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BioScientifica, Journal of Endocrinology, 3(226), p. X1, 2015

DOI: 10.1530/joe-14-0474e

BioScientifica, Journal of Endocrinology, 3(224), p. 303-313, 2015

DOI: 10.1530/joe-14-0474

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TWIST1 and TWIST2 regulate glycogen storage and inflammatory genes in skeletal muscle

Journal article published in 2015 by Jonathan M. Mudry, Julie Massart ORCID, Ferenc L. M. Szekeres, Anna Krook
This paper is made freely available by the publisher.
This paper is made freely available by the publisher.

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Abstract

TWIST proteins are important for development of embryonic skeletal muscle and play a role in the metabolism of tumor and white adipose tissue. The impact of TWIST on metabolism in skeletal muscle is incompletely studied. Our aim was to assess the impact of TWIST1 and TWIST2 overexpression on glucose and lipid metabolism. In intact mouse muscle, overexpression of Twist reduced total glycogen content without altering glucose uptake. Expression of TWIST1 or TWIST2 reducedPdk4mRNA, while increasing mRNA levels ofIl6,Tnfα, andIl1β. Phosphorylation of AKT was increased and protein abundance of acetyl CoA carboxylase (ACC) was decreased in skeletal muscle overexpressing TWIST1 or TWIST2. Glycogen synthesis and fatty acid oxidation remained stable in C2C12 cells overexpressing TWIST1 or TWIST2. Finally, skeletal muscle mRNA levels remain unaltered inob/obmice, type 2 diabetic patients, or in healthy subjects before and after 3 months of exercise training. Collectively, our results indicate that TWIST1 and TWIST2 are expressed in skeletal muscle. Overexpression of these proteins impacts proteins in metabolic pathways and mRNA level of cytokines. However, skeletal muscle levels of TWIST transcripts are unaltered in metabolic diseases.