Involvement of TLR3-Dependent PGES Expression in Immunosuppression by Human Bone Marrow Mesenchymal Stem Cells

作者：Kim Dae Seong; Lee Whi Hyeong; Lee Myoung Woo^*; Park Hyun Jin; Jang In Keun; Lee Ji Won; Sung Ki Woong; Koo Hong Hoe; Yoo Keon Hee^*

来源：Stem Cell Reviews, 2018, 14(2): 286-293.

DOI：10.1007/s12015-017-9793-6

• Mesenchymal stem cell
• Cyclooxygenase 2
• Prostaglandin E synthase
• Prostaglandin E-2
• Immunosuppression

Human mesenchymal stem cells (MSCs) are known for their prostaglandin E-2 (PGE(2))-mediated immunosuppressive function but the precise molecular mechanisms underlying PGE(2) biosynthesis during inflammation have not been completely elucidated. In this study, we have investigated the involvement of PGE(2) pathway members in PGE(2) production by bone marrow (BM)-MSCs in response to inflammatory stimuli, and their role in immunosuppression mediated by BM-MSCs. We found that IFN-gamma and TNF-alpha increased cyclooxygenase (COX)-2 expression but not that of prostaglandin E synthase (PGES), or PGE(2) production. On the other hand, the toll like receptor 3 (TLR3) stimulant poly(I:C) increased expression of both COX-2 and PGES, resulting in a significant increase in PGE(2) levels. This effect was reversed upon COX-2 inhibition with indomethacin or PGES downregulation by siRNA. Reduced PGE(2) levels decreased MSC's capacity to inhibit hPBMC proliferation. In addition, administration of MSCs with inhibited PGES expression into mice with graft-versus-host disease (GVHD) did not reduce mortality. In summary, the present study reveals that upregulation of PGES via TLR3 is critical for BM-MSCs-mediated immunosuppression by PGE(2) secretion via the COX-2/PGE(2) pathway. These results provide a basis for understanding the molecular mechanisms underlying the PGE(2)-mediated immunosuppressive properties of MSCs.

• 出版日期2018-4