Datasets | Category | Treg source | Type | TotalDEGs | CS up | /DEGs% | CS down | /DEGs% |
---|---|---|---|---|---|---|---|---|
GSE50096 | Lymphoid | Skeletal muscle injured 2w spleen | Array | 308 | 48 | 15.58 | 14 | 4.55 |
GSE50096 | Lymphoid | Skeletal muscle injured 4d spleen | Array | 313 | 47 | 15.02 | 12 | 3.83 |
E-MTAB-7961 | Non-lymphoid | Fibrosis kidney | RNA-seq | 2440 | 179 | 7.34 | 71 | 2.91 |
E-MTAB-7961 | Non-lymphoid | Regeneration kidney | RNA-seq | 2608 | 265 | 10.16 | 86 | 3.30 |
GSE50096 | Non-lymphoid | Skeletal muscle injured 2w muscle | Array | 539 | 74 | 13.73 | 27 | 5.01 |
GSE50096 | Non-lymphoid | Skeletal muscle injured 4d muscle | Array | 465 | 49 | 10.54 | 39 | 8.39 |
CS, canonical secretome; DEG, differentially expressed gene.
IPA analysis was performed to identify upregulated canonical secretome pathways in benign disease tissues (cut off: p < 0.05 and |Z-score| >= 2). In the benign disease Treg groups, a total of 24 activated pathways were enriched ( Supplementary Table 5 ). Most of the canonical secretome pathways were specific in E-MTAB-7961 kidney regeneration Treg, including Hepatic Fibrosis Signaling Pathway, PDGF Signaling, VEGF Signaling, and VEGF Family Ligand-Receptor Interactions, which functions were related to the tissue repair. IL-6 Signaling was specifically enriched in GSE50096 muscle injury 4D Treg, which was Treg in the muscle during the acute reaction phase after muscle injury.