An abnormal triglyceride-rich lipoprotein containing excess sialylated apolipoprotein C-III
- PMID: 7076853
- PMCID: PMC370147
- DOI: 10.1172/jci110532
An abnormal triglyceride-rich lipoprotein containing excess sialylated apolipoprotein C-III
Abstract
An abnormal triglyceride-rich lipoprotein has been isolated from some patients with chronic renal failure or severe hypertriglyceridemia. The abnormal lipoprotein was characterized by an increased content of apolipoprotein (apo) C-III-2 (57.5% of total apo C-III peptides compared with 35.5% for controls, P less than 0.001) as characterized by isoelectric focusing and scanning densitometry. As determined by a substrate competition assay, the abnormal lipoprotein was a less efficient substrate for purified bovine milk lipoprotein lipase than control lipoproteins. Neuraminidase digestion of abnormal or control lipoprotein resulted in a reduction of the apo C-III-2 band with a corresponding increase in the region of apo C-III-0, which suggests that the increased content of apo C-III-2 in the abnormal is due to excessive sialylation of the C-III peptide. Limited incubation of the abnormal lipoproteins with neuraminidase caused a partial loss of sialic acid and resulted in a triglyceride-rich lipoprotein with a normal C-III-2:C-III-1 ratio. This preparation displayed normal substrate interaction with lipoprotein lipase. Three severely hypertriglyceridemic patients with the abnormal lipoprotein showed a marked reduction in serum triglyceride concentration, which is associated with a reversion to a normal C-peptide profile after dietary therapy. The results suggest that the extent of sialylation of the apo C-III peptide carried on triglyceride-rich lipoproteins may be critical for their interaction with lipoprotein lipase.
Similar articles
-
Effect of heparin-induced lipolysis on the distribution of apolipoprotein e among lipoprotein subclasses. Studies with patients deficient in hepatic triglyceride lipase and lipoprotein lipase.J Clin Invest. 1985 Feb;75(2):710-21. doi: 10.1172/JCI111751. J Clin Invest. 1985. PMID: 3973025 Free PMC article.
-
Quantitation of human apolipoprotein C-III and its subspecie by radioimmunoassay and analytical isoelectric focusing: abnormal plasma triglyceride-rich lipoprotein apolipoprotein C-III subspecie concentrations in hypertriglyceridemia.J Lipid Res. 1981 Jul;22(5):800-10. J Lipid Res. 1981. PMID: 7288286
-
Hypertriglyceridaemia associated with an abnormal triglyceride-rich lipoprotein carrying excess apolipoprotein C-III-2.Lancet. 1979 Sep 29;2(8144):667-71. doi: 10.1016/s0140-6736(79)92068-3. Lancet. 1979. PMID: 90760
-
Apolipoprotein C-III and hepatic triglyceride-rich lipoprotein production.Curr Opin Lipidol. 2012 Jun;23(3):206-212. doi: 10.1097/MOL.0b013e328352dc70. Curr Opin Lipidol. 2012. PMID: 22510806 Review.
-
The sialylation of plasma lipoproteins.Atherosclerosis. 2001 Jan;154(1):1-13. doi: 10.1016/s0021-9150(00)00697-3. Atherosclerosis. 2001. PMID: 11137077 Review.
Cited by
-
Apo CIII Proteoforms, Plasma Lipids, and Cardiovascular Risk in MESA.Arterioscler Thromb Vasc Biol. 2023 Aug;43(8):1560-1571. doi: 10.1161/ATVBAHA.123.319035. Epub 2023 Jun 15. Arterioscler Thromb Vasc Biol. 2023. PMID: 37317850
-
Systematic Assessment of Protein C-Termini Mutated in Human Disorders.Biomolecules. 2023 Feb 12;13(2):355. doi: 10.3390/biom13020355. Biomolecules. 2023. PMID: 36830724 Free PMC article.
-
The known unknowns of apolipoprotein glycosylation in health and disease.iScience. 2022 Aug 28;25(9):105031. doi: 10.1016/j.isci.2022.105031. eCollection 2022 Sep 16. iScience. 2022. PMID: 36111253 Free PMC article. Review.
-
Cardiovascular Disease Risk in Children With Chronic Kidney Disease: Impact of Apolipoprotein C-II and Apolipoprotein C-III.Front Pediatr. 2021 Aug 12;9:706323. doi: 10.3389/fped.2021.706323. eCollection 2021. Front Pediatr. 2021. PMID: 34458211 Free PMC article.
-
The Roles of ApoC-III on the Metabolism of Triglyceride-Rich Lipoproteins in Humans.Front Endocrinol (Lausanne). 2020 Jul 28;11:474. doi: 10.3389/fendo.2020.00474. eCollection 2020. Front Endocrinol (Lausanne). 2020. PMID: 32849270 Free PMC article. Review.
References
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Medical
Research Materials
