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Choice of factors and medium impinge on success of ESC to TSC conversion
The first lineage separation in mammalian development occurs when totipotent cells of the zygote give rise to the inner cell mass and the trophectoderm. The lineages are strictly separated by an epigenetic barrier. In vitro derivatives of these lineages embryonic stem cells (ESC) and trophoblast ste...
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Published in: | Placenta (Eastbourne) 2020-01, Vol.90, p.128-137 |
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description | The first lineage separation in mammalian development occurs when totipotent cells of the zygote give rise to the inner cell mass and the trophectoderm. The lineages are strictly separated by an epigenetic barrier. In vitro derivatives of these lineages embryonic stem cells (ESC) and trophoblast stem cells (TSC) are used to study the requirements needed to overcome the barrier in ESC to TSC conversion approaches.
Different combinations of TSC transcription factors were induced in ESC for three days. Cells were kept in TS medium with fetal bovine serum (FBS) or the chemically defined TX medium. Obtained cells were analysed for OCT4 levels, TSC surface marker levels, expression of TSC markers and methylation status of Elf5, Oct4 and Nanog promoters. Further, long-term culture stability and in vitro and in vivo differentiation was tested.
Overexpression of Gata3, Eomes, Tfap2c, Ets2 and Cdx2 in ESC resulted in induction of TSC fate. Overexpression of Cdx2 or four factors (Gata3, Eomes, Tfap2c and Ets2) resulted in complete conversion only when cells were cultured in TX medium. The obtained induced TSC (iTSC) display characteristics of bona fide TSC in terms of marker expression and promoter methylation patterns. The generated converted cells were shown to display self-renewal and to be capable to differentiate into TSC derivatives in vitro and in vivo.
Gata3, Eomes, Tfap2c, Ets2 and Cdx2 overexpression in ESC resulted in stable iTSC fate independent of culture conditions. For four factors or Cdx2 alone, TX medium is required for complete TSC conversion.
•In TX medium induction of Gata3, Eomes, Tfap2c, Ets2 reprograms ESC to TSC.•In regular TS medium Cdx2 needs to be added to the four-factor cocktail.•TX medium facilitates ESC to TSC conversion.•Transgene activation of three days is sufficient.•Conversion continues past transgene activation. |
doi_str_mv | 10.1016/j.placenta.2019.12.017 |
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Different combinations of TSC transcription factors were induced in ESC for three days. Cells were kept in TS medium with fetal bovine serum (FBS) or the chemically defined TX medium. Obtained cells were analysed for OCT4 levels, TSC surface marker levels, expression of TSC markers and methylation status of Elf5, Oct4 and Nanog promoters. Further, long-term culture stability and in vitro and in vivo differentiation was tested.
Overexpression of Gata3, Eomes, Tfap2c, Ets2 and Cdx2 in ESC resulted in induction of TSC fate. Overexpression of Cdx2 or four factors (Gata3, Eomes, Tfap2c and Ets2) resulted in complete conversion only when cells were cultured in TX medium. The obtained induced TSC (iTSC) display characteristics of bona fide TSC in terms of marker expression and promoter methylation patterns. The generated converted cells were shown to display self-renewal and to be capable to differentiate into TSC derivatives in vitro and in vivo.
Gata3, Eomes, Tfap2c, Ets2 and Cdx2 overexpression in ESC resulted in stable iTSC fate independent of culture conditions. For four factors or Cdx2 alone, TX medium is required for complete TSC conversion.
