Table 2.
Number of protein-coding DEGs identified by differential expression analysis in CTL and ALK1-mutated ECFCs and HMVECs
| Comparison | ECFCs | HMVECs | ||||
|---|---|---|---|---|---|---|
| Total DEGs | Upregulated | Downregulated | Total DEGs | Upregulated | Downregulated | |
| CTL NS vs B9 | 828 | 456 | 372 | 704 | 366 | 338 |
| CTL NS vs B10 | 787 | 418 | 369 | 481 | 225 | 256 |
| CTL B9 vs B10 | 0 | 0 | 0 | 2 | 0 | 2 |
| MUT NS vs B9 | 604 | 310 | 294 | 295 | 158 | 137 |
| MUT NS vs B10 | 564 | 278 | 286 | 206 | 90 | 116 |
| MUT B9 vs B10 | 0 | 0 | 0 | 0 | 0 | 0 |
| CTL NS vs MUT NS | 28 | 11 | 17 | 1261 | 528 | 733 |
| CTL B9 vs MUT B9 | 19 | 6 | 13 | 1262 | 502 | 760 |
| CTL B10 vs MUT B10 | 30 | 7 | 23 | 1164 | 503 | 661 |
3 CTL ECFCs and 2 ALK1-mutated ECFCs (MUT-H1–H2) or 3 CTL HMVECs and 2 ALK1-mutated HMVECs (MUT-P1–P2) were stimulated or not with BMP9 or BMP10 (10 ng/mL) for 18 h. The experiment was repeated three times to generate technical replicates, after which bulk RNA-seq analysis was performed using DESeq2 package with an absolute log2 fold change threshold of 1 (llog2FCl ≥ 1) and a adjusted p-value ≤ 0.05 (Benjamini–Hochberg procedure). Data show protein coding DEGS analyzed by NS non-stimulated, B9 BMP9-stimulated, B10 BMP10-stimulated