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An RNAi Screen Reveals an Essential Role for HIPK4 in Human Skin Epithelial Differentiation from iPSCs
Molecular mechanisms responsible for the development of human skin epithelial cells are incompletely understood. As a consequence, the efficiency to establish a pure skin epithelial cell population from human induced pluripotent stem cells (hiPSCs) remains poor. Using an approach including RNAi and...
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Published in: | Stem cell reports 2017-10, Vol.9 (4), p.1234-1245 |
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description | Molecular mechanisms responsible for the development of human skin epithelial cells are incompletely understood. As a consequence, the efficiency to establish a pure skin epithelial cell population from human induced pluripotent stem cells (hiPSCs) remains poor. Using an approach including RNAi and high-throughput imaging of early epithelial cells, we identified candidate kinases involved in their differentiation from hiPSCs. Among these, we found HIPK4 to be an important inhibitor of this process. Indeed, its silencing increased the amount of generated skin epithelial precursors at an early time point, increased the amount of generated keratinocytes at a later time point, and improved growth and differentiation of organotypic cultures, allowing for the formation of a denser basal layer and stratification with the expression of several keratins. Our data bring substantial input regarding regulation of human skin epithelial differentiation and for improving differentiation protocols from pluripotent stem cells.
•High-throughput RNAi screen setup during human skin epithelial differentiation•Identification of HIPK4 as a crucial blocker of human skin epithelial differentiation•Improvement of human organotypic epithelial cultures after HIPK4 silencing
In this article, Larribère and colleagues establish a high-throughput RNAi screen on induced pluripotent stem cell-derived epithelial cells. This screen led to the identification of HIPK4 as a crucial blocker of human skin epithelial differentiation. Indeed, HIPK4 silencing increased the amount of early generated skin epithelial precursors, increased the amount of generated keratinocytes, and improved the differentiation of organotypic cultures. |
doi_str_mv | 10.1016/j.stemcr.2017.08.023 |
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•High-throughput RNAi screen setup during human skin epithelial differentiation•Identification of HIPK4 as a crucial blocker of human skin epithelial differentiation•Improvement of human organotypic epithelial cultures after HIPK4 silencing
In this article, Larribère and colleagues establish a high-throughput RNAi screen on induced pluripotent stem cell-derived epithelial cells. This screen led to the identification of HIPK4 as a crucial blocker of human skin epithelial differentiation. Indeed, HIPK4 silencing increased the amount of early generated skin epithelial precursors, increased the amount of generated keratinocytes, and improved the differentiation of organotypic cultures.</description><identifier>ISSN: 2213-6711</identifier><identifier>EISSN: 2213-6711</identifier><identifier>DOI: 10.1016/j.stemcr.2017.08.023</identifier><identifier>PMID: 28966120</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Cell Differentiation - genetics ; Cell Line ; Cells, Cultured ; development ; differentiation ; Enzyme Activation ; Epithelial Cells - cytology ; Epithelial Cells - metabolism ; epithelium ; Gene Silencing ; High-Throughput Screening Assays ; HIPK4 ; Humans ; Induced Pluripotent Stem Cells - cytology ; Induced Pluripotent Stem Cells - metabolism ; iPSC ; keratinocytes ; Keratinocytes - cytology ; Keratinocytes - metabolism ; Organ Culture Techniques ; organotypic culture ; Protein-Serine-Threonine Kinases - genetics ; RNA Interference ; RNAi screen ; skin ; stem cell</subject><ispartof>Stem cell reports, 2017-10, Vol.9 (4), p.1234-1245</ispartof><rights>2017 The Author(s)</rights><rights>Copyright © 2017 The Author(s). Published by Elsevier Inc. All rights reserved.</rights><rights>2017 The Author(s) 2017</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c529t-3ee31748f2301603d0fbc8868243625d8531dabee1c5697dca0dd0be80b279693</citedby><cites>FETCH-LOGICAL-c529t-3ee31748f2301603d0fbc8868243625d8531dabee1c5697dca0dd0be80b279693</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC5639458/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S2213671117303806$$EHTML$$P50$$Gelsevier$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,881,3535,27903,27904,45759,53769,53771</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/28966120$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Larribère, Lionel</creatorcontrib><creatorcontrib>Galach, Marta</creatorcontrib><creatorcontrib>Novak, Daniel</creatorcontrib><creatorcontrib>Arévalo, Karla</creatorcontrib><creatorcontrib>Volz, Hans Christian</creatorcontrib><creatorcontrib>Stark, Hans-Jürgen</creatorcontrib><creatorcontrib>Boukamp, Petra</creatorcontrib><creatorcontrib>Boutros, Michael</creatorcontrib><creatorcontrib>Utikal, Jochen</creatorcontrib><title>An RNAi Screen Reveals an Essential Role for HIPK4 in Human Skin Epithelial Differentiation from iPSCs</title><title>Stem cell reports</title><addtitle>Stem Cell Reports</addtitle><description>Molecular mechanisms responsible for the development of human skin epithelial cells are incompletely understood. As a consequence, the efficiency to establish a pure skin epithelial cell population from human induced pluripotent stem cells (hiPSCs) remains poor. Using an approach including RNAi and high-throughput imaging of early epithelial cells, we identified candidate kinases involved in their differentiation from hiPSCs. Among these, we found HIPK4 to be an important inhibitor of this process. Indeed, its silencing increased the amount of generated skin epithelial precursors at an early time point, increased the amount of generated keratinocytes at a later time point, and improved growth and differentiation of organotypic cultures, allowing for the formation of a denser basal layer and stratification with the expression of several keratins. Our data bring substantial input regarding regulation of human skin epithelial differentiation and for improving differentiation protocols from pluripotent stem cells.
