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金属蛋白酶组织抑制剂-4在小鼠卵巢中的定位与时间调控

Localization and temporal regulation of tissue inhibitor of metalloproteinases-4 in mouse ovary.

作者信息

Bu Shumin, Cao Chenfu, Yang Yongjun, Miao Chenglin, Hu Zeng, Cao Yujing, Sang Qingxiang Amy, Duan Enkui

机构信息

State Key Laboratory of Reproductive Biology, Institute of Zoology, Chinese Academy of Sciences, Beijing, China.

出版信息

Reproduction. 2006 Jun;131(6):1099-107. doi: 10.1530/rep.1.00810.

Abstract

Tissue inhibitors of metalloproteinases (TIMPs) are potential regulators of tissue remodeling in the ovary. The aim of the present study was to examine the localization and temporal regulation of TIMP-4 protein in the mouse ovary. An induced superovulation model (eCG/hCG) was employed in immature mice to evaluate TIMP-4 protein expression profiles in ovaries collected during the follicular phase, the pre ovulatory period, and the luteal lifespan. Immunofluorescence results indicated that TIMP-4 protein was localized to theca of both antral and preovulatory follicles and adjacent ovarian stroma. After the initiation of luteinization with hCG, TIMP-4 was observed within the luteinizing granulosa cells and persisted throughout the lifespan of the corpus luteum. In the cycling ovary, TIMP-4 signaling localized to corpus luteum from previous estrous cycles, the theca of preovulatory follicles, and appeared to be lower in newly forming corpus luteum. Western analysis further showed that the levels of TIMP-4 increased significantly during the luteinization process of granulosa cells, but no significant change was found among all corpus luteum stages. A putative regulatory mechanism of TIMP-4 expression was identified utilizing an in vitro model. Treatment of cultured granulosa cells with hCG significantly augmented TIMP-4 protein expression levels. Together our data indicate that the luteinization process of granulosa cells is associated with up-regulation of TIMP-4 and that TIMP-4 might play an essential role in maintenance of the luteal function during the whole lifespan of corpus luteum.

摘要

金属蛋白酶组织抑制剂(TIMPs)是卵巢组织重塑的潜在调节因子。本研究的目的是检测TIMP-4蛋白在小鼠卵巢中的定位和时间调控。在未成熟小鼠中采用诱导超排卵模型(eCG/hCG),以评估在卵泡期、排卵前期和黄体期收集的卵巢中TIMP-4蛋白的表达谱。免疫荧光结果表明,TIMP-4蛋白定位于窦状卵泡和排卵前卵泡的膜细胞以及相邻的卵巢基质。用hCG启动黄体化后,在黄体化的颗粒细胞中观察到TIMP-4,并在黄体的整个生命周期中持续存在。在周期性卵巢中,TIMP-4信号定位于前一个发情周期的黄体、排卵前卵泡的膜细胞,而在新形成的黄体中似乎较低。蛋白质免疫印迹分析进一步表明,在颗粒细胞黄体化过程中TIMP-4水平显著升高,但在所有黄体阶段之间未发现显著变化。利用体外模型确定了TIMP-4表达的一种假定调节机制。用hCG处理培养的颗粒细胞可显著提高TIMP-4蛋白表达水平。我们的数据共同表明,颗粒细胞的黄体化过程与TIMP-4的上调有关,并且TIMP-4可能在黄体整个生命周期的黄体功能维持中起重要作用。

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