Transfer of MHC-class-I molecules among liver sinusoidal cells facilitates hepatic immune surveillance

被引:25
作者
Schoelzel, Katrin [1 ,2 ]
Schildberg, Frank A. [1 ,2 ]
Welz, Meike [1 ,2 ]
Boerner, Carolin [1 ,2 ]
Geiger, Sergej [1 ,2 ]
Kurts, Christian [1 ,2 ]
Heikenwaelder, Mathias [3 ,4 ]
Knolle, Percy A. [1 ,2 ,5 ]
Wohlleber, Dirk [1 ,2 ]
机构
[1] Univ Bonn, Inst Mol Med, Bonn, Germany
[2] Univ Bonn, Inst Expt Immunol, Bonn, Germany
[3] Tech Univ Munich, Inst Virol, D-81667 Munich, Germany
[4] Helmholtz Zentrum Munchen, Munich, Germany
[5] Tech Univ Munich, Inst Mol Immunol, D-81667 Munich, Germany
关键词
LSEC; HSC; Cross-presentation; MHC-I; CROSS-PRESENTATION; DENDRITIC CELLS; T-CELLS; STELLATE CELLS; ENDOTHELIAL-CELLS; TOLERANCE INDUCTION; ANTIGEN; CD8(+); TROGOCYTOSIS; ACTIVATION;
D O I
10.1016/j.jhep.2014.04.028
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background & Aims: In the liver, antigen-presenting cell populations such as Kupffer cells, liver dendritic cells, and liver sinusoidal endothelial cells (LSECs) participate through cross-presentation to CD8 T cells (CTLs) in hepatic immune-regulation and immune-surveillance. The participation of hepatic stellate cells (HSCs) in immune regulation is controversial. Here we studied HSC's contribution to antiviral CTL immunity. Methods: Flow cytometric analysis of MHC-I molecules at the cell surface of liver cells from mice with cell-type restricted MHC-I expression. Mice with HSC-restricted MHC-I expression were infected with a hepatotropic virus and analyzed for development of viral hepatitis after CTL transfer. Results: HSCs transferred MHC-I molecules to LSECs and these molecules were employed for LSEC cross-presentation to CTLs. Such transfer of MHC-I molecules was sufficient to support in vivo LSEC cross-presentation of soluble antigens to CTLs. Importantly, this transfer of MHC-I molecules contributed to anti-viral CTL immunity leading to development of immune-mediated hepatitis. Conclusions: Our findings demonstrate transfer of MHC-I molecules among sinusoidal liver cell populations as a potent mechanism to increase anti-viral CTL effector function. The transfer of MHC-I molecules from HSCs supplies LSECs with additional MHC-I molecules for their own cell-intrinsic cross-presentation. Such cross-allocation of MHC-I molecules in liver cell populations is distinct from cross-dressing that occurs among immune cell populations in lymphoid tissues where peptide-loaded MHC-I molecules are transferred. Our findings thus reveal a novel mechanism that increases local cross-presentation and CTL effector function in the liver, which may be instrumental for immune-surveillance during viral infection of antigen-presenting liver cells. (C) 2014 European Association for the Study of the Liver. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:600 / 608
页数:9
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