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修饰后的脂蛋白提供脂类物质,调节树突状细胞的免疫功能。

Modified lipoproteins provide lipids that modulate dendritic cell immune function.

机构信息

Université de Lyon, France.

出版信息

Biochimie. 2013 Jan;95(1):103-8. doi: 10.1016/j.biochi.2012.08.006. Epub 2012 Aug 20.

Abstract

Both physiological and pathological situations can result in biochemical changes of low-density lipoproteins (LDL). Because they can deliver signals to dendritic cells (DC), these modified lipoproteins now appear as regulators of the immune response. Among these modified lipoproteins, oxidized LDL (oxLDL) that accumulate during inflammatory conditions have been extensively studied. Numerous studies have shown that oxLDL induce the maturation of DC, enhancing their ability to activate IFNγ secretion by T cells. LDL treated by secreted phospholipase A(2) also promote DC maturation. Among the bioactive lipids generated by oxidation or phospholipase treatment of LDL, lysophosphatidylcholine (LPC) and some saturated fatty acids induce DC maturation whereas some unsaturated fatty acids or oxidized derivatives have opposite effects. Among other factors, the nuclear receptor peroxisome-proliferator activated receptor γ (PPARγ) plays a crucial role in this regulation. Non-modified lipoproteins also contribute to the regulation of DC function, suggesting that the balance between native and modified lipoproteins, as well as the biochemical nature of the LDL modifications, can regulate the activation threshold of DC. Here we discuss two pathological situations in which the impact of LDL modifications on inflammation and immunity could play an important role. During atherosclerosis, modified LDL accumulating in the arterial intima may interfere with DC maturation and function, promoting a Th1 immune response and a local inflammation favoring the development of the pathology. In patients chronically infected, the hepatitis C virus (HCV) interferes with lipoprotein metabolism resulting in the production of infectious modified lipoproteins. These lipo-viral-particles (LVP) are modified low-density lipoproteins containing viral material that can alter DC maturation and affect specific toll-like receptor signaling. In conclusion, lipoprotein modifications play an important role in the regulation of immunity by delivering signals of danger to DC and modulating their function.

摘要

生理和病理情况都可能导致低密度脂蛋白(LDL)的生化变化。由于它们可以向树突状细胞(DC)传递信号,这些修饰的脂蛋白现在似乎是免疫反应的调节剂。在这些修饰的脂蛋白中,在炎症条件下积累的氧化低密度脂蛋白(oxLDL)已经得到了广泛的研究。许多研究表明,oxLDL 诱导 DC 成熟,增强其激活 IFNγ分泌 T 细胞的能力。由分泌型磷脂酶 A2 处理的 LDL 也促进 DC 成熟。在 LDL 氧化或磷脂酶处理产生的生物活性脂质中,溶血磷脂酰胆碱(LPC)和一些饱和脂肪酸诱导 DC 成熟,而一些不饱和脂肪酸或氧化衍生物则具有相反的作用。在其他因素中,核受体过氧化物酶体增殖物激活受体 γ(PPARγ)在这种调节中起着至关重要的作用。非修饰的脂蛋白也有助于调节 DC 功能,这表明天然和修饰的脂蛋白之间的平衡,以及 LDL 修饰的生化性质,可以调节 DC 的激活阈值。在这里,我们讨论了两种病理情况,即 LDL 修饰对炎症和免疫的影响可能发挥重要作用。在动脉粥样硬化中,在动脉内膜中积累的修饰 LDL 可能干扰 DC 成熟和功能,促进 Th1 免疫反应和局部炎症,有利于病理学的发展。在慢性感染的患者中,丙型肝炎病毒(HCV)干扰脂蛋白代谢,导致产生感染性修饰的脂蛋白。这些脂蛋白病毒颗粒(LVP)是含有病毒物质的修饰的低密度脂蛋白,可改变 DC 成熟并影响特定的 toll 样受体信号。总之,脂蛋白修饰通过向 DC 传递危险信号并调节其功能,在免疫调节中起着重要作用。

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