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Anguita-Ruiz, A.* ; Bustos-Aibar, M.* ; Plaza-Díaz, J.* ; Méndez-Gutiérrez, A.* ; Alcalá-Fdez, J.* ; Aguilera, C.M.* ; Ruiz Ojeda, F.J.

Omics approaches in adipose tissue and skeletal muscle addressing the role of extracellular matrix in obesity and metabolic dysfunction.

Int. J. Mol. Sci. 22:2756 (2021)
Publ. Version/Full Text Research data DOI PMC
Open Access Gold
Creative Commons Lizenzvertrag
Extracellular matrix (ECM) remodeling plays important roles in both white adipose tissue (WAT) and the skeletal muscle (SM) metabolism. Excessive adipocyte hypertrophy causes fibro-sis, inflammation, and metabolic dysfunction in adipose tissue, as well as impaired adipogenesis. Similarly, disturbed ECM remodeling in SM has metabolic consequences such as decreased insulin sensitivity. Most of described ECM molecular alterations have been associated with DNA sequence variation, alterations in gene expression patterns, and epigenetic modifications. Among others, the most important epigenetic mechanism by which cells are able to modulate their gene expression is DNA methylation. Epigenome-Wide Association Studies (EWAS) have become a powerful approach to identify DNA methylation variation associated with biological traits in humans. Likewise, Genome-Wide Association Studies (GWAS) and gene expression microarrays have allowed the study of whole-genome genetics and transcriptomics patterns in obesity and metabolic diseases. The aim of this review is to explore the molecular basis of ECM in WAT and SM remodeling in obesity and the consequences of metabolic complications. For that purpose, we reviewed scientific literature including all omics approaches reporting genetic, epigenetic, and transcriptomic (GWAS, EWAS, and RNA-seq or cDNA arrays) ECM-related alterations in WAT and SM as associated with metabolic dysfunction and obesity.
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Publication type Article: Journal article
Document type Review
Corresponding Author
Keywords Adipose Tissue ; Epigenetic ; Extracellular Matrix ; Genetics ; Obesity ; Skeletal Muscle ; Transcriptomic
ISSN (print) / ISBN 1422-0067
e-ISSN 1661-6596
Quellenangaben Volume: 22, Issue: 5, Pages: , Article Number: 2756 Supplement: ,
Publisher MDPI
Publishing Place Basel
Non-patent literature Publications
Reviewing status Peer reviewed
Grants Junta de Andalucia (PAIDI, 2020)
"Ramon-Areces Foundation", Spain
doctorate contract i-PFIS: Doctorados IIS-empresa en ciencias y tecnologias de la salud
doctorate fellowship Formacion del Profesorado Universitario