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Journal of Lipid Research, Vol 29, 915-923, Copyright © 1988 by Lipid Research, Inc.
MM Hussain, NL Bucher, B Faris, C Franzblau and VI Zannis
We have studied the synthesis, modification, and secretion of rat apoE in
primary cultures of neonatal aortic smooth muscle cells and adult rat
hepatocytes. The cultures were pulsed with [35S]methionine and the
intracellular and secreted apoE were immunoprecipitated and analyzed by
two-dimensional isoelectric focusing/polyacrylamide gel electrophoresis and
autoradiography. A short pulse (10 min) showed the presence of a major
unmodified apoE form in both cultures. This form comigrated on
two-dimensional gels with the major rat plasma apoE isoprotein. A longer
pulse (15-120 min) resulted in the progressive appearance of
intracellularly modified apoE isoproteins in both cultures. The apoE
secreted by aortic smooth muscle cells consisted exclusively of sialated
apoE isoproteins that were sensitive to neuraminidase treatment. In
contrast, the apoE secreted by primary cultures of adult rat hepatocytes,
organ cultures of neonatal rat liver, as well as rat plasma apoE, contained
several minor modified isoproteins. Nascent apoE secreted by the aortic
smooth muscle cell cultures floats in the density range of 1.09 to 1.186
g/ml. We conclude that aortic smooth muscle cells can synthesize and
secrete sialated apoE isoproteins associated with nascent lipoproteins
floating in the high density lipoprotein region.
ARTICLES
Tissue-specific posttranslational modification of rat apoE. Synthesis of sialated apoE forms by neonatal rat aortic smooth muscle cells
Department of Biochemistry, Boston University Medical School, Boston, MA 02118.
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