[No authors listed]
The present study investigated the role of tissue inhibitor of matrix metalloproteinaseâ3 (TIMPâ3) in regulating the proliferation, migration, apoptosis and activity of matrix metalloproteinase (MMP)â2 and â9, during the development of an atherosclerotic abdominal artery aneurysm (AAA). Experiments were conducted using rabbit AAA neck (NA) smooth muscle cells (SMCs), to investigate the potential for TIMPâ3 to be used as a novel stent coating in preventing aortic dilation adjacent to the AAA. The atherosclerotic AAA model was induced in New Zealand white rabbits via a 6âweek highâcholesterol diet, followed by incubation of the targeted aortic region with elastase. SMCs were isolated from the aorta adjacent to the aneurysm 30 days after AAA model induction, and stimulated with 3, 10, 30 or 100 ng/ml TIMPâ3. Cell proliferation was investigated using Cell Counting Kitâ8 reagent, migration was examined using a Boyden chamber assay and apoptotic rate was analyzed using the Annexin Vâfluorescein isothiocyanate Apoptosis Detection kit. Gelatin zymography and ELISA were used to measure the activity of MMPâ2 and MMPâ9, and the expression of tumor necrosis factorâα (TNFâα), respectively. Analysis of cell proliferation indicated that 10, 30 and 100 ng/ml TIMPâ3 reduced cell viability. Cell migration was decreased by 10, 30 and 100 ng/ml TIMPâ3. MMPâ2 activity was inhibited by 10, 30 and 100 ng/ml TIMPâ3, and MMPâ9 activity was suppressed by 30 and 100 ng/ml TIMPâ3. The protein levels of secreted TNFâα were reduced by 10, 30 and 100 ng/ml TIMPâ3. The present study demonstrated the ability of 30 and 100 ng/ml TIMPâ3 to attenuate migration and proliferation, and to inhibit the activity of MMPâ2, MMPâ9 and TNFâα secretion of NA SMCs. In conclusion, TIMPâ3 may be considered a potential therapeutic drug for use in a novel drugâeluting stent, to attenuate the progressive dilation of the aortic NA.
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