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J Transl Med. 2016 Feb 2;14:34. doi: 10.1186/s12967-016-0794-z.

Paracrine effects of TLR4-polarised mesenchymal stromal cells are mediated by extracellular vesicles.

Author information

1
Stem Cell Biology and Regenerative Medicine Group, Reading School of Pharmacy, University of Reading, Whiteknights Campus, PO Box 226, Reading, RG6 6AP, UK. m.zeuner@pgr.reading.ac.uk.
2
School of Biological Sciences, University of Reading, Whiteknights Campus, Reading, UK. ketan.patel@reading.ac.uk.
3
Freiburg Institute for Advanced Studies (FRIAS), University of Freiburg, Albertstr. 19, 79104, Freiburg, Germany. ketan.patel@reading.ac.uk.
4
Interdisciplinary Center for Clinical Research Aachen (IZKF Aachen), RWTH Aachen University, Aachen, Germany. Bernd.Denecke@rwth-aachen.de.
5
Institute for Transfusion Medicine, University Hospital Essen, University Duisburg-Essen, Essen, Germany. Bernd.Giebel@uk-essen.de.
6
Stem Cell Biology and Regenerative Medicine Group, Reading School of Pharmacy, University of Reading, Whiteknights Campus, PO Box 226, Reading, RG6 6AP, UK. d.widera@reading.ac.uk.

Abstract

Mesenchymal stromal cells (MSCs) are adult stem cells able to give rise to bone, cartilage and fat cells. In addition, they possess immunomodulatory and immunosuppressive properties that are mainly mediated through secretion of extracellular vesicles (EVs). In a previous issue of Journal of Translational Medicine, Ti and colleagues demonstrated that preconditioning of MSCs with bacterial lipopolysaccharides results in secretion of EVs that can polarise macrophages towards anti-inflammatory M2 phenotype. Moreover, the authors suggest that EVs of ​lipopolysaccharide (LPS)-treated MSCs are superior to EVs of untreated MSCs concerning their ability to support wound healing. Our commentary critically discusses parallel efforts of other laboratories to generate conditioned media from stem cells for therapeutic applications, and highlights impact and significance of the study of Ti et al. Finally, we summarise its limitations and spotlight areas that need to be addressed to better define the underlying molecular mechanisms.

PMID:
26838370
PMCID:
PMC4735950
DOI:
10.1186/s12967-016-0794-z
[Indexed for MEDLINE]
Free PMC Article

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