Maeda A, Fadeel B
Division of Molecular Toxicology, Institute of Environmental Medicine, Karolinska Institutet, Stockholm, Sweden.
Cell Death Dis. 2014 Jul 3;5(7):e1312. doi: 10.1038/cddis.2014.277.
Necrosis leads to the release of so-called damage-associated molecular patterns (DAMPs), which may provoke inflammatory responses. However, the release of organelles from dying cells, and the consequences thereof have not been documented before. We demonstrate here that mitochondria are released from cells undergoing tumor necrosis factor-α (TNF-α)-induced, receptor-interacting protein (RIP)1-dependent necroptosis, a form of programmed necrosis. The released, purified mitochondria were determined to be intact as they did not emit appreciable amounts of mitochondrial DNA (mtDNA). Pharmacological inhibition of dynamin-related protein 1 (Drp1) prevented mitochondrial fission in TNF-α-triggered cells, but this did not block necroptosis nor the concomitant release of mitochondria. Importantly, primary human macrophages and dendritic cells engulfed mitochondria from necroptotic cells leading to modulation of macrophage secretion of cytokines and induction of dendritic cell maturation. Our results show that intact mitochondria are released from necroptotic cells and suggest that these organelles act as bona fide danger signals.
坏死会导致所谓的损伤相关分子模式(DAMPs)的释放,这可能引发炎症反应。然而,之前尚未有关于死亡细胞中细胞器的释放及其后果的记录。我们在此证明,线粒体从经历肿瘤坏死因子-α(TNF-α)诱导的、受体相互作用蛋白(RIP)1依赖性坏死性凋亡(一种程序性坏死形式)的细胞中释放出来。所释放并纯化的线粒体被确定为完整的,因为它们没有释放出大量的线粒体DNA(mtDNA)。对动力相关蛋白1(Drp1)的药理学抑制可防止TNF-α触发的细胞中的线粒体分裂,但这并不阻断坏死性凋亡,也不阻止线粒体的伴随释放。重要的是,原代人巨噬细胞和树突状细胞会吞噬坏死性凋亡细胞中的线粒体,从而导致巨噬细胞细胞因子分泌的调节以及树突状细胞成熟的诱导。我们的结果表明,完整的线粒体从坏死性凋亡细胞中释放出来,并表明这些细胞器作为真正的危险信号发挥作用。