Schwarzer E, Skorokhod O A, Barrera V, Arese P
Department of Genetics, Biology and Biochemistry, University of Torino, Via Santena 5 bis, 10126 Torino, Italy.
Parassitologia. 2008 Jun;50(1-2):143-5.
In vitro, human monocytes avidly ingest hemozoin (HZ) that modifies a number of monocyte functions. Inhibitory effects: inhibition of: PMA-elicited respiratory burst, ability to killing and repeat phagocytosis, activity of NADPH-oxidase and PKC, expression of ICAM-1, integrin-CD11c, MHC-class-II (IFN-gamma-mediated), differentiation to functional, antigen-presenting dendritic cells. Stimulatory effects: increase in phagocytosis-related respiratory burst and accumulation of lipoperoxidation products; induction of metalloproteinase-9 and pro-inflammatory cytokines and chemokines. Mechanism of action: HZ generates by nonenzymatic catalysis large amounts of lipoperoxidation products, such as monohydroxy derivatives of arachidonic (HETE) and linoleic (HODE) acid, and 4-hydroxynonenal (HNE). Several HZ effects were reproduced by supplementation with plausible concentrations of HETE or HNE, the first most likely via interaction with PPAR-receptors, the second via adduct or crosslinks formation with critical targets.
在体外,人类单核细胞能大量摄取疟原虫色素(HZ),而疟原虫色素会改变多种单核细胞功能。抑制作用:抑制佛波醇酯(PMA)诱导的呼吸爆发、杀伤和重复吞噬能力、NADPH氧化酶和蛋白激酶C(PKC)的活性、细胞间黏附分子-1(ICAM-1)、整合素-CD11c、MHC-II类分子(IFN-γ介导)的表达,以及向功能性抗原呈递树突状细胞的分化。刺激作用:吞噬相关呼吸爆发增加和脂质过氧化产物积累;诱导金属蛋白酶-9以及促炎细胞因子和趋化因子。作用机制:疟原虫色素通过非酶催化产生大量脂质过氧化产物,如花生四烯酸(HETE)和亚油酸(HODE)的单羟基衍生物,以及4-羟基壬烯醛(HNE)。补充合理浓度的HETE或HNE可重现疟原虫色素的多种效应,前者最有可能通过与过氧化物酶体增殖物激活受体(PPAR)相互作用,后者则通过与关键靶点形成加合物或交联来实现。