Single-cell transcriptomic analysis reveals altered mitochondrial and protein translation signatures in murine HSPCs. (A) Timeline of GW4869 (or DMSO) treatment in ex vivo cultured murine HSPCs (n = 3 biologic replicates per treatment/condition) before 10x Genomics single-cell RNA sequencing. (B) Proportions of mitochondrial over total genes sequenced per cell across treatment groups and time points. (C) In silico fluorescence-activated cell sorter–like annotations of stem and progenitor cell populations identified across conditions in single-cell RNA sequencing analyses. (D) Uniform manifold approximation and projections of ST-HSCs in HSPCCon and HSPCGW at 24-hour time point. Bubble heatmaps of significant hallmark gene sets enriched in HSPCGW at 24 hours (E) and 120 hours (F). (G) Violin plots of top differentially expressed genes in ST-HSCGW. Refer to supplemental Figures 3 and 4.

Single-cell transcriptomic analysis reveals altered mitochondrial and protein translation signatures in murine HSPCs. (A) Timeline of GW4869 (or DMSO) treatment in ex vivo cultured murine HSPCs (n = 3 biologic replicates per treatment/condition) before 10x Genomics single-cell RNA sequencing. (B) Proportions of mitochondrial over total genes sequenced per cell across treatment groups and time points. (C) In silico fluorescence-activated cell sorter–like annotations of stem and progenitor cell populations identified across conditions in single-cell RNA sequencing analyses. (D) Uniform manifold approximation and projections of ST-HSCs in HSPCCon and HSPCGW at 24-hour time point. Bubble heatmaps of significant hallmark gene sets enriched in HSPCGW at 24 hours (E) and 120 hours (F). (G) Violin plots of top differentially expressed genes in ST-HSCGW. Refer to supplemental Figures 3 and 4.

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