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Total glucosides of paeony improves the immunomodulatory capacity of MSCs partially via the miR-124/STAT3 pathway in oral lichen planus.
- Source :
-
Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie [Biomed Pharmacother] 2018 Sep; Vol. 105, pp. 151-158. Date of Electronic Publication: 2018 May 29. - Publication Year :
- 2018
-
Abstract
- Mesenchymal stem cells (MSCs) have been used clinically and experimentally to relieve severe immune-related diseases due to their immunomodulatory properties, but these are impaired by inflammation. Oral lichen planus (OLP) is a T cell-mediated chronic inflammatory mucosal disease. In the present study, we found MSCs from OLP with higher expression of interleukin (IL)-6, tumour necrosis factor alpha (TNF-α), transforming growth factor beta (TGF-β) and IL-10 compared with control. Total glucosides of paeony (TGP) significantly improves the immunomodulatory function of MSCs by inhibiting IL-6 and TNF-α expression and increasing TGF-β and IL-10 expression. Moreover, TGP can downregulate p-STAT3 expression through upregulation of miR-124. The changes of IL-6, TGF-β and p-STAT3 were further confirmed by overexpression and knockdown of miR-124 in MSCs. Taken together, the immune-regulating function of MSCs can be improved by TGP via the miR-124/STAT3 pathway.<br /> (Copyright © 2018. Published by Elsevier Masson SAS.)
- Subjects :
- Adult
Cells, Cultured
Cytokines genetics
Cytokines immunology
Female
Glucosides isolation & purification
Humans
Lichen Planus, Oral immunology
Lichen Planus, Oral metabolism
Male
Mesenchymal Stem Cells immunology
Mesenchymal Stem Cells metabolism
Middle Aged
Signal Transduction
Glucosides therapeutic use
Immunomodulation drug effects
Lichen Planus, Oral drug therapy
Mesenchymal Stem Cells drug effects
MicroRNAs metabolism
Paeonia chemistry
STAT3 Transcription Factor metabolism
Subjects
Details
- Language :
- English
- ISSN :
- 1950-6007
- Volume :
- 105
- Database :
- MEDLINE
- Journal :
- Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie
- Publication Type :
- Academic Journal
- Accession number :
- 29852392
- Full Text :
- https://doi.org/10.1016/j.biopha.2018.05.076