Fu Chunfeng,Huang Wei,Liang Xi,Hu Ning,K-L Paul Sung,Xie Jing,Chen Rongfu,Wang Chunli,Lin Liangbo,Wang Zhiqiang,Chen Cheng.Effect of titanium particles and inflammatory cytokines on MMP-2 expression in human knee joint synovial cells[J].J Amry Med Univ (J Third Mil Med Univ),2013,35(16):1676-1679.
Fu Chunfeng,Huang Wei,Liang Xi,Hu Ning,K-L Paul Sung,Xie Jing,Chen Rongfu,Wang Chunli,Lin Liangbo,Wang Zhiqiang,Chen Cheng.Effect of titanium particles and inflammatory cytokines on MMP-2 expression in human knee joint synovial cells[J].J Amry Med Univ (J Third Mil Med Univ),2013,35(16):1676-1679.DOI:
Effect of titanium particles and inflammatory cytokines on MMP-2 expression in human knee joint synovial cells
Objective To determine the effect of titanium (Ti) particles
and cytokines TNF-α and IL-1β on the expression and activity of MMP-2 in human synovial cells so as to explore the probable mechanism of post-operative osteolysis of metal-on-metal total joint arthroplasty in human synovial cells induced by Ti particles. Methods Human synovial cells were freshly isolated and cultured from normal knee joint synovium
and then those at passage 4 were treated with Ti particles in size of ≥10
5-10
and ≤5 μm respectively for 12
24
48 or 72 h. TNF-α
and IL-1β at different doses were used to treat the cells in presence
or absence of Ti particles for above time periods. Gelatin zymography was performed to detect the activity of MMP-2 in the cell supernatant. Results Compared with the cells without any treatment
the expression level of MMP-2 treated by Ti particles in size of ≤5 μm was significantly increased by 4 times
that treated by Ti particles
TNF-α
and IL-1β respectively or combined of any 2 agents were also increased significantly (
P
0.01)
and that treated by the combination of the 3 agents were most significantly higher (P0.01). Ti particles
TNF-α
and IL-1β induced the stimulation of MMP-2 activities in human knee joint synovial cells
and exerted synergetic effect. Conclusion Synovial cells may be involved in aseptic loosening after metal-on-metal arthroplasty through increasing the degradation of bone matrix and declining of osseous support structure mechanics.