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正常小鼠、基质溶素缺陷小鼠和基质溶解素-1缺陷小鼠子宫中基质金属蛋白酶家族成员的协同表达

Coordinate expression of matrix metalloproteinase family members in the uterus of normal, matrilysin-deficient, and stromelysin-1-deficient mice.

作者信息

Rudolph-Owen L A, Hulboy D L, Wilson C L, Mudgett J, Matrisian L M

机构信息

Department of Cell Biology, Vanderbilt University Medical School, Nashville, Tennessee 37232, USA.

出版信息

Endocrinology. 1997 Nov;138(11):4902-11. doi: 10.1210/endo.138.11.5478.

Abstract

The expression patterns of matrix metalloproteinase (MMP) family members during the murine estrous cycle and postpartum uterine involution were analyzed, and the consequence of removing specific MMPs during uterine functions was determined using mice deficient in either matrilysin (MAT) or stromelysin-1 (STR-1). In wild-type animals, MAT, STR-1, STR-2, STR-3, and gelatinase A were consistently expressed during the most active phases of the estrous cycle, estrus and proestrus. The messenger RNA for these MMPs as well as collagenase-3 and the tissue inhibitors of metalloproteinases were also expressed during uterine involution, as determined by Northern analysis and in situ hybridization. Notably, MAT, STR-2, and collagenase-3 messenger RNA levels were elevated at early times of involution and rapidly decreased with time, whereas the transcripts for other MMPs remained elevated throughout the involution process. Involution proceeded normally in mice lacking MAT or STR-1; however, the expression of STR-1 and STR-2 was dramatically up-regulated in MAT nullizygous mice, and the expression of MAT and STR-2 was moderately up-regulated in STR-1-deficient animals. We conclude that the concerted action of several MMPs is likely to play an important role in the remodeling of the postpartum uterus, and that mechanisms that compensate for the loss of a specific MMP during this process appear to exist.

摘要

分析了基质金属蛋白酶(MMP)家族成员在小鼠发情周期和产后子宫复旧过程中的表达模式,并使用基质溶素(MAT)或基质溶解素-1(STR-1)缺陷的小鼠确定了在子宫功能过程中去除特定MMP的后果。在野生型动物中,MAT、STR-1、STR-2、STR-3和明胶酶A在发情周期的最活跃阶段,即发情期和动情前期持续表达。通过Northern分析和原位杂交确定,这些MMP以及胶原酶-3和金属蛋白酶组织抑制剂的信使核糖核酸在子宫复旧过程中也有表达。值得注意的是,MAT、STR-2和胶原酶-3的信使核糖核酸水平在复旧早期升高,并随时间迅速下降,而其他MMP的转录本在整个复旧过程中保持升高。MAT或STR-1缺失的小鼠子宫复旧正常;然而,STR-1和STR-2的表达在MAT纯合缺失小鼠中显著上调,而MAT和STR-2的表达在STR-1缺陷动物中适度上调。我们得出结论,几种MMP的协同作用可能在产后子宫重塑中起重要作用,并且在此过程中似乎存在补偿特定MMP缺失的机制。

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