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TP53调节Gata1红系细胞中的氧化应激。

TP53 Modulates Oxidative Stress in Gata1 Erythroid Cells.

作者信息

Kramer Ashley C, Weber Jenna, Zhang Ying, Tolar Jakub, Gibbens Ying Y, Shevik Margaret, Lund Troy C

机构信息

Division of Pediatric Blood and Marrow Transplantation, University of Minnesota, Minneapolis, MN 55455, USA.

Minnesota Supercomputing Institute, University of Minnesota, Minneapolis, MN 55455, USA.

出版信息

Stem Cell Reports. 2017 Feb 14;8(2):360-372. doi: 10.1016/j.stemcr.2016.12.025. Epub 2017 Jan 26.

Abstract

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.

摘要

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。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1a20/5312256/d1eb4e56baa5/gr1.jpg

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