| Literature DB >> 27167148 |
Jia Ng1, Kim Hynes1, Gregory White1,2, Kisha Nandini Sivanathan2,3, Kate Vandyke4,5,6, Peter Mark Bartold1, Stan Gronthos7,8.
Abstract
MSC-like populations derived from induced pluripotent stem cells (iPSC-MSC) serve as an alternative stem cell source due to their high proliferative capacity. In this study, we assessed the immunomodulatory potential of iPSC-MSC generated from periodontal ligament (PDL) and gingival (GF) tissue. The iPSC-MSC lines exhibited a similar level of suppression of mitogen-stimulated peripheral blood mononuclear cells (PBMNC) proliferation compared to their respective parental fibroblast populations in vitro. Moreover, iPSC-MSC demonstrated the ability to suppress T-cells effector cells, Th1/Th2/Th17 populations, and increase levels of Treg cells. In order to investigate the mechanisms involved, expression of common MSC-derived soluble factors known to supress lymphocyte proliferation were assessed in iPSC-MSC cultured with PBMNC with direct cell-cell contact or separated in transwells. Real-time PCR analysis of factors known to be involved in MSC mediated immune regulation, found a general trend of elevated IDO1 and IL6 transcript levels in iPSC-MSC lines and their respective primary cells co-cultured with activated PBMNC, with a wide range of gene expression levels between the different mesenchymal cell types. The results suggest that different iPSC-MSC may be useful as a potential alternative source of cells for future clinical use in therapeutic applications because of their potent immunosuppressive properties. J. Cell. Biochem. 117: 2844-2853, 2016.Entities:
Keywords: GINGIVAL FIBROBLASTS; MESENCHYMAL STEM CELL; PERIODONTAL LIGAMENT CELL; T-CELLS; iPSC
Mesh:
Substances:
Year: 2016 PMID: 27167148 DOI: 10.1002/jcb.25596
Source DB: PubMed Journal: J Cell Biochem ISSN: 0730-2312 Impact factor: 4.429