•In TX medium induction of Gata3, Eomes, Tfap2c, Ets2 reprograms ESC to TSC.•In regular TS medium Cdx2 needs to be added to the four-factor cocktail.•TX medium facilitates ESC to TSC conversion.•Transgene activation of three days is sufficient.•Conversion continues past transgene activation.</description><identifier>ISSN: 0143-4004</identifier><identifier>EISSN: 1532-3102</identifier><identifier>DOI: 10.1016/j.placenta.2019.12.017</identifier><identifier>PMID: 32056544</identifier><language>eng</language><publisher>Netherlands: Elsevier Ltd</publisher><subject>Animals ; Cell Culture Techniques ; Cell Differentiation - physiology ; Cell Lineage - physiology ; Chemically defined medium ; Culture Media ; Direct cell fate conversion ; Embryonic stem cells ; Embryonic Stem Cells - cytology ; Lineage barrier ; Mice ; Trophoblast stem cells ; Trophoblasts - cytology</subject><ispartof>Placenta (Eastbourne), 2020-01, Vol.90, p.128-137</ispartof><rights>2019 Elsevier Ltd</rights><rights>Copyright © 2019 Elsevier Ltd. All rights reserved.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c416t-c34d8dd1d92c85fbcd9087ad1086707677dd765640c47a552a394f3bacbdfb343</citedby><cites>FETCH-LOGICAL-c416t-c34d8dd1d92c85fbcd9087ad1086707677dd765640c47a552a394f3bacbdfb343</cites><orcidid>0000-0001-8272-0076</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/32056544$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Kaiser, Franziska</creatorcontrib><creatorcontrib>Kubaczka, Caroline</creatorcontrib><creatorcontrib>Graf, Monika</creatorcontrib><creatorcontrib>Langer, Nina</creatorcontrib><creatorcontrib>Langkabel, Jan</creatorcontrib><creatorcontrib>Arévalo, Lena</creatorcontrib><creatorcontrib>Schorle, Hubert</creatorcontrib><title>Choice of factors and medium impinge on success of ESC to TSC conversion</title><title>Placenta (Eastbourne)</title><addtitle>Placenta</addtitle><description>The first lineage separation in mammalian development occurs when totipotent cells of the zygote give rise to the inner cell mass and the trophectoderm. The lineages are strictly separated by an epigenetic barrier. In vitro derivatives of these lineages embryonic stem cells (ESC) and trophoblast stem cells (TSC) are used to study the requirements needed to overcome the barrier in ESC to TSC conversion approaches.
Different combinations of TSC transcription factors were induced in ESC for three days. Cells were kept in TS medium with fetal bovine serum (FBS) or the chemically defined TX medium. Obtained cells were analysed for OCT4 levels, TSC surface marker levels, expression of TSC markers and methylation status of Elf5, Oct4 and Nanog promoters. Further, long-term culture stability and in vitro and in vivo differentiation was tested.
Overexpression of Gata3, Eomes, Tfap2c, Ets2 and Cdx2 in ESC resulted in induction of TSC fate. Overexpression of Cdx2 or four factors (Gata3, Eomes, Tfap2c and Ets2) resulted in complete conversion only when cells were cultured in TX medium. The obtained induced TSC (iTSC) display characteristics of bona fide TSC in terms of marker expression and promoter methylation patterns. The generated converted cells were shown to display self-renewal and to be capable to differentiate into TSC derivatives in vitro and in vivo.
Gata3, Eomes, Tfap2c, Ets2 and Cdx2 overexpression in ESC resulted in stable iTSC fate independent of culture conditions. For four factors or Cdx2 alone, TX medium is required for complete TSC conversion.
•In TX medium induction of Gata3, Eomes, Tfap2c, Ets2 reprograms ESC to TSC.•In regular TS medium Cdx2 needs to be added to the four-factor cocktail.•TX medium facilitates ESC to TSC conversion.•Transgene activation of three days is sufficient.•Conversion continues past transgene activation.</description><subject>Animals</subject><subject>Cell Culture Techniques</subject><subject>Cell Differentiation - physiology</subject><subject>Cell Lineage - physiology</subject><subject>Chemically defined medium</subject><subject>Culture Media</subject><subject>Direct cell fate conversion</subject><subject>Embryonic stem cells</subject><subject>Embryonic Stem Cells - cytology</subject><subject>Lineage barrier</subject><subject>Mice</subject><subject>Trophoblast stem cells</subject><subject>Trophoblasts - cytology</subject><issn>0143-4004</issn><issn>1532-3102</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><recordid>eNqFkMtOwzAQRS0EouXxC1WWbBLGzzQ7UMVLQmIBrC1n7ICrJi52gsTf46rAltUs5ty5mkPIgkJFgarLdbXdGHTDaCoGtKkoq4DWB2ROJWclp8AOyRyo4KUAEDNyktIaABpB2TGZcQZSSSHm5H71Hjy6InRFZ3AMMRVmsEXvrJ_6wvdbP7zl7VCkCdGltANvnlfFGIqXPDAMny4mH4YzctSZTXLnP_OUvN7evKzuy8enu4fV9WOJgqqxRC7s0lpqG4ZL2bVoG1jWxlJYqhpqVdfW1koqAShqIyUzvBEdbw22tmu54KfkYn93G8PH5NKoe5_QbTZmcGFKmnEpG6FA8YyqPYoxpBRdp7fR9yZ-aQp6Z1Gv9a9FvbOoKdPZYg4ufjqmNpv4i_1qy8DVHnD500_vok7o3YDZWnQ4ahv8fx3fRI2Fcw</recordid><startdate>20200115</startdate><enddate>20200115</enddate><creator>Kaiser, Franziska</creator><creator>Kubaczka, Caroline</creator><creator>Graf, Monika</creator><creator>Langer, Nina</creator><creator>Langkabel, Jan</creator><creator>Arévalo, Lena</creator><creator>Schorle, Hubert</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>7X8</scope><orcidid>https://orcid.org/0000-0001-8272-0076</orcidid></search><sort><creationdate>20200115</creationdate><title>Choice