Mattsson L, Johansson H, Ottosson M, Bondjers G, Wiklund O
Wallenberg Laboratory for Cardiovascular Research, Department of Medicine I, University of Gothenburg, Sweden.
J Clin Invest. 1993 Oct;92(4):1759-65. doi: 10.1172/JCI116764.
The expression of lipoprotein lipase (LPL) mRNA and the LPL activity were studied in macrophages (CD14 positive) from human atherosclerotic tissue. Macrophages were isolated after collagenase digestion by immunomagnetic isolation. About 90% of the cells were foam cells with oil red O positive lipid droplets. To analyze the mRNA expression, PCR with specific primers for LPL was used. Arterial macrophages were analyzed directly after isolation and the data showed low expression of LPL mRNA when compared with monocyte-derived macrophages. To induce the expression of LPL mRNA in macrophages, PMA was used. When incubating arterial macrophages with PMA for 24 h we could not detect any increase in LPL mRNA levels. Similarly, the cells secreted very small amounts of LPL even after PMA stimulation. In conclusion, these studies show a very low expression of LPL mRNA in the CD14-positive macrophage-derived foam cells isolated from human atherosclerotic tissue. These data suggest that the CD14-positive cells are a subpopulation of foam cells that express low levels of lipoprotein lipase, and the lipid content could be a major factor for downregulation of LPL. However, the cells were isolated from advanced atherosclerotic lesions, and these findings may not reflect the situation in early fatty streaks.
在取自人类动脉粥样硬化组织的巨噬细胞(CD14阳性)中,研究了脂蛋白脂肪酶(LPL)mRNA的表达及LPL活性。巨噬细胞经胶原酶消化后通过免疫磁珠分离法进行分离。约90%的细胞为油红O阳性脂滴的泡沫细胞。为分析mRNA表达,使用了针对LPL的特异性引物进行PCR。动脉巨噬细胞分离后直接进行分析,数据显示与单核细胞衍生的巨噬细胞相比,LPL mRNA表达较低。为诱导巨噬细胞中LPL mRNA的表达,使用了佛波酯(PMA)。当用PMA孵育动脉巨噬细胞24小时时,我们未检测到LPL mRNA水平有任何增加。同样,即使在PMA刺激后,细胞分泌的LPL量也非常少。总之,这些研究表明,从人类动脉粥样硬化组织分离出的CD14阳性巨噬细胞衍生的泡沫细胞中,LPL mRNA表达非常低。这些数据表明,CD14阳性细胞是脂蛋白脂肪酶表达水平低的泡沫细胞亚群,脂质含量可能是LPL下调的主要因素。然而,这些细胞是从晚期动脉粥样硬化病变中分离出来的,这些发现可能无法反映早期脂肪条纹中的情况。