MODULATING EFFECTS OF BILE-SALT HYDROPHOBICITY ON BILE SECRETION OF THE MAJOR PROTEIN OF THE BILE LIPOPROTEIN COMPLEX

Bile lipids are secreted in association with a newly identified major apoprotein called anionic polypeptide fraction-calcium binding protein (APF-CBP), which is synthesized in the hepatocytes and has been detec ted in both bile and plasma and characterized. The secretion of the li pids in bile depends both on the concentration and the hydrophobicity of the bile salts (BS) secreted. The present study was undertaken to d etermine whether the synthesis and the secretion of APF-CBP are simila rly regulated by BS, using two methods. The synthesis and secretion of labelled, newly synthesized APF-CBP by isolated rat hepatocytes were monitored by solid-phase immunoassay. For this purpose, hepatocytes we re incubated with either glycodeoxycholate (GDC) or taurocholate (TC). The synthesis and secretion of labelled, newly synthesized APF-CBP by perfused rat liver were measured by immunological enzyme-linked assay (ELISA) upon perfusing the liver with either GDC or TC. We found that (i) the synthesis and the secretion of APF-CBP were increased during either TC or GDC perfusion, but the increase was more pronounced with TC; (ii) in GDC perfusion the APF-CBP levels measured were more closel y related to the levels of bile salts and not to phospholipid levels, (iii) when the two bile salts were perfused in reverse order, i.e., fi rst GDC and then TC, the secretion of APF-CBP in bile decreased when G DC was perfused, but increased when TC was perfused. Similar results w ere obtained in experiments with isolated hepatocytes. The data sugges t that the hydrophobicity of the BS used in the infusion modulates the synthesis and secretion of APF-CBP. In the liver, the pool of APF-CBP can be modified by BS and responds rapidly to BS stimulation.