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Atonal homolog 8/Math6 regulates differentiation and maintenance of skeletal muscle

Atonal Homolog 8 (Atoh8) belongs to a large superfamily of transcriptional regulators called basic helix-loop-helix (bHLH) transcription factors. Atoh8 (murine homolog “Math6”) has been shown to be involved in organogenesis during murine embryonic development. We have previously identified the expre...

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Autores principales: Divvela, Satya Srirama Karthik, Offei, Eric Bekoe, Suerland, Florian, Revuelta García, David, Kwiatkowski, Julia, Balakrishnan-Renuka, Ajeesh, Bohne, Pauline, Böing, Marion, Morosan-Puopolo, Gabriela, Mark, Melanie D., Brand-Saberi, Beate
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9438786/
https://www.ncbi.nlm.nih.gov/pubmed/36060799
http://dx.doi.org/10.3389/fcell.2022.950414
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author Divvela, Satya Srirama Karthik
Offei, Eric Bekoe
Suerland, Florian
Revuelta García, David
Kwiatkowski, Julia
Balakrishnan-Renuka, Ajeesh
Bohne, Pauline
Böing, Marion
Morosan-Puopolo, Gabriela
Mark, Melanie D.
Brand-Saberi, Beate
author_facet Divvela, Satya Srirama Karthik
Offei, Eric Bekoe
Suerland, Florian
Revuelta García, David
Kwiatkowski, Julia
Balakrishnan-Renuka, Ajeesh
Bohne, Pauline
Böing, Marion
Morosan-Puopolo, Gabriela
Mark, Melanie D.
Brand-Saberi, Beate
author_sort Divvela, Satya Srirama Karthik
collection PubMed
description Atonal Homolog 8 (Atoh8) belongs to a large superfamily of transcriptional regulators called basic helix-loop-helix (bHLH) transcription factors. Atoh8 (murine homolog “Math6”) has been shown to be involved in organogenesis during murine embryonic development. We have previously identified the expression of Atoh8 during skeletal myogenesis in chicken where we described its involvement in hypaxial myotome formation suggesting a regulatory role of Atoh8 in skeletal muscle development. Within the current study, we analyzed the effect of the loss of function of Atoh8 in murine primary myoblasts and during differentiation of pluripotent stem cells into myotubes, and the effect of its gain of function in C2C12 cells. Based on the observed results, we conclude that Atoh8 regulates myoblast proliferation via modulating myostatin signaling. Further, our data revealed a reduced muscle mass, strength and fiber size with significant changes to the muscle fiber type suggesting atrophy in skeletal muscle of Atoh8 mutants. We further report that Atoh8 knockout mice suffer from a condition similar to ambient hypoxia which may be the primary cause of the phenotype. Altogether, this study shows the significance of Atoh8 not only in myogenesis but also in the maintenance of skeletal muscle.
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spelling pubmed-94387862022-09-03 Atonal homolog 8/Math6 regulates differentiation and maintenance of skeletal muscle Divvela, Satya Srirama Karthik Offei, Eric Bekoe Suerland, Florian Revuelta García, David Kwiatkowski, Julia Balakrishnan-Renuka, Ajeesh Bohne, Pauline Böing, Marion Morosan-Puopolo, Gabriela Mark, Melanie D. Brand-Saberi, Beate Front Cell Dev Biol Cell and Developmental Biology Atonal Homolog 8 (Atoh8) belongs to a large superfamily of transcriptional regulators called basic helix-loop-helix (bHLH) transcription factors. Atoh8 (murine homolog “Math6”) has been shown to be involved in organogenesis during murine embryonic development. We have previously identified the expression of Atoh8 during skeletal myogenesis in chicken where we described its involvement in hypaxial myotome formation suggesting a regulatory role of Atoh8 in skeletal muscle development. Within the current study, we analyzed the effect of the loss of function of Atoh8 in murine primary myoblasts and during differentiation of pluripotent stem cells into myotubes, and the effect of its gain of function in C2C12 cells. Based on the observed results, we conclude that Atoh8 regulates myoblast proliferation via modulating myostatin signaling. Further, our data revealed a reduced muscle mass, strength and fiber size with significant changes to the muscle fiber type suggesting atrophy in skeletal muscle of Atoh8 mutants. We further report that Atoh8 knockout mice suffer from a condition similar to ambient hypoxia which may be the primary cause of the phenotype. Altogether, this study shows the significance of Atoh8 not only in myogenesis but also in the maintenance of skeletal muscle. Frontiers Media S.A. 2022-08-16 /pmc/articles/PMC9438786/ /pubmed/36060799 http://dx.doi.org/10.3389/fcell.2022.950414 Text en Copyright © 2022 Divvela, Offei, Suerland, Revuelta García, Kwiatkowski, Balakrishnan-Renuka, Bohne, Böing, Morosan-Puopolo, Mark and Brand-Saberi. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Cell and Developmental Biology
Divvela, Satya Srirama Karthik
Offei, Eric Bekoe
Suerland, Florian
Revuelta García, David
Kwiatkowski, Julia
Balakrishnan-Renuka, Ajeesh
Bohne, Pauline
Böing, Marion
Morosan-Puopolo, Gabriela
Mark, Melanie D.
Brand-Saberi, Beate
Atonal homolog 8/Math6 regulates differentiation and maintenance of skeletal muscle
title Atonal homolog 8/Math6 regulates differentiation and maintenance of skeletal muscle
title_full Atonal homolog 8/Math6 regulates differentiation and maintenance of skeletal muscle
title_fullStr Atonal homolog 8/Math6 regulates differentiation and maintenance of skeletal muscle
title_full_unstemmed Atonal homolog 8/Math6 regulates differentiation and maintenance of skeletal muscle
title_short Atonal homolog 8/Math6 regulates differentiation and maintenance of skeletal muscle
title_sort atonal homolog 8/math6 regulates differentiation and maintenance of skeletal muscle
topic Cell and Developmental Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9438786/
https://www.ncbi.nlm.nih.gov/pubmed/36060799
http://dx.doi.org/10.3389/fcell.2022.950414
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