On the association of lipid rafts to the spectrin skeleton in human erythrocytes

被引:28
作者
Ciana, Annarita [1 ]
Achilli, Cesare [1 ]
Balduini, Cesare [1 ]
Minetti, Giampaolo [1 ]
机构
[1] Univ Pavia, Dept Biochem, I-27100 Pavia, Italy
来源
BIOCHIMICA ET BIOPHYSICA ACTA-BIOMEMBRANES | 2011年 / 1808卷 / 01期
关键词
Detergent-resistant membranes; Polymorphonuclear granulocytes; Neutrophil elastase; Cathepsin G; Eglin; DFP; p55; Carbonate; Membrane skeleton; Gelatin zymography; DETERGENT-RESISTANT MEMBRANES; ELECTROPHORETIC ANALYSIS; POLYACRYLAMIDE GELS; BINDING-SITES; PROTEINS; CELLS; ANKYRIN; PLASMA; BLOOD; METALLOPROTEINASES;
D O I
10.1016/j.bbamem.2010.08.019
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Lipid rafts are local inhomogeneities in the composition of the plasma membrane of living cells, that are enriched in sphingolipids and cholesterol in a liquid-ordered state, and proteins involved in receptor-mediated signalling. Interactions between lipid rafts and the cytoskeleton have been observed in various cell types. They are isolated as a fraction of the plasma membrane that resists solubilization by nonionic detergents at 4 degrees C (detergent-resistant membranes, DRMs). We have previously described that DRMs are anchored to the spectrin-based membrane skeleton in human erythrocytes and can be released by increasing the pH and ionic strength of the solubilization medium with sodium carbonate. It was unexplained why this carbonate treatment was necessary and why this requirement was not reported by other workers in this area. We show here that when contaminating leukocytes are present in erythrocyte preparations that are subjected to detergent treatment, the isolation of DRMs can occur without the requirement for carbonate treatment. This is due to the uncontrolled breakdown of erythrocyte membrane components by hydrolases that are released from contaminating neutrophils that lead to proteolytic disruption of the supramolecular assembly of the membrane skeleton. Results presented here corroborate the concept that DRMs are anchored to the membrane skeleton through electrostatic interactions that most likely involve the spectrin molecule. (C) 2010 Elsevier B.V. All rights reserved.
引用
收藏
页码:183 / 190
页数:8
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