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. 2021 May 18;12:678201. doi: 10.3389/fimmu.2021.678201
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.