro. |
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Human artificial oral mucosa was generated in the laboratory using fibrin-agarose biomaterials. As controls, we used human native normal oral mucosa and embryonic oral tissues. Our results demonstrated that human embryonic oral tissues tended to express CK8 and CK19. In contrast, monolayered bioengineered oral mucosa did not show any CK expression by immunohistochemistry, whereas bilayered and multilayered artificial oral mucosa showed several markers of stratified epithelia, but did not express CK10. These results suggest that the CK expression pattern is strongly dependent on the maturation state of the artificial tissues and that the CK expression profile of our model of artificial oral mucosa was partially similar to that of the non-keratinized human adult oral mucosa. However, the expression of CK8 by the artificial oral mucosa suggests that these samples correspond to an early stage of development while kept in vitro.</description><identifier>ISSN: 0391-3988</identifier><identifier>EISSN: 1724-6040</identifier><identifier>DOI: 10.1177/039139880903201002</identifier><identifier>PMID: 19943232</identifier><language>eng</language><publisher>United States</publisher><subject>Bioartificial Organs ; Cell Differentiation ; Cells, Cultured ; Fibrin - chemistry ; Gene Expression Profiling - methods ; Gene Expression Regulation, Developmental ; Humans ; Immunohistochemistry ; Keratin-10 - genetics ; Keratin-19 - genetics ; Keratin-8 - genetics ; Keratins - genetics ; Keratins - metabolism ; Mouth Mucosa - cytology ; Mouth Mucosa - embryology ; Mouth Mucosa - metabolism ; Oligonucleotide Array Sequence Analysis ; RNA, Messenger - metabolism ; Sepharose - chemistry ; Tissue Engineering - methods ; Tissue Scaffolds</subject><ispartof>International journal of artificial organs, 2009-10, Vol.32 (10), p.711-719</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c368t-5c2832f0574cb39db3a1ef933dd4607ab68ca7d35b2ea9796d10e0d8fd3277e73</citedby><cites>FETCH-LOGICAL-c368t-5c2832f0574cb39db3a1ef933dd4607ab68ca7d35b2ea9796d10e0d8fd3277e73</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/19943232$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Garzon, Ingrid</creatorcontrib><creatorcontrib>Serrato, Deyanira</creatorcontrib><creatorcontrib>Roda, Olga</creatorcontrib><creatorcontrib>Del Carmen Sanchez-Quevedo, Maria</creatorcontrib><creatorcontrib>Gonzales-Jaranay, Maximino</creatorcontrib><creatorcontrib>Moreu, Gerardo</creatorcontrib><creatorcontrib>Nieto-Aguilar, Renato</creatorcontrib><creatorcontrib>Alaminos, Miguel</creatorcontrib><creatorcontrib>Campos, Antonio</creatorcontrib><title>In vitro cytokeratin expression profiling of human oral mucosa substitutes developed by tissue engineering</title><title>International journal of artificial organs</title><addtitle>Int J Artif Organs</addtitle><description>In this work we performed a study of cytokeratin (CK) expression profiling on human artificial oral mucosa developed in vitro by tissue engineering at different stages of maturation (from immature to well-developed stages) at the protein and mRNA levels. Human artificial oral mucosa was generated in the laboratory using fibrin-agarose biomaterials. As controls, we used human native normal oral mucosa and embryonic oral tissues. Our results demonstrated that human embryonic oral tissues tended to express CK8 and CK19. In contrast, monolayered bioengineered oral mucosa did not show any CK expression by immunohistochemistry, whereas bilayered and multilayered artificial oral mucosa showed several markers of stratified epithelia, but did not express CK10. These results suggest that the CK expression pattern is strongly dependent on the maturation state of the artificial tissues and that the CK expression profile of our model of artificial oral mucosa was partially similar to that of the non-keratinized human adult oral mucosa. However, the expression of CK8 by the artificial oral mucosa suggests that these samples correspond to an early stage of development while kept in vitro.</description><subject>Bioartificial Organs</subject><subject>Cell Differentiation</subject><subject>Cells, Cultured</subject><subject>Fibrin - chemistry</subject><subject>Gene Expression Profiling - methods</subject><subject>Gene Expression Regulation, Developmental</subject><subject>Humans</subject><subject>Immunohistochemistry</subject><subject>Keratin-10 - genetics</subject><subject>Keratin-19 - genetics</subject><subject>Keratin-8 - genetics</subject><subject>Keratins - genetics</subject><subject>Keratins - metabolism</subject><subject>Mouth Mucosa - cytology</subject><subject>Mouth Mucosa - embryology</subject><subject>Mouth Mucosa - metabolism</subject><subject>Oligonucleotide Array Sequence Analysis</subject><subject>RNA, Messenger - metabolism</subject><subject>Sepharose - chemistry</subject><subject>Tissue Engineering - methods</subject><subject>Tissue Scaffolds</subject><issn>0391-3988</issn><issn>1724-6040</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2009</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNplkDtPwzAURi0EoqXwBxiQN6aAH4kdj6jiJVVigTly7JviksTBdir672nUSgxMdznf0dVB6JqSO0qlvCdcUa7KkijCGaGEsBM0p5LlmSA5OUXzCcgmYoYuYtwQQkWeF-doRpXKOeNsjjavPd66FDw2u-S_IOjkegw_Q4AYne_xEHzjWtevsW_w59jpHvugW9yNxkeN41jH5NKYIGILW2j9ABbXO5xcjCNg6NeuBwh7wSU6a3Qb4ep4F-jj6fF9-ZKt3p5flw-rzHBRpqwwrOSsIYXMTc2Vrbmm0CjOrc0FkboWpdHS8qJmoJVUwlICxJaN5UxKkHyBbg_e_evfI8RUdS4aaFvdgx9jJXlOCyXERLIDaYKPMUBTDcF1OuwqSqopcfU_8X50c9SPdQf2b3Jsyn8BqVt46A</recordid><startdate>20091001</startdate><enddate>20091001</enddate><creator>Garzon, Ingrid</creator><creator>Serrato, Deyanira</creator><creator>Roda, Olga</creator><creator>Del