Essaji Yasmin, Yang Yanbo, Albert Carolyn J, Ford David A, Brown Robert J
Department of Biochemistry, Memorial University of Newfoundland, St. John's, NL, A1B 3X9, Canada.
Department of Biochemistry and Molecular Biology, School of Medicine, and Center for Cardiovascular Research, Saint Louis University, St. Louis, MO 63104, USA.
Lipids. 2013 Aug;48(8):769-778. doi: 10.1007/s11745-013-3810-6. Epub 2013 Jun 22.
Macrophages express lipoprotein lipase (LPL) and endothelial lipase (EL) within atherosclerotic plaques; however, little is known about how lipoprotein hydrolysis products generated by these lipases might affect macrophage cell signalling pathways. We hypothesized that hydrolysis products affect macrophage cell signalling pathways associated with atherosclerosis. To test our hypothesis, we incubated differentiated THP-1 macrophages with products from total lipoprotein hydrolysis by recombinant LPL or EL. Using antibody arrays, we found that the phosphorylation of six receptor tyrosine kinases and three signalling nodes--most associated with atherosclerotic processes--was increased by LPL derived hydrolysis products. EL derived hydrolysis products only increased the phosphorylation of tropomyosin-related kinase A, which is also implicated in playing a role in atherosclerosis. Using electrospray ionization-mass spectrometry, we identified the species of triacylglycerols and phosphatidylcholines that were hydrolyzed by LPL and EL, and we identified the fatty acids liberated by gas chromatography-mass spectrometry. To determine if the total liberated fatty acids influenced signalling pathways, we incubated differentiated THP-1 macrophages with a mixture of the fatty acids that matched the concentrations of liberated fatty acids from total lipoproteins by LPL, and we subjected cell lysates to antibody array analyses. The analyses showed that only the phosphorylation of Akt was significantly increased in response to fatty acid treatment. Overall, our study shows that macrophages display potentially pro-atherogenic signalling responses following acute treatments with LPL and EL lipoprotein hydrolysis products.
巨噬细胞在动脉粥样硬化斑块中表达脂蛋白脂肪酶(LPL)和内皮脂肪酶(EL);然而,关于这些脂肪酶产生的脂蛋白水解产物如何影响巨噬细胞信号通路,人们知之甚少。我们推测水解产物会影响与动脉粥样硬化相关的巨噬细胞信号通路。为了验证我们的假设,我们用重组LPL或EL对总脂蛋白进行水解产生的产物孵育分化的THP-1巨噬细胞。使用抗体阵列,我们发现LPL衍生的水解产物增加了六种受体酪氨酸激酶和三个信号节点(大多数与动脉粥样硬化过程相关)的磷酸化。EL衍生的水解产物仅增加了原肌球蛋白相关激酶A的磷酸化,该激酶也与动脉粥样硬化的发生有关。通过电喷雾电离质谱,我们确定了被LPL和EL水解的三酰甘油和磷脂酰胆碱的种类,并通过气相色谱-质谱法鉴定了释放的脂肪酸。为了确定总释放脂肪酸是否影响信号通路,我们用与LPL从总脂蛋白中释放的脂肪酸浓度相匹配的脂肪酸混合物孵育分化的THP-1巨噬细胞,并对细胞裂解物进行抗体阵列分析。分析表明,仅Akt的磷酸化在脂肪酸处理后显著增加。总体而言,我们的研究表明,巨噬细胞在用LPL和EL脂蛋白水解产物进行急性处理后显示出潜在的促动脉粥样硬化信号反应。