Reconstruction of three-dimensional human skin model composed of dendritic cells, keratinocytes and fibroblasts utilizing a handy scaffold of collagen vitrigel membrane
We previously we attempted to make a three-dimensional human skin model consisting of three different cells, dendritic cells, keratinocytes and fibroblasts (KDF-Skin) to evaluate immunoreactions in human skin; however, this model had various problems; for example (1) the incubation period for the co...
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Veröffentlicht in: | Toxicology in vitro 2009-03, Vol.23 (2), p.333-337 |
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description | We previously we attempted to make a three-dimensional human skin model consisting of three different cells, dendritic cells, keratinocytes and fibroblasts (KDF-Skin) to evaluate immunoreactions in human skin; however, this model had various problems; for example (1) the incubation period for the construction of this model is long (about three weeks); (2) to construct the collagen gel, high amounts of fibroblasts are needed; and (3) the horny layer of keratinocytes in this skin model is thinner than that of keratinocytes in real human skin.
In order to overcome these problems, a new three-dimensional human skin model utilizing a handy scaffold of collagen vitrigel membrane (VG-KDF-Skin) was constructed. As a result, after 14 days incubation, the epidermis layer of normal human keratinocytes was thicker than the keratinocyte layer of KDF-Skin. The incubation period for VG-KDF-Skin construction was 7 days shorter than that of KDF-Skin, and the number of fibroblasts needed to seed VG-KDF-Skin was four times fewer than that of KDF-Skin. After the application of sensitizers such as DNCB, VG-KDF-Skin induced the expression of CD86 and cytokine release.
These results suggest that the new three-dimensional human skin model consisting of dendritic cells, keratinocytes, fibroblasts and collagen vitrigel membrane was more useful for alternative animal testing than the KDF-Skin model. |
doi_str_mv | 10.1016/j.tiv.2008.12.003 |
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In order to overcome these problems, a new three-dimensional human skin model utilizing a handy scaffold of collagen vitrigel membrane (VG-KDF-Skin) was constructed. As a result, after 14 days incubation, the epidermis layer of normal human keratinocytes was thicker than the keratinocyte layer of KDF-Skin. The incubation period for VG-KDF-Skin construction was 7 days shorter than that of KDF-Skin, and the number of fibroblasts needed to seed VG-KDF-Skin was four times fewer than that of KDF-Skin. After the application of sensitizers such as DNCB, VG-KDF-Skin induced the expression of CD86 and cytokine release.
These results suggest that the new three-dimensional human skin model consisting of dendritic cells, keratinocytes, fibroblasts and collagen vitrigel membrane was more useful for alternative animal testing than the KDF-Skin model.</description><identifier>ISSN: 0887-2333</identifier><identifier>EISSN: 1879-3177</identifier><identifier>DOI: 10.1016/j.tiv.2008.12.003</identifier><identifier>PMID: 19121381</identifier><language>eng</language><publisher>England: Elsevier Ltd</publisher><subject>Animal Testing Alternatives ; B7-2 Antigen - metabolism ; CD86 ; Cell Culture Techniques - methods ; Cells, Cultured ; Coculture Techniques - methods ; Collagen Type I - chemistry ; Collagen vitrigel membrane ; Cytokines - metabolism ; Dendritic cells ; Dendritic Cells - cytology ; Dendritic Cells - drug effects ; Dendritic Cells - metabolism ; Fibroblasts - cytology ; Fibroblasts - drug effects ; Fibroblasts - metabolism ; Gels ; Humans ; Irritants - toxicity ; Keratinocytes - cytology ; Keratinocytes - drug effects ; Keratinocytes - metabolism ; Membranes, Artificial ; Models, Biological ; Skin sensitization ; Skin, Artificial ; Three-dimensional human skin model ; Time Factors ; Tissue Scaffolds</subject><ispartof>Toxicology in vitro, 2009-03, Vol.23 (2), p.333-337</ispartof><rights>2008 Elsevier Ltd</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c448t-6b6347565597f6fc907defdcff27398448008c22f858139634624d90875c1e513</citedby><cites>FETCH-LOGICAL-c448t-6b6347565597f6fc907defdcff27398448008c22f858139634624d90875c1e513</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0887233308002889$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3537,27901,27902,65306</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/19121381$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Uchino, T.</creatorcontrib><creatorcontrib>Takezawa, T.</creatorcontrib><creatorcontrib>Ikarashi, Y.</creatorcontrib><title>Reconstruction of three-dimensional human skin model composed of dendritic cells, keratinocytes and fibroblasts utilizing a handy scaffold of collagen vitrigel membrane</title><title>Toxicology in vitro</title><addtitle>Toxicol In Vitro</addtitle><description>We previously we attempted to make a three-dimensional human skin model consisting of three different cells, dendritic cells, keratinocytes and fibroblasts (KDF-Skin) to evaluate immunoreactions in human skin; however, this model had various problems; for example (1) the incubation period for the construction of this model is long (about three weeks); (2) to construct the collagen gel, high amounts of fibroblasts are needed; and (3) the horny layer of keratinocytes in this skin model is thinner than that of keratinocytes in real human skin.