Carmen Sanchez-Quevedo, Maria</creator><creator>Gonzales-Jaranay, Maximino</creator><creator>Moreu, Gerardo</creator><creator>Nieto-Aguilar, Renato</creator><creator>Alaminos, Miguel</creator><creator>Campos, Antonio</creator><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>7X8</scope></search><sort><creationdate>20091001</creationdate><title>In vitro cytokeratin expression profiling of human oral mucosa substitutes developed by tissue engineering</title><author>Garzon, Ingrid ; Serrato, Deyanira ; Roda, Olga ; Del Carmen Sanchez-Quevedo, Maria ; Gonzales-Jaranay, Maximino ; Moreu, Gerardo ; Nieto-Aguilar, Renato ; Alaminos, Miguel ; Campos, Antonio</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c368t-5c2832f0574cb39db3a1ef933dd4607ab68ca7d35b2ea9796d10e0d8fd3277e73</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2009</creationdate><topic>Bioartificial Organs</topic><topic>Cell Differentiation</topic><topic>Cells, Cultured</topic><topic>Fibrin - chemistry</topic><topic>Gene Expression Profiling - methods</topic><topic>Gene Expression Regulation, Developmental</topic><topic>Humans</topic><topic>Immunohistochemistry</topic><topic>Keratin-10 - genetics</topic><topic>Keratin-19 - genetics</topic><topic>Keratin-8 - genetics</topic><topic>Keratins - genetics</topic><topic>Keratins - metabolism</topic><topic>Mouth Mucosa - cytology</topic><topic>Mouth Mucosa - embryology</topic><topic>Mouth Mucosa - metabolism</topic><topic>Oligonucleotide Array Sequence Analysis</topic><topic>RNA, Messenger - metabolism</topic><topic>Sepharose - chemistry</topic><topic>Tissue Engineering - methods</topic><topic>Tissue Scaffolds</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Garzon, Ingrid</creatorcontrib><creatorcontrib>Serrato, Deyanira</creatorcontrib><creatorcontrib>Roda, Olga</creatorcontrib><creatorcontrib>Del Carmen Sanchez-Quevedo, Maria</creatorcontrib><creatorcontrib>Gonzales-Jaranay, Maximino</creatorcontrib><creatorcontrib>Moreu, Gerardo</creatorcontrib><creatorcontrib>Nieto-Aguilar, Renato</creatorcontrib><creatorcontrib>Alaminos, Miguel</creatorcontrib><creatorcontrib>Campos, Antonio</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>International journal of artificial organs</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Garzon, Ingrid</au><au>Serrato, Deyanira</au><au>Roda, Olga</au><au>Del Carmen Sanchez-Quevedo, Maria</au><au>Gonzales-Jaranay, Maximino</au><au>Moreu, Gerardo</au><au>Nieto-Aguilar, Renato</au><au>Alaminos, Miguel</au><au>Campos, Antonio</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>In vitro cytokeratin expression profiling of human oral mucosa substitutes developed by tissue engineering</atitle><jtitle>International journal of artificial organs</jtitle><addtitle>Int J Artif Organs</addtitle><date>2009-10-01</date><risdate>2009</risdate><volume>32</volume><issue>10</issue><spage>711</spage><epage>719</epage><pages>711-719</pages><issn>0391-3988</issn><eissn>1724-6040</eissn><abstract>In this work we performed a study of cytokeratin (CK) expression profiling on human artificial oral mucosa developed in vitro by tissue engineering at different stages of maturation (from immature to well-developed stages) at the protein and mRNA levels. Human artificial oral mucosa was generated in the laboratory using fibrin-agarose biomaterials. As controls, we used human native normal oral mucosa and embryonic oral tissues. Our results demonstrated that human embryonic oral tissues tended to express CK8 and CK19. In contrast, monolayered bioengineered oral mucosa did not show any CK expression by immunohistochemistry, whereas bilayered and multilayered artificial oral mucosa showed several markers of stratified epithelia, but did not express CK10. These results suggest that the CK expression pattern is strongly dependent on the maturation state of the artificial tissues and that the CK expression profile of our model of artificial oral mucosa was partially similar to that of the non-keratinized human adult oral mucosa. However, the expression of CK8 by the artificial oral mucosa suggests that these samples correspond to an early stage of development while kept in vitro.</abstract><cop>United States</cop><pmid>19943232</pmid><doi>10.1177/039139880903201002</doi><tpages>9</tpages></addata></record> |
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subjects | Bioartificial Organs Cell Differentiation Cells, Cultured Fibrin - chemistry Gene Expression Profiling - methods Gene Expression Regulation, Developmental Humans Immunohistochemistry Keratin-10 - genetics Keratin-19 - genetics Keratin-8 - genetics Keratins - genetics Keratins - metabolism Mouth Mucosa - cytology Mouth Mucosa - embryology Mouth Mucosa - metabolism Oligonucleotide Array Sequence Analysis RNA, Messenger - metabolism Sepharose - chemistry Tissue Engineering - methods Tissue Scaffolds |
title | In vitro cytokeratin expression profiling of human oral mucosa substitutes developed by tissue engineering |
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