Gewählte Publikation:
Menzel, HJ; Dieplinger, H; Lackner, C; Hoppichler, F; Lloyd, JK; Muller, DR; Labeur, C; Talmud, PJ; Utermann, G.
Abetalipoproteinemia with an ApoB-100-lipoprotein(a) glycoprotein complex in plasma. Indication for an assembly defect.
J Biol Chem. 1990; 265(2):981-986
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- Co-Autor*innen der Med Uni Graz
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Lackner Karoline
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- Abstract:
- Patients with autosomal recessive abetalipoproteinemia (ABL) lack in their plasma all lipoproteins containing apolipoprotein (apo)B-100 or B-48. Previous studies have suggested that this is due to the complete absence of apoB. We have investigated whether such patients (n = 10) are able to secrete the lipoprotein(a) (Lp(a] glycoprotein (apo(a] which, in normal plasma, exists as a complex with low density lipoproteins containing apoB-100 (Lp(a) lipoprotein). All 10 patients had reduced but detectable apo(a) levels in plasma (mean, 0.49 mg/dl; range, 0.2-2.03 mg/dl) but no Lp(a) lipoprotein. However, we also detected small amounts (0.2-2.8 mg/dl) of apoB in all patients with ABL. The apoB in the ABL patients had the size of apoB-100 and occurred as a lipid-poor complex with the Lp(a) glycoprotein in a fraction of density 1.22 g/ml. This material may represent partially assembled Lp(a) lipoprotein. There was also uncomplexed apo(a) and apoB-100 in the ABL plasma. The distribution and relative concentration of both proteins in the density fraction greater than 1.06 g/ml varied among patients. The data suggest that in ABL, the assembly of apoB-containing lipoproteins is defective and that apoB-100 may be secreted without its full lipid complement when complexed with apo(a).
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Abetalipoproteinemia - blood
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Adolescent - blood
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Adult - blood
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Apolipoprotein B-100 - blood
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Apolipoproteins A - blood
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Apolipoproteins B - blood
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Blotting, Western - blood
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Chromatography, Affinity - blood
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Electrophoresis, Polyacrylamide Gel - blood
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Enzyme-Linked Immunosorbent Assay - blood
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Glycoproteins - blood
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Humans - blood
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Pedigree - blood
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Ultracentrifugation - blood