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Institute of Hematology, the First Hospital Affiliated to Zhejiang University of Chinese Medicine,Hangzhou,China
纸质出版日期:2012,
网络出版日期:2012-8-2,
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Yin, Lm., Wang, X., Qian, Xd. et al. Effects of Panax notoginseng saponins on proliferation and differentiation in NIH3T3 cells., Chin. J. Integr. Med. 18, 616–620 (2012). https://doi.org/10.1007/s11655-012-1179-7
Li-ming Yin, Xiao Wang, Xu-dai Qian, et al. Effects of Panax notoginseng saponins on proliferation and differentiation in NIH3T3 cells[J]. Chinese Journal of Integrative Medicine, 2012,18(8):616-620.
Yin, Lm., Wang, X., Qian, Xd. et al. Effects of Panax notoginseng saponins on proliferation and differentiation in NIH3T3 cells., Chin. J. Integr. Med. 18, 616–620 (2012). https://doi.org/10.1007/s11655-012-1179-7 DOI:
Li-ming Yin, Xiao Wang, Xu-dai Qian, et al. Effects of Panax notoginseng saponins on proliferation and differentiation in NIH3T3 cells[J]. Chinese Journal of Integrative Medicine, 2012,18(8):616-620. DOI: 10.1007/s11655-012-1179-7.
To investigate the effects of Panax notoginseng saponins (PNS) on the proliferation and differentiation in NIH3T3 cells. NIH3T3 cells were treated by various concentrations of PNS 0
0.05
0.10
0.20
and 0.40 g/L. The vitality and proliferation potential of cells were detected by 3-(4
5-dimethylthiazol-2-yl)-2
5-diphenyltetrazolium bromide (MTT) assay
the alkaline phosphatase (ALP) activity was measured by p-nitrophenyl phosphate (pNPP) assay
and the mineralization formation ability was tested for the cellular differentiation toward osteoblast
as well as the expression level of phosphorylated extracellular signal-regulated kinase1/2(P-ERK1/2)
extracellular signal-regulated kinase1/2 (ERK1/2) protein kinase was analyzed by Western blot with total cell lysate of NIH3T3 cells treated by PNS. Both MTT and pNPP assay showed that optical density (OD) values were increased in response to PNS treatment at a dose-dependent pattern. The mineralization formation ability was enhanced in PNS-treated NIH3T3 cells compared with untreated cells. Meanwhile
the expression level of P-ERK1/2 protein kinase was up-regulated in PNS-treated NIH3T3 cells
while
the expression level of ERK1/2 protein kinase revealed no obvious difference with or without PNS treated cells. PNS could pay a role to promote the proliferation and differentiation in NIH3T3 cells by means of up-regulation of P-ERK1/2 protein kinase.
To investigate the effects of Panax notoginseng saponins (PNS) on the proliferation and differentiation in NIH3T3 cells. NIH3T3 cells were treated by various concentrations of PNS 0
0.05
0.10
0.20
and 0.40 g/L. The vitality and proliferation potential of cells were detected by 3-(4
5-dimethylthiazol-2-yl)-2
5-diphenyltetrazolium bromide (MTT) assay
the alkaline phosphatase (ALP) activity was measured by p-nitrophenyl phosphate (pNPP) assay
and the mineralization formation ability was tested for the cellular differentiation toward osteoblast
as well as the expression level of phosphorylated extracellular signal-regulated kinase1/2(P-ERK1/2)
extracellular signal-regulated kinase1/2 (ERK1/2) protein kinase was analyzed by Western blot with total cell lysate of NIH3T3 cells treated by PNS. Both MTT and pNPP assay showed that optical density (OD) values were increased in response to PNS treatment at a dose-dependent pattern. The mineralization formation ability was enhanced in PNS-treated NIH3T3 cells compared with untreated cells. Meanwhile
the expression level of P-ERK1/2 protein kinase was up-regulated in PNS-treated NIH3T3 cells
while
the expression level of ERK1/2 protein kinase revealed no obvious difference with or without PNS treated cells. PNS could pay a role to promote the proliferation and differentiation in NIH3T3 cells by means of up-regulation of P-ERK1/2 protein kinase.
panax notoginseng saponinsNIH3T3 cellsosteoblastextracellular signal-regulated kinase protein kinase
panax notoginseng saponinsNIH3T3 cellsosteoblastextracellular signal-regulated kinase protein kinase
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