Faculty Opinions recommendation of Matrix metalloproteinase-1 decorated polymersomes, a surface-active extracellular matrix therapeutic, potentiates collagen degradation and attenuates early liver fibrosis.

Author(s):  
Ralf Weiskirchen
2003 ◽  
Vol 124 (2) ◽  
pp. 445-458 ◽  
Author(s):  
Yuji Iimuro ◽  
Toshihiro Nishio ◽  
Taisuke Morimoto ◽  
Takashi Nitta ◽  
Branko Stefanovic ◽  
...  

2003 ◽  
Vol 120 (5) ◽  
pp. 842-848 ◽  
Author(s):  
Suzanne E.G. Fligiel ◽  
James Varani ◽  
Subhash C. Datta ◽  
Sewon Kang ◽  
Gary J. Fisher ◽  
...  

2014 ◽  
Vol 2014 ◽  
pp. 1-10 ◽  
Author(s):  
Guo-fu Huang ◽  
Jing Zou ◽  
Jing Shi ◽  
Dong-you Zhang ◽  
Hong-fen Pen ◽  
...  

The present study was aimed at determining if the electroacupuncture (EA) is able to protect degenerated disc in vivo. New Zealand white rabbits (n=40) were used for the study. The rabbits were randomly assigned to four groups. EA intervention was applied to one of the four groups. Magnetic resonance imaging and Pfirrmann’s classification were obtained for each group to evaluate EA treatment on the intervertebral disc degeneration. Discs were analyzed using immunofluorescence for the labeling of collagens 1 and 2, bone morphogenetic protein-2 (BMP-2), matrix metalloproteinase-13 (MMP-13), and tissue inhibitor of matrix metalloproteinase-1 (TIMP-1). For protein expression analysis, western blot was used for biglycan and decorin. Outcomes indicated that EA intervention decreased the grades compared with the compressed disc. Immunofluorescence analysis showed a significant increase of collagens 1 and 2, TIMP-1, and BMP-2 positive cells, in contrast to MMP-13 after EA treatment for 28 days. The protein expression showed a sign of regeneration that decorin and biglycan were upregulated. It was concluded that EA contributed to the extracellular matrix (ECM) anabolic processes and increased the ECM components. MMPs and their inhibitors involved in the mechanism of EA intervention on ECM decreased disc. It kept a dynamic balance between ECM synthesis and degradation.


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