Proteomic analysis revealed different responses to hypergravity of soleus and extensor digitorum longus muscles in mice.


Journal

Journal of proteomics
ISSN: 1876-7737
Titre abrégé: J Proteomics
Pays: Netherlands
ID NLM: 101475056

Informations de publication

Date de publication:
15 04 2020
Historique:
received: 22 11 2019
revised: 30 01 2020
accepted: 12 02 2020
pubmed: 18 2 2020
medline: 22 6 2021
entrez: 17 2 2020
Statut: ppublish

Résumé

Investigating protein abundance profiles is important to understand the differences in the slow and fast skeletal muscle characteristics. The profiles in soleus (Sol) and extensor digitorum longus (EDL) muscles in mice exposed to 1 g or 3 g for 28 d were compared. The biological implications of the profiles revealed that hypergravity exposure activated a larger number of pathways involved in protein synthesis in Sol. In contrast, the inactivation of signalling pathways involved in oxidative phosphorylation were conspicuous in EDL. These results suggested that the reactivity of molecular pathways in Sol and EDL differed. Additionally, the levels of spermidine synthase and spermidine, an important polyamine for cell growth, increased in both muscles following hypergravity exposure, whereas the level of spermine oxidase (SMOX) increased in EDL alone. The SMOX level was negatively correlated with spermine content, which is involved in muscle atrophy, and was higher in EDL than Sol, even in the 1 g group. These results indicated that the contribution of SMOX to the regulation of spermidine and spermine contents in Sol and EDL differed. However, contrary to expectations, the difference in the SMOX level did not have a significant impact on the growth of these muscles following hypergravity exposure. SIGNIFICANCE: The skeletal muscle-specific protein abundance profiles result in differences in the characteristics of slow and fast skeletal muscles. We investigated differences in the profiles in mouse slow-twitch Sol and fast-twitch EDL muscles following 28-d of 1 g and 3 g exposure by LC-MS/MS analysis and label-free quantitation. A two-step solubilisation of the skeletal muscle proteins increased the coverage of proteins identified by LC-MS/MS analysis. Additionally, this method reduced the complexity of samples more easily than protein or peptide fractionation by SDS-PAGE and offline HPLC while maintaining the high operability of samples and was reproducible. A larger number of hypergravity-responsive proteins as well as a prominent increase in the wet weights was observed in Sol than EDL muscles. The biological implications of the difference in the protein abundance profiles in 1 g and 3 g groups revealed that the reactivity of each molecular pathway in Sol and EDL muscles to hypergravity exposure differed significantly. In addition, we found that the biosynthetic and interconversion pathway of polyamines, essential factors for cell growth and survival in mammals, was responsive to hypergravity exposure; spermidine and spermine contents in Sol and EDL muscles were regulated by different mechanisms even in the 1 g group. However, our results indicated that the difference in the mechanism regulating polyamine contents is unlikely to have a significant effect on the differences in Sol and EDL muscle growth following hypergravity exposure.

Identifiants

pubmed: 32061808
pii: S1874-3919(20)30054-3
doi: 10.1016/j.jprot.2020.103686
pii:
doi:

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

103686

Informations de copyright

Copyright © 2020 Elsevier B.V. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of Competing Interest We declare that none of the authors have competing financial or non-financial interests.

Auteurs

Takashi Ohira (T)

Advanced Medical Research Center, Yokohama City University, Kanagawa, Japan.

Yoko Ino (Y)

Advanced Medical Research Center, Yokohama City University, Kanagawa, Japan.

Yusuke Nakai (Y)

Advanced Medical Research Center, Yokohama City University, Kanagawa, Japan.

Hironobu Morita (H)

Department of Physiology, Gifu University Graduate School of Medicine, Gifu, Japan.

Ayuko Kimura (A)

Advanced Medical Research Center, Yokohama City University, Kanagawa, Japan.

Yoichi Kurata (Y)

Advanced Medical Research Center, Yokohama City University, Kanagawa, Japan.

Hiroyuki Kagawa (H)

Advanced Medical Research Center, Yokohama City University, Kanagawa, Japan.

Mitsuo Kimura (M)

Advanced Medical Research Center, Yokohama City University, Kanagawa, Japan.

Kenji Egashira (K)

Advanced Medical Research Center, Yokohama City University, Kanagawa, Japan.

Shunsuke Moriya (S)

Department of Advanced Research for Biomolecules, Tokyo Metropolitan Institute of Medical Science, Tokyo, Japan.

Kyoko Hiramatsu (K)

Department of Advanced Research for Biomolecules, Tokyo Metropolitan Institute of Medical Science, Tokyo, Japan.

Masao Kawakita (M)

Department of Advanced Research for Biomolecules, Tokyo Metropolitan Institute of Medical Science, Tokyo, Japan.

Yayoi Kimura (Y)

Advanced Medical Research Center, Yokohama City University, Kanagawa, Japan. Electronic address: ykimura@yokohama-cu.ac.jp.

Hisashi Hirano (H)

Advanced Medical Research Center, Yokohama City University, Kanagawa, Japan. Electronic address: hirano@yokohama-cu.ac.jp.

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