Acta Pharmacologica Sinica (2009) 30: 435-441; doi: 10.1038/aps.2009.21; published online 23rd March 2009

 
Original Article
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Sinomenine influences capacity for invasion and migration in activated human monocytic THP-1 cells by inhibiting the expression of MMP-2, MMP-9, and CD147
 

Yang-qiong OU, Li-hua CHEN, Xue-jun LI, Zhi-bin LIN, Wei-dong LI *

Department of Pharmacology, School of Basic Medical Sciences, Peking University Health Science Center , Beijing 100191, China

 

Aim: The aim of this study was to investigate the mechanism of the effects of Sinomenine (SIN) on the invasion and migration ability of activated human monocytic THP-1 cells (A-THP-1).  Sinomenine is a pure alkaloid extracted from the Chinese medical plant Sinomenium acutum. 

Methods: Human monocytic THP-1 cells were induced to differentiate into macrophages with phorbol 12-myristate 13-acetate (PMA).  Cells were treated with different concentrations of SIN.  The invasion and migration ability of cells was tested by in vitro transwell assays.  The levels of CD147 and MMPs were evaluated by flow cytometric analysis and zymographic analysis, respectively.  The mRNA expression of CD147, MMP-2, and MMP-9 was measured by RT-PCR.  

Results: The invasion and migration ability of A-THP-1 cells was significantly inhibited by SIN in a concentration-dependent fashion; at the same time, the levels of CD147, MMP-2, and MMP-9 were markedly down-regulated.  This inhibitory effect was most notable at concentrations of 0.25 mmol/L and 1.00 mmol/L (P<0.01).  

 

Conclusion: A possible mechanism of the inhibitory effect of SIN on cell invasion and migration ability is repression of the expression of MMP-2 and MMP-9, which strongly correlates with the inhibition of CD147 activity.  
 

Keywords: sinomenine; rheumatoid arthritis; invasion; migration; CD147; MMP-2; MMP-9

 

The authors are very grateful to Prof jian-hui LIANG and Dr Michael A McNutt for revising this paper.

 

* Correspondence to Wei-dong LI. 
E-maillwdpharma@126.com
Received 2008-12-19   Accepted 2009-02-10

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