Abstract
In the present study, we demonstrated that gadolinium-containing particles formed in cell culture medium acted as a biologically active entity to mediate cell cycle progression in NIH3T3 cells. The particles were observed to accumulate at the cell surface by scanning electron microscopy. Energy-dispersive X-ray analysis was undertaken and confirmed that gadolinium was incorporated in the agglomerated particles. Moreover, the smaller gadolinium particles exhibited a stronger cell-cycle-promoting effect than the larger ones, but they shared the common signaling pathways. Both extracellular signal regulated kinase and phosphatidylinositol 3-kinase signaling pathways were activated by gadolinium-containing particles and may account for their proliferation-promoting effect on NIH3T3 cells. Furthermore, the study showed that the free gadolinium ion released from gadolinium-containing particles may be responsible for the proliferation effect. This study will be helpful to clarify the biological effect of the insoluble species formed from Gd3+ as well as other multivalent metal ions under physiological conditions and will help to improve their medical applications.
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Abbreviations
- DMEM:
-
Dulbecco’s modified Eagle’s medium
- DTS:
-
Dispersion Technology Software
- EDX:
-
Energy-dispersive X-ray
- ERK:
-
Extracellular-signal-regulated kinase
- JNK:
-
c-Jun N-terminal kinase
- MAPK:
-
Mitogen-activated protein kinase
- MTT:
-
3-(4,5-Dimethylthiazoyl-2-yl)-2,5-diphenyltetrazolium bromide
- NSF:
-
Nephrogenic systemic fibrosis
- PBS:
-
Phosphate-buffered saline
- PI3K:
-
Phosphatidylinositol 3-kinase
- pRb:
-
Retinoblastoma tumor suppressor protein
- ROS:
-
Reactive oxygen species
- SEM:
-
Scanning electron microscopy
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This work was supported by the National Natural Science Foundation of China (20637010).
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Li, JX., Liu, JC., Wang, K. et al. Gadolinium-containing bioparticles as an active entity to promote cell cycle progression in mouse embryo fibroblast NIH3T3 cells. J Biol Inorg Chem 15, 547–557 (2010). https://doi.org/10.1007/s00775-010-0622-5
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DOI: https://doi.org/10.1007/s00775-010-0622-5