of factors and medium impinge on success of ESC to TSC conversion</title><author>Kaiser, Franziska ; Kubaczka, Caroline ; Graf, Monika ; Langer, Nina ; Langkabel, Jan ; Arévalo, Lena ; Schorle, Hubert</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c416t-c34d8dd1d92c85fbcd9087ad1086707677dd765640c47a552a394f3bacbdfb343</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>Animals</topic><topic>Cell Culture Techniques</topic><topic>Cell Differentiation - physiology</topic><topic>Cell Lineage - physiology</topic><topic>Chemically defined medium</topic><topic>Culture Media</topic><topic>Direct cell fate conversion</topic><topic>Embryonic stem cells</topic><topic>Embryonic Stem Cells - cytology</topic><topic>Lineage barrier</topic><topic>Mice</topic><topic>Trophoblast stem cells</topic><topic>Trophoblasts - cytology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kaiser, Franziska</creatorcontrib><creatorcontrib>Kubaczka, Caroline</creatorcontrib><creatorcontrib>Graf, Monika</creatorcontrib><creatorcontrib>Langer, Nina</creatorcontrib><creatorcontrib>Langkabel, Jan</creatorcontrib><creatorcontrib>Arévalo, Lena</creatorcontrib><creatorcontrib>Schorle, Hubert</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>Placenta (Eastbourne)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kaiser, Franziska</au><au>Kubaczka, Caroline</au><au>Graf, Monika</au><au>Langer, Nina</au><au>Langkabel, Jan</au><au>Arévalo, Lena</au><au>Schorle, Hubert</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Choice of factors and medium impinge on success of ESC to TSC conversion</atitle><jtitle>Placenta (Eastbourne)</jtitle><addtitle>Placenta</addtitle><date>2020-01-15</date><risdate>2020</risdate><volume>90</volume><spage>128</spage><epage>137</epage><pages>128-137</pages><issn>0143-4004</issn><eissn>1532-3102</eissn><abstract>The first lineage separation in mammalian development occurs when totipotent cells of the zygote give rise to the inner cell mass and the trophectoderm. The lineages are strictly separated by an epigenetic barrier. In vitro derivatives of these lineages embryonic stem cells (ESC) and trophoblast stem cells (TSC) are used to study the requirements needed to overcome the barrier in ESC to TSC conversion approaches.
Different combinations of TSC transcription factors were induced in ESC for three days. Cells were kept in TS medium with fetal bovine serum (FBS) or the chemically defined TX medium. Obtained cells were analysed for OCT4 levels, TSC surface marker levels, expression of TSC markers and methylation status of Elf5, Oct4 and Nanog promoters. Further, long-term culture stability and in vitro and in vivo differentiation was tested.
Overexpression of Gata3, Eomes, Tfap2c, Ets2 and Cdx2 in ESC resulted in induction of TSC fate. Overexpression of Cdx2 or four factors (Gata3, Eomes, Tfap2c and Ets2) resulted in complete conversion only when cells were cultured in TX medium. The obtained induced TSC (iTSC) display characteristics of bona fide TSC in terms of marker expression and promoter methylation patterns. The generated converted cells were shown to display self-renewal and to be capable to differentiate into TSC derivatives in vitro and in vivo.
Gata3, Eomes, Tfap2c, Ets2 and Cdx2 overexpression in ESC resulted in stable iTSC fate independent of culture conditions. For four factors or Cdx2 alone, TX medium is required for complete TSC conversion.
•In TX medium induction of Gata3, Eomes, Tfap2c, Ets2 reprograms ESC to TSC.•In regular TS medium Cdx2 needs to be added to the four-factor cocktail.•TX medium facilitates ESC to TSC conversion.•Transgene activation of three days is sufficient.•Conversion continues past transgene activation.</abstract><cop>Netherlands</cop><pub>Elsevier Ltd</pub><pmid>32056544</pmid><doi>10.1016/j.placenta.2019.12.017</doi><tpages>10</tpages><orcidid>https://orcid.org/0000-0001-8272-0076</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Animals Cell Culture Techniques Cell Differentiation - physiology Cell Lineage - physiology Chemically defined medium Culture Media Direct cell fate conversion Embryonic stem cells Embryonic Stem Cells - cytology Lineage barrier Mice Trophoblast stem cells Trophoblasts - cytology |
title | Choice of factors and medium impinge on success of ESC to TSC conversion |
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