Review Article

Extracellular Vesicles: Evolving Factors in Stem Cell Biology

Table 1

Stem cell signatures expressed and secreted in EVs.

ComponentsStem cell type/sourceReference

Nanog, Oct-4, HoxB4 and Rex-1ESCs[37]
CD105CSCs, MSCs[38, 97]
Prominin-1/CD133HPCs, melanocytes[39, 40]
KITMast/stem cells[42]
WNTFibroblasts, DLBCL[43, 44, 96]
β-cateninHEK[45]
Stem-cell antigen-1MSCs[97]
TGF-β1Fibroblasts, epithelial cells[98]
TIA, TIAR, HuR, Stau1, Stau2, RPS29, and Ago2MSCs[54]
KGFMSCs[99]
Oct4 and Sox2 mRNAsESCs[62]
IGF-1R mRNAMSCs[100]
DEFA3, HBB, ITGA2B, and ITGB3 mRNAsHPCs[101]
VEGFMSCs[68]
PDGFR-β, TIMP 1 and 2, sphingomyelin, lactic acid, and glutamic acidMSCs[69]
CD34MSCs[102]
E-cadherinMSCs[103]
Bcl-2MSCs[104]
NEPMSCs[105]

ESCs: embryonic stem cells, CSCs: cancer stem cells, MSC: mesenchymal stem cells, HPCs: haematopoietic precursor cells, DLBCL: diffuse large B-cell lymphoma, HEK: human embryonic kidney cells, KIT: mast/stem cell growth factor receptor, IGF-1R: growth factor receptor, TGF-β1: transforming growth factor beta 1, KGF: keratinocyte growth factor, ITGA; integrin alpha, VEGF: vascular endothelial growth factor, PDGFR-β: platelet-derived growth factor receptor beta, TIMP: tissue inhibitor of metalloproteinase, and NEP: neprilysin.