In order to overcome these problems, a new three-dimensional human skin model utilizing a handy scaffold of collagen vitrigel membrane (VG-KDF-Skin) was constructed. As a result, after 14 days incubation, the epidermis layer of normal human keratinocytes was thicker than the keratinocyte layer of KDF-Skin. The incubation period for VG-KDF-Skin construction was 7 days shorter than that of KDF-Skin, and the number of fibroblasts needed to seed VG-KDF-Skin was four times fewer than that of KDF-Skin. After the application of sensitizers such as DNCB, VG-KDF-Skin induced the expression of CD86 and cytokine release.
These results suggest that the new three-dimensional human skin model consisting of dendritic cells, keratinocytes, fibroblasts and collagen vitrigel membrane was more useful for alternative animal testing than the KDF-Skin model.</description><subject>Animal Testing Alternatives</subject><subject>B7-2 Antigen - metabolism</subject><subject>CD86</subject><subject>Cell Culture Techniques - methods</subject><subject>Cells, Cultured</subject><subject>Coculture Techniques - methods</subject><subject>Collagen Type I - chemistry</subject><subject>Collagen vitrigel membrane</subject><subject>Cytokines - metabolism</subject><subject>Dendritic cells</subject><subject>Dendritic Cells - cytology</subject><subject>Dendritic Cells - drug effects</subject><subject>Dendritic Cells - metabolism</subject><subject>Fibroblasts - cytology</subject><subject>Fibroblasts - drug effects</subject><subject>Fibroblasts - metabolism</subject><subject>Gels</subject><subject>Humans</subject><subject>Irritants - toxicity</subject><subject>Keratinocytes - cytology</subject><subject>Keratinocytes - drug effects</subject><subject>Keratinocytes - metabolism</subject><subject>Membranes, Artificial</subject><subject>Models, Biological</subject><subject>Skin sensitization</subject><subject>Skin, Artificial</subject><subject>Three-dimensional human skin model</subject><subject>Time Factors</subject><subject>Tissue Scaffolds</subject><issn>0887-2333</issn><issn>1879-3177</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2009</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kcuOFCEUhonROO3oA7gxrFxZJZe6UHFlJt6SSUyMrgkFh256KGiB6qR9Ih9T2u7EnSsS-M7POedD6CUlLSV0eLtvizu2jBDRUtYSwh-hDRXj1HA6jo_RhggxNoxzfoOe5bwnhPSCkafohk6UUS7oBv3-BjqGXNKqi4sBR4vLLgE0xi0Qcr1SHu_WRQWcH1zASzTgsY7LIWYwZ9xAMMkVp7EG7_Mb_ABJFReiPhXIWAWDrZtTnL3KJeO1OO9-ubDFCu_q4wlnrayN_m-Yjt6rLQR8dCW5bf1qgWVOKsBz9MQqn-HF9bxFPz5--H73ubn_-unL3fv7RnedKM0wD7wb-6Hvp9EOVk9kNGCNtpaNfBKVqdvSjFnRC8qnCg-sMxMRY68p9JTfoteX3EOKP1fIRS4unyerPcQ1S0Z4x6aBVJBeQJ1izgmsPCS3qHSSlMizHrmXVY8865GUyaqn1ry6hq_zAuZfxdVHBd5dAKgjHh0kmbWDoMG4BLpIE91_4v8AUp2j9w</recordid><startdate>20090301</startdate><enddate>20090301</enddate><creator>Uchino, T.</creator><creator>Takezawa, T.</creator><creator>Ikarashi, Y.</creator><general>Elsevier Ltd</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>7T5</scope><scope>7U7</scope><scope>C1K</scope><scope>H94</scope></search><sort><creationdate>20090301</creationdate><title>Reconstruction of three-dimensional human skin model composed of dendritic cells, keratinocytes and fibroblasts utilizing a handy scaffold of collagen vitrigel membrane</title><author>Uchino, T. ; Takezawa, T. ; Ikarashi, Y.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c448t-6b6347565597f6fc907defdcff27398448008c22f858139634624d90875c1e513</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2009</creationdate><topic>Animal Testing Alternatives</topic><topic>B7-2 Antigen - metabolism</topic><topic>CD86</topic><topic>Cell Culture Techniques - methods</topic><topic>Cells, Cultured</topic><topic>Coculture Techniques - methods</topic><topic>Collagen Type I - chemistry</topic><topic>Collagen vitrigel membrane</topic><topic>Cytokines - metabolism</topic><topic>Dendritic cells</topic><topic>Dendritic Cells - cytology</topic><topic>Dendritic Cells - drug effects</topic><topic>Dendritic Cells - metabolism</topic><topic>Fibroblasts - cytology</topic><topic>Fibroblasts - drug effects</topic><topic>Fibroblasts - metabolism</topic><topic>Gels</topic><topic>Humans</topic><topic>Irritants - toxicity</topic><topic>Keratinocytes - cytology</topic><topic>Keratinocytes - drug effects</topic><topic>Keratinocytes - metabolism</topic><topic>Membranes, Artificial</topic><topic>Models, Biological</topic><topic>Skin sensitization</topic><topic>Skin, Artificial</topic><topic>Three-dimensional human skin model</topic><topic>Time Factors</topic><topic>Tissue Scaffolds</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Uchino, T.