Activation of Kupffer cells inhibits tumor growth in a murine model system

TitleActivation of Kupffer cells inhibits tumor growth in a murine model system
Publication TypeJournal Article
Year of Publication2002
AuthorsChen GG, Lau WY, Lai PB, Chun YS, Chak EC, Leung BC, Lam IK, Lee JF, Chui AK
JournalInt J Cancer
Volume99
Issue5
Pagination713 - 20
Date PublishedJun 10
Accession Number12115505
KeywordsAnimals, Apoptosis, Blotting, Western, Caspases / metabolism, DNA Damage, Glioma / pathology / prevention & control, Immunohistochemistry, Interferon Type II / analysis, Kupffer Cells / *physiology, Mice, Mice, Inbred BALB C, Mice, Nude, Neoplasm Transplantation, Neoplasms, Experimental / pathology / *prevention & control, Nitric Oxide / analysis, Proto-Oncogene Proteins c-bcl-2 / analysis, Rats, Research Support, Non-U.S. Gov't, Tumor Necrosis Factor-alpha / analysis
Abstract

Kupffer cells, a liver organ-specific macrophage, play an important role in preventing the development of malignant tumors. The mechanism responsible for their tumoricidal activities is not completely known. In our study, we established in vivo models involving a rat malignant cell line, rat Kupffer cells and tumor implantation in nude mice. A series of relevant in vitro experiments were also carried out to determine possible pathways. LPS-activated Kupffer cells produced significant amounts of NO, TNFalpha and IFNgamma. Malignant cells treated with either Kupffer cells or culture supernatant of the activated Kupffer cells had an increase in caspase-8 activity. Implanted tumors originated from malignant cells treated with either Kupffer cells or culture supernatant of the activated Kupffer cells grew much smaller than those from malignant cells without treatment or treated with control supernatants. The alteration of anti-apoptotic Bcl-2 was inversely associated with the change of pro-apoptotic caspase-8 and their levels in the tumor tissues matched the size of the tumors and treatments they received. It appeared that the above changes resulted in an increase in cellular DNA damage and apoptosis seen in malignant cells. Therefore, Kupffer cells execute their anti-tumor effect via increasing the production of NO, TNFalpha and IFNgamma and these cytotoxic molecules inhibit the growth of tumor by damaging cellular DNA and inducing apoptosis that was featured by downregulation of Bcl-2 but upregulation of caspase-8.

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