L transcription factors, e.g., PPARG, ELF3, GATA3, MXD1, and TFAP2A. A few marker genes were expressed significantly higher in the <40-m fraction than in the >70-m fraction (VTCN1, LAMA1, GABRP, and ITGB6).A Comparison of the Transcriptome Profiles of ESC-Derived STB with STB Generated from Cytotrophoblast Isolated from Term Placenta.When cytotrophoblast isolated from term placentas (PHTu) SIS3 web underwent differentiation and formed STB (PHTd), there was the expected rise in expression of the genes, such as CGA, CGB, PGF, ERVWR-1, and PSG family members, which are anticipated markers of STB (SI Appendix, Fig. S3B). A few other trophoblast signature genes were down-regulated during the differentiation process, among them OVOL1 and ERVFRD-1. The former is a key transcription factor regulating fusion of progenitor cytotrophoblast (26), whereas ERVFRD-1 (formerly called syncytin-2) has CI-1011MedChemExpress CI-1011 recently been proposed to be a more important facilitator of trophoblast fusion than ERVW-1 (syncytin-1) (27). Presumably once cell fusion had begun, these two genes became quickly down-regulated in PHTd. We then made a comparison between the >70-m size fraction STB generated from ESCs and PHTd formed from fusion of PHTu cells. The majority of trophoblast marker genes showed no more than a twofold difference in log2 expression values between the two types of STB (Fig. 5C). Some were expressed equivalently (gray bar in Fig. 5C). However, others were highly enriched in one cell type versus the other. For example, transcripts for GABRP, SLC38A3, LAMA1, and VTCN1, the transcription factor HEYYabe et al.and the chemokine CCR2 were barely detectable in the PHTd fraction, although significantly expressed in ESCd >70 cells. The genes encoding LHB family members, (LHB, CGB, CGB5, CGB8, and CGB7), as well as CGA, although significantly up-regulated in PHTd relative to PHTu (SI Appendix, Fig. S3B), were much more strongly expressed in the >70-m size fraction derived from ESCs (ESCd >70) (Fig. 6). By contrast, a cohort of other genes, including KRT7, GPR56, CLIC3, NUPR1, and PSG4, were expressed significantly higher in placental STB (PHTd) than in the the >70-m size fraction (ESCd >70) derived from ESCs (Fig. 5C). Other highly expressed genes with biased expression toward PHTd relative to ESCd >70 cells and that have been linked to placental trophoblast function but are not shown in Fig. 5C, include CSH1 (placental lactogen), B2M (beta-2 microglobulin), ENG (endoglin), ALPP (placental alkaline phosphatase), PPARG, SPINT1 (Kunitz type 1 serine peptidase inhibitor), PSG family members (PSG1? PSG11; pregnancy-specific 1 glycoproteins), and LGALS family members (LGALS1, 3, 8, 9, 13, and 14; L-galectins). Overall, this comparison indicated many similarities between the two cell types but also some major differences. Additional distinctions are explored in the following sections.Yabe et al.A Comparison of the Expression of Transporter Genes in ESCd >70 and STB Generated from PHTd. A major function of placental STBis in transport of solutes to and from the conceptus, especially involving the SLC and ABC transporter families. There are 492 genes in the human SLC superfamily. Of these, RNA-seq revealed that 254 were measurably expressed (cutoff FKPM value >1) in the ESCd >70 cells and 231 in the PHTd cells. The expression of the top 25 SLC genes in terms of transcriptome abundance are shown in SI Appendix, Fig. S4A. Although the majority of these genes showed quite similar levels of exp.L transcription factors, e.g., PPARG, ELF3, GATA3, MXD1, and TFAP2A. A few marker genes were expressed significantly higher in the <40-m fraction than in the >70-m fraction (VTCN1, LAMA1, GABRP, and ITGB6).A Comparison of the Transcriptome Profiles of ESC-Derived STB with STB Generated from Cytotrophoblast Isolated from Term Placenta.When cytotrophoblast isolated from term placentas (PHTu) underwent differentiation and formed STB (PHTd), there was the expected rise in expression of the genes, such as CGA, CGB, PGF, ERVWR-1, and PSG family members, which are anticipated markers of STB (SI Appendix, Fig. S3B). A few other trophoblast signature genes were down-regulated during the differentiation process, among them OVOL1 and ERVFRD-1. The former is a key transcription factor regulating fusion of progenitor cytotrophoblast (26), whereas ERVFRD-1 (formerly called syncytin-2) has recently been proposed to be a more important facilitator of trophoblast fusion than ERVW-1 (syncytin-1) (27). Presumably once cell fusion had begun, these two genes became quickly down-regulated in PHTd. We then made a comparison between the >70-m size fraction STB generated from ESCs and PHTd formed from fusion of PHTu cells. The majority of trophoblast marker genes showed no more than a twofold difference in log2 expression values between the two types of STB (Fig. 5C). Some were expressed equivalently (gray bar in Fig. 5C). However, others were highly enriched in one cell type versus the other. For example, transcripts for GABRP, SLC38A3, LAMA1, and VTCN1, the transcription factor HEYYabe et al.and the chemokine CCR2 were barely detectable in the PHTd fraction, although significantly expressed in ESCd >70 cells. The genes encoding LHB family members, (LHB, CGB, CGB5, CGB8, and CGB7), as well as CGA, although significantly up-regulated in PHTd relative to PHTu (SI Appendix, Fig. S3B), were much more strongly expressed in the >70-m size fraction derived from ESCs (ESCd >70) (Fig. 6). By contrast, a cohort of other genes, including KRT7, GPR56, CLIC3, NUPR1, and PSG4, were expressed significantly higher in placental STB (PHTd) than in the the >70-m size fraction (ESCd >70) derived from ESCs (Fig. 5C). Other highly expressed genes with biased expression toward PHTd relative to ESCd >70 cells and that have been linked to placental trophoblast function but are not shown in Fig. 5C, include CSH1 (placental lactogen), B2M (beta-2 microglobulin), ENG (endoglin), ALPP (placental alkaline phosphatase), PPARG, SPINT1 (Kunitz type 1 serine peptidase inhibitor), PSG family members (PSG1? PSG11; pregnancy-specific 1 glycoproteins), and LGALS family members (LGALS1, 3, 8, 9, 13, and 14; L-galectins). Overall, this comparison indicated many similarities between the two cell types but also some major differences. Additional distinctions are explored in the following sections.Yabe et al.A Comparison of the Expression of Transporter Genes in ESCd >70 and STB Generated from PHTd. A major function of placental STBis in transport of solutes to and from the conceptus, especially involving the SLC and ABC transporter families. There are 492 genes in the human SLC superfamily. Of these, RNA-seq revealed that 254 were measurably expressed (cutoff FKPM value >1) in the ESCd >70 cells and 231 in the PHTd cells. The expression of the top 25 SLC genes in terms of transcriptome abundance are shown in SI Appendix, Fig. S4A. Although the majority of these genes showed quite similar levels of exp.
