A novel method to reconstruct epithelial tissue using high-purity keratinocyte lineage cells induced from human embryonic stem cells
The treatment of oral mucosa defect such as autologous oral mucosa caused by resection of oral mucosa carcinoma is still not ideal in clinical practice. However, Tissue engineering gives us the possibility to solve this problem. As we all know, Human embryonic stem cells (hESCs) have the ability to...
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Veröffentlicht in: | Cell cycle (Georgetown, Tex.) Tex.), 2019-02, Vol.18 (3), p.264-273 |
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creator | Zhao, Houming Shao, Yanxiong Li, Hanqing Zhou, Haiwen |
description | The treatment of oral mucosa defect such as autologous oral mucosa caused by resection of oral mucosa carcinoma is still not ideal in clinical practice. However, Tissue engineering gives us the possibility to solve this problem. As we all know, Human embryonic stem cells (hESCs) have the ability to give rise to various cell types. We can take advantage of the totipotency of human embryonic stem cells to acquire keratinocytes. Directing the epithelial differentiation of hESCs can provide seed cells for the construction of epithelium tissue by tissue engineering. But, how to get high purity keratinocytes by induced stem cells then Applied to tissue engineering mucosa is an important challenge. We described a novel method to directly induce hESCs to differentiate into keratinocytes. Retinoic acid, ascorbic acid, and bone morphogenetic protein induced hESCs to differentiate into cells that highly expressed cytokeratin (CK)14. Our findings suggest that the retinoic acid, ascorbic acid and bone morphogenetic proteins induced hESCs to form high purity keratinocyte cell populations. In addition, we found that the highly pure keratinocyte populations reconstructed artificial tissue resembling epithelial tissue when inoculated in vitro on a biological scaffold. |
doi_str_mv | 10.1080/15384101.2018.1555118 |
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However, Tissue engineering gives us the possibility to solve this problem. As we all know, Human embryonic stem cells (hESCs) have the ability to give rise to various cell types. We can take advantage of the totipotency of human embryonic stem cells to acquire keratinocytes. Directing the epithelial differentiation of hESCs can provide seed cells for the construction of epithelium tissue by tissue engineering. But, how to get high purity keratinocytes by induced stem cells then Applied to tissue engineering mucosa is an important challenge. We described a novel method to directly induce hESCs to differentiate into keratinocytes. Retinoic acid, ascorbic acid, and bone morphogenetic protein induced hESCs to differentiate into cells that highly expressed cytokeratin (CK)14. Our findings suggest that the retinoic acid, ascorbic acid and bone morphogenetic proteins induced hESCs to form high purity keratinocyte cell populations. 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However, Tissue engineering gives us the possibility to solve this problem. As we all know, Human embryonic stem cells (hESCs) have the ability to give rise to various cell types. We can take advantage of the totipotency of human embryonic stem cells to acquire keratinocytes. Directing the epithelial differentiation of hESCs can provide seed cells for the construction of epithelium tissue by tissue engineering. But, how to get high purity keratinocytes by induced stem cells then Applied to tissue engineering mucosa is an important challenge. We described a novel method to directly induce hESCs to differentiate into keratinocytes. Retinoic acid, ascorbic acid, and bone morphogenetic protein induced hESCs to differentiate into cells that highly expressed cytokeratin (CK)14. Our findings suggest that the retinoic acid, ascorbic acid and bone morphogenetic proteins induced hESCs to form high purity keratinocyte cell populations. In addition, we found that the highly pure keratinocyte populations reconstructed artificial tissue resembling epithelial tissue when inoculated in vitro on a biological scaffold.