Abstract

Hepatic lipase, a glycoprotein synthesized and secreted by the hepatocyte, binds to sinusoidal endothelium where it is involved in metabolism of lipoprotein phospholipid and triglyceride. To better understand the regulation of hepatic lipase, we investigated the synthesis, post-translational processing, and secretion of the enzyme by isolated rat hepatocytes. Metabolically labeled [35S]methionine hepatic lipase protein, produced by the collagenase-dispersed hepatocytes, was immunoisolated from detergent-solubilized cells and incubation medium at designated times, using a polyclonal rabbit anti-rat hepatic lipase antibody raised against hepatic lipase purified to homogeneity from rat liver post-heparin perfusates. Following polyacrylamide gel electrophoresis and fluorography, radiolabeled hepatic lipase was quantitated by densitometry. Newly synthesized hepatic lipase was rapidly secreted and accumulated in the medium as a 59,000-dalton protein in a manner consistent with a constitutive process. An intracellular 53,000-dalton precursor of the mature 59,000-dalton hepatic lipase was identified by immunoprecipitation. The 53,000-dalton form could also be generated by endoglycosidase digestion of the secreted 59,000-dalton protein. In pulse-chase experiments, the 53,000-dalton protein was converted into the 59,000-dalton form. A 47,000-dalton form of hepatic lipase was immunoisolated from cell lysates only after tunicamycin treatment and could be generated from the secreted 59,000-dalton enzyme by prolonged endoglycosidase digestion. These data show that hepatic lipase is synthesized and rapidly secreted by isolated rat hepatocytes. Further, an intracellular 47,000-dalton precursor peptide can be identified after tunicamycin treatment, which may represent the hepatic lipase polypeptide, presumably after removal of its signal sequence; a 53,000-dalton partially glycosylated peptide exists as a major precursor form in the cell; and the mature 59,000-dalton hepatic lipase is present in the hepatocyte, but it is rapidly secreted.

Highlights

  • From the Departmentsof 7Obstetrics and Gynecologyand of $Pathology and Laboratory Medicine, Universityof Pennsylvania and the §Department of Physwlogy/Bwchemistry,Medical College of Pennsylvania, Philadelphia, Pennsylvania 19104-4283

  • It hsaisnce creted by the hepatocyte, binds to sinusoidal endothelium where it isinvolved in metabolism of lipoprotein phospholipid and triglyceride

  • To better understand the regulation of hepatic lipase, we investigated the synthesis, post-translationalprocessing, and secretion of the enzyme by isolated rat hepatocytes

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Summary

Hepatic Lipase

Labeled [36S]methioninehepatic lipase protein, produced by the collagenase-dispersed hepatocytes, was immunoisolated from detergent-solubilized cells and incubation medium at designated times, using a polyclonal rabbitanti-rat hepatic lipaseantibody raised against hepatic lipase purified to homogeneity from rat liver post-heparin perfusates. That hepatic lipase is synthesized and rapidly secreted Hepaticlipase from several species has been purified to by isolated rat hepatocytes. N-Glycosidase F Digestion of Hepatic Lipase-For hydrolysis of asparagine-linked oligosaccharides,isolated hepatocytes were prepared, incubated in Dulbecco's modified Eagle's medium containing [:''S]methionine, and hepaticlipase was immunoisolated asdescribed above from 150 pl of medium of an isolated hepatocyte suspension after 4 h of incubation.Hepatic lipase was dissociatedfrom the immunoprecipitate by the addition of 30 pl of 0.0625 M Tris, pH8.6, containing 2% SDS, and the mixture was heated a t 90 "C for 3 min, followed by centrifugation a t 8000 X g for 10 min.

RESULTS AND DISCUSSION
MW X
SynthesainsSdecretion of HepatLicipase by IsolatReHdatepatocytes
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