Shaikh Saame Raza, Dumaual Alfred C, Castillo Alicia, LoCascio Daniel, Siddiqui Rafat A, Stillwell William, Wassall Stephen R
Department of Biology, Indiana University-Purdue University, Indianapolis, Indiana 46202-5132, USA.
Biophys J. 2004 Sep;87(3):1752-66. doi: 10.1529/biophysj.104.044552.
We have previously suggested that the omega-3 polyunsaturated fatty acid, docosahexaenoic acid (DHA) may in part function by enhancing membrane lipid phase separation into lipid rafts. Here we further tested for differences in the molecular interactions of an oleic (OA) versus DHA-containing phospholipid with sphingomyelin (SM) and cholesterol (CHOL) utilizing (2)H NMR spectroscopy, differential scanning calorimetry, atomic force microscopy, and detergent extractions in model bilayer membranes. (2)H NMR and DSC (differential scanning calorimetry) established the phase behavior of the OA-containing 1-[(2)H(31)]palmitoyl-2-oleoyl-sn-glycero-3-phosphoethanolamine (16:0-18:1PE-d(31))/SM (1:1) and the DHA-containing 1-[(2)H(31)]palmitoyl-2-docosahexaenoyl-sn-glycero-3-phosphoethanolamine (16:0-22:6PE-d(31))/SM (1:1) in the absence and presence of equimolar CHOL. CHOL was observed to affect the OA-containing phosphatidylethanolamine (PE) more than the DHA-containing PE, as exemplified by >2 x greater increase in order measured for the perdeuterated palmitic chain in 16:0-18:1PE-d(31)/SM (1:1) compared to 16:0-22:6PE-d(31)/SM (1:1) bilayers in the liquid crystalline phase. Atomic force microscopy (AFM) experiments showed less lateral phase separation between 16:0-18:1PE-rich and SM/CHOL-rich raft domains in 16:0-18:1PE/SM/CHOL (1:1:1) bilayers than was observed when 16:0-22:6PE replaced 16:0-18:1PE. Differences in the molecular interaction of 16:0-18:1PE and 16:0-22:6PE with SM/CHOL were also found using biochemical detergent extractions. In the presence of equimolar SM/CHOL, 16:0-18:1PE showed decreased solubilization in comparison to 16:0-22:6PE, indicating greater phase separation with the DHA-PE. Detergent experiments were also conducted with cardiomyocytes fed radiolabeled OA or DHA. Although both OA and DHA were found to be largely detergent solubilized, the amount of OA that was found to be associated with raft-rich detergent-resistant membranes exceeded DHA by almost a factor of 2. We conclude that the OA-PE phase separates from rafts far less than DHA-PE, which may have implications for cellular signaling.
我们之前曾提出,ω-3多不饱和脂肪酸二十二碳六烯酸(DHA)可能部分通过增强膜脂质相分离形成脂筏来发挥作用。在此,我们利用(2)H核磁共振光谱、差示扫描量热法、原子力显微镜和去污剂提取法,进一步测试了含油酸(OA)与含DHA的磷脂与鞘磷脂(SM)和胆固醇(CHOL)在模型双层膜中的分子相互作用差异。(2)H核磁共振和差示扫描量热法确定了在不存在和存在等摩尔CHOL的情况下,含OA的1-[(2)H(31)]棕榈酰-2-油酰-sn-甘油-3-磷酸乙醇胺(16:0-18:1PE-d(31))/SM(1:1)和含DHA的1-[(2)H(31)]棕榈酰-2-二十二碳六烯酰-sn-甘油-3-磷酸乙醇胺(16:0-22:6PE-d(31))/SM(1:1)的相行为。观察到CHOL对含OA的磷脂酰乙醇胺(PE)的影响大于对含DHA的PE的影响,例如,在液晶相中,16:0-18:1PE-d(31)/SM(1:1)双层膜中全氘代棕榈酸链的有序度增加幅度比16:0-22:6PE-d(31)/SM(1:1)双层膜大2倍以上。原子力显微镜(AFM)实验表明,在16:0-18:1PE/SM/CHOL(1:1:1)双层膜中,富含16:0-18:1PE的区域与富含SM/CHOL的脂筏区域之间的横向相分离比用16:0-22:6PE取代16:0-18:1PE时观察到的要少。使用生化去污剂提取法也发现了16:0-18:1PE和16:0-22:6PE与SM/CHOL分子相互作用的差异。在等摩尔SM/CHOL存在的情况下,与16:0-22:6PE相比,16:0-18:1PE的溶解减少,表明与DHA-PE的相分离更大。还用放射性标记的OA或DHA喂养心肌细胞进行了去污剂实验。虽然发现OA和DHA在很大程度上都能被去污剂溶解,但发现与富含脂筏的抗去污剂膜相关的OA量比DHA几乎多一倍。我们得出结论,OA-PE与脂筏的相分离远少于DHA-PE,这可能对细胞信号传导有影响。