共 36 条
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.
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页码:600 / 608
页数:9
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