SEPARATION AND CHARACTERIZATION OF HUMAN SERUM CHYLOMICRONS

РАЗДЕЛЕНИЕ И ХАРАКТЕРИСТИКА ХИЛОМИКРОНОВ СЫВОРОТКИ ЧЕЛОВЕКА
Angelo M. Scanu, Irvine H. Page
1959-03-01

clearing factor activityhuman serum chylomicronslipoprotein characterizationserum lipoproteinsultracentrifugation
Chylomicrons were separated by low and high speed ultracentrifugation from lipemic sera of human subjects in the absorptive phase. The final chylomicron preparation was free from other serum components and contained a small constant amount of protein, approximately 2 per cent of the chylomicron fraction. Electrophoresis, immunochemical analysis, and absorption experiments identified the protein component as derived from a mixture of beta and alpha(1) serum lipoproteins. Large aliquots of an emulsion of serum freed of chylomicrons and coconut oil were incubated at 37 degrees C. for 2 hours and ultracentrifuged as in the preparation of chylomicrons. The fat particles now showed the presence of minute amounts of beta and alpha(1) serum lipoproteins in almost the same proportion as found in chylomicrons. "Finger prints" of delipidized samples of chylomicrons and particles from serum-coconut oil emulsion gave similar, although not identical patterns. The data on "clearing factor" activity corroborated the finding that serum alpha(1) lipoproteins are contained in chylomicrons and particles from serum-coconut oil emulsion. These two lipide particles, partially delipidized, were both able to activate a "clearing factor" system in vitro, a property exhibited only by intact or partially delipidized alpha(1) serum lipoproteins. Clearing activity was satisfactorily determined by using an emulsion of coconut oil mixed in agar as a substrate to give an opaque gel, in which the diffusing enzyme showed its activity by areas of clearing. The results obtained by this technique were in agreement with those based on fall in optical density and non-esterified fatty acid production. Chemical analysis of serum chylomicrons showed a concentration of cholesterol and phospholipides higher than could be accounted for by the attached beta and alpha(1) serum lipoproteins. On the basis of these results the assumption is made that in the blood stream small amounts of serum lipoproteins, by a process of adsorption, form a complex with the absorbed triglycerides, cholesterol, and phospholipides, to produce chylomicrons.
1
Chylomicrons and coconut-oil emulsion particles activated an in vitro clearing-factor system, consistent with their content of intact or partially delipidized alpha(1) lipoproteins.
2
Chylomicrons contained more cholesterol and phospholipides than could be explained by their associated beta and alpha(1) lipoproteins, suggesting additional lipid incorporation or association in the bloodstream.
3
Human serum chylomicrons were purified by low- and high-speed ultracentrifugation, yielding preparations free of other serum components.
4
Purified chylomicrons contained approximately 2% protein, identified immunochemically and electrophoretically as a mixture of beta and alpha(1) serum lipoproteins.
5
Serum-free-of-chylomicrons emulsions incubated with coconut oil formed particles containing beta and alpha(1) lipoproteins in proportions similar to those in chylomicrons.

Human serum chylomicrons and coconut-oil emulsion fat particles

Protein composition, lipoprotein association, lipid composition, and in vitro clearing-factor activation of the particles

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1959-03-01
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Angelo M. Scanu
Irvine H. Page
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