A study of the abnormal lipoproteins in abetalipoproteinemia
Autor: | A W Kruski, Angelo M. Scanu, C T Lim, H J Kayden, L P Aggerbeck |
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Rok vydání: | 1974 |
Předmět: |
Adult
Male medicine.medical_specialty Adolescent Lipoproteins Blood serum Internal medicine medicine Humans Distribution (pharmacology) Centrifugation Child Apolipoproteins B chemistry.chemical_classification Circular Dichroism Abetalipoproteinemia General Medicine Metabolism medicine.disease Lipids Lipoproteins LDL Apolipoproteins Endocrinology Enzyme Biochemistry chemistry Electrophoresis Polyacrylamide Gel Female lipids (amino acids peptides and proteins) Ultracentrifuge Lipoproteins HDL Research Article Lipoprotein |
Zdroj: | Journal of Clinical Investigation. 53:440-453 |
ISSN: | 0021-9738 |
DOI: | 10.1172/jci107578 |
Popis: | The serum lipoproteins of five patients with abetalipoproteinemia (ABL) were separated by ultracentrifugation and then analyzed either intact or after delipidation. In accord with previous findings, all of the patients lacked serum particles with the characteristics of normal low-density lipoproteins (LDL) and of the LDL apoprotein as assessed by immunochemical methods. Each patient exhibited on every examination an abnormal particle, "LDL", which had the flotational properties of LDL, the polypeptide makeup of high-density lipoproteins HDL, the spectral and morphological characteristics of neither LDL nor HDL, and a relatively low content of cholesteryl esters. The HDL were abnormal in having a marked decrease in their total plasma content, an altered proportion of the subclasses HDL2 and HDL3, and a peculiar polypeptide distribution, comprising both normal and additional components, usually not seen in normal controls. The patients also exhibited a decrease of plasma lecithin-cholesterol acyl transferase (LCAT) activity which probably accounted for the low content of cholesteryl esters in both "LDL" and HDL, and in turn for the unusual appearance of "LDL" on electron microscopy. It is concluded that ABL is a disorder affecting all serum lipoprotein classes. Whether the abetalipoproteinemia previously described and noted in the current studies is related to or independent of the abnormalities observed in the other lipoproteins was not established. How the deficiency of LCAT activity, observed in all patients studied, contributed to some of the observed structural lipoprotein abnormalities also remained undetermined. |
Databáze: | OpenAIRE |
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