Although the role of CD8 as a supplier of lck is unchallenged, its role in contributing to the formation of a stable complex between class I molecules and the TCR, as well as its role as an adhesion molecule, is less clear. To address the role of CD8/MHC-I interactions, we generated tetramers compos
Recently primed CD8+ T cells entering the liver induce hepatocytes to interact with naïve CD8+ T cells in the mouse
✍ Scribed by Nektarios Dikopoulos; Ursula Wegenka; Andrea Kröger; Hansjörg Hauser; Reinhold Schirmbeck; Jörg Reimann
- Publisher
- John Wiley and Sons
- Year
- 2004
- Tongue
- English
- Weight
- 411 KB
- Volume
- 39
- Category
- Article
- ISSN
- 0270-9139
No coin nor oath required. For personal study only.
✦ Synopsis
Large number of T cells traffic through the liver. In order to examine the effects of such traffic on the phenotype of hepatocytes, we vaccinated mice using DNA vaccines encoding antigens with MHC class I-binding epitopes. Small numbers of activated CD8 ؉ T blasts (10 5 -10 6 / liver) changed the surface phenotype and cytokine expression profile of hepatocytes (HCs).
HCs upregulate surface expression of major histocompatibility complex (MHC) class I molecules and CD1d but not MHC class II molecules
Qa-1, CD80, CD86, CD54, or CD95; in addition, they expressed/secreted interleukin (IL)-10 and IL-4 but not IL-1, IL-6, IL-13, interferon (IFN)-␥, tumor necrosis factor (TNF), IL-4, or IL-27 (i.e., they acquire the HC* phenotype). HCs* (but not HCs) induced specific activation, proliferation, and IFN-␥, TNF, and IL-13 release of cocultured naı ¨ve CD8 ؉ T cells. In contrast to the specific activation of naı ¨ve CD8 ؉ T cells by dendritic cells (DCs), specific CD8 ؉ T cell activation by HC* was not down-modulated by IFN-␣. Only recently activated CD8 ؉ T blasts (but not recently activated CD4 ؉ T blasts or activated cells of the innate immune system, including natural killer T [NKT] cells) induced the HC* phenotype that is prominent from day 10 to day 20 postvaccination (i.e., time points at which peak numbers of recently primed CD8 ؉ T blasts are found in the liver). In conclusion, recently activated CD8 ؉ T blasts that enter the liver postimmunization in small numbers can transiently modulate the phenotype of HC, allowing them to activate naı ¨ve CD8 ؉ T cells with unrelated specificities. (HEPATOLOGY 2004;39: 1256 -1266.
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