Assessment and Imaging of Intracellular Magnesium in SaOS-2 Osteosarcoma Cells and Its Role in Proliferation.
Cell Cycle
/ drug effects
Cell Death
/ drug effects
Cell Line, Tumor
Cell Proliferation
/ drug effects
Cell Survival
/ drug effects
Diagnostic Imaging
Humans
Intracellular Space
/ chemistry
Magnesium
/ pharmacology
Microtubule-Associated Proteins
/ metabolism
Osteosarcoma
/ diagnostic imaging
Phosphorylation
/ drug effects
Signal Transduction
/ drug effects
TOR Serine-Threonine Kinases
/ metabolism
cell cycle
mTOR
magnesium
osteosarcoma
Journal
Nutrients
ISSN: 2072-6643
Titre abrégé: Nutrients
Pays: Switzerland
ID NLM: 101521595
Informations de publication
Date de publication:
20 Apr 2021
20 Apr 2021
Historique:
received:
14
03
2021
revised:
15
04
2021
accepted:
17
04
2021
entrez:
30
4
2021
pubmed:
1
5
2021
medline:
27
5
2021
Statut:
epublish
Résumé
Magnesium is an essential nutrient involved in many important processes in living organisms, including protein synthesis, cellular energy production and storage, cell growth and nucleic acid synthesis. In this study, we analysed the effect of magnesium deficiency on the proliferation of SaOS-2 osteosarcoma cells. When quiescent magnesium-starved cells were induced to proliferate by serum addition, the magnesium content was 2-3 times lower in cells maintained in a medium without magnesium compared with cells growing in the presence of the ion. Magnesium depletion inhibited cell cycle progression and caused the inhibition of cell proliferation, which was associated with mTOR hypophosphorylation at Serine 2448. In order to map the intracellular magnesium distribution, an analytical approach using synchrotron-based X-ray techniques was applied. When cell growth was stimulated, magnesium was mainly localized near the plasma membrane in cells maintained in a medium without magnesium. In non-proliferating cells growing in the presence of the ion, high concentration areas inside the cell were observed. These results support the role of magnesium in the control of cell proliferation, suggesting that mTOR may represent an important target for the antiproliferative effect of magnesium. Selective control of magnesium availability could be a useful strategy for inhibiting osteosarcoma cell growth.
Identifiants
pubmed: 33923895
pii: nu13041376
doi: 10.3390/nu13041376
pmc: PMC8073505
pii:
doi:
Substances chimiques
MAP1LC3A protein, human
0
Microtubule-Associated Proteins
0
TOR Serine-Threonine Kinases
EC 2.7.11.1
Magnesium
I38ZP9992A
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
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