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椎间盘退变过程中MMP-2活性增加与MMP-14水平相关。

Increased MMP-2 activity during intervertebral disc degeneration is correlated to MMP-14 levels.

作者信息

Rutges J P H J, Kummer J A, Oner F C, Verbout A J, Castelein R J M, Roestenburg H J A, Dhert W J A, Creemers L B

机构信息

Department of Orthopaedics, University Medical Centre, Utrecht, The Netherlands.

出版信息

J Pathol. 2008 Mar;214(4):523-30. doi: 10.1002/path.2317.

Abstract

Intervertebral disc (IVD) degeneration is associated with the increased expression of several matrix metalloproteinases (MMPs), in particular MMP-2. However, little is known about the actual activity of MMP-2 in healthy and degenerated discs, or what mechanisms are involved in its activation. A major activation pathway involves complex formation with MMP-14 and a tissue inhibitor of metalloproteinases-2 (TIMP-2). In a series of 56 human IVDs, obtained at autopsy and graded according to the Thompson score (I-V), we analysed whether MMP-2 activity was increased in different stages of IVD degeneration and to what extent activation was related to the production of MMP-14 and TIMP-2. MMP-2 activation and production were quantified by gelatin zymography. Immunohistochemical staining of MMP-14 and TIMP-2 was quantified with a video overlay-based system. A positive correlation was observed between the amount of active MMP-2 and pro-MMP-2 and degeneration grade (p < 0.001, correlation coefficient (CC) 0.557; and p < 0.001, CC 0.556, respectively). MMP-2 activity correlated positively with MMP-14 and less strongly with TIMP-2 (p = 0.001, CC 0.436; and p = 0.03, CC 0.288, respectively). Moreover, immunopositivity for MMP-14 correlated to degeneration grade (p = 0.002, CC 0.398). IVD degeneration was associated with the activity of MMP-2 and the correlation of its activation with MMP-14 production suggests MMP-14 activates MMP-2 during degeneration. As MMP-14 is capable of activating several other enzymes that are also thought to be involved in IVD degeneration, it may be a key mediator of the degenerative process.

摘要

椎间盘(IVD)退变与多种基质金属蛋白酶(MMPs)的表达增加有关,尤其是MMP-2。然而,关于MMP-2在健康和退变椎间盘中的实际活性,以及其激活涉及何种机制,人们了解甚少。一条主要的激活途径涉及与MMP-14和金属蛋白酶组织抑制剂-2(TIMP-2)形成复合物。在一系列56个经尸检获得并根据汤普森评分(I-V级)分级的人类IVD中,我们分析了MMP-2活性在IVD退变的不同阶段是否增加,以及激活程度与MMP-14和TIMP-2产生的关系。通过明胶酶谱法对MMP-2的激活和产生进行定量。用基于视频叠加的系统对MMP-14和TIMP-2进行免疫组织化学染色定量。观察到活性MMP-2和前体MMP-2的量与退变程度呈正相关(分别为p < 0.001,相关系数(CC)0.557;以及p < 0.001,CC 0.556)。MMP-2活性与MMP-14呈正相关,与TIMP-2的相关性较弱(分别为p = 0.001,CC 0.436;以及p = 0.03,CC 0.288)。此外,MMP-14的免疫阳性与退变程度相关(p = 0.002,CC 0.398)。IVD退变与MMP-2的活性相关,其激活与MMP-14产生的相关性表明MMP-14在退变过程中激活MMP-2。由于MMP-14能够激活其他几种也被认为参与IVD退变的酶,它可能是退变过程的关键介质。

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