Effects of Simulated Microgravity on Muscle Stem Cells Activity.


Journal

Cellular physiology and biochemistry : international journal of experimental cellular physiology, biochemistry, and pharmacology
ISSN: 1421-9778
Titre abrégé: Cell Physiol Biochem
Pays: Germany
ID NLM: 9113221

Informations de publication

Date de publication:
05 Aug 2020
Historique:
accepted: 18 07 2020
entrez: 5 8 2020
pubmed: 5 8 2020
medline: 13 1 2021
Statut: ppublish

Résumé

The study of the effects of simulated microgravity on primary cultures of human satellite cells represents a reliable model for identifying the biomolecular processes involved in mechanic load-related muscle mass loss. Therefore, this study aims to investigate the role of myostatin and Bone Morphogenetic Protein-2 in human satellite cells response to simulated microgravity condition. In order to identify the main molecules involved in the phenomena of degeneration/regeneration of muscle tissue related to the alteration of mechanic load, we performed a morphological and immunohistochemical study on 27 muscle biopsies taken from control, osteoporotic and osteoarthritic patients, underwent hip arthroplasty. For each patient, we set up primary satellite cell cultures subjected to normogravity and simulated microgravity (110h) regimens. Cellular functionality has been studied through a morphological evaluation performed by optical microscopy, and an ultrastructural evaluation carried out by transmission electron microscopy. Furthermore, we evaluated the expression of Bone Morphogenetic Protein-2 and myostatin through immunocytochemical reactions. Our results showed that in the very early phases of simulated microgravity condition the satellite cells are more active than those subjected to the normogravity regime, as demonstrated by both the increase in the number of myotubes and the significant increase in the expression of Bone Morphogenetic Protein-2 in all experimental groups. However, with prolongated exposure to simulated microgravity regime (>72h), satellite cells and new formed myotubes underwent to cell death. It is important to note that, in early phases, simulated microgravity can stimulate the formation of new myotubes from satellite cells derived by osteoporotic patients. Furthermore, we observed that simulated microgravity can induce changes in myostatin expression levels by group-dependent variations. The results obtained allowed us to hypothesize a possible molecular mechanism of response to simulated microgravity, confirming the importance of Bone Morphogenetic Protein-2 and myostatin in the physio-pathogenesis of muscle tissue. In addition, these data can lay the foundation for new therapeutic approached in the prevention/cure of osteoporosis and sarcopenia.

Sections du résumé

BACKGROUND/AIMS OBJECTIVE
The study of the effects of simulated microgravity on primary cultures of human satellite cells represents a reliable model for identifying the biomolecular processes involved in mechanic load-related muscle mass loss. Therefore, this study aims to investigate the role of myostatin and Bone Morphogenetic Protein-2 in human satellite cells response to simulated microgravity condition.
METHODS METHODS
In order to identify the main molecules involved in the phenomena of degeneration/regeneration of muscle tissue related to the alteration of mechanic load, we performed a morphological and immunohistochemical study on 27 muscle biopsies taken from control, osteoporotic and osteoarthritic patients, underwent hip arthroplasty. For each patient, we set up primary satellite cell cultures subjected to normogravity and simulated microgravity (110h) regimens. Cellular functionality has been studied through a morphological evaluation performed by optical microscopy, and an ultrastructural evaluation carried out by transmission electron microscopy. Furthermore, we evaluated the expression of Bone Morphogenetic Protein-2 and myostatin through immunocytochemical reactions.
RESULTS RESULTS
Our results showed that in the very early phases of simulated microgravity condition the satellite cells are more active than those subjected to the normogravity regime, as demonstrated by both the increase in the number of myotubes and the significant increase in the expression of Bone Morphogenetic Protein-2 in all experimental groups. However, with prolongated exposure to simulated microgravity regime (>72h), satellite cells and new formed myotubes underwent to cell death. It is important to note that, in early phases, simulated microgravity can stimulate the formation of new myotubes from satellite cells derived by osteoporotic patients. Furthermore, we observed that simulated microgravity can induce changes in myostatin expression levels by group-dependent variations.
CONCLUSION CONCLUSIONS
The results obtained allowed us to hypothesize a possible molecular mechanism of response to simulated microgravity, confirming the importance of Bone Morphogenetic Protein-2 and myostatin in the physio-pathogenesis of muscle tissue. In addition, these data can lay the foundation for new therapeutic approached in the prevention/cure of osteoporosis and sarcopenia.

Identifiants

pubmed: 32749090
doi: 10.33594/000000252
doi:

Substances chimiques

BMP2 protein, human 0
Bone Morphogenetic Protein 2 0
Myostatin 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

736-747

Subventions

Organisme : ASI (Italian Space Agency)
Pays : Italy
Organisme : Center of Space BioMedicine - "Tor Vergata" University of Rome
Pays : Italy

Informations de copyright

© Copyright by the Author(s). Published by Cell Physiol Biochem Press.

Déclaration de conflit d'intérêts

The authors declare that they have no competing interests.

Auteurs

Umberto Tarantino (U)

Department of Clinical Sciences and Translational Medicine, "Tor Vergata" University of Rome, Rome, Italy.
Department of Orthopaedics and Traumatology, "Policlinico Tor Vergata" Foundation, Rome, Italy.
Center of Space BioMedicine, "Tor Vergata" University of Rome, Rome, Italy.

Ida Cariati (I)

Department of Clinical Sciences and Translational Medicine, "Tor Vergata" University of Rome, Rome, Italy, Ida.Cariati@uniroma2.it.
Center of Space BioMedicine, "Tor Vergata" University of Rome, Rome, Italy.
PhD Students' Program in Medical-Surgical Biotechnologies and Translational Medicine, "Tor Vergata" University of Rome, Rome, Italy.

Mario Marini (M)

Center of Space BioMedicine, "Tor Vergata" University of Rome, Rome, Italy.
Department of Medicine of Systems, "Tor Vergata" University of Rome, Rome, Italy.

Giovanna D'Arcangelo (G)

Center of Space BioMedicine, "Tor Vergata" University of Rome, Rome, Italy.
Department of Medicine of Systems, "Tor Vergata" University of Rome, Rome, Italy.

Virginia Tancredi (V)

Center of Space BioMedicine, "Tor Vergata" University of Rome, Rome, Italy.
Department of Medicine of Systems, "Tor Vergata" University of Rome, Rome, Italy.

Matteo Primavera (M)

Department of Clinical Sciences and Translational Medicine, "Tor Vergata" University of Rome, Rome, Italy.
Department of Orthopaedics and Traumatology, "Policlinico Tor Vergata" Foundation, Rome, Italy.

Riccardo Iundusi (R)

Department of Clinical Sciences and Translational Medicine, "Tor Vergata" University of Rome, Rome, Italy.
Department of Orthopaedics and Traumatology, "Policlinico Tor Vergata" Foundation, Rome, Italy.

Elena Gasbarra (E)

Department of Clinical Sciences and Translational Medicine, "Tor Vergata" University of Rome, Rome, Italy.
Department of Orthopaedics and Traumatology, "Policlinico Tor Vergata" Foundation, Rome, Italy.

Manuel Scimeca (M)

Center of Space BioMedicine, "Tor Vergata" University of Rome, Rome, Italy.
Department of Biomedicine and Prevention, "Tor Vergata" University of Rome, Rome, Italy.

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Classifications MeSH