羊膜早破时基质金属蛋白酶2活性的变化。

Atsuyuki Ota, Hisashi Yonemoto, Akimasa Someya, Shigeru Itoh, Katsuyuki Kinoshita, Isao Nagaoka
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引用次数: 19

摘要

目的:基质金属蛋白酶(mmp)如MMP-3和MMP-9的蛋白水解活性升高与足月胎膜早破有关。然而,目前尚不清楚MMP-2是否与胎膜早破有关。在本研究中,为了阐明MMP-2的作用,我们评估了MMP-2的活性以及前MMP-2、膜型1 (MT1)-MMP和组织金属蛋白酶抑制剂(TIMP)-1在膜早破中的表达。方法:29例无产(剖宫产;CS, n = 10),产程(正常分娩;ND, n = 10)和胎膜早破时的分娩(PROM, n = 9)。通过测量MMP-2特异性底物的消化,分光光度法测定了MMP-2的活性。Western免疫印迹法检测pro-MMP-2、MT1-MMP、TIMP-1水平。结果:MMP-2在胎膜早破中活性明显高于CS和ND (P)。结论:MMP-2 pro-MMP-2和MT1-MMP表达增加,TIMP-1表达降低可能导致MMP-2活性增加,而MMP-2参与胎膜细胞外基质(ECM)的降解,从而诱导胎膜在足月早破。
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Changes in matrix metalloproteinase 2 activities in amniochorions during premature rupture of membranes.

Objective: Increased proteolytic activities of matrix metalloproteinases (MMPs) such as MMP-3 and MMP-9 are associated with premature rupture of membranes at term. However, it is unclear whether MMP-2 is involved in the premature rupture of membranes. In this study, to elucidate the role of MMP-2, we evaluated the activity of MMP-2 and also the expression of pro-MMP-2, membrane type 1 (MT1)-MMP and tissue inhibitor of metalloproteinase (TIMP)-1 in premature rupture of membranes.

Methods: Amniochorions were prepared from 29 subjects with no labor (cesarean section; CS, n = 10), labor (normal delivery; ND, n = 10), and labor during premature rupture of membranes (PROM, n = 9). MMP-2 activity was spectrophotometrically assayed by measuring the digestion of an MMP-2-specific substrate. The levels of pro-MMP-2, MT1-MMP and TIMP-1 were determined by Western immunoblotting.

Results: The activity of MMP-2 in PROM was significantly higher than that in CS and ND (P <.05). In addition, the levels of MT1-MMP, an activator of MMP-2, were higher in PROM than in CS and ND. In contrast, the level of TIMP-1, an inhibitor of MMP-2 was substantially lower in PROM than CS and ND. Moreover, the levels of pro-MMP-2 were increased more significantly in PROM and ND than in CS (P <.05).

Conclusion: Our results suggest that the increased expression of pro-MMP-2 and MT1-MMP and decreased expression of TIMP-1 may result in the increased activity of MMP-2, which is involved in the degradation of extracellular matrix (ECM) of fetal membrane, thereby inducing the premature rupture of membranes at term.

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