2019
DOI: 10.1016/j.jtemb.2019.08.001
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The effects of zinc treatment on matrix metalloproteinases: A systematic review

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Cited by 35 publications
(17 citation statements)
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“…After zinc doping, the amount of VEGF released from the endothelial cells on the TiO 2 nanotubes surface increased further because the matrix metalloproteinase (MMP) in endothelial cells is a kind of extracellular protein hydrolase with zinc ions and calcium ions dependence. It can promote the release of VEGF from the endothelial cells, thus enhancing the adhesion and proliferation of endothelial cells . Because more zinc ions are released from the surface of TNT-50Zn, they can promote the synthesis of MMP and further release more VEGF.…”
Section: Results and Discussionmentioning
confidence: 99%
“…After zinc doping, the amount of VEGF released from the endothelial cells on the TiO 2 nanotubes surface increased further because the matrix metalloproteinase (MMP) in endothelial cells is a kind of extracellular protein hydrolase with zinc ions and calcium ions dependence. It can promote the release of VEGF from the endothelial cells, thus enhancing the adhesion and proliferation of endothelial cells . Because more zinc ions are released from the surface of TNT-50Zn, they can promote the synthesis of MMP and further release more VEGF.…”
Section: Results and Discussionmentioning
confidence: 99%
“…The degradation rate of implanted TM-doped cryogels was in the order: Zn > Cu > Co ≄ Ctrl ( Figure 8 , 1 ). The profound promoting effect of the Zn dopant is apparently associated with this TM activity as a key cofactor of different MMPs, including MMP-1, MMP-3, MMP-8, MMP-13, MMP-2, and MMP-9 [ 75 ]. The peptidase activity of MMP-1 and MMP-9 can be also promoted by Cu [ 38 ] in accordance with some lesser effect of the latter dopant.…”
Section: Discussionmentioning
confidence: 99%
“…In addition, bioactive compounds that are more rapidly released can diffuse through the extracellular fluid helping cell proliferation and matrix formation [ 60 , 61 ]. The presence of Zn 2+ in the extracellular environment has been related to the activation of matrix metalloproteases responsible for the degradation of the cartilage matrix by proteolysis and is closely related to osteoarthritis mechanisms [ 41 , 62 ]. However, there is a therapeutic concentration range of Zn 2+ (0.015 to 6.5 ÎŒg/mL) in which this element can have the opposite effect inhibiting the activity of these enzymes [ 63 ].…”
Section: Discussionmentioning
confidence: 99%