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Exosomes secreted by mesenchymal stem cells promote endothelial cell angiogenesis by transferring miR-125a.
- Source :
-
Journal of cell science [J Cell Sci] 2016 Jun 01; Vol. 129 (11), pp. 2182-9. - Publication Year :
- 2016
-
Abstract
- Angiogenesis plays crucial roles in various physiological processes including wound healing and tissue repair. It requires a tight interaction between endothelial cells and their surrounding environment. Mesenchymal stem cells (MSCs), one of the non-endothelial cell types present in the perivascular environment, have been shown to secret exosomes to modulate intercellular communications between MSCs and their target cells. In this study, we initially isolated exosomes secreted by human adipose-derived MSCs (adMSC-Exo) and examined their roles in angiogenesis. We found that adMSC-Exo could be taken up by endothelial cells and significantly promote angiogenesis in vitro and in vivo Further study showed that miR-125a was enriched in adMSC-Exo, and repressed the expression of the angiogenic inhibitor delta-like 4 (DLL4) by targeting its 3' untranslated region. Additionally, adMSC-Exo and its exosomal transferred miR-125a could repress DLL4 expression and modulate endothelial cell angiogenesis through promoting formation of endothelial tip cells. In conclusion, our study indicates that adMSC-Exo can transfer miR-125a to endothelial cells and promote angiogenesis by repressing DLL4. adMSC-Exo, as a pro-angiogenic factor, might be a promising candidate for therapeutical tissue repair.<br /> (© 2016. Published by The Company of Biologists Ltd.)
- Subjects :
- Adaptor Proteins, Signal Transducing
Adipose Tissue cytology
Animals
Base Sequence
Calcium-Binding Proteins
Cell Separation
Exosomes ultrastructure
Intercellular Signaling Peptides and Proteins metabolism
Male
Mesenchymal Stem Cells cytology
Mice, Inbred BALB C
Mice, Nude
MicroRNAs genetics
Exosomes metabolism
Human Umbilical Vein Endothelial Cells metabolism
Mesenchymal Stem Cells metabolism
MicroRNAs metabolism
Neovascularization, Physiologic
Subjects
Details
- Language :
- English
- ISSN :
- 1477-9137
- Volume :
- 129
- Issue :
- 11
- Database :
- MEDLINE
- Journal :
- Journal of cell science
- Publication Type :
- Academic Journal
- Accession number :
- 27252357
- Full Text :
- https://doi.org/10.1242/jcs.170373