17β-estradiol upregulates oxytocin and the oxytocin receptor in C2C12 myotubes

Background The endocrinology of skeletal muscle is highly complex and many issues about hormone action in skeletal muscle are still unresolved. Aim of the work is to improve our knowledge on the relationship between skeletal muscle and 17β-estradiol. Methods The skeletal muscle cell line C2C12 was t...

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Main Authors: Enrica Berio, Sara Divari, Laura Starvaggi Cucuzza, Bartolomeo Biolatti, Francesca Tiziana Cannizzo
Format: Article
Language:English
Published: PeerJ Inc. 2017-03-01
Series:PeerJ
Subjects:
Online Access:https://peerj.com/articles/3124.pdf
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spelling doaj-db33e79d5630462d9a42fae2f4109f6f2020-11-24T20:59:23ZengPeerJ Inc.PeerJ2167-83592017-03-015e312410.7717/peerj.312417β-estradiol upregulates oxytocin and the oxytocin receptor in C2C12 myotubesEnrica Berio0Sara Divari1Laura Starvaggi Cucuzza2Bartolomeo Biolatti3Francesca Tiziana Cannizzo4Department of Veterinary Science, University of Turin, Grugliasco, Torino, ItalyDepartment of Veterinary Science, University of Turin, Grugliasco, Torino, ItalyDepartment of Veterinary Science, University of Turin, Grugliasco, Torino, ItalyDepartment of Veterinary Science, University of Turin, Grugliasco, Torino, ItalyDepartment of Veterinary Science, University of Turin, Grugliasco, Torino, ItalyBackground The endocrinology of skeletal muscle is highly complex and many issues about hormone action in skeletal muscle are still unresolved. Aim of the work is to improve our knowledge on the relationship between skeletal muscle and 17β-estradiol. Methods The skeletal muscle cell line C2C12 was treated with 17β-estradiol, the oxytocin peptide and a combination of the two hormones. The mRNA levels of myogenic regulatory factors, myosin heavy chain, oxytocin, oxytocin receptor and adipogenic factors were analysed in C2C12 myotubes. Results It was demonstrated that C2C12 myoblasts and myotubes express oxytocin and its receptor, in particular the receptor levels physiologically increase in differentiated myotubes. Myotubes treated with 17β-estradiol overexpressed oxytocin and oxytocin receptor genes by approximately 3- and 29-fold, respectively. A decrease in the expression of fatty acid binding protein 4 (0.62-fold), a fat metabolism-associated gene, was observed in oxytocin-treated myotubes. On the contrary, fatty acid binding protein 4 was upregulated (2.66-fold) after the administration of the combination of 17β-estradiol and oxytocin. 17β-estradiol regulates oxytocin and its receptor in skeletal muscle cells and they act in a synergic way on fatty acid metabolism. Discussion Oxytocin and its receptor are physiologically regulated along differentiation. 17β-estradiol regulates oxytocin and its receptor in skeletal muscle cells. 17β-estradiol and oxytocin act in a synergic way on fatty acid metabolism. A better understanding of the regulation of skeletal muscle homeostasis by estrogens and oxytocin peptide could contribute to increase our knowledge of muscle and its metabolism.https://peerj.com/articles/3124.pdfEstrogenOxytocinSkeletal muscle cellGene expression regulation
collection DOAJ
language English
format Article
sources DOAJ
author Enrica Berio
Sara Divari
Laura Starvaggi Cucuzza
Bartolomeo Biolatti
Francesca Tiziana Cannizzo
spellingShingle Enrica Berio
Sara Divari
Laura Starvaggi Cucuzza
Bartolomeo Biolatti
Francesca Tiziana Cannizzo
17β-estradiol upregulates oxytocin and the oxytocin receptor in C2C12 myotubes
PeerJ
Estrogen
Oxytocin
Skeletal muscle cell
Gene expression regulation
author_facet Enrica Berio
Sara Divari
Laura Starvaggi Cucuzza
Bartolomeo Biolatti
Francesca Tiziana Cannizzo
author_sort Enrica Berio
title 17β-estradiol upregulates oxytocin and the oxytocin receptor in C2C12 myotubes
title_short 17β-estradiol upregulates oxytocin and the oxytocin receptor in C2C12 myotubes
title_full 17β-estradiol upregulates oxytocin and the oxytocin receptor in C2C12 myotubes
title_fullStr 17β-estradiol upregulates oxytocin and the oxytocin receptor in C2C12 myotubes
title_full_unstemmed 17β-estradiol upregulates oxytocin and the oxytocin receptor in C2C12 myotubes
title_sort 17β-estradiol upregulates oxytocin and the oxytocin receptor in c2c12 myotubes
publisher PeerJ Inc.
series PeerJ
issn 2167-8359
publishDate 2017-03-01
description Background The endocrinology of skeletal muscle is highly complex and many issues about hormone action in skeletal muscle are still unresolved. Aim of the work is to improve our knowledge on the relationship between skeletal muscle and 17β-estradiol. Methods The skeletal muscle cell line C2C12 was treated with 17β-estradiol, the oxytocin peptide and a combination of the two hormones. The mRNA levels of myogenic regulatory factors, myosin heavy chain, oxytocin, oxytocin receptor and adipogenic factors were analysed in C2C12 myotubes. Results It was demonstrated that C2C12 myoblasts and myotubes express oxytocin and its receptor, in particular the receptor levels physiologically increase in differentiated myotubes. Myotubes treated with 17β-estradiol overexpressed oxytocin and oxytocin receptor genes by approximately 3- and 29-fold, respectively. A decrease in the expression of fatty acid binding protein 4 (0.62-fold), a fat metabolism-associated gene, was observed in oxytocin-treated myotubes. On the contrary, fatty acid binding protein 4 was upregulated (2.66-fold) after the administration of the combination of 17β-estradiol and oxytocin. 17β-estradiol regulates oxytocin and its receptor in skeletal muscle cells and they act in a synergic way on fatty acid metabolism. Discussion Oxytocin and its receptor are physiologically regulated along differentiation. 17β-estradiol regulates oxytocin and its receptor in skeletal muscle cells. 17β-estradiol and oxytocin act in a synergic way on fatty acid metabolism. A better understanding of the regulation of skeletal muscle homeostasis by estrogens and oxytocin peptide could contribute to increase our knowledge of muscle and its metabolism.
topic Estrogen
Oxytocin
Skeletal muscle cell
Gene expression regulation
url https://peerj.com/articles/3124.pdf
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