Departamento de Bioquímica, Instituto de Biologia, Universidade Estadual de Campinas, Cid. Univ. Zeferino Vaz s/n, C.P. 6109, CEP 13083-970, Campinas, SP, Brazil.
J Membr Biol. 2010 Apr;234(3):195-205. doi: 10.1007/s00232-010-9246-5. Epub 2010 Mar 26.
Transient lateral microdomains or lipid rafts play important roles in many physiological membrane-mediated cell processes. Detergent-resistant membranes (DRMs) are good models for the study of lipid rafts. Here we report that DRMs can be obtained by treating human erythrocytes with the nonionic detergents Triton X-100 or octaethylene glycol monododecyl ether (C(12)E(8)) at 37 degrees C, and by treatment at 4 degrees C of cholesterol-depleted erythrocytes. Electron paramagnetic resonance with spin labels inserted at different membrane depths (5- and 16-doxyl stearic acids, 5-SASL and 16-SASL) were used to measure the order parameter (S) of the cell membranes and DRMs. We previously reported significantly higher S values in DRMs with respect to intact erythrocyte membranes. Here we show that higher S values were still measurable in DRMs prepared from intact erythrocytes at 37 degrees C, or from cholesterol-depleted cells at 4 degrees C, for both detergents. For 5-SASL only, increased S values were measured in 4 degrees C DRMs obtained from cholesterol-depleted versus intact erythrocytes. Flotillin-2, a protein marker of lipid rafts, was found in DRMs from intact cells in trace amounts but it was sensitively increased in C(12)E(8) DRMs prepared at 4 degrees C from cholesterol-depleted erythrocytes, while the membrane-skeletal proteins spectrin and actin were excluded from both Triton X-100 and C(12)E(8) DRMs. However, contrary to the 4 degrees C treatment results, flotillin-2 and stomatin were not resistant to Triton X-100 and C(12)E(8) treatment at physiological temperature. The role of cholesterol in DRMs formation is discussed and the results presented provide further support for the use of C(12)E(8) to the study of DRMs.
瞬时横向微区或脂质筏在许多生理膜介导的细胞过程中起着重要作用。去污剂抗性膜(DRM)是研究脂质筏的良好模型。在这里,我们报告说,DRM 可以通过在 37°C 下用非离子去污剂 Triton X-100 或辛基聚乙二醇单十二醚(C(12)E(8))处理人红细胞,以及通过在 4°C 下处理胆固醇耗尽的红细胞来获得。用插入不同膜深度的自旋标记物(5-和 16-二氧代硬脂酸,5-SASL 和 16-SASL)进行电子顺磁共振,以测量细胞膜和 DRM 的序参数(S)。我们之前报道过,与完整的红细胞膜相比,DRM 中的 S 值显着更高。在这里,我们表明,对于两种去污剂,用 37°C 从完整的红细胞或 4°C 从胆固醇耗尽的细胞制备的 DRM 中仍可测量到更高的 S 值。仅对于 5-SASL,从胆固醇耗尽的红细胞而不是完整的红细胞获得的 4°C DRMs 中测量到的 S 值增加。 flotillin-2 是脂质筏的蛋白质标志物,在完整细胞的 DRMs 中痕量存在,但在从胆固醇耗尽的红细胞中在 4°C 用 C(12)E(8)制备的 DRMs 中,它的含量敏感增加,而膜骨架蛋白血影蛋白和肌动蛋白则被排除在 Triton X-100 和 C(12)E(8)DRM 之外。然而,与 4°C 处理结果相反, flotillin-2 和 stomatin 对 Triton X-100 和 C(12)E(8)在生理温度下的处理不具有抗性。讨论了胆固醇在 DRM 形成中的作用,并且提供的结果进一步支持使用 C(12)E(8)来研究 DRM。