School of Biological Sciences, University of Northern Colorado, Greeley, CO 80639, United States.
School of Biological Sciences, University of Northern Colorado, Greeley, CO 80639, United States.
Biochim Biophys Acta Biomembr. 2017 Dec;1859(12):2413-2419. doi: 10.1016/j.bbamem.2017.09.012. Epub 2017 Sep 11.
Fish oil is a rich source of omega-3 fatty acids which disrupt lipid microdomain structure and affect mobility of the prostaglandin F (FP) receptor in bovine luteal cells. The objectives of this study were to determine the effects of individual omega-3 fatty acids, eicosapentaenoic acid (EPA) and docosahexaenoic acid (DHA) on 1) membrane fatty acid composition, 2) lipid microdomain structure, and 3) lateral mobility of the FP receptor in bovine luteal cells. Ovaries were collected from a local abattoir (n=5/experiment). The corpus luteum was resected and enzymatically digested using collagenase to generate a mixed luteal cell population. In all experiments, luteal cells were treated with 0, 1, 10 or 100μM EPA or DHA for 72h to allow incorporation of fatty acids into membrane lipids. Results from experiment 1 show that culturing luteal cells in the presence of EPA or DHA increased these luteal fatty acids. In experiment 2, both EPA and DHA increased spatial distribution of lipid microdomains in a dose-dependent manner. Single particle tracking results from experiment 3 show that increasing both EPA and DHA concentrations increased micro- and macro-diffusion coefficients, increased domain size, and decreased residence time of FP receptors. Collectively, results from this study demonstrate similar effects of EPA and DHA on lipid microdomain structure and lateral mobility of FP receptors in cultured bovine luteal cells. Moreover, only 10μM of either fatty acid was needed to mimic the effects of fish oil.
鱼油是ω-3 脂肪酸的丰富来源,可破坏脂质微区结构并影响牛黄体细胞中前列腺素 F(FP)受体的流动性。本研究的目的是确定单一的 ω-3 脂肪酸,二十碳五烯酸(EPA)和二十二碳六烯酸(DHA)对以下方面的影响:1)膜脂肪酸组成,2)脂质微区结构,以及 3)牛黄体细胞中 FP 受体的侧向流动性。从当地屠宰场(n=5/实验)收集卵巢。切除黄体并使用胶原酶进行酶消化,以产生混合黄体细胞群。在所有实验中,黄体细胞均用 0、1、10 或 100μM EPA 或 DHA 处理 72h,以允许脂肪酸掺入膜脂质中。实验 1 的结果表明,在培养黄体细胞时添加 EPA 或 DHA 会增加这些黄体脂肪酸。在实验 2 中,EPA 和 DHA 均以剂量依赖的方式增加了脂质微区的空间分布。实验 3 的单颗粒追踪结果表明,增加 EPA 和 DHA 浓度会增加微扩散和宏观扩散系数,增加域大小,并减少 FP 受体的停留时间。总之,这项研究的结果表明,EPA 和 DHA 对培养的牛黄体细胞中脂质微区结构和 FP 受体的侧向流动性具有相似的影响。此外,仅需 10μM 的脂肪酸即可模拟鱼油的作用。