Topic
Sterol
About: Sterol is a research topic. Over the lifetime, 8117 publications have been published within this topic receiving 309926 citations. The topic is also known as: sterols & sterol lipids.
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TL;DR: Using a double isotopic steady state in animals fed cholesterol-7a-H3 and implanted with cholester01-4-C’~, it has been possible to demonstrate that the major portion of fecal cholesterol of endogenous origin is derived from or is in equilibrium with that of the blood.
132 citations
TL;DR: It is demonstrated that two inducible ATP-binding cassette (ABC) transporters mediate nonvesicular movement of PM sterol to the endoplasmic reticulum (ER) in Saccharomyces cerevisiae and that Aus1p and Pdr11p facilitate sterol uptake by increasing the cycling of sterol between the PM and ER.
132 citations
TL;DR: By chromatography on a silicic acid column, artificial lipid mixtures and plasma lipids have been separated into fractions composed mainly of the sterol esters, triglycerides, sterols, fatty acids and phospholipids.
Abstract: SummaryBy chromatography on a silicic acid column, artificial lipid mixtures and plasma lipids have been separated into fractions composed mainly of the following groups: sterol esters, triglycerides, sterols, fatty acids and phospholipids. By this tech-nic eleostearic acid is found exclusively in the triglyceride fraction after having been fed as the methyl ester.
132 citations
TL;DR: Increasing evidence obtained with model and isolated cell membranes, transfected cells, genetic mutants, and gene-ablated mice suggests that proteins such as caveolin, sterol carrier protein-2 (SCP-2), Niemann-Pick C1 protein, steroidogenic acute regulatory protein (StAR), and other intracellular proteins mediate intrACEllular cholesterol transfer.
Abstract: Cellular cholesterol homeostasis is a balance of influx, catabolism and synthesis, and efflux. Unlike vascular lipoprotein cholesterol transport, intracellular cholesterol trafficking is only beginning to be resolved. Exogenous cholesterol and cholesterol ester enter cells via the low-density lipoprotein (LDL) receptor/lysosomal and less so by nonvesicular, high-density lipoprotein (HDL) receptor/caveolar pathways. However, the mechanism(s) whereby cholesterol enters the lysosomal membrane, translocates, and transfers out of the lysosome to the cell interior are unknown. Likewise, the steps whereby cholesterol enters the cytofacial leaflet of the plasma membrane caveolae, rapidly translocates, leaves the exofacial leaflet, and transfers to extracellular HDL are unclear. Increasing evidence obtained with model and isolated cell membranes, transfected cells, genetic mutants, and gene-ablated mice suggests that proteins such as caveolin, sterol carrier protein-2 (SCP-2), Niemann-Pick C1 protein, steroidogenic acute regulatory protein (StAR), and other intracellular proteins mediate intracellular cholesterol transfer. While these proteins bind cholesterol and/or interact with cholesterol-rich membrane microdomains (e.g., caveolae, rafts, and annuli), their relative contributions to direct molecular versus vesicular cholesterol transfer remain to be resolved. The formation, regulation, and role of membrane microdomains in regulating cholesterol uptake/efflux and trafficking are unclear. Some cholesterol-binding proteins exert opposing effects on cellular cholesterol uptake/efflux, transfer of cholesterol out of the lysosomal membrane, and/or intracellular cholesterol trafficking to select membranous organelles. Resolving these cholesterol pathways and the role of membrane cholesterol microdomains is essential to our understanding not only of processes that affect cholesterol metabolism, but also of the abnormal regulation that may lead to disease (diabetes, obesity, atherosclerosis, neutral lipid storage, Niemann-Pick C, congenital lipoid adrenal hyperplasia, etc.).
131 citations
TL;DR: What is known about these processes and the dynamics of cholesterol in the vertebrate retina are reviewed and some future avenues of research in this area are indicated.
131 citations