Author(s)
Author(s): Liu Xiaoping, Yu Zhongjie, Jiang Shasha, Wang Yi, Yang Tongxi, Wang Chunxue
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DOI: 10.18483/ijSci.925
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a 91-102
Volume 5 - Feb 2016
Abstract
BMSCs were isolated, cultured and proliferated in vitro. The proliferation of mouse BMSCs treated with different concentrations of LPS and NNK were detected by MTT assay, the expression of NF-κB and CUGBP1 in the BMSCs were analyzed by Immunocytochemistry assay and Western Blot. MTT results shown that different concentrations of LPS and NNK could promote the proliferation of BMSCs and the promotion effect of LPS12.5μg/ml, NNK10μg/ml and LPS12.5μg/ml combined NNK 10μg/ml was much more significant than others. Immunocytochemistry and Western Blot revealed that the location and the expression level of NF-κB and CUGBP1 in BMSCs treated with LPS and NNK were changed with different incubation time. The highest expression of NF-κB was detected at the LPS48h, NNK24h and LPS combined NNK24h and significant difference can be seen in-group compared. The highest expression of CUGBP1 was LPS96h, NNK48h and LPS combined NNK24h and significant difference can be seen in-group compared. The irritation of LPS and NNK on the proliferation of mouse BMSCs may mediate by up-regulating the expression of NF-κB and CUGBP1.
Keywords
Bone Marrow Stem Cells (BMSCs), Cell proliferation, NF-κB, CUGBP1.
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