Abstract | OBJECTIVE: METHODS: MSCs were separated by percoll cell separating medium (density 1.073 g/cm3). After being cultured and transferred, the cells were divided into a control group, a low-dose group (10(-7) mol/L PCB126) and a high-dose group (10(-6) mol/L PCB126). The cellular growth rate and the expression of c-fos and c-jun protein were analyzed by MTT, immunofluorescence chemical assay, RT-PCR and Western blot. RESULTS: The cellular growth rate in the low-and high-dose group were 13.8% and 19.1% at 12 h, 31.5% and 36.1% at 24 h, 42.5% and 43.6% at 48 h, respectively (P < 0.01). The positive rates of c-fos expression in the low-and high-dose groups were 54.6% and 51.3% at 12 h, and 83.2% and 73.0% at 24 h. The expression of c-fos mRNA detected by RT-PCR was upregulated at 30 min and 1h in PCB126 groups. The expression of c-jun mRNA were much higher in PCB126 groups than that in the control group. The expression of c-fos and c-jun protein was upregulated in the low-and high-dose groups at 12 h and 24 h. CONCLUSION:
PCB126 could promote the proliferation of MSCs and upregulate the expression of cancer associated gene c-fos and c-jun. The effect of PCB126 on the function of MSCs might be associated with the abnormal expression of c-fos and c-jun gene.
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Authors | Hongbin Zhao, Jianfeng Wang, Xu Wang, Juzi Dong, Huanfa Zhou, Yinshu Yang |
Journal | Wei sheng yan jiu = Journal of hygiene research
(Wei Sheng Yan Jiu)
Vol. 41
Issue 2
Pg. 180-4, 190
(Mar 2012)
ISSN: 1000-8020 [Print] China |
PMID | 22611921
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Chemical References |
- Environmental Pollutants
- Proto-Oncogene Proteins c-fos
- Proto-Oncogene Proteins c-jun
- RNA, Messenger
- Polychlorinated Biphenyls
- 3,4,5,3',4'-pentachlorobiphenyl
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Topics |
- Animals
- Bone Marrow Cells
(cytology)
- Environmental Pollutants
(toxicity)
- Female
- Male
- Mesenchymal Stem Cells
(cytology, metabolism)
- Polychlorinated Biphenyls
(toxicity)
- Proto-Oncogene Proteins c-fos
(genetics, metabolism)
- Proto-Oncogene Proteins c-jun
(genetics, metabolism)
- RNA, Messenger
(genetics, metabolism)
- Rats
- Rats, Wistar
- Up-Regulation
(drug effects)
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