By J. Gauldie (auth.), M. B. Pepys MA, MD, PhD, FRCP, MCRPath (eds.)
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A number of phorbol ester inducible nuclear proteins have been identified. These include AP-1, AP-2, AP-3, and NFKB. NFKB has yet to be demonstrated in tissues that normally express SAA. Factors in cell-types other than B-, T- and He La cells have been identified that possess very similar DNA-binding properties to NFKB, but have higher affinity to slightly different sequences. Moreover, the PMA inducible factor AP-3 is able to bind an identical sequence in SV40, but has slightly different binding characteristics from NFKB (Chiu et al.
Thus this upstream sequence of human SAA g9 enhances transcription of a heterologous gene, and is regulated by PMA via a transcription factor. Experiments are in progress to see whether PMA will induce transcription of the whole gene via this mechanism. Cytokine Control of SAA Expression The acute phase response results in a dramatic change in the expression of a group of serum proteins. These changes can be induced in vivo and in vitro by treatment with individual or combinations of cytokines.
1981; Ades et al. Systems for the Study of the Acute Phase Response 31 1982; Pepys and Baltz 1983; Robey and Jones 1986). It appears that their function during APR is to exert a feedback control on the activation of monocytes and lymphocytes. In conclusion, APR can be considered a sort of unspecific first-aid defence of the organism against a broad array of disrupting events. It is important to stress that the APR phenomenon is species-specific (Kushner 1982; Fey and Fuller 1987). The proteins involved differ from species to species.
