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Biogenesis of Lp(a) in transgenic mouse hepatocytes
Author(s) -
White Ann L.
Publication year - 1997
Publication title -
clinical genetics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.543
H-Index - 102
eISSN - 1399-0004
pISSN - 0009-9163
DOI - 10.1111/j.1399-0004.1997.tb04350.x
Subject(s) - biogenesis , endoplasmic reticulum , secretion , apolipoprotein b , microbiology and biotechnology , transgene , hepatocyte , genetically modified mouse , lipoprotein , secretory protein , biology , cell , lipid droplet , biochemistry , chemistry , cholesterol , in vitro , gene
Lipoprotein(a) [Lp(a)] biogenesis was examined in primary cultures of hepatocytes isolated from mice transgenic for both human apolipoprotein(a) [apo(a)] and human apoB. Steady‐state and pulse‐chase labeling experiments demonstrated that newly synthesized human apo(a) had a prolonged residence time (˜60 min) in the endoplasmic reticulum (ER) before maturation and secretion. Apo(a) was inefficiently secreted by the hepatocytes and a large portion of the protein was retained and degraded intracellularly. Apo(a) exhibited a prolonged and complex folding pathway in the ER, which included incorporation of apo(a) into high molecular weight, disulfide‐linked aggregates. These folding characteristics could account for long ER residence time and inefficient secretion of apo(a). Mature apo(a) bound via its kringle domains to the hepatocyte cell surface before appearing in the culture medium. Apo(a) could be released from the cell surface by apoB‐containing lipoproteins. These studies are consistent with a model in which the efficiency of posttranslational processing of apo(a) strongly influences human plasma Lp(a) levels, and suggest that cell surface assembly may be one pathway of human Lpfa) production in vivo. Transgenic mouse hepatocytes thus provide a valuable model system with which to study factors regulating human Lp(a) biogenesis.