Cantoni Orazio, Tommasini Ilaria, Cerioni Liana
Istituto di Farmacologia e Farmacognosia, Università degli Studi di Urbino Carlo Bo, Urbino, Italy.
Methods Enzymol. 2008;441:73-82. doi: 10.1016/S0076-6879(08)01205-6.
Cells belonging to the monocyte/macrophage lineage are in general highly resistant to peroxynitrite. Resistance is not dependent on the scavenging of peroxynitrite itself, or of other secondary reactive species, but is rather associated with the prompt activation of a survival signaling leading to the prevention of toxicity in cells otherwise committed to mitochondrial permeability transition (MPT)-dependent necrosis. The signaling pathway is triggered by cytosolic phospholipase A2-released arachidonic acid, leading to the sequential activation of 5-lipoxygenase (5-LO) and protein kinase C alpha, an event associated with the cytosolic accumulation of Bad. Hence, inhibition of 5-LO (or that of any of the aforementioned enzymes involved in the signaling cascade) was associated with the mitochondrial accumulation of Bad and Bax and with a rapid MPT-dependent toxicity. These results contribute to the definition of the mechanism(s) whereby monocytes/macrophages survive to peroxynitrite in inflamed tissues and provide insights for the development of novel anti-inflammatory therapies based on the suppression of inflammatory cell survival.
一般来说,属于单核细胞/巨噬细胞谱系的细胞对过氧亚硝酸盐具有高度抗性。这种抗性并不依赖于过氧亚硝酸盐本身或其他次级反应性物质的清除,而是与一种存活信号的迅速激活相关,该信号可防止细胞发生依赖线粒体通透性转换(MPT)的坏死毒性。该信号通路由胞质磷脂酶A2释放的花生四烯酸触发,导致5-脂氧合酶(5-LO)和蛋白激酶Cα的顺序激活,这一事件与Bad的胞质积累有关。因此,抑制5-LO(或信号级联中涉及的上述任何一种酶)与Bad和Bax在线粒体中的积累以及快速的MPT依赖性毒性有关。这些结果有助于明确单核细胞/巨噬细胞在炎症组织中对过氧亚硝酸盐产生抗性的机制,并为基于抑制炎症细胞存活的新型抗炎疗法的开发提供思路。