Beneficial effects of cytokine induced hyperlipidemia.

K R Feingold, I Hardardóttir, C Grunfeld
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Abstract

Infection, inflammation and trauma induce marked changes in the plasma levels of a wide variety of proteins (acute phase response), and these changes are mediated by cytokines. The acute phase response is thought to be beneficial to the host. The host's response to injury also results in dramatic alterations in lipid metabolism and circulating lipoprotein levels which are mediated by cytokines. A large number of cytokines including TNF, the interleukins, and the interferons increase serum triglyceride levels. This rapid increase (1-2 h) is predominantly due to an increase in hepatic VLDL secretion while the late increase may be due to a variety of factors including increased hepatic production of VLDL or delayed clearance secondary to a decrease in lipoprotein lipase activity and/or apolipoprotein E levels on VLDL. In animals other than primates, cytokines also increase serum cholesterol levels, most likely by increasing hepatic cholesterol. Cytokines increase hepatic cholesterol synthesis by stimulating HMG CoA reductase gene expression and decrease hepatic cholesterol catabolism by inhibiting cholesterol 7 alpha-hydroxylase, the key enzyme in bile acid synthesis. Injury and/or cytokines also decrease HDL cholesterol levels and induce alterations in the composition of HDL. The content of SAA and apolipoprotein J increase, apolipoprotein A1 may decrease, and the cholesterol ester content decreases while free cholesterol increases. Additionally, key proteins involved in HDL metabolism are altered by cytokines; LCAT activity, hepatic lipase activity, and CETP levels decrease. These changes in lipid and lipoprotein metabolism may be beneficial in a number of ways including: lipoproteins competing with viruses for cellular receptors, apolipoproteins neutralizing viruses, lipoproteins binding and targeting parasites for destruction, apolipoproteins lysing parasites, redistribution of nutrients to cells involved in the immune response and/or tissue repair, and lipoproteins binding toxic agents and neutralizing their harmful effects. Thus, cytokines induce marked changes in lipid metabolism that lead to hyperlipidemia which represents part of the innate immune response and may be beneficial to the host.

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细胞因子诱导高脂血症的有益作用。
感染、炎症和创伤会引起血浆中多种蛋白质水平的显著变化(急性期反应),这些变化是由细胞因子介导的。急性期反应被认为对宿主有益。宿主对损伤的反应也导致由细胞因子介导的脂质代谢和循环脂蛋白水平的显著改变。大量的细胞因子包括TNF,白细胞介素和干扰素增加血清甘油三酯水平。这种快速的增加(1-2小时)主要是由于肝脏VLDL分泌的增加,而后期的增加可能是由于多种因素,包括肝脏VLDL生成的增加或继发于脂蛋白脂肪酶活性和/或VLDL载脂蛋白E水平下降的延迟清除。在灵长类动物以外的动物中,细胞因子也会增加血清胆固醇水平,很可能是通过增加肝脏胆固醇来实现的。细胞因子通过刺激HMG CoA还原酶基因表达增加肝脏胆固醇合成,通过抑制胆汁酸合成关键酶胆固醇7 α -羟化酶降低肝脏胆固醇分解代谢。损伤和/或细胞因子也会降低高密度脂蛋白胆固醇水平并诱导高密度脂蛋白组成的改变。SAA和载脂蛋白J含量升高,载脂蛋白A1含量可能降低,胆固醇酯含量降低,游离胆固醇升高。此外,参与HDL代谢的关键蛋白被细胞因子改变;LCAT活性、肝脂肪酶活性和CETP水平降低。脂质和脂蛋白代谢的这些变化可能在许多方面是有益的,包括:脂蛋白与病毒竞争细胞受体,载脂蛋白中和病毒,脂蛋白结合并靶向寄生虫进行破坏,载脂蛋白溶解寄生虫,营养物质重新分配到参与免疫反应和/或组织修复的细胞,脂蛋白结合有毒物质并中和它们的有害影响。因此,细胞因子引起脂质代谢的显著变化,导致高脂血症,这是先天免疫反应的一部分,可能对宿主有益。
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