Department of Chemical Engineering and Materials Science, Michigan State University, East Lansing, MI 48824, USA.
Exp Cell Res. 2010 Mar 10;316(5):716-27. doi: 10.1016/j.yexcr.2009.12.008. Epub 2009 Dec 21.
Saturated free fatty acids (FFAs), e.g. palmitate, have long been shown to induce toxicity and cell death in various types of cells. In this study, we demonstrate that cAMP synergistically amplifies the effect of palmitate on the induction of cell death in human hepatocellular carcinoma cell line, HepG2 cells. Elevation of cAMP level in palmitate-treated cells led to enhanced mitochondrial fragmentation, mitochondrial reactive oxygen species (ROS) generation and mitochondrial biogenesis. Mitochondrial fragmentation precedes mitochondrial ROS generation and mitochondrial biogenesis, and may contribute to mitochondrial ROS overproduction and subsequent mitochondrial biogenesis. Fragmentation of mitochondria also facilitated the release of cytotoxic mitochondrial proteins, such as Smac, from the mitochondria and subsequent activation of caspases. However, cell death induced by palmitate and cAMP was caspase-independent and mainly necrotic.
饱和游离脂肪酸(FFAs),如棕榈酸,长期以来一直被证明会在各种类型的细胞中诱导毒性和细胞死亡。在这项研究中,我们证明 cAMP 协同放大了棕榈酸对人肝癌细胞系 HepG2 细胞死亡诱导的作用。在棕榈酸处理的细胞中升高 cAMP 水平导致线粒体片段化、线粒体活性氧(ROS)生成和线粒体生物发生增强。线粒体片段化先于线粒体 ROS 生成和线粒体生物发生,可能导致线粒体 ROS 过度产生和随后的线粒体生物发生。线粒体的片段化也促进了细胞色素 c 等细胞毒性线粒体蛋白从线粒体中释放出来,随后激活了半胱天冬酶。然而,棕榈酸和 cAMP 诱导的细胞死亡是 caspase 非依赖性的,主要是坏死性的。