directly by activating the matrix metalloproteinases (MMPs), Urokinase plasminogen activator (uPA) generates interstitial collagenase, and stromelysin. 4,5 Between them plasmin, a process inhibited by plasminogen-activator these enzymes are capable of degrading most matrix compoinhibitor (PAI)-1 and
In vivo immune modulatory activity of hepatic stellate cells in mice
β Scribed by Cheng-Hsu Chen; Liang-Mou Kuo; Yigang Chang; Wenhan Wu; Christina Goldbach; Mark A. Ross; Donna B. Stolz; Liepin Chen; John J. Fung; Lin Lu; Shiguang Qian
- Publisher
- John Wiley and Sons
- Year
- 2006
- Tongue
- English
- Weight
- 919 KB
- Volume
- 44
- Category
- Article
- ISSN
- 0270-9139
No coin nor oath required. For personal study only.
β¦ Synopsis
Accumulating data suggest that hepatic tolerance, initially demonstrated by spontaneous acceptance of liver allografts in many species, results from an immune regulatory activity occurring in the liver. However, the responsible cellular and molecular components have not been completely understood. We have recently described profound T cell inhibitory activity of hepatic stellate cells (HSCs) in vitro. In this study, we demonstrate in vivo evidence of immune modulatory activity of HSCs in mice using an islet transplantation model. Co-transplanted HSCs effectively protected islet allografts from rejection, forming a multi-layered capsule, which reduced allograft immunocyte infiltrates by enhancement of apoptotic death. The immune modulation by HSCs appeared to be a local effect, and regulated by inducible expression of B7-H1, an inhibitory molecule of B7 family. This may reflect an intrinsic mechanism of immune inhibition mediated by liver-derived tissue cells. In conclusion, these results may lead to better understanding of liver immunobiology and development of new strategies for treatment of liver diseases.
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## Abstract The authors have demonstrated a strong Tβcell inhibitory activity of hepatic stellate cells (HSC), which may participate in the establishment of hepatic tolerance. The underlying mechanism is not completely understood. This study showed that intercellular adhesion molecule 1 (ICAMβ1) wa
## Abstract Hepatic tolerance is demonstrated by spontaneous acceptance of liver allografts in mice. Hepatic dendritic cells (DC) play a crucial role in determining immunity or tolerance. In this study, we adopted an approach to transfect gene(s) into the mouse liver by tailβvein injection of plasm
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