•High-throughput RNAi screen setup during human skin epithelial differentiation•Identification of HIPK4 as a crucial blocker of human skin epithelial differentiation•Improvement of human organotypic epithelial cultures after HIPK4 silencing
In this article, Larribère and colleagues establish a high-throughput RNAi screen on induced pluripotent stem cell-derived epithelial cells. This screen led to the identification of HIPK4 as a crucial blocker of human skin epithelial differentiation. Indeed, HIPK4 silencing increased the amount of early generated skin epithelial precursors, increased the amount of generated keratinocytes, and improved the differentiation of organotypic cultures.</description><subject>Cell Differentiation - genetics</subject><subject>Cell Line</subject><subject>Cells, Cultured</subject><subject>development</subject><subject>differentiation</subject><subject>Enzyme Activation</subject><subject>Epithelial Cells - cytology</subject><subject>Epithelial Cells - metabolism</subject><subject>epithelium</subject><subject>Gene Silencing</subject><subject>High-Throughput Screening Assays</subject><subject>HIPK4</subject><subject>Humans</subject><subject>Induced Pluripotent Stem Cells - cytology</subject><subject>Induced Pluripotent Stem Cells - metabolism</subject><subject>iPSC</subject><subject>keratinocytes</subject><subject>Keratinocytes - cytology</subject><subject>Keratinocytes - metabolism</subject><subject>Organ Culture Techniques</subject><subject>organotypic culture</subject><subject>Protein-Serine-Threonine Kinases - genetics</subject><subject>RNA Interference</subject><subject>RNAi screen</subject><subject>skin</subject><subject>stem cell</subject><issn>2213-6711</issn><issn>2213-6711</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><sourceid>DOA</sourceid><recordid>eNp9kU1vEzEQhlcIRKvSf4CQj1wS_LVe-4IUhZREVKVq4Gx57XHrsLsO9iYS_x6nKf244ItH43ee8cxbVe8JnhJMxKfNNI_Q2zSlmDRTLKeYslfVKaWETURDyOtn8Ul1nvMGl6MUoZy8rU6oVEIQik8rPxvQzdUsoLVNACWGPZguIzOgRc4wjMF06CZ2gHxMaLm6_sZRGNBy1xfF-lcJF9sw3kF30H0J3kO6LxpDHJBPsUfhej3P76o3vmDh_OE-q35eLH7Ml5PL719X89nlxNZUjRMGwEjDpaesTImZw761UgpJORO0drJmxJkWgNhaqMZZg53DLUjc0kYJxc6q1ZHrotnobQq9SX90NEHfJ2K61SaNwXagheSOkLb13iuuACuieNNYLAUvS2ttYX0-sra7tgdny1zJdC-gL1-GcKdv417XgileywL4-ABI8fcO8qj7kC10nRkg7rIuDeuGKCVZkfKj1KaYcwL_2IZgfXBcb_TRcX1wXGOpi-Ol7MPzLz4W_fP3aQYoS98HSDrbAIMFFxLYsWwl_L_DX9RcvTg</recordid><startdate>20171010</startdate><enddate>20171010</enddate><creator>Larribère, Lionel</creator><creator>Galach, Marta</creator><creator>Novak, Daniel</creator><creator>Arévalo, Karla</creator><creator>Volz, Hans Christian</creator><creator>Stark, Hans-Jürgen</creator><creator>Boukamp, Petra</creator><creator>Boutros, Michael</creator><creator>Utikal, Jochen</creator><general>Elsevier Inc</general><general>Elsevier</general><scope>6I.</scope><scope>AAFTH</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>7X8</scope><scope>5PM</scope><scope>DOA</scope></search><sort><creationdate>20171010</creationdate><title>An RNAi Screen Reveals an Essential Role for HIPK4 in Human Skin Epithelial Differentiation from iPSCs</title><author>Larribère, Lionel ; Galach, Marta ; Novak, Daniel ; Arévalo, Karla ; Volz, Hans Christian ; Stark, Hans-Jürgen ; Boukamp, Petra ; Boutros, Michael ; Utikal, Jochen</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c529t-3ee31748f2301603d0fbc8868243625d8531dabee1c5697dca0dd0be80b279693</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>Cell Differentiation - genetics</topic><topic>Cell Line</topic><topic>Cells, Cultured</topic><topic>development</topic><topic>differentiation</topic><topic>Enzyme Activation</topic><topic>Epithelial Cells - cytology</topic><topic>Epithelial Cells - metabolism</topic><topic>epithelium</topic><topic>Gene Silencing</topic><topic>High-Throughput Screening Assays</topic><topic>HIPK4</topic><topic>Humans</topic><topic>Induced Pluripotent Stem Cells - cytology</topic><topic>Induced Pluripotent Stem Cells - metabolism</topic><topic>iPSC</topic><topic>keratinocytes</topic><topic>Keratinocytes - cytology</topic><topic>Keratinocytes - metabolism</topic><topic>Organ Culture Techniques</topic><topic>organotypic