Serpin-6 expression protects embryonic stem cells from lysis by antigen-specific CTL

被引:42
作者
Abdullah, Zeinab
Saric, Tomo
Kashkar, Hamid
Baschuk, Nikola
Yazdanpanah, Benjamin
Fleischmann, Bernd K.
Hescheler, Juergen
Kroenke, Martin
Utermoehlen, Olaf
机构
[1] Univ Cologne, Inst Med Microbiol Immunol & Hyg, Ctr Med, D-50935 Cologne, Germany
[2] Univ Cologne, Inst Neurophysiol, Ctr Med, D-50935 Cologne, Germany
[3] Univ Bonn, Inst Physiol 1, Life & Brain Ctr, D-5300 Bonn, Germany
[4] Univ Cologne, Ctr Mol Med, D-50935 Cologne, Germany
关键词
D O I
10.4049/jimmunol.178.6.3390
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The immune response to embryonic stem (ES) cells is still poorly understood. In this study, we addressed the adaptive cellular immune response to undifferentiated and differentiated ES cells infected with lymphocytic choriomeningitis virus (LCMV), a vertically transmitted pathogen in mice and humans. In contrast to the prevailing view, we found that undifferentiated and differentiated murine ES cells express MHC class I molecules, although at low levels. When cocultured with LCMV-infected ES cells, syngeneic but not allogeneic LCMV-specific CTL secrete IFN-gamma. Strikingly, LCMV-specific CTL do not efficiently kill LCMV-infected ES cells. ES cells showed high-level expression of the serine protease inhibitor 6, an endogenous inhibitor of the CTL-derived cytotoxic effector molecule granzyme B. Down-regulation of serpin-6 by RNA interference sensitized ES cells for CTL-induced cell death. The results of this study suggest that LCMV-infected murine ES cells present viral Ags and are recognized by LCMV-specific CTL in a MHC class I-restricted manner, yet resist CTL-mediated lysis through high-level expression of serine protease inhibitor 6.
引用
收藏
页码:3390 / 3399
页数:10
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