Recycling of apolipoprotein E in mouse liver

Sergio Fazio, MacRae F. Linton, Alyssa H. Hasty, Larry L. Swift

Research output: Contribution to journalArticle

44 Citations (Scopus)

Abstract

Following the internalization of low density lipoprorein (LDL) by the LDL receptor within cells, both the lipid and the protein components of LDL are completely degraded within the lysosomes. Remnant lipoproteins are also internalized by cells via the LDL receptor as well as other receptors, but the events following the internalization of these complexes, which use apolipoprotein E (apoE) as their ligand for receptor capture, have not been defined. There is evidence that apoE-containing β-very low density lipoproteins follow differential intracellular routing depending on their size and apoE content and that apoE internalized with lipoproteins can be resecreted by cultured hepatocytes and fibroblasts. In the present studies, we addressed the question of apoE sparing or recycling as a physiologic phenomenon. Remnant lipoproteins (d <1.019 g/ml) from normal mouse plasma were iodinated and injected into normal C57BL/6 mice. Livers were collected at 10, 30, 60, and 120 min after injection, and hepatic Golgi fractions were prepared for gel electrophoresis analysis. Golgi preparations were analyzed for galactosyltransferase enrichment (>40-fold above cell homogehate) and by appearance of the Golgi stacks and vesicles on electron microscopy. Iodinated apoE was consistently found in the Golgi fractions peaking at 10 min and disappearing by 2 h after injection. Although traces of apoB48 were present in the Golgi fractions, the apoE/apoB ratio in the Golgi was 50-fold higher compared with serum. Quantitatively similar results were obtained when the very low density lipoprotein remnants were injected into mice deficient in either apoE or the LDL receptor, indicating that the phenomenon of apoE recycling is not influenced by the production of endogenous apoE and is not dependent on the presence of LDL receptors. In addition, radioactive apoE in the Golgi fractions was part of d = 1.019-1.21 g/ml complexes, indicating an association of recycled apoE with either newly formed lipoproteins or the internalized complexes. These studies show that apoE recycling is a physiologic phenomenon in vivo and establish the presence of a unique pathway of intracellular processing of apoE-containing remnant lipoproteins.

Original languageEnglish (US)
Pages (from-to)8247-8253
Number of pages7
JournalJournal of Biological Chemistry
Volume274
Issue number12
DOIs
StatePublished - Mar 19 1999
Externally publishedYes

Fingerprint

Recycling
Apolipoproteins E
Liver
Lipoproteins
VLDL Lipoproteins
Apolipoprotein B-48
Apolipoproteins B
Fibroblasts
Lysosomes
Electron microscopy
Hepatocytes
Electron Microscopy

ASJC Scopus subject areas

  • Biochemistry

Cite this

Recycling of apolipoprotein E in mouse liver. / Fazio, Sergio; Linton, MacRae F.; Hasty, Alyssa H.; Swift, Larry L.

In: Journal of Biological Chemistry, Vol. 274, No. 12, 19.03.1999, p. 8247-8253.

Research output: Contribution to journalArticle

Fazio, Sergio ; Linton, MacRae F. ; Hasty, Alyssa H. ; Swift, Larry L. / Recycling of apolipoprotein E in mouse liver. In: Journal of Biological Chemistry. 1999 ; Vol. 274, No. 12. pp. 8247-8253.
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