نتایج جستجو برای: apoa

تعداد نتایج: 2181  

Journal: :Arteriosclerosis, Thrombosis, and Vascular Biology 2005

Journal: :Arteriosclerosis, thrombosis, and vascular biology 2000
W Velez-Carrasco A H Lichtenstein Z Li G G Dolnikowski S Lamon-Fava F K Welty E J Schaefer

The purpose of our study was to investigate high density lipoprotein (HDL) apolipoprotein (apo) A-I and apoA-II kinetics in a state of constant feeding after a primed-constant infusion of [5,5, 5-(2)H(3)]L-leucine in 32 normolipidemic older men and postmenopausal women (aged 41 to 79 years). ApoA-I and apoA-II were isolated from plasma HDL, and enrichment was determined by gas chromatography/ma...

Journal: :Journal of lipid research 2007
Shen Qu German Perdomo Dongming Su Fiona M D'Souza Neil S Shachter H Henry Dong

Apolipoprotein A-V (apoA-V) and apoC-III are exchangeable constituents of VLDL and HDL. ApoA-V counteracts the effect of apoC-III on triglyceride (TG) metabolism with poorly defined mechanisms. To better understand the effects of apoA-V on TG and cholesterol metabolism, we delivered apoA-V cDNA into livers of hypertriglyceridemic APOC3 transgenic mice by adenovirus-mediated gene transfer. In re...

Journal: :The Journal of biological chemistry 1989
Z H Beg J A Stonik J M Hoeg S J Demosky T Fairwell H B Brewer

In vitro phosphorylation of purified human plasma apolipoprotein A-I (apoA-I) by a recently characterized Ca2+/calmodulin-dependent kinase (Beg, Z. H., Stonik, J. A., and Brewer, H. B., Jr. (1987) J. Biol. Chem. 262, 13228-13240) was time-, Ca2+-, and calmodulin-dependent. Maximal phosphorylation of human apoA-I revealed a stoichiometry of approximately 1 mol of PO4/mol of apoA-I. Phosphorylati...

2012
Dong Won Yi Dong Wook Jeong Sang Yeoup Lee Seok Man Son Yang Ho Kang

BACKGROUND Apolipoprotein A-II (apoA-II) is the second-most abundant apolipoprotein in human high-density lipoprotein and its role in cardio metabolic risk is not entirely clear. It has been suggested to have poor anti-atherogenic or even pro-atherogenic properties, but there are few studies on the possible role of apoA-II in Asian populations. The aim of this study is to evaluate the role of a...

2014
Sophie Stukas Jerome Robert Michael Lee Iva Kulic Michael Carr Katherine Tourigny Jianjia Fan Dhananjay Namjoshi Kalistyne Lemke Nicole DeValle Jeniffer Chan Tammy Wilson Anna Wilkinson Rafi Chapanian Jayachandran N. Kizhakkedathu John R. Cirrito Michael N. Oda Cheryl L. Wellington

BACKGROUND Brain lipoprotein metabolism is dependent on lipoprotein particles that resemble plasma high-density lipoproteins but that contain apolipoprotein (apo) E rather than apoA-I as their primary protein component. Astrocytes and microglia secrete apoE but not apoA-I; however, apoA-I is detectable in both cerebrospinal fluid and brain tissue lysates. The route by which plasma apoA-I enters...

Journal: :The Biochemical journal 2012
Shobini Jayaraman Giorgio Cavigiolio Olga Gursky

HDL (high-density lipoproteins) remove cell cholesterol and protect from atherosclerosis. The major HDL protein is apoA-I (apolipoprotein A-I). Most plasma apoA-I circulates in lipoproteins, yet ~5% forms monomeric lipid-poor/free species. This metabolically active species is a primary cholesterol acceptor and is central to HDL biogenesis. Structural properties of lipid-poor apoA-I are unclear ...

Journal: :Journal of lipid research 1988
P de Knijff M Rosseneu U Beisiegel W de Keersgieter R R Frants L M Havekes

Recently, we determined the apolipoprotein E (apoE) phenotype distribution in 2,000 randomly selected 35-year-old male individuals by slab gel isoelectric focusing of delipidated plasma samples, followed by immunoblotting using anti-apoE antiserum. These blots have been successfully re-used for immunovisualization of apoA-IV isoelectric focusing patterns. In a population sample of 1,393 individ...

Journal: :The Journal of biological chemistry 2004
Maxime Denis Bassam Haidar Michel Marcil Michel Bouvier Larbi Krimbou Jacques Genest

The dynamics of ABCA1-mediated apoA-I lipidation were investigated in intact human fibroblasts induced with 22(R)-hydroxycholesterol and 9-cis-retinoic acid (stimulated cells). Specific binding parameters of (125)I-apoA-I to ABCA1 at 37 degrees C were determined: K(d) = 0.65 microg/ml, B(max) = 0.10 ng/microg cell protein. Lipid-free apoA-I inhibited the binding of (125)I-apoA-I to ABCA1 more e...

Journal: :Translational research : the journal of laboratory and clinical medicine 2013
Hamid Moradi Hamid M Said Nosratola D Vaziri

Chronic kidney disease is associated with premature death from cardiovascular disease, which is, in part, driven by high density lipoprotein deficiency and dysfunction. One of the main causes of high density lipoprotein deficiency in chronic kidney disease is diminished plasma apolipoprotein (Apo)A-I level. Plasma ApoA-I is reduced in dialysis patients and hepatic ApoA-I messenger RNA (mRNA) is...

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