| Datasets | Category | Treg source | Type | TotalDEG | Exo up | /DEG% | Exo down | /DEG% |
|---|---|---|---|---|---|---|---|---|
| GSE50096 | Lymphoid | Skeletal muscle injured 2w spleen | Array | 308 | 96 | 31.17 | 28 | 9.09 |
| GSE50096 | Lymphoid | Skeletal muscle injured 4d spleen | Array | 313 | 115 | 36.74 | 22 | 7.03 |
| E-MTAB-7961 | Non-lymphoid | Fibrosis kidney | RNA-seq | 2440 | 379 | 15.53 | 109 | 4.47 |
| E-MTAB-7961 | Non-lymphoid | Regeneration kidney | RNA-seq | 2365 | 541 | 22.88 | 131 | 5.54 |
| GSE50096 | Non-lymphoid | Skeletal muscle injured 2w muscle | Array | 539 | 147 | 27.27 | 75 | 13.91 |
| GSE50096 | Non-lymphoid | Skeletal muscle injured 4d muscle | Array | 465 | 94 | 20.22 | 101 | 21.72 |
IPA analysis was performed to identify upregulated commonly shared exosome pathways in benign disease tissue Treg. A total of 111 exosome pathways were enriched in benign disease Treg groups including 32 commonly shared and 79 specific pathways. The 71 of 79 specifically enriched pathways were in E-MTAN-7961 Treg. Vitamin-C Transport and Th2 Pathways were enriched in GSE50096 2W spleen Treg. TREM1 Signaling was enriched in GSE50096 4D spleen Treg. PTEN Signaling was enriched in GSE50096 4D muscle Treg. Dendritic Cell Maturation, Apelin Endothelial Signaling Pathway, and Bladder Cancer Signaling were enriched in E-MTAB-7961 fibrosis Treg. The 71 specifically enriched pathways in E-MTAB-7961 regeneration Treg were shown in Supplementary Table 6B . (cut off: p < 0.05 and |Z-score| >= 2).