Induction of tumour necrosis factor and interferon-γ in cultured murine splenocytes by the antivascular agent DMXAA and its metabolites
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- 作者：Wang ; Liang-Chuan S. ; Reddy ; Charu B. ; Baguley ; Bruce C. ; Kestell ; Philip ; Sutherland ; Rachel ; et. al.
- 关键词：DMXAA ; 5 ; 6-dimethylxanthenone-4-acetic acid ; TNF ; tumour necrosis factor ; IFN ; interferon ; IP-10 ; interferon-inducible protein-10 ; PBL ; peripheral blood leucocytes ; LPS ; lipopolysaccharide ; MEM ; modified essential medium ; DMXAA-G ; DMXAA-glucuronide ; 6-OH-
- 刊名：Biochemical Pharmacology
- 出版年：2004
- 出版时间：March 1, 2004
- 年：2004
- 卷：67
- 期：5
- 页码：937-945
- 全文大小：161 K
文摘
The induction of haemorrhagic necrosis by 5,6-dimethylxanthenone-4-acetic acid (DMXAA) in transplantable murine tumours depends on the in situ synthesis of cytokines, particularly tumour necrosis factor (TNF). Since the in vivo action of DMXAA would be greatly clarified by the development of an in vitro model, we investigated whether DMXAA could induce cytokines in cultured murine splenocytes. DMXAA alone induced low amounts of TNF with an optimal concentration of 10μg/mL and an optimal time of 4hr. When combined with low concentrations of lipopolysaccharide, deactivated-lipopolysaccharide (dLPS) or phorbol-12-myristate-13-acetate that did not elicit TNF production alone, synergistic TNF production was obtained. DMXAA also induced interferon-γ at an optimal dose of 300μg/mL, but the addition of dLPS had no further effect. Decreasing culture pH, although not changing the optimal concentrations for stimulation, increased both TNF and interferon-γ production in response to DMXAA. The major DMXAA metabolites, DMXAA-glucuronide and 6-hydroxy-5-methylxanthenone-4-acetic acid, did not induce either cytokine alone, in combination with dLPS or at low pH. The results indicate that DMXAA rather than a metabolite is responsible for cytokine induction and suggest that the microenvironment of the tumour may be responsible for the observed selective induction of cytokines in tumour tissue.