</creatorcontrib><creatorcontrib>Takezawa, T.</creatorcontrib><creatorcontrib>Ikarashi, Y.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Immunology Abstracts</collection><collection>Toxicology Abstracts</collection><collection>Environmental Sciences and Pollution Management</collection><collection>AIDS and Cancer Research Abstracts</collection><jtitle>Toxicology in vitro</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Uchino, T.</au><au>Takezawa, T.</au><au>Ikarashi, Y.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Reconstruction of three-dimensional human skin model composed of dendritic cells, keratinocytes and fibroblasts utilizing a handy scaffold of collagen vitrigel membrane</atitle><jtitle>Toxicology in vitro</jtitle><addtitle>Toxicol In Vitro</addtitle><date>2009-03-01</date><risdate>2009</risdate><volume>23</volume><issue>2</issue><spage>333</spage><epage>337</epage><pages>333-337</pages><issn>0887-2333</issn><eissn>1879-3177</eissn><abstract>We previously we attempted to make a three-dimensional human skin model consisting of three different cells, dendritic cells, keratinocytes and fibroblasts (KDF-Skin) to evaluate immunoreactions in human skin; however, this model had various problems; for example (1) the incubation period for the construction of this model is long (about three weeks); (2) to construct the collagen gel, high amounts of fibroblasts are needed; and (3) the horny layer of keratinocytes in this skin model is thinner than that of keratinocytes in real human skin.
In order to overcome these problems, a new three-dimensional human skin model utilizing a handy scaffold of collagen vitrigel membrane (VG-KDF-Skin) was constructed. As a result, after 14 days incubation, the epidermis layer of normal human keratinocytes was thicker than the keratinocyte layer of KDF-Skin. The incubation period for VG-KDF-Skin construction was 7 days shorter than that of KDF-Skin, and the number of fibroblasts needed to seed VG-KDF-Skin was four times fewer than that of KDF-Skin. After the application of sensitizers such as DNCB, VG-KDF-Skin induced the expression of CD86 and cytokine release.
These results suggest that the new three-dimensional human skin model consisting of dendritic cells, keratinocytes, fibroblasts and collagen vitrigel membrane was more useful for alternative animal testing than the KDF-Skin model.</abstract><cop>England</cop><pub>Elsevier Ltd</pub><pmid>19121381</pmid><doi>10.1016/j.tiv.2008.12.003</doi><tpages>5</tpages></addata></record> |
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subjects | Animal Testing Alternatives B7-2 Antigen - metabolism CD86 Cell Culture Techniques - methods Cells, Cultured Coculture Techniques - methods Collagen Type I - chemistry Collagen vitrigel membrane Cytokines - metabolism Dendritic cells Dendritic Cells - cytology Dendritic Cells - drug effects Dendritic Cells - metabolism Fibroblasts - cytology Fibroblasts - drug effects Fibroblasts - metabolism Gels Humans Irritants - toxicity Keratinocytes - cytology Keratinocytes - drug effects Keratinocytes - metabolism Membranes, Artificial Models, Biological Skin sensitization Skin, Artificial Three-dimensional human skin model Time Factors Tissue Scaffolds |
title | Reconstruction of three-dimensional human skin model composed of dendritic cells, keratinocytes and fibroblasts utilizing a handy scaffold of collagen vitrigel membrane |
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