Epigenetic reprogramming of H3K4me3 in adipose-derived stem cells by HFS diet consumption leads to a disturbed transcriptomic profile in adipocytes

Author:

Pérez Berenice1ORCID,Torre-Villalvazo Iván1,Wilson-Verdugo Martí2,Lau-Corona Dana1,Muciño-Olmos Erick23,Coutiño-Hernández Diana1,Noriega-López Lilia1,Resendis-Antonio Osbaldo3,Valdés Víctor Julián2,Torres Nimbe1ORCID,Tovar Armando R.1ORCID

Affiliation:

1. Departamento de Fisiología de la Nutrición, Instituto Nacional de Ciencias Médicas y Nutrición Salvador Zubirán, Mexico City, Mexico

2. Departamento de Biología Celular, Instituto de Fisiología Celular, Universidad Nacional Autónoma de México, Mexico City, Mexico

3. Laboratorio de Biología de Sistemas, Coordinación de la Investigación Científica - Red de Apoyo a la Investigación - Centro de Ciencias de la Complejidad, Universidad Nacional Autónoma de México & Instituto Nacional de Medicina Genómica, Mexico City, Mexico

Abstract

Obesity is associated with the development of chronic diseases like metabolic syndrome and type 2 diabetes, and adipose tissue plays a crucial role. In a rat model, our study reveals how an obesogenic environment primes adipocyte precursor cells, leading to epigenetic changes that affect inflammation, adipogenesis, and mitochondrial activity after differentiation. We highlight the importance of histone modifications, especially the trimethylation of histone H3 to lysine 4 (H3K4me3), showing its influence on adipocyte expression profiles.

Funder

Instituto Nacional de Ciências Médicas y Nutricion Salvador Zubiran

Publisher

American Physiological Society

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