Department of Laboratory Animal Science, Shanghai Jiao Tong University School of Medicine, 280 South Chongqing Road, Shanghai 200025, China.
Shanghai Institute of Endocrinology and Metabolism, Shanghai Key Laboratory for Endocrine Tumors, Rui-Jin Hospital, Shanghai Jiao Tong University School of Medicine, 197 Rui-Jin 2nd Road, Shanghai 200025, China.
Cell Metab. 2016 Apr 12;23(4):735-43. doi: 10.1016/j.cmet.2016.01.014. Epub 2016 Feb 18.
Both epidemiologic and experimental animal studies demonstrate that chronic psychological stress exerts adverse effects on the initiation and/or progression of many diseases. However, intergenerational effects of this environmental information remains poorly understood. Here, using a C57BL/6 mouse model of restraint stress, we show that offspring of stressed fathers exhibit hyperglycemia due to enhanced hepatic gluconeogenesis and elevated expression of PEPCK. Mechanistically, we identify an epigenetic alteration at the promoter region of the Sfmbt2 gene, a maternally imprinted polycomb gene, leading to a downregulation of intronic microRNA-466b-3p, which post-transcriptionally inhibits PEPCK expression. Importantly, hyperglycemia in F1 mice is reversed by RU486 treatment in fathers, and dexamethasone administration in F0 mice phenocopies the roles of restraint stress. Thus, we provide evidence showing the effects of paternal psychological stress on the regulation of glucose metabolism in offspring, which may have profound implications for our understanding of health and disease risk inherited from fathers.
流行病学和实验动物研究都表明,慢性心理压力对许多疾病的发生和/或发展都有不良影响。然而,这种环境信息的代际效应仍知之甚少。在这里,我们使用束缚应激的 C57BL/6 小鼠模型,发现应激父亲的后代表现出高血糖,这是由于肝糖异生增强和 PEPCK 表达升高所致。从机制上讲,我们在 Sfmbt2 基因(一种母系印记的多梳基因)的启动子区域发现了一种表观遗传改变,导致内含子 microRNA-466b-3p 的下调,从而转录后抑制 PEPCK 的表达。重要的是,RU486 处理父代可以逆转 F1 代小鼠的高血糖,而 F0 代小鼠给予地塞米松处理则可模拟束缚应激的作用。因此,我们提供的证据表明,父代心理压力对后代葡萄糖代谢的调节作用,这可能对我们理解从父亲那里遗传的健康和疾病风险具有深远意义。