Alpha Mangostin promotes myogenic differentiation of C2C12 mouse myoblast cells.
Animals
Cell Differentiation
/ drug effects
Cell Line
Cell Survival
/ drug effects
Enzyme Activation
/ drug effects
Extracellular Signal-Regulated MAP Kinases
/ metabolism
Mice
Mitochondria
/ drug effects
Muscle Development
/ drug effects
MyoD Protein
/ metabolism
Myoblasts
/ cytology
Proto-Oncogene Proteins c-akt
/ metabolism
Xanthones
/ pharmacology
C2C12
Differentiation
MyoD
Myoblast
Myogenin
α-Mangostin
Journal
Biochemical and biophysical research communications
ISSN: 1090-2104
Titre abrégé: Biochem Biophys Res Commun
Pays: United States
ID NLM: 0372516
Informations de publication
Date de publication:
12 07 2020
12 07 2020
Historique:
received:
11
03
2020
accepted:
24
04
2020
pubmed:
2
6
2020
medline:
14
1
2021
entrez:
2
6
2020
Statut:
ppublish
Résumé
Mangosteen, a fruit mainly produced in Southeast Asia, has been used as food and as an antipyretic and for treating skin diseases. The xanthones contained in mangosteen have many physiological activities including melanin suppression and anticancer activities, but little is known about the physiological effects of the most abundant xanthone, α-mangostin (α-MG) on myoblasts. In this study, we applied α-MG to C2C12 cells that had been induced to differentiate using 2% HS, and analyzed the physiological action of α-MS and the underlying mechanism in the context of myogenic differentiation. α-MG increased the survival rate of C2C12 cells in a concentration-dependent manner. Analysis of the morphological changes in the cells showed that α-MG significantly enhanced the myogenic differentiation of C2C12 myoblasts, whereas the mitochondrial number was only slightly affected. Expression analysis of differentiation-related proteins in C2C12 cells revealed that α-MG promoted the expression of MyoD and Myogenin. Thus, the present study revealed that α-MG improves the survival and myogenic differentiation of C2C12 myoblasts.
Identifiants
pubmed: 32475640
pii: S0006-291X(20)30868-8
doi: 10.1016/j.bbrc.2020.04.128
pii:
doi:
Substances chimiques
MyoD Protein
0
Xanthones
0
Proto-Oncogene Proteins c-akt
EC 2.7.11.1
Extracellular Signal-Regulated MAP Kinases
EC 2.7.11.24
mangostin
U6RIV93RU1
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
193-198Informations de copyright
Copyright © 2020 Elsevier Inc. All rights reserved.
Déclaration de conflit d'intérêts
Declaration of competing interest On behalf of all authors, the corresponding author states that there are no conflicts of interest.