La3+-promoted proliferation is interconnected with apoptosis in NIH 3T3 cells
Siwang Yu1, Lan Yuan, Xiaoda Yang
1Department of Chemical Biology and Joint Laboratory of Peking University & The Hong Kong Polytechnic University, School of Pharmaceutical Sciences, Peking University Health Science Center, Beijing 100083, People's Republic of China.
Lanthanum ions (La3+) promote NIH 3T3 cell proliferation and apoptosis by altering cell cycle progression. This dual effect is mediated through extracellular signal-regulated kinase (ERK) signaling, suggesting a coordinated relationship between cell growth and death.
Area of Science:
- Cell Biology
- Biochemistry
- Toxicology
Background:
- Lanthanum ion (La3+) is known to influence cellular processes.
- Previous studies suggest La3+ affects cell proliferation and apoptosis.
- The precise mechanisms of La3+ on cell cycle regulation remain under investigation.
Purpose of the Study:
- To investigate the effects of lanthanum ion (La3+) on NIH 3T3 cell proliferation and apoptosis.
- To elucidate the role of cell cycle alterations and extracellular signal-regulated kinase (ERK) signaling in La3+-induced cellular responses.
- To explore the potential interconnection between proliferation and apoptosis induced by La3+.
Main Methods:
- Treatment of NIH 3T3 cells with varying concentrations of La3+.
- Cell cycle analysis using flow cytometry.
- Western blot analysis to detect phosphorylated extracellular signal-regulated kinase (p-ERK).
- Inhibition of ERK phosphorylation using PD98059.
Main Results:
- La3+ promoted both proliferation and apoptosis of NIH 3T3 cells at identical concentrations.
- La3+ facilitated cell cycle progression from G1 to S phase, but these proliferating cells eventually underwent apoptosis.
- La3+ induced ERK phosphorylation, and inhibiting this phosphorylation with PD98059 suppressed both proliferation and apoptosis.
- La3+-induced proliferation and apoptosis were correlated with cell cycle alterations.
Conclusions:
- Lanthanum ion (La3+) exhibits a dual role in NIH 3T3 cells, promoting both proliferation and apoptosis.
- The observed effects are linked to cell cycle modulation and are dependent on extracellular signal-regulated kinase (ERK) signaling.
- These findings support the hypothesis that cell proliferation and apoptosis are intrinsically coordinated processes.
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