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