Cantoni Orazio, Tommasini Ilaria, Cerioni Liana, Palomba Letizia, Carloni Elisa, Guidarelli Andrea
Istituto di Farmacologia e Farmacognosia, Università degli Studi di Urbino Carlo Bo, Via S. Chiara, Urbino (PU) 27-61029, Italy.
Comp Biochem Physiol A Mol Integr Physiol. 2005 Oct;142(2):118-23. doi: 10.1016/j.cbpb.2005.05.037. Epub 2005 Jun 17.
Peroxynitrite, a highly reactive nitrogen species, promotes in U937 cells (a promonocytic cell line) a mitochondrial permeability transition (MPT)-dependent necrosis. An initial event triggered by peroxynitrite (i.e., inhibition of complex III of the mitochondrial respiratory chain) is responsible for the time-dependent formation of H(2)O(2), essential for the occurrence of cell death. Otherwise non-toxic concentrations of peroxynitrite nevertheless commit cells to MPT-dependent necrosis, which is however prevented by a cytoprotective signaling driven by arachidonic acid (AA) released by the cytosolic PLA(2) isoform. Interestingly, the mechanism whereby delayed formation of H(2)O(2) promotes toxicity in cells exposed to intrinsically toxic concentrations of peroxynitrite is independent of the accumulation of additional damage. Cell death is in fact mediated by inhibition of the AA-dependent cytoprotective signaling. Exogenous AA, however, prevented toxicity also under these conditions. An additional point to be made is that the major findings obtained using U937 cells were reproduced in different cell types belonging to the monocyte/macrophage lineage. Hence, within the context of the inflammatory response, monocytes and macrophages may cope with peroxynitrite by using AA, a signaling molecule largely available at the inflammatory sites.
过氧亚硝酸盐是一种高反应性氮物种,可在U937细胞(一种前单核细胞系)中促进依赖线粒体通透性转换(MPT)的坏死。过氧亚硝酸盐引发的初始事件(即线粒体呼吸链复合物III的抑制)导致H(2)O(2)的时间依赖性形成,这对细胞死亡的发生至关重要。否则,无毒浓度的过氧亚硝酸盐仍会使细胞发生依赖MPT的坏死,不过由胞质磷脂酶A(2)同工型释放的花生四烯酸(AA)驱动的细胞保护信号可阻止这种坏死。有趣的是,在暴露于内在毒性浓度过氧亚硝酸盐的细胞中,H(2)O(2)的延迟形成促进毒性的机制与额外损伤的积累无关。细胞死亡实际上是由AA依赖性细胞保护信号的抑制介导的。然而,在这些条件下,外源性AA也可预防毒性。另一个要点是,使用U937细胞获得的主要发现也在属于单核细胞/巨噬细胞谱系的不同细胞类型中得到了重现。因此,在炎症反应的背景下,单核细胞和巨噬细胞可能通过使用AA来应对过氧亚硝酸盐,AA是炎症部位大量存在的一种信号分子。