The long term objective of the research proposed is the explication of the distribution, dynamics and function of cholesterol in mammalian cell membranes. Although cholesterol is a major constituent of plasma membrances, its precise disposition and function are to a large degree unknown. The mechanisms of cholesterol transfer between tissues and plasma and between biological membrances ae unknown. The literature contains proposals for mechanisms of unmediated transfer which fall into two categories: diffusion through the aqueous phase and transfer during the formation of a collision complex. These mechanisms can be distinguished from the dependence of transfer rate on concentration of donor and acceptor. We shall examine the exchange of [3H]-cholesterol between red cells themselves and between red cells, sonicated liposomes and plasma lipoproteins to determine the mechanism of cholesterol transfer. We shall use cholesterol oxidase, an enzyme which catalyzes cholesterol oxidation, as a probe to study cholesterol distribution and transfer between the plasma membrane and internal organelles of cultured cells. Our previous studies showed that cholesterol enrichment of red cells to just above the physiological levels leads to membrane reorganization. A study of the molecular basis of this change is proposed. We showed previously that cholesterol transmembrane movement in red cells is extremely rapid. We now propose studies at subzero temperature to examine how rapid this motion is and to determine the transbilayer distribution of cholesterol in the red cell membrane. The rapid transmembrane movement of cholesterol may lie at the heart of its function. We shall examine the hypothesis that redistribution of cholesterol across the membrane occurs in response to stress such as that imposed by shape deformation or the incorporation at the outer membrane leaflet of an exogenous molecule such as lysolecithin. In these studies the antibiotic filipin, which forms complexes with sterols, will be used as a probe for cholesterol distribution.

Agency
National Institute of Health (NIH)
Institute
National Heart, Lung, and Blood Institute (NHLBI)
Type
Research Project (R01)
Project #
5R01HL028448-05
Application #
3339820
Study Section
Hematology Subcommittee 2 (HEM)
Project Start
1981-06-01
Project End
1987-05-31
Budget Start
1985-06-01
Budget End
1986-05-31
Support Year
5
Fiscal Year
1985
Total Cost
Indirect Cost
Name
Rush University
Department
Type
Schools of Medicine
DUNS #
City
Chicago
State
IL
Country
United States
Zip Code
60612
Lange, Yvonne; Ye, Jin; Steck, Theodore L (2014) Essentially all excess fibroblast cholesterol moves from plasma membranes to intracellular compartments. PLoS One 9:e98482
Lange, Yvonne; Tabei, S M Ali; Ye, Jin et al. (2013) Stability and stoichiometry of bilayer phospholipid-cholesterol complexes: relationship to cellular sterol distribution and homeostasis. Biochemistry 52:6950-9
Lange, Yvonne; Ye, Jin; Steck, Theodore L (2012) Activation mobilizes the cholesterol in the late endosomes-lysosomes of Niemann Pick type C cells. PLoS One 7:e30051
Steck, Theodore L; Lange, Yvonne (2010) Cell cholesterol homeostasis: mediation by active cholesterol. Trends Cell Biol 20:680-7
Lange, Yvonne; Ye, Jin; Duban, Mark-Eugene et al. (2009) Activation of membrane cholesterol by 63 amphipaths. Biochemistry 48:8505-15
Lange, Yvonne; Steck, Theodore L; Ye, Jin et al. (2009) Regulation of fibroblast mitochondrial 27-hydroxycholesterol production by active plasma membrane cholesterol. J Lipid Res 50:1881-8
Lange, Yvonne; Steck, Theodore L (2008) Cholesterol homeostasis and the escape tendency (activity) of plasma membrane cholesterol. Prog Lipid Res 47:319-32
Lange, Yvonne; Ye, Jin; Steck, Theodore L (2007) Scrambling of phospholipids activates red cell membrane cholesterol. Biochemistry 46:2233-8