Literature DB >> 24043462

CD39-mediated effect of human bone marrow-derived mesenchymal stem cells on the human Th17 cell function.

Jong Joo Lee1, Hyun Jeong Jeong, Mee Kum Kim, Won Ryang Wee, Won Woo Lee, Seung U Kim, Changmin Sung, Yung Hun Yang.   

Abstract

This study investigated the immune-modulatory effects of human bone marrow-derived mesenchymal stem cells (hBMSCs) on human Th17 cell function through the CD39-mediated adenosine-producing pathway. The suppressive effects of hBMSCs were evaluated by assessing their effects on the proliferation of Th17 cells and the secretion of interferon (IFN)-γ and interleukin (IL)-17A by Th17 cells with or without anti-CD39 treatment. Changes in CD39 and CD73 expression on the T cells with or without co-culture of hBMSCs were evaluated by flow cytometry. hBMSCs effectively suppressed the proliferation of Th17 cells and the secretion of both IL-17A and IFN-γ from Th17 cells using by both flow cytometry and ELISA, while anti-CD39 treatment significantly reduced the inhibitory effects of hBMSCs on the proliferation and secretion of the Th17 cells. The hBMSCs induced increased expression of the CD39 and CD73 on T cells correlated with the suppressive function of hBMSCs, which was accompanied by increased adenosine production. Our data suggests that hBMSCs can effectively suppress immune responses of the Th17 cells via the CD39-CD73-mediated adenosine-producing pathway.

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Year:  2013        PMID: 24043462      PMCID: PMC4040175          DOI: 10.1007/s11302-013-9385-0

Source DB:  PubMed          Journal:  Purinergic Signal        ISSN: 1573-9538            Impact factor:   3.765


  29 in total

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6.  Mesenchymal stromal cells up-regulate CD39 and increase adenosine production to suppress activated T-lymphocytes.

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Review 7.  Mechanisms of T-cell immunosuppression by mesenchymal stromal cells: what do we know so far?

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Review 8.  The role of purinergic receptors in stem cell differentiation.

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Review 10.  Comparing the Immunomodulatory Properties of Bone Marrow, Adipose Tissue, and Birth-Associated Tissue Mesenchymal Stromal Cells.

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