Transcriptome Analyses of In Vitro Exercise Models by Clenbuterol Supplementation or Electrical Pulse Stimulation

Exercise has beneficial effects on human health and is affected by two different pathways; motoneuron and endocrine. For the advancement of exercise research, <i>in vitro</i> exercise models are essential. We established two <i>in vitro</i> exercise models using C2C12 myotube...

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Autores principales: Taku Fukushima, Miho Takata, Ayano Kato, Takayuki Uchida, Takeshi Nikawa, Iori Sakakibara
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Publicado: MDPI AG 2021
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spelling oai:doaj.org-article:a09847db25b04dd4b68369f3bceb88f02021-11-11T15:24:13ZTranscriptome Analyses of In Vitro Exercise Models by Clenbuterol Supplementation or Electrical Pulse Stimulation10.3390/app1121104362076-3417https://doaj.org/article/a09847db25b04dd4b68369f3bceb88f02021-11-01T00:00:00Zhttps://www.mdpi.com/2076-3417/11/21/10436https://doaj.org/toc/2076-3417Exercise has beneficial effects on human health and is affected by two different pathways; motoneuron and endocrine. For the advancement of exercise research, <i>in vitro</i> exercise models are essential. We established two <i>in vitro</i> exercise models using C2C12 myotubes; EPS (electrical pulse stimulation) for a motoneuron model and clenbuterol, a specific β2 adrenergic receptor agonist, treatment for an endocrine model. For clenbuterol treatment, we found that <i>Ppargc1a</i> was induced only in low glucose media (1 mg/mL) using a 1-h treatment of 30 ng/mL clenbuterol. Global transcriptional changes of clenbuterol treatment were analyzed by RNA-seq and gene ontology analyses and indicated that mitogenesis and the PI3K-Akt pathway were enhanced, which is consistent with the effects of exercise. Cxcl1 and Cxcl5 were identified as candidate myokines induced by adrenaline. As for the EPS model, we compared 1 Hz of 1-pulse EPS and 1 Hz of 10-pulse EPS for 24 h and determined <i>Myh</i> gene expressions. Ten-pulse EPS induced higher <i>Myh2</i> and <i>Myh7</i> expression. Global transcriptional changes of 10-pulse EPS were also analyzed using RNA-seq, and gene ontology analyses indicated that CaMK signaling and hypertrophy pathways were enhanced, which is also consistent with the effects of exercise. In this paper, we provided two transcriptome results of <i>in vitro</i> exercise models and these databases will contribute to advances in exercise research.Taku FukushimaMiho TakataAyano KatoTakayuki UchidaTakeshi NikawaIori SakakibaraMDPI AGarticletranscriptomeskeletal muscleexerciseRNA-seqEPSadrenalineTechnologyTEngineering (General). Civil engineering (General)TA1-2040Biology (General)QH301-705.5PhysicsQC1-999ChemistryQD1-999ENApplied Sciences, Vol 11, Iss 10436, p 10436 (2021)
institution DOAJ
collection DOAJ
language EN
topic transcriptome
skeletal muscle
exercise
RNA-seq
EPS
adrenaline
Technology
T
Engineering (General). Civil engineering (General)
TA1-2040
Biology (General)
QH301-705.5
Physics
QC1-999
Chemistry
QD1-999
spellingShingle transcriptome
skeletal muscle
exercise
RNA-seq
EPS
adrenaline
Technology
T
Engineering (General). Civil engineering (General)
TA1-2040
Biology (General)
QH301-705.5
Physics
QC1-999
Chemistry
QD1-999
Taku Fukushima
Miho Takata
Ayano Kato
Takayuki Uchida
Takeshi Nikawa
Iori Sakakibara
Transcriptome Analyses of In Vitro Exercise Models by Clenbuterol Supplementation or Electrical Pulse Stimulation
description Exercise has beneficial effects on human health and is affected by two different pathways; motoneuron and endocrine. For the advancement of exercise research, <i>in vitro</i> exercise models are essential. We established two <i>in vitro</i> exercise models using C2C12 myotubes; EPS (electrical pulse stimulation) for a motoneuron model and clenbuterol, a specific β2 adrenergic receptor agonist, treatment for an endocrine model. For clenbuterol treatment, we found that <i>Ppargc1a</i> was induced only in low glucose media (1 mg/mL) using a 1-h treatment of 30 ng/mL clenbuterol. Global transcriptional changes of clenbuterol treatment were analyzed by RNA-seq and gene ontology analyses and indicated that mitogenesis and the PI3K-Akt pathway were enhanced, which is consistent with the effects of exercise. Cxcl1 and Cxcl5 were identified as candidate myokines induced by adrenaline. As for the EPS model, we compared 1 Hz of 1-pulse EPS and 1 Hz of 10-pulse EPS for 24 h and determined <i>Myh</i> gene expressions. Ten-pulse EPS induced higher <i>Myh2</i> and <i>Myh7</i> expression. Global transcriptional changes of 10-pulse EPS were also analyzed using RNA-seq, and gene ontology analyses indicated that CaMK signaling and hypertrophy pathways were enhanced, which is also consistent with the effects of exercise. In this paper, we provided two transcriptome results of <i>in vitro</i> exercise models and these databases will contribute to advances in exercise research.
format article
author Taku Fukushima
Miho Takata
Ayano Kato
Takayuki Uchida
Takeshi Nikawa
Iori Sakakibara
author_facet Taku Fukushima
Miho Takata
Ayano Kato
Takayuki Uchida
Takeshi Nikawa
Iori Sakakibara
author_sort Taku Fukushima
title Transcriptome Analyses of In Vitro Exercise Models by Clenbuterol Supplementation or Electrical Pulse Stimulation
title_short Transcriptome Analyses of In Vitro Exercise Models by Clenbuterol Supplementation or Electrical Pulse Stimulation
title_full Transcriptome Analyses of In Vitro Exercise Models by Clenbuterol Supplementation or Electrical Pulse Stimulation
title_fullStr Transcriptome Analyses of In Vitro Exercise Models by Clenbuterol Supplementation or Electrical Pulse Stimulation
title_full_unstemmed Transcriptome Analyses of In Vitro Exercise Models by Clenbuterol Supplementation or Electrical Pulse Stimulation
title_sort transcriptome analyses of in vitro exercise models by clenbuterol supplementation or electrical pulse stimulation
publisher MDPI AG
publishDate 2021
url https://doaj.org/article/a09847db25b04dd4b68369f3bceb88f0
work_keys_str_mv AT takufukushima transcriptomeanalysesofinvitroexercisemodelsbyclenbuterolsupplementationorelectricalpulsestimulation
AT mihotakata transcriptomeanalysesofinvitroexercisemodelsbyclenbuterolsupplementationorelectricalpulsestimulation
AT ayanokato transcriptomeanalysesofinvitroexercisemodelsbyclenbuterolsupplementationorelectricalpulsestimulation
AT takayukiuchida transcriptomeanalysesofinvitroexercisemodelsbyclenbuterolsupplementationorelectricalpulsestimulation
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AT iorisakakibara transcriptomeanalysesofinvitroexercisemodelsbyclenbuterolsupplementationorelectricalpulsestimulation
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