1. 甘肃省中医院
2. 甘肃省中医药研究院
3. 甘肃中医药大学
纸质出版:2019
移动端阅览
[1]谢兴文,李应福,李宁,李盛华,宋敏.不同浓度麝香含药血清对骨髓间充质干细胞增殖、分化的影响[J].中医杂志,2019,60(01):57-61.
XIE Xingwen, LI Yingfu, LI Ning, et al. Effects of Different Concentrations of Moschus-containing Serum on Proliferation and Differentiation of Bone Marrow Mesenchymal Stem Cells[J]. Journal of Traditional Chinese Medicine2019, 60(1): 57-61.
[1]谢兴文,李应福,李宁,李盛华,宋敏.不同浓度麝香含药血清对骨髓间充质干细胞增殖、分化的影响[J].中医杂志,2019,60(01):57-61. DOI: 10.13288/j.11-2166/r.2019.01.014.
XIE Xingwen, LI Yingfu, LI Ning, et al. Effects of Different Concentrations of Moschus-containing Serum on Proliferation and Differentiation of Bone Marrow Mesenchymal Stem Cells[J]. Journal of Traditional Chinese Medicine2019, 60(1): 57-61. DOI: 10.13288/j.11-2166/r.2019.01.014.
目的探讨不同浓度麝香对骨髓间充质干细胞(BMSCs)增殖和定向成骨、成脂诱导分化的影响。方法 60只SD大鼠随机分为麝香高、中、低剂量组及空白对照组
每组15只。麝香高、中、低剂量组分别给予麝香16. 8、8. 4、4. 2μl/100 g灌胃
每日1次
连续8天
分别制备不同浓度麝香含药血清及空白血清。另取15只SD大鼠利用全骨髓贴壁筛选法分离BMSCs
培养至第3代
通过细胞形态学观察、细胞表型鉴定、成骨及成脂诱导分化方法鉴定BMSCs。利用不同浓度麝香含药血清和空白血清干预BMSCs
检测各组细胞不同时间细胞增殖率、碱性磷酸酶(ALP)活性、Ⅰ型胶原免疫荧光染色、钙化结节数及脂肪细胞转化率。结果与空白血清组同时间比较
麝香低剂量血清组在第2、3、4、5、7天
麝香中剂量血清组在第1、5天细胞增殖率均升高;麝香低剂量血清组在第2、4、6、8天
麝香中剂量血清组在第4、8天
麝香高剂量血清组在第2、8天ALP活性升高;除麝香高剂量血清组钙化结节数外
各组钙化结节数和脂肪细胞转化率亦升高(P <0. 05或P <0. 01)。与麝香低剂量血清组比较
麝香高剂量血清组在第1、3、5、7天
麝香中剂量血清组在第1、5天细胞增殖率降低
在第6、8天ALP活性降低
钙化结节数及脂肪细胞转化率亦降低(P <0. 05)。麝香高、中、低剂量血清组Ⅰ型胶原细胞阳性表达依次增强
空白血清组细胞阳性表达很弱或几乎未见。结论麝香可以促进BMSCs增殖并诱导其定向分化
以4. 2μl/100 g浓度效果最好。
Objective To investigate the effects of different concentrations of Moschus on the proliferation and osteogenesis and adipogenic differentiation of bone marrow mesenchymal stem cells( BMSCs). Methods A total of60 SD rats were randomly divided into blank control group and Moschus high
medium
low dose groups
with 15 groups in each group. The Moschus high
medium
low dose groups were respectively given 16. 8
8. 4
4. 2 μl/100 g Moschus once a day
for 8 consecutive days to prepare different concentrations of Moschus-containing serum and blank serum. BMSCs were isolated from other 15 SD rats by whole bone marrow adherence screening method
and cultured to the third generation. BMSCs were identified by cell morphology observation
cell phenotype identification
osteogenic and adipogenic differentiation methods. BMSCs were treated with different concentrations of Moschus-containing serum and blank serum. The cell proliferation rate
alkaline phosphatase( ALP) activity
type I collagen immunofluorescence staining
calcification nodules and adipocyte conversion rate were measured at different time points.Results Compared with the blank serum group at the same time
the cell proliferation rate of the murine low-dose serum group was increased on the 2 nd
3 rd
4 th
5 th
and 7 th day
and it was also increased in the medium group on the 1 st and 5 th day. The ALP activity of the Moschus low-dose serum group was increased on the 2 nd
4 th
6 th and8 th days
and that of the Moschus high-dose serum group was increase as well on the 2 nd and 8 th days
and it was increased on the 4 th and 8 th days in the Moschus medium-dose serum group. Except the number of calcified nodules in the high-dose serum group
the number of calcified nodules and adipocyte conversion rate in each group also were increased( P < 0. 05 or P < 0. 01). Compared with the Moschus low-dose serum group
the cell proliferation rate of the Moschus high-dose serum group on the 1 st
3 rd
5 th
and 7 th days
and of the Moschus medium dose serum group on the 1 st and 5 th days was decreased
and the ALP activity on the 6 th and 8 th days was decreased. The number of calcified nodules and the conversion rate of adipocytes were also decreased( P < 0. 05). The positive expression of type I collagen cells in the high
medium and low doses of Moschus increased in turn
and the positive expression of blank serum group cells was weak or almost absent. Conclusion Moschus can promote the proliferation of BMSCs and induce their differentiation
the best effect occured at the concentration of 4. 2 μL/100 g.
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