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TIMP-3 通过降低 MMP-2 和 MMP-9 的活性以及减少 TNF-α 的表达,抑制了兔粥样硬化 AAA 主动脉颈中 SMC 的增殖和迁移。

TIMP‑3 suppresses the proliferation and migration of SMCs from the aortic neck of atherosclerotic AAA in rabbits, via decreased MMP‑2 and MMP‑9 activity, and reduced TNF‑α expression.

机构信息

Department of Interventional Radiology, First Affiliated Hospital of China Medical University, Shenyang, Liaoning 110001, P.R. China.

Key Laboratory of Diagnostic Imaging and Interventional Radiology of Liaoning Province, First Affiliated Hospital of China Medical University, Shenyang, Liaoning 110001, P.R. China.

出版信息

Mol Med Rep. 2018 Aug;18(2):2061-2067. doi: 10.3892/mmr.2018.9224. Epub 2018 Jun 26.

Abstract

The present study investigated the role of tissue inhibitor of matrix metalloproteinase‑3 (TIMP‑3) in regulating the proliferation, migration, apoptosis and activity of matrix metalloproteinase (MMP)‑2 and ‑9, 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 TIMP‑3 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 6‑week high‑cholesterol 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 TIMP‑3. Cell proliferation was investigated using Cell Counting Kit‑8 reagent, migration was examined using a Boyden chamber assay and apoptotic rate was analyzed using the Annexin V‑fluorescein isothiocyanate Apoptosis Detection kit. Gelatin zymography and ELISA were used to measure the activity of MMP‑2 and MMP‑9, and the expression of tumor necrosis factor‑α (TNF‑α), respectively. Analysis of cell proliferation indicated that 10, 30 and 100 ng/ml TIMP‑3 reduced cell viability. Cell migration was decreased by 10, 30 and 100 ng/ml TIMP‑3. MMP‑2 activity was inhibited by 10, 30 and 100 ng/ml TIMP‑3, and MMP‑9 activity was suppressed by 30 and 100 ng/ml TIMP‑3. The protein levels of secreted TNF‑α were reduced by 10, 30 and 100 ng/ml TIMP‑3. The present study demonstrated the ability of 30 and 100 ng/ml TIMP‑3 to attenuate migration and proliferation, and to inhibit the activity of MMP‑2, MMP‑9 and TNF‑α secretion of NA SMCs. In conclusion, TIMP‑3 may be considered a potential therapeutic drug for use in a novel drug‑eluting stent, to attenuate the progressive dilation of the aortic NA.

摘要

本研究旨在探讨组织金属蛋白酶抑制剂 3(TIMP-3)在调控基质金属蛋白酶(MMP)-2 和 -9 的增殖、迁移、凋亡和活性方面的作用,这些作用发生在腹主动脉瘤(AAA)的发展过程中。实验采用兔 AAA 颈部(NA)平滑肌细胞(SMCs)进行,以研究 TIMP-3 作为一种新型支架涂层用于预防 AAA 附近主动脉扩张的潜力。新西兰白兔通过 6 周的高胆固醇饮食诱导动脉粥样硬化性 AAA 模型,然后用弹性酶孵育靶向主动脉区域。在 AAA 模型诱导后 30 天,从动脉瘤附近的主动脉分离 SMCs,并以 3、10、30 或 100ng/ml TIMP-3 刺激。使用 Cell Counting Kit-8 试剂检测细胞增殖,Boyden 室测定迁移率,Annexin V-荧光素异硫氰酸酯凋亡检测试剂盒分析凋亡率。明胶酶谱和 ELISA 分别用于测量 MMP-2 和 MMP-9 的活性和肿瘤坏死因子-α(TNF-α)的表达。细胞增殖分析表明,10、30 和 100ng/ml TIMP-3 降低了细胞活力。10、30 和 100ng/ml TIMP-3 减少了细胞迁移。10、30 和 100ng/ml TIMP-3 抑制 MMP-2 活性,30 和 100ng/ml TIMP-3 抑制 MMP-9 活性。10、30 和 100ng/ml TIMP-3 降低了分泌的 TNF-α的蛋白水平。本研究表明,30 和 100ng/ml TIMP-3 能够减弱 NA SMC 的迁移和增殖,并抑制 MMP-2、MMP-9 和 TNF-α 的活性和分泌。总之,TIMP-3 可能被认为是一种有前途的治疗药物,可用于新型药物洗脱支架,以减轻主动脉 NA 的进行性扩张。

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