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.

Animal studies have shown that the nutritional status of parents can predispose the offspring to obesity and obesity-related diseases. Here the authors show that cardiac dysfunction induced by a high-fat diet persists for two generations in Drosophila, and that targeted expression of ATGL/bmm in the offspring, as well as inhibition of H3K27 trimethylation, is cardioprotective.

Details

Title
Intergenerational inheritance of high fat diet-induced cardiac lipotoxicity in Drosophila
Author
Guida, Maria Clara 1 ; Birse, Ryan Tyge 2 ; Dall’Agnese Alessandra 3 ; Toto Paula Coutinho 1 ; Diop Soda Balla 1 ; Mai Antonello 4 ; Adams, Peter D 1 ; Puri, Pier Lorenzo 5   VIAFID ORCID Logo  ; Bodmer Rolf 1 

 Sanford-Burnham-Prebys Medical Discovery Institute, Development, Aging and Regeneration Program, La Jolla, USA (GRID:grid.479509.6) (ISNI:0000 0001 0163 8573) 
 Sanford-Burnham-Prebys Medical Discovery Institute, Development, Aging and Regeneration Program, La Jolla, USA (GRID:grid.479509.6) (ISNI:0000 0001 0163 8573) ; Biocompatibles Inc., West Conshohocken, USA (GRID:grid.479509.6) 
 Sanford-Burnham-Prebys Medical Discovery Institute, Development, Aging and Regeneration Program, La Jolla, USA (GRID:grid.479509.6) (ISNI:0000 0001 0163 8573) ; Whitehead Institute for Biomedical Research, Cambridge, USA (GRID:grid.116068.8) (ISNI:0000 0001 2341 2786) 
 Sapienza Università di Roma, Rome, Italy (GRID:grid.7841.a) 
 Sanford-Burnham-Prebys Medical Discovery Institute, Development, Aging and Regeneration Program, La Jolla, USA (GRID:grid.479509.6) (ISNI:0000 0001 0163 8573) ; IRCCS Fondazione Santa Lucia, Rome, Italy (GRID:grid.417778.a) (ISNI:0000 0001 0692 3437) 
Publication year
2019
Publication date
Jan 2019
Publisher
Nature Publishing Group
e-ISSN
20411723
Source type
Scholarly Journal
Language of publication
English
ProQuest document ID
2167021413
Copyright
This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.