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Effects of Kupffer cell-depletion on Concanavalin A-induced hepatitis.
- Source :
-
Cellular immunology [Cell Immunol] 2008 Jan; Vol. 251 (1), pp. 25-30. Date of Electronic Publication: 2008 Mar 28. - Publication Year :
- 2008
-
Abstract
- TNF-alpha, IFN-gamma, IL-4, and MIP-2 are known to be involved in Con A-induced hepatitis. Although Kupffer cells are reportedly involved in TNF-alpha production, it is largely unknown whether or not Kupffer cells also play a role in the production of other cytokines, such as IFN-gamma, IL-4, and MIP-2. In this study we examined the liver injury and the levels of plasma cytokines, including above four cytokines, KC, and IL-10 in Kupffer cell-depleted mice obtained through administration of liposome-encapsulated dichloromethylene bisphosphonate. The liver injury was significantly suppressed in Kupffer cell-depleted mice, as assessed as to the plasma ALT level and histochemistry. The cytokine levels were also significantly suppressed in such mice except for those of IFN-gamma, which was slightly suppressed at 12h, and IL-10, which was not significantly suppressed at any time. Apoptosis was also significantly suppressed in such mice, as found immunohistochemically with anti-ssDNA Ab. Taken together, these results suggest that Kupffer cells are involved in the production of MIP-2, KC, IL-4, and TNF-alpha in Con A-induced hepatitis, thereby contributing to the liver injury either directly or indirectly.
- Subjects :
- Animals
Apoptosis drug effects
Chemical and Drug Induced Liver Injury immunology
Clodronic Acid toxicity
Disease Models, Animal
Immunohistochemistry
Kupffer Cells drug effects
Liposomes
Male
Mice
Chemical and Drug Induced Liver Injury pathology
Concanavalin A
Cytokines blood
Kupffer Cells metabolism
Kupffer Cells pathology
Subjects
Details
- Language :
- English
- ISSN :
- 1090-2163
- Volume :
- 251
- Issue :
- 1
- Database :
- MEDLINE
- Journal :
- Cellular immunology
- Publication Type :
- Academic Journal
- Accession number :
- 18374909
- Full Text :
- https://doi.org/10.1016/j.cellimm.2008.02.003