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Ebola, Nipah, and Andes viruses each exert different effects on hPSC-derived ECs A) Experimental summary. h: hour. B) Replication of Andes, Nipah, and Ebola viruses in hPSC-derived artery and vein ECs, as assayed by qPCR for viral genomes in the culture media. Statistics: unpaired t-test. Error bars: SEM. **P<0.01. n.s.: not significant. †: extensive cell death. C) Bulk RNA-seq of interferon and interferon-stimulated gene expression in hPSC-derived artery and vein ECs 6, 12, 24, and 48 hours after infection with Sendai, Andes, Nipah, and Ebola viruses. Fold change relative to uninfected cells is depicted. D) Bulk RNA-seq of inflammatory cytokine gene expression in hPSC-derived artery and vein ECs 6, 12, 24, and 48 hours after infection with Sendai, Andes, Nipah, and Ebola viruses. Fold change relative to uninfected cells is depicted. E) Summary of the present study. F) Bulk-RNA-seq of hPSC-derived artery ECs 6, 12, 24, and 48 hours after infection with Ebola, Andes, and Sendai viruses, or left uninfected (mock control). Error bars: SEM. G) <t>IFNβ</t> protein secretion by hPSC-derived artery ECs after 24 or 48 hours of infection by Ebola, Andes, and Sendai viruses, or left uninfected (mock control), as measured by <t>ELISA.</t> Statistics: unpaired t-test. **P<0.01. H) Bulk-RNA-seq of hPSC-derived artery ECs 6, 12, 24, and 48 hours after infection with Ebola, Andes, and Sendai viruses, or left uninfected (mock control). Error bars: SEM. Related to Figures S7 and S8.
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Ebola, Nipah, and Andes viruses each exert different effects on hPSC-derived ECs A) Experimental summary. h: hour. B) Replication of Andes, Nipah, and Ebola viruses in hPSC-derived artery and vein ECs, as assayed by qPCR for viral genomes in the culture media. Statistics: unpaired t-test. Error bars: SEM. **P<0.01. n.s.: not significant. †: extensive cell death. C) Bulk RNA-seq of interferon and interferon-stimulated gene expression in hPSC-derived artery and vein ECs 6, 12, 24, and 48 hours after infection with Sendai, Andes, Nipah, and Ebola viruses. Fold change relative to uninfected cells is depicted. D) Bulk RNA-seq of inflammatory cytokine gene expression in hPSC-derived artery and vein ECs 6, 12, 24, and 48 hours after infection with Sendai, Andes, Nipah, and Ebola viruses. Fold change relative to uninfected cells is depicted. E) Summary of the present study. F) Bulk-RNA-seq of hPSC-derived artery ECs 6, 12, 24, and 48 hours after infection with Ebola, Andes, and Sendai viruses, or left uninfected (mock control). Error bars: SEM. G) IFNβ protein secretion by hPSC-derived artery ECs after 24 or 48 hours of infection by Ebola, Andes, and Sendai viruses, or left uninfected (mock control), as measured by ELISA. Statistics: unpaired t-test. **P<0.01. H) Bulk-RNA-seq of hPSC-derived artery ECs 6, 12, 24, and 48 hours after infection with Ebola, Andes, and Sendai viruses, or left uninfected (mock control). Error bars: SEM. Related to Figures S7 and S8.

Journal: bioRxiv

Article Title: A human arteriovenous differentiation roadmap reveals vein developmental mechanisms and vascular effects of viruses

doi: 10.1101/2025.10.11.681838

Figure Lengend Snippet: Ebola, Nipah, and Andes viruses each exert different effects on hPSC-derived ECs A) Experimental summary. h: hour. B) Replication of Andes, Nipah, and Ebola viruses in hPSC-derived artery and vein ECs, as assayed by qPCR for viral genomes in the culture media. Statistics: unpaired t-test. Error bars: SEM. **P<0.01. n.s.: not significant. †: extensive cell death. C) Bulk RNA-seq of interferon and interferon-stimulated gene expression in hPSC-derived artery and vein ECs 6, 12, 24, and 48 hours after infection with Sendai, Andes, Nipah, and Ebola viruses. Fold change relative to uninfected cells is depicted. D) Bulk RNA-seq of inflammatory cytokine gene expression in hPSC-derived artery and vein ECs 6, 12, 24, and 48 hours after infection with Sendai, Andes, Nipah, and Ebola viruses. Fold change relative to uninfected cells is depicted. E) Summary of the present study. F) Bulk-RNA-seq of hPSC-derived artery ECs 6, 12, 24, and 48 hours after infection with Ebola, Andes, and Sendai viruses, or left uninfected (mock control). Error bars: SEM. G) IFNβ protein secretion by hPSC-derived artery ECs after 24 or 48 hours of infection by Ebola, Andes, and Sendai viruses, or left uninfected (mock control), as measured by ELISA. Statistics: unpaired t-test. **P<0.01. H) Bulk-RNA-seq of hPSC-derived artery ECs 6, 12, 24, and 48 hours after infection with Ebola, Andes, and Sendai viruses, or left uninfected (mock control). Error bars: SEM. Related to Figures S7 and S8.

Article Snippet: Media was then thawed, and the concentration of secreted interferon-β (IFNβ) protein in the 2:1 diluted media was quantified using the Human IFNβ Quantikine QuicKit ELISA Kit (R&D Systems, QK410), as described previously and as per the manufacturer’s instructions.

Techniques: Derivative Assay, RNA Sequencing, Gene Expression, Infection, Control, Enzyme-linked Immunosorbent Assay