J. Lipid Res.
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Journal of Lipid Research, Vol. 42, 60-69, January 2001
Copyright © 2001 by Lipid Research, Inc.


Original Article

Determinants of human apolipoprotein [a] secretion from mouse hepatocyte cultures

Jin Wanga, Jennifer Boedekera, Helen H. Hobbsb,c, and Ann L. Whitea
a Center for Human Nutrition, University of Texas Southwestern Medical Center at Dallas, Dallas, TX
b Departments of Internal Medicine, University of Texas Southwestern Medical Center at Dallas, Dallas, TX
c Molecular Genetics, University of Texas Southwestern Medical Center at Dallas, Dallas, TX

Correspondence to: Ann L. White, To whom correspondence should be addressed.

Efforts to develop an in vitro model system to analyze apolipoprotein [a] (apo[a]) gene transcription, mRNA translation, and protein secretion have been complicated by the limited tissue and species distribution of apo[a] and the presence of regulatory DNA sequences remote from the apo[a] transcription start site. In the current study we examined primary hepatocytes cultured from apo[a] transgenic mice as a model system for analyzing apo[a] biogenesis. Hepatocytes from mice transgenic for a yeast artificial chromosome (YAC) encoding the entire apo[a] gene in its own genomic context (YAC-apo[a] hepatocytes) were unable to maintain apo[a] expression beyond 48 h of culture. This suggests that the apo[a] promoter was not active in cultured YAC-apo[a] hepatocytes. In contrast, apo[a] expression was maintained for at least 7 days in hepatocytes cultured from mice transgenic for an apo[a] cDNA under control of the mouse transferrin promoter (transferrin-apo[a] hepatocytes). Pulse-chase experiments established that more than 80% of apo[a] synthesized by both transferrin-apo[a] and YAC-apo[a] hepatocytes was degraded prior to secretion, independently of the coexpression of human apoB.

Thus, low secretion efficiency appears to be a general characteristic of human apo[a] proteins in mouse liver. Apo[a] secretion was increased somewhat (from 18% to 32%) in the presence of lipoprotein-containing serum. Transformed cell lines derived from transferrin apo[a] hepatocytes retained characteristics of apo[a] secretion similar to those observed in primary cells. Primary and transformed apo[a] transgenic hepatocytes may provide valuable additional models with which to study posttranslational mechanisms regulating apo[a] secretion. Wang, J., J. Boedeker, H. H. Hobbs, and A. L. White. Determinants of human apolipoprotein [a] secretion from mouse hepatocyte cultures. J. Lipid Res. 2001. 42: 60;–69.

Supplementary key words: apolipoprotein B, endoplasmic reticulum, lipoprotein [a], proteasome, transcription, transformed liver cell lines


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