Stem Cell Program, Division of Experimental Hematology and Cancer Biology, Cincinnati Children's Hospital Medical Center, Cincinnati, OH.
Division of Immunobiology, Cincinnati Children's Hospital Medical Center, Cincinnati, OH.
J Exp Med. 2018 Feb 5;215(2):627-644. doi: 10.1084/jem.20170690. Epub 2017 Dec 27.
Obesity is a chronic organismal stress that disrupts multiple systemic and tissue-specific functions. In this study, we describe the impact of obesity on the activity of the hematopoietic stem cell (HSC) compartment. We show that obesity alters the composition of the HSC compartment and its activity in response to hematopoietic stress. The impact of obesity on HSC function is progressively acquired but persists after weight loss or transplantation into a normal environment. Mechanistically, we establish that the oxidative stress induced by obesity dysregulates the expression of the transcription factor Gfi1 and that increased expression is required for the abnormal HSC function induced by obesity. These results demonstrate that obesity produces durable changes in HSC function and phenotype and that elevation of Gfi1 expression in response to the oxidative environment is a key driver of the altered HSC properties observed in obesity. Altogether, these data provide phenotypic and mechanistic insight into durable hematopoietic dysregulations resulting from obesity.
肥胖是一种慢性的机体应激,会破坏多个系统和组织特异性功能。在这项研究中,我们描述了肥胖对造血干细胞(HSC)池活性的影响。我们表明,肥胖会改变 HSC 池的组成及其对造血应激的反应。肥胖对 HSC 功能的影响是逐渐获得的,但在减肥或移植到正常环境后仍然存在。从机制上讲,我们确定肥胖引起的氧化应激会使转录因子 Gfi1 的表达失调,而表达增加是肥胖引起的异常 HSC 功能所必需的。这些结果表明,肥胖会导致 HSC 功能和表型发生持久变化,并且对氧化环境的 Gfi1 表达升高是肥胖导致 HSC 特性改变的关键驱动因素。总的来说,这些数据为肥胖引起的持久造血失调提供了表型和机制上的深入了解。