Survival pathways triggered by peroxynitrite in cells belonging to the monocyte/macrophage lineage

被引:6
|
作者
Cantoni, O [1 ]
Tommasini, H [1 ]
Cerioni, L [1 ]
Palomba, L [1 ]
Carloni, E [1 ]
Guidarelli, A [1 ]
机构
[1] Univ Urbino Carlo Bo, Ist Farmacol & Farmacognosia, I-61029 Urbino, PU, Italy
来源
COMPARATIVE BIOCHEMISTRY AND PHYSIOLOGY A-MOLECULAR & INTEGRATIVE PHYSIOLOGY | 2005年 / 142卷 / 02期
关键词
peroxynitrite; cytosolic phospholipase A(2); arachidonic acid; H2O2; mitochondrial permeability transition; necrosis; DNA damage; U937; cells; monocytes; macrophages;
D O I
10.1016/j.cbpb.2005.05.037
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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 H2O2, 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 H2O2 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. (C) 2005 Elsevier Inc. All rights reserved.
引用
收藏
页码:118 / 123
页数:6
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