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Overexpression of Human Apolipoprotein B-100 in Transgenic Rabbits Results in Increased Levels of LDL and Decreased Levels of HDL
Abstract
Abstract In this study, an 80-kb human genomic DNA fragment spanning the human apoB gene was used to generate transgenic New Zealand White rabbits that expressed human apoB-100. The concentration of human apoB in the plasma of the transgenic rabbits ranged between 5 and 100 mg/dL. The transgenic rabbits had nearly threefold elevations in the plasma levels of triglycerides and cholesterol compared with nontransgenic controls. Nearly all the cholesterol and human apoB in the plasma was in the LDL fraction. Pronounced triglyceride enrichment of the LDL fraction was a striking feature of human apoB overexpression in the transgenic rabbits, in which the LDL fraction contained more than 75% of the plasma triglycerides. The triglyceride-enriched LDL particles were smaller and more dense than the native rabbit LDL and contained markedly increased amounts of apoE and apoC-III. In the nontransgenic control animals most of the triglycerides were in the VLDL, and most of the apoE and apoC-III were in the VLDL and HDL fractions. In addition to increased LDL levels, overexpression of human apoB in rabbits resulted in lower plasma levels of HDL cholesterol and apoA-I. In our prior studies on transgenic mice expressing human apoB, we documented triglyceride-rich LDL and reduced levels of HDL cholesterol. These prior findings in mice, together with the present findings in transgenic rabbits, suggest that triglyceride-rich LDL and lowered levels of HDL cholesterol may be hallmark features of apoB overexpression.
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Overexpression of apo B100 results in increased VLDL secretion and plasma LDL levels in rabbits.
“Overexpression of apo B100 results in increased VLDL secretion and plasma LDL levels in rabbits.7”
From (Pro)renin Receptor Inhibition Reprograms Hepatic Lipid Metabolism and Protects Mice From Diet-Induced Obesity and Hepatosteatosis (2018) · cites this paper as [7]
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Metadata
- Authors
- Fan, J., McCormick, S. P. A., Krauss, R. M., Taylor, S., Quan, R., Taylor, J. M., & Young, S. G.
- Affiliations
- From the Gladstone Institute of Cardiovascular Disease (J.F., S.P.A.M., S.T., R.Q., J.M.T., S.G.Y.), San Francisco; the Cardiovascular Research Institute (J.F., S.P.A.M., J.M.T., S.G.Y.), University of California, San Francisco; the Lawrence Berkeley Laboratory (R.M.K.), University of California, Berkeley; and the Departments of Physiology (J.M.T.) and Medicine (S.G.Y.), University of California, San Francisco.
- Venue
- Arteriosclerosis, Thrombosis, and Vascular Biology
- Published
- 1995-11
- Volume
- 15
- Issue
- 11
- Pages
- 1889-1899
- ISSN
- 1079-5642
- 1524-4636
- Cited by
- 53
- References
- 1
- Language
- en
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