culture</topic><topic>Protein-Serine-Threonine Kinases - genetics</topic><topic>RNA Interference</topic><topic>RNAi screen</topic><topic>skin</topic><topic>stem cell</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Larribère, Lionel</creatorcontrib><creatorcontrib>Galach, Marta</creatorcontrib><creatorcontrib>Novak, Daniel</creatorcontrib><creatorcontrib>Arévalo, Karla</creatorcontrib><creatorcontrib>Volz, Hans Christian</creatorcontrib><creatorcontrib>Stark, Hans-Jürgen</creatorcontrib><creatorcontrib>Boukamp, Petra</creatorcontrib><creatorcontrib>Boutros, Michael</creatorcontrib><creatorcontrib>Utikal, Jochen</creatorcontrib><collection>ScienceDirect Open Access Titles</collection><collection>Elsevier:ScienceDirect:Open Access</collection><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><collection>Directory of Open Access Journals</collection><jtitle>Stem cell reports</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Larribère, Lionel</au><au>Galach, Marta</au><au>Novak, Daniel</au><au>Arévalo, Karla</au><au>Volz, Hans Christian</au><au>Stark, Hans-Jürgen</au><au>Boukamp, Petra</au><au>Boutros, Michael</au><au>Utikal, Jochen</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>An RNAi Screen Reveals an Essential Role for HIPK4 in Human Skin Epithelial Differentiation from iPSCs</atitle><jtitle>Stem cell reports</jtitle><addtitle>Stem Cell Reports</addtitle><date>2017-10-10</date><risdate>2017</risdate><volume>9</volume><issue>4</issue><spage>1234</spage><epage>1245</epage><pages>1234-1245</pages><issn>2213-6711</issn><eissn>2213-6711</eissn><abstract>Molecular mechanisms responsible for the development of human skin epithelial cells are incompletely understood. As a consequence, the efficiency to establish a pure skin epithelial cell population from human induced pluripotent stem cells (hiPSCs) remains poor. Using an approach including RNAi and high-throughput imaging of early epithelial cells, we identified candidate kinases involved in their differentiation from hiPSCs. Among these, we found HIPK4 to be an important inhibitor of this process. Indeed, its silencing increased the amount of generated skin epithelial precursors at an early time point, increased the amount of generated keratinocytes at a later time point, and improved growth and differentiation of organotypic cultures, allowing for the formation of a denser basal layer and stratification with the expression of several keratins. Our data bring substantial input regarding regulation of human skin epithelial differentiation and for improving differentiation protocols from pluripotent stem cells.
•High-throughput RNAi screen setup during human skin epithelial differentiation•Identification of HIPK4 as a crucial blocker of human skin epithelial differentiation•Improvement of human organotypic epithelial cultures after HIPK4 silencing
In this article, Larribère and colleagues establish a high-throughput RNAi screen on induced pluripotent stem cell-derived epithelial cells. This screen led to the identification of HIPK4 as a crucial blocker of human skin epithelial differentiation. Indeed, HIPK4 silencing increased the amount of early generated skin epithelial precursors, increased the amount of generated keratinocytes, and improved the differentiation of organotypic cultures.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>28966120</pmid><doi>10.1016/j.stemcr.2017.08.023</doi><tpages>12</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Cell Differentiation - genetics Cell Line Cells, Cultured development differentiation Enzyme Activation Epithelial Cells - cytology Epithelial Cells - metabolism epithelium Gene Silencing High-Throughput Screening Assays HIPK4 Humans Induced Pluripotent Stem Cells - cytology Induced Pluripotent Stem Cells - metabolism iPSC keratinocytes Keratinocytes - cytology Keratinocytes - metabolism Organ Culture Techniques organotypic culture Protein-Serine-Threonine Kinases - genetics RNA Interference RNAi screen skin stem cell |
title | An RNAi Screen Reveals an Essential Role for HIPK4 in Human Skin Epithelial Differentiation from iPSCs |
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