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杂合子家族性高胆固醇血症患者的巨噬细胞脂蛋白脂肪酶表达增加。

Macrophage lipoprotein lipase expression is increased in patients with heterozygous familial hypercholesterolemia.

作者信息

Beauchamp Marie-Claude, Letendre Elaine, Renier Geneviève

机构信息

CHUM Research Centre and Metabolic Clinic, Notre-Dame Hospital, Montreal Quebec, Canada.

出版信息

J Lipid Res. 2002 Feb;43(2):215-22.

Abstract

FH is associated with accelerated atherosclerosis. Based on the crucial role of macrophage LPL in atherogenesis, we determined in the present study macrophage LPL expression in patients with FH. Monocytes isolated from 13 FH patients and 13 control subjects were differentiated into macrophages by culturing the cells for 9 days in 20% autologous or heterologous serum. Macrophages of patients with FH cultured in their own sera showed a significant increase in LPL mRNA levels, extracellular LPL mass, and activity compared with macrophages of control subjects. Although these alterations positively correlated with the levels of serum platelet-derived growth factor-BB (PDGF-BB) in FH subjects, increased LPL secretion by cultured FH macrophages was reduced neither by immunoneutralizing FH serum with an anti-PDGF-BB antibody, nor by culturing these cells in sera from control subjects. With the exception of LPL, levels of other cytokines and 8-isoprostane were not increased in the supernatants of macrophages of FH patients. Serum from FH patients also enhances the levels of LPL secreted by macrophages from control subjects. Immunoneutralization of FH serum with an anti-PDGF-BB antibody totally reversed this alteration. Overall, this study demonstrates that macrophages from FH subjects overproduce LPL and that PDGF present in the serum from FH patients stimulates LPL secretion by control macrophages. These findings suggest that macrophage LPL induction in patients with FH might be related to the increased atherogenesis observed in these subjects.

摘要

家族性高胆固醇血症(FH)与动脉粥样硬化加速有关。基于巨噬细胞脂蛋白脂肪酶(LPL)在动脉粥样硬化发生中的关键作用,我们在本研究中测定了FH患者巨噬细胞LPL的表达。从13例FH患者和13例对照受试者中分离出的单核细胞,通过在20%自体或异体血清中培养9天分化为巨噬细胞。与对照受试者的巨噬细胞相比,在自身血清中培养的FH患者的巨噬细胞LPL mRNA水平、细胞外LPL质量和活性显著增加。尽管这些改变与FH受试者血清血小板衍生生长因子-BB(PDGF-BB)水平呈正相关,但用抗PDGF-BB抗体免疫中和FH血清,或在对照受试者的血清中培养这些细胞,均不能降低培养的FH巨噬细胞增加的LPL分泌。除LPL外,FH患者巨噬细胞上清液中其他细胞因子和8-异前列腺素水平并未升高。FH患者的血清也可提高对照受试者巨噬细胞分泌的LPL水平。用抗PDGF-BB抗体免疫中和FH血清可完全逆转这种改变。总体而言,本研究表明,FH受试者的巨噬细胞过度产生LPL,且FH患者血清中的PDGF可刺激对照巨噬细胞分泌LPL。这些发现提示,FH患者巨噬细胞LPL的诱导可能与这些受试者中观察到的动脉粥样硬化增加有关。

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