Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Pivot Concepts:
Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Target Concepts:
Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Query: UMLS:C0242339 (
dyslipidemia
)
13,927
document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)
Intracellular cholesterol transport proteins move cholesterol to different subcellular compartments and thereby regulate its final metabolic fate. In hepatocytes, for example, delivery of high-density lipoprotein (HDL)-associated cholesterol for bile acid synthesis or secretion into bile facilitates cholesterol elimination from the body (anti-atherogenic effect), whereas delivery for esterification and subsequent incorporation into apolipoprotein B-containing atherogenic lipoproteins (
e.g.
very-low-density lipoprotein (VLDL)) enhances cholesterol secretion into the systemic circulation (pro-atherogenic effect). Intracellular cholesterol transport proteins such as
sterol carrier protein-2
(
SCP2
) should, therefore, play a role in regulating these pro- or anti-atherosclerotic processes. Here, we sought to evaluate the effects of
SCP2
deficiency on the development of diet-induced atherosclerosis. We generated LDLR
-/-
mice deficient in
SCP2
/SCPx (LS) and examined the effects of this deficiency on Western diet-induced atherosclerosis.
SCP2
/SCPx deficiency attenuated atherosclerosis in LS mice by >80% and significantly reduced plasma cholesterol and triglyceride levels. Investigation of the likely underlying mechanisms revealed a significant reduction in intestinal cholesterol absorption (given as an oral gavage) in
SCP2
/SCPx-deficient mice. Consistently, siRNA-mediated knockdown of
SCP2
in intestinal cells significantly reduced cholesterol uptake. Furthermore, hepatic triglyceride/VLDL secretion from the liver or hepatocytes isolated from
SCP2
/SCPx-deficient mice was significantly reduced. These results indicate an important regulatory role for
SCP2
deficiency in attenuating diet-induced atherosclerosis by limiting intestinal cholesterol absorption and decreasing hepatic triglyceride/VLDL secretion. These findings suggest targeted inhibition of
SCP2
as a potential therapeutic strategy to reduce Western diet-induced
dyslipidemia
and atherosclerosis.
...
PMID:Sterol carrier protein-2 deficiency attenuates diet-induced dyslipidemia and atherosclerosis in mice. 2970 Jan 17