JIA Chunrong1, FENG Xinghua2, LIU Hongxiao2, et al. Effect of Bushen Qiangji Granules on Fibroblast Proliferation,Cycle,and Apoptosis Induced by Cell Factors in Ankylosing Spondylitis[J]. Journal of Traditional Chinese Medicine2011, 52(20): 1766-1770.
JIA Chunrong1, FENG Xinghua2, LIU Hongxiao2, et al. Effect of Bushen Qiangji Granules on Fibroblast Proliferation,Cycle,and Apoptosis Induced by Cell Factors in Ankylosing Spondylitis[J]. Journal of Traditional Chinese Medicine2011, 52(20): 1766-1770.DOI: 10.13288/j.11-2166/r.2011.20.030.
Effect of Bushen Qiangji Granules on Fibroblast Proliferation,Cycle,and Apoptosis Induced by Cell Factors in Ankylosing Spondylitis
Objective To explore the effect and mechanism of Bushen Qiangji Granules(Granules for reinforcing the kidney to strengthen the spine) on ankylosing spondylitis(AS).Methods The fibroblasts of AS hip-joint capsule cultured in vitro
as the experimental subjects
were divided into normal group
AS control group
AS cell factor induction group(AS induction group)
AS rabbit blank serum group
Bushen Qiangji Granules small-dose
medium-dose
and large-dose groups
and salicylazosulfapyridine(SASP) control group.Through the induction of bone morphogenetic protein(BMP) and transformation growth factor-β(TGF-β)
the effect of Bushen Qiangji Granules on fibroblast proliferation(5 samples
acid phosphatase staining)
period(3 samples
PI flow cytometry)
and apoptosis rate(3 samples
Annexin V flow cytometry) induced by cell factors was observed.Results Affected by the Bushen Qiangji medicinal serum
the proliferation of fibroblasts in AS induced by cell factors was significantly inhibited(P
<
0.01).The ratio of G
0
/G
1
stage of fibroblasts was significantly increased(P
<
0.05).The ratio of S stage of fibroblasts was decreased(P
<
0.01).And the early and late apoptosis rates of fibroblasts were all increased to different degrees(P
<
0.01).Conclusion Through inhibiting the effect of cell factors on the proliferation
period
and apoptosis of fibroblasts
Bushen Qiangji Granules can control the further differentiation of fibroblasts to osteoblasts.