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高脂饮食诱导的果蝇心脏脂肪毒性的代际遗传。

Intergenerational inheritance of high fat diet-induced cardiac lipotoxicity in Drosophila.

机构信息

Development, Aging and Regeneration Program, Sanford-Burnham-Prebys Medical Discovery Institute, 10901 N. Torrey Pines Road, La Jolla, CA, 92037, USA.

Biocompatibles Inc., 300 Four Falls Corporate Center, 300 Conshohocken State Road, West Conshohocken, PA, 19428-2998, USA.

出版信息

Nat Commun. 2019 Jan 14;10(1):193. doi: 10.1038/s41467-018-08128-3.

Abstract

Obesity is strongly correlated with lipotoxic cardiomyopathy, heart failure and thus mortality. The incidence of obesity has reached alarming proportions worldwide, and increasing evidence suggests that the parents' nutritional status may predispose their offspring to lipotoxic cardiomyopathy. However, to date, mechanisms underlying intergenerational heart disease risks have yet to be elucidated. Here we report that cardiac dysfunction induced by high-fat-diet (HFD) persists for two subsequent generations in Drosophila and is associated with reduced expression of two key metabolic regulators, adipose triglyceride lipase (ATGL/bmm) and transcriptional cofactor PGC-1. We provide evidence that targeted expression of ATGL/bmm in the offspring of HFD-fed parents protects them, and the subsequent generation, from cardio-lipotoxicity. Furthermore, we find that intergenerational inheritance of lipotoxic cardiomyopathy correlates with elevated systemic H3K27 trimethylation. Lowering H3K27 trimethylation genetically or pharmacologically in the offspring of HFD-fed parents prevents cardiac pathology. This suggests that metabolic homeostasis is epigenetically regulated across generations.

摘要

肥胖与脂肪毒性心肌病、心力衰竭乃至死亡率密切相关。肥胖的发生率在全球范围内已达到惊人的比例,越来越多的证据表明,父母的营养状况可能使后代易患脂肪毒性心肌病。然而,迄今为止,代际心脏病风险的机制仍未阐明。在这里,我们报告高脂肪饮食(HFD)诱导的心脏功能障碍在果蝇中持续存在于两代之后,并与两种关键代谢调节剂脂肪甘油三酯脂肪酶(ATGL/bmm)和转录共激活因子 PGC-1 的表达减少有关。我们提供的证据表明,HFD 喂养父母后代中 ATGL/bmm 的靶向表达可保护它们及其后代免受心脏脂肪毒性的影响。此外,我们发现脂肪毒性心肌病的代际遗传与全身性 H3K27 三甲基化水平升高有关。在 HFD 喂养父母的后代中降低 H3K27 三甲基化的遗传或药理学水平可预防心脏病变。这表明代谢稳态在代际间是通过表观遗传调控的。

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