Kramer Ashley C, Weber Jenna, Zhang Ying, Tolar Jakub, Gibbens Ying Y, Shevik Margaret, Lund Troy C
Division of Pediatric Blood and Marrow Transplantation, University of Minnesota, Minneapolis, MN 55455, USA.
Minnesota Supercomputing Institute, University of Minnesota, Minneapolis, MN 55455, USA.
Stem Cell Reports. 2017 Feb 14;8(2):360-372. doi: 10.1016/j.stemcr.2016.12.025. Epub 2017 Jan 26.
Metabolism of oxidative stress is necessary for cellular survival. We have previously utilized the zebrafish as a model of the oxidative stress response. In this study, we found that gata1-expressing erythroid cells contributed to a significant proportion of total-body oxidative stress when animals were exposed to a strong pro-oxidant. RNA-seq of zebrafish under oxidative stress revealed the induction of tp53. Zebrafish carrying tp53 with a mutation in its DNA-binding domain were acutely sensitive to pro-oxidant exposure and displayed significant reactive oxygen species (ROS) and tp53-independent erythroid cell death resulting in an edematous phenotype. We found that a major contributing factor to ROS was increased basal mitochondrial respiratory rate without reserve. These data add to the concept that tp53, while classically a tumor suppressor and cell-cycle regulator, has additional roles in controlling cellular oxidative stress.
氧化应激的代谢对于细胞存活是必要的。我们之前利用斑马鱼作为氧化应激反应的模型。在本研究中,我们发现当动物暴露于强促氧化剂时,表达gata1的红细胞对全身氧化应激有很大比例的贡献。氧化应激下斑马鱼的RNA测序揭示了tp53的诱导。携带DNA结合域发生突变的tp53的斑马鱼对促氧化剂暴露极为敏感,并表现出显著的活性氧(ROS)和不依赖tp53的红细胞死亡,导致水肿表型。我们发现ROS的一个主要促成因素是基础线粒体呼吸速率无储备地增加。这些数据进一步支持了这样的概念,即tp53虽然传统上是一种肿瘤抑制因子和细胞周期调节因子,但在控制细胞氧化应激方面还有其他作用。