| First Author | Li Y | Year | 2015 |
| Journal | J Immunol | Volume | 195 |
| Issue | 6 | Pages | 2648-56 |
| PubMed ID | 26246140 | Mgi Jnum | J:303447 |
| Mgi Id | MGI:6512206 | Doi | 10.4049/jimmunol.1500139 |
| Citation | Li Y, et al. (2015) Hepatic Stellate Cells Inhibit T Cells through Active TGF-beta1 from a Cell Surface-Bound Latent TGF-beta1/GARP Complex. J Immunol 195(6):2648-56 |
| abstractText | Hepatic stellate cells (HSCs) inhibit T cells, a process that could help the liver to maintain its immunoprivileged status. HSCs secrete latent TGF-beta1, but the detailed mechanisms by which latent TGF-beta1 is activated and whether it plays any role in HSC-mediated T cell suppression remain unclear. Glycoprotein A repetitions predominant (GARP) is a surface marker of activated regulatory T cells. GARP binds latent TGF-beta1 for its activation, which is critical for regulatory T cells to suppress effector T cells; however, it is still unclear whether GARP is present on HSCs and whether it has any impact on HSC function. In this study, we found that TGF-beta1(+/-) HSCs, which produce reduced levels of TGF-beta1, showed decreased potency in inhibiting T cells. We also found that pharmaceutical or genetic inhibition of the TGF-beta1 signaling pathway reduced the T cell-inhibiting activity of HSCs. Additionally, using isolated primary HSCs, we demonstrated that GARP was constitutively expressed on HSCs. Blocking GARP function or knocking down GARP expression significantly impaired the potency of HSCs to suppress the proliferation of and IFN-gamma production from activated T cells, suggesting that GARP is important for HSCs to inhibit T cells. These results demonstrate the unexpected presence of GARP on HSCs and its significance in regard to the ability of HSCs to activate latent TGF-beta1 and thereby inhibit T cells. Our study reveals a new mechanism for HSC-mediated immune regulation and potentially for other conditions, such as liver fibrosis, that involve HSC-secreted TGF-beta1. |