</description><subject>Cell Differentiation</subject><subject>Cell Lineage</subject><subject>Cells, Cultured</subject><subject>Embryonic Stem Cells - cytology</subject><subject>Human embryonic stem cell</subject><subject>Humans</subject><subject>induced differentiation</subject><subject>keratinocyte</subject><subject>Keratinocytes - cytology</subject><subject>Keratinocytes - ultrastructure</subject><subject>Research Paper</subject><subject>tissue engineering</subject><subject>Tissue Engineering - methods</subject><issn>1538-4101</issn><issn>1551-4005</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kcuO1DAQRS0EYoaBTwB5ySaNHceJs0GMRrykkdjA2nI75Y7Bj8aPQdnz4STqnhFsWFVJdepWXV2EXlKyo0SQN5Qz0VFCdy2hYkc555SKR-hy7WjTEcIfbz0TzQZdoGc5fyekFcNIn6ILRnjPOiIu0e9rHOIdOOyhzHHCJeIEOoZcUtUFw9GWGZxVDhebcwVcsw0HPNvD3BxrsmXBPyCpYkPUSwHsbAB1AKzBuYxtmKqGCZsUPZ6rVwGD36clBqtxLuBP3HP0xCiX4cW5XqFvH95_vfnU3H75-Pnm-rbRXS9KMwwaqOFcqNX66mAUwjAYdD_2hk68JZPig-lJR8YeCBgiYJj40IHYQzdwzq7Q25Puse49TBpCScrJY7JepUVGZeW_k2BneYh3smdiVW1XgddngRR_VshFeps3CypArFm2lAvOWzGyFeUnVKeYcwLzcIYSuSUo7xOUW4LynOC69-rvHx-27iNbgXcnwAYTk1e_YnKTLGpxMZmkgrZZsv_f-AMBcq5a</recordid><startdate>20190201</startdate><enddate>20190201</enddate><creator>Zhao, Houming</creator><creator>Shao, Yanxiong</creator><creator>Li, Hanqing</creator><creator>Zhou, Haiwen</creator><general>Taylor & Francis</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>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0003-3883-1275</orcidid></search><sort><creationdate>20190201</creationdate><title>A novel method to reconstruct epithelial tissue using high-purity keratinocyte lineage cells induced from human embryonic stem cells</title><author>Zhao, Houming ; Shao, Yanxiong ; Li, Hanqing ; Zhou, Haiwen</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c468t-77ce1f558a384056988f3e7c696f1d520da57f604096e0ef08e7d574e8be47553</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>Cell Differentiation</topic><topic>Cell Lineage</topic><topic>Cells, Cultured</topic><topic>Embryonic Stem Cells - cytology</topic><topic>Human embryonic stem cell</topic><topic>Humans</topic><topic>induced differentiation</topic><topic>keratinocyte</topic><topic>Keratinocytes - cytology</topic><topic>Keratinocytes - ultrastructure</topic><topic>Research Paper</topic><topic>tissue engineering</topic><topic>Tissue Engineering - methods</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Zhao, Houming</creatorcontrib><creatorcontrib>Shao, Yanxiong</creatorcontrib><creatorcontrib>Li, Hanqing</creatorcontrib><creatorcontrib>Zhou, Haiwen</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><collection>PubMed Central (Full Participant titles)</collection><jtitle>Cell cycle (Georgetown, Tex.)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Zhao, Houming</au><au>Shao, Yanxiong</au><au>Li, Hanqing</au><au>Zhou, Haiwen</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>A novel method to reconstruct epithelial tissue using high-purity keratinocyte lineage cells induced from human embryonic stem cells</atitle><jtitle>Cell cycle (Georgetown, Tex.)</jtitle><addtitle>Cell Cycle</addtitle><date>2019-02-01</date><risdate>2019</risdate><volume>18</volume><issue>3</issue><spage>264</spage><epage>273</epage><pages>264-273</pages><issn>1538-4101</issn><eissn>1551-4005</eissn><abstract>The treatment of oral mucosa defect such as autologous oral mucosa caused by resection of oral mucosa carcinoma is still not ideal in clinical practice. However, Tissue engineering gives us the possibility to solve this problem. As we all know, Human embryonic stem cells (hESCs) have the ability to give rise to various cell types. We can take advantage of the totipotency of human embryonic stem cells to acquire keratinocytes. Directing the epithelial differentiation of hESCs can provide seed cells for the construction of epithelium tissue by tissue engineering. But, how to get high purity keratinocytes by induced stem cells then Applied to tissue engineering mucosa is an important challenge. We described a novel method to directly induce hESCs to differentiate into keratinocytes. Retinoic acid, ascorbic acid, and bone morphogenetic protein induced hESCs to differentiate into cells that highly expressed cytokeratin (CK)14. Our findings suggest that the retinoic acid, ascorbic acid and bone morphogenetic proteins induced hESCs to form high purity keratinocyte cell populations. 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subjects | Cell Differentiation Cell Lineage Cells, Cultured Embryonic Stem Cells - cytology Human embryonic stem cell Humans induced differentiation keratinocyte Keratinocytes - cytology Keratinocytes - ultrastructure Research Paper tissue engineering Tissue Engineering - methods |
title | A novel method to reconstruct epithelial tissue using high-purity keratinocyte lineage cells induced from human embryonic stem cells |
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