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纸质出版日期:2013
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苏晓慧, 孔祥英, 吴文彬, 等. 风湿清对RANKL诱导的RAW264.7细胞向破骨细胞分化的影响[J]. 中国实验方剂学杂志, 2013,19(4):173-176.
SU Xiao-hui, KONG Xiang-ying, WU Wen-bin, et al. Effects of Fengshiqing on Osteoclast Differentiation of RAW264.7 Cells Induced by RANKL[J]. Chinese journal of experimental traditional medical formulae, 2013, 19(4): 173-176.
苏晓慧, 孔祥英, 吴文彬, 等. 风湿清对RANKL诱导的RAW264.7细胞向破骨细胞分化的影响[J]. 中国实验方剂学杂志, 2013,19(4):173-176. DOI:
SU Xiao-hui, KONG Xiang-ying, WU Wen-bin, et al. Effects of Fengshiqing on Osteoclast Differentiation of RAW264.7 Cells Induced by RANKL[J]. Chinese journal of experimental traditional medical formulae, 2013, 19(4): 173-176. DOI:
目的: 通过观察风湿清(Fengshiqing
FSQ)含药血清对RAW264.7细胞向破骨细胞分化及细胞分泌骨免疫相关因子肿瘤坏死因子α (TNF-α)和白介素-17 (IL-17)的影响
初步探讨FSQ缓解类风湿性关节炎(RA)骨破坏的机制。 方法: 5%
10%
15% 3个不同体积分数的FSQ含药血清与核因子-κB受体活化因子配体(receptor activator for nuclear factor-κB ligand
RANKL)诱导的RAW264.7共孵育6 d
抗酒石酸酸性磷酸酶(TRAP)染色观察TRAP阳性多核细胞的形成;FSQ含药血清(5%
10%
15%)与白介素-1β(IL-1β)诱导的RAW264.7细胞共孵育24 h后收集细胞上清液
ELISA方法检测TNF-α和IL-17的含量。 结果: RANKL诱导RAW264.7细胞形成TRAP阳性多核细胞
IL-1β诱导TNF-α和IL-17在RAW264.7细胞中异常高表达
5%~15% FSQ含药血清能剂量依赖地降低TRAP阳性细胞数;10%和15%的FSQ含药血清能显著抑制TNF-α (P<0.05)以及IL-17(P<0.01)的表达量。 结论: FSQ能抑制破骨前体细胞向破骨细胞分化
降低TNF-α和IL-17在RAW264.7细胞中的异常高表达
这可能是FSQ抑制骨破坏治疗RA的作用机制之一。
Objective: To observe the effect of Fengshiqing (FSQ) on osteoclast differentiation of RAW264.7 cells induced by receptor activator for nuclear factor-κB ligand
RANKL(RANKL) and the secretion of bone-related immune factor tumor necrosis factor-α(TNF-α)
interleukin-17(IL-17) in RAW264.7 cells. Method: RAW264.7 cells induced by RANKL were cultured with three variable volume fraction (5%
10%
15%) of serum containing FSQ in vitro 6 days. The influence of FSQ on osteoclast (RAW264.7 induced by RANKL) differentiation was observed by tartrate-resistant acid phosphatase(TRAP) staining. RAW264.7 cells induced by IL-1β were cultured with three variable volume fraction of serum containing FSQ in vitro 24 hours
level of TNF-α
IL-17 in cell culture supernatant was examined by ELISA. Result: RANKL could induce RAW264.7 cell to form TRAP positive multinucleated cells
IL-1β could induce abnormally high expression of TNF-α and IL-17 in RAW264.7 cells. Variable volume fraction (5%
10%
15%) of serum containing FSQ could decrease the number of TRAP-positive cells dose-dependently. In addition
FSQ (10%
15%) also suppressed the expression of IL-17(P<0.01) and TNF-α (P<0.05). Conclusion: FSQ has notable inhibiting effect on osteoclast differentiation of preosteoclast cells and suppressing expression of IL-17 and TNF-α in RAW264.7 cells induced by IL-1β
which may be a part of the mechanism of FSQ for treating rheumatoid arthritis.
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