Immune-regulation of the apolipoprotein A-I/C-III/A-IV gene cluster in experimental inflammation
Apolipoprotein A-IV is a member of the apo A-I/C-III/A-IV gene cluster. In order to investigate its hypothetical coordinated regulation, an acute phase was induced in pigs by turpentine oil injection. The hepatic expression of the gene cluster as well as the plasma levels of apolipoproteins were mon...
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Veröffentlicht in: | Cytokine (Philadelphia, Pa.) Pa.), 2005-07, Vol.31 (1), p.52-63 |
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Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | Apolipoprotein A-IV is a member of the
apo A-I/C-III/A-IV gene cluster. In order to investigate its hypothetical coordinated regulation, an acute phase was induced in pigs by turpentine oil injection. The hepatic expression of the gene cluster as well as the plasma levels of apolipoproteins were monitored at different time periods. Furthermore, the involvement of the inflammatory mediators' interleukins 1 and 6 and tumor necrosis factor in the regulation of this gene cluster was tested in cultured pig hepatocytes, incubated with those mediators and
apo A-I/C-III/A-IV gene cluster expression at the mRNA level was measured. In response to turpentine oil-induced inflammation, a decreased hepatic
apo A-IV mRNA expression was observed (independent of
apo A-I and
apo C-III mRNA) not correlating with the plasma protein levels. The distribution of plasma apo A-IV experienced a shift from HDL to larger particles. In contrast, the changes in
apo A-I and
apo C-III mRNA were reflected in their corresponding plasma levels. Addition of cytokines to cultured pig hepatocytes also decreased
apo A-IV and
apo A-I mRNA levels. All these results show that the down-regulation of apolipoprotein
A-I and
A-IV messages in the liver may be mediated by interleukin 6 and TNF-α. The well-known HDL decrease found in many different acute-phase responses also appears in the pig due to the decreased expression of apolipoprotein A-I and the enlargement of the apolipoprotein A-IV-containing HDL. |
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ISSN: | 1043-4666 1096-0023 |
DOI: | 10.1016/j.cyto.2005.03.002 |