Kinetics of cholesterol and phospholipid exchange between Mycoplasma gallisepticum cells and lipid vesicles. Alterations in membrane cholesterol and protein content

• Published in: The Journal of biological chemistry Vol. 259; no. 1; pp. 441 - 448
• Main Authors: Clejan, S, Bittman, R
• Format: Journal Article
• Language: English
• Published: Bethesda, MD Elsevier Inc 10.01.1984; American Society for Biochemistry and Molecular Biology
• Subjects: Biological and medical sciences; Cell membranes. Ionic channels. Membrane pores; Cell structures and functions; Cholesterol - metabolism; Cross-Linking Reagents - pharmacology; Dimethyl Sulfoxide - pharmacology; Fundamental and applied biological sciences. Psychology; Kinetics; Maleimides - pharmacology; Membrane Proteins - metabolism; Molecular and cellular biology; Molecular Weight; Mycoplasma - metabolism; Phospholipids - metabolism; Vesicle; Mycoplasmatales; Membrane protein; Plasma membrane; Phospholipid; Exchange reaction; Metabolism; Cholesterol; Mycoplasma gallisepticum
• ISSN: 0021-9258; 1083-351X
• DOI: 10.1016/S0021-9258(17)43680-5

The kinetics of exchange of radiolabeled cholesterol and phospholipids between intact Mycoplasma gallisepticum cells and unilamellar lipid vesicles were investigated over a wide range of cholesterol/phospholipid molar ratio. The change in cholesterol/phospholipid molar ratio was achieved by adapting the sterol-requiring M. gallisepticum to grow in cholesterol-poor media, providing cells with decreased unesterified cholesterol content. At least 90% of the cholesterol molecules in unsealed M. gallisepticum membranes underwent exchange at 37 degrees C as a single kinetic pool in the presence of albumin (2%, w/v). However, we observed biphasic exchange kinetics with intact cells, indicating that cholesterol translocation from the inner to outer monolayers was rate-limiting in the exchange process. Approximately 50% of the cholesterol molecules were localized in each kinetic pool, independent of the cholesterol/phospholipid molar ratio in the cells and vesicles. A striking change in the kinetic parameters for cholesterol exchange occurred between 20 and 26 mol % cholesterol; for example, when the cholesterol/phospholipid molar ratio was decreased from 0.36 to 0.25, the half-time for equilibration of the two cholesterol pools at 37 degrees C decreased from 4.6 +/- 0.5 to 2.5 +/- 0.1 h. Phospholipid exchange rates were also enhanced on decreasing the membrane cholesterol content. The ability of cholesterol to modulate its own exchange rate, as well as that of phospholipids, is suggested to arise from the sterol's ability to regulate membrane lipid order. Extensive chemical modification of the membrane surface by cross-linking of some of the protein constituents with 1,4-phenylenedimaleimide decreased the cholesterol exchange rate. Depletion of membrane proteins by treatment of growing cultures with chloramphenicol increased the cholesterol exchange rate, possibly because of removal of some of the protein mass that may impede lipid translocation. The observations that phospholipid exchange was one order of magnitude slower than cholesterol exchange and that dimethyl sulfoxide, potassium thiocyanate, and potassium salicylate enhanced the cholesterol exchange rate are consistent with a mechanism involving lipid exchange by diffusion through the aqueous phase.