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Pyridoxal-5'-Phosphate Promotes Immunomodulatory Function of Adipose-Derived Mesenchymal Stem Cells through Indoleamine 2,3-Dioxygenase-1 and TLR4/NF- κ B Pathway.
- Source :
-
Stem cells international [Stem Cells Int] 2019 Nov 25; Vol. 2019, pp. 3121246. Date of Electronic Publication: 2019 Nov 25 (Print Publication: 2019). - Publication Year :
- 2019
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Abstract
- Adipose-derived mesenchymal stem cells (A-MSCs) are promising cellular therapies for the treatment of immune-mediated diseases. Non-gene editing technologies can improve the immune regulatory function of A-MSCs. Our preliminary experiments revealed that an active form of vitamin B6-pyridoxal-5'-phosphate (PLP)-plays an important role in regulating gene expression and cytokine secretion in A-MSCs in vivo . To further clarify the effect of PLP on receptors and cytokines related to the immune regulatory function of A-MSCs, a series of experiments were designed to verify the relationships between PLP and A-MSCs in vitro . Initially, A-MSCs were obtained, and cytokine secretion and the expression of IDO1, NF- κ B, and Toll-like receptors in PLP-stimulated A-MSCs were evaluated. In addition, coculture was used to detect A-MSCs-mediated apoptosis of CD3 <superscript>+</superscript> CD8 <superscript>+</superscript> T lymphocytes. These results showed that A-MSCs stimulated with PLP were highly proliferative, consistent with their pluripotent capacity. Further, the surface receptors TLR3, TLR4, IDO1, and NF- κ B were upregulated, while TLR6 was downregulated. Concurrently, A-MSCs preconditioned with PLP had the greatest inhibitory effect on CD3 <superscript>+</superscript> CD8 <superscript>+</superscript> T lymphocyte proliferation, indicating that PLP altered the immune regulatory function of A-MSCs through the regulation of TLRs and IDO1 expression.<br />Competing Interests: The authors report no conflict of interest.<br /> (Copyright © 2019 Cong Li et al.)
Details
- Language :
- English
- ISSN :
- 1687-966X
- Volume :
- 2019
- Database :
- MEDLINE
- Journal :
- Stem cells international
- Publication Type :
- Academic Journal
- Accession number :
- 31885603
- Full Text :
- https://doi.org/10.1155/2019/3121246