Curry Thomas E, Wheeler Sarah E
Department of Obstetrics & Gynecology, University of Kentucky, Lexington 40536, USA.
Biol Reprod. 2002 Dec;67(6):1943-51. doi: 10.1095/biolreprod.102.003681.
The present study determined the ovarian cellular localization of the mRNA for the tissue inhibitors of metalloproteinases (TIMPs) during pseudopregnancy in the rat. Pseudopregnancy was induced by eCG/hCG stimulation. At Day 1 of pseudopregnancy, intense reaction product for TIMP-1 mRNA was observed surrounding the developing corpus luteum (CL), with less intense expression present in granulosa-lutein cells. With continued luteal development, the TIMP-1 mRNA encircling the CL was lost, although low levels of expression were found within the CL. For TIMP-2 mRNA, intense reaction product was observed surrounding the developing CL but, unlike TIMP-1, was present in granulosa-lutein cells, with high levels near the center of the CL. The localization pattern of TIMP-2 mRNA was unchanged through the latter stages of pseudopregnancy. TIMP-3 mRNA expression was strikingly different from the other TIMPs. At Day 1 of pseudopregnancy, intense reaction product for TIMP-3 mRNA was observed in granulosa-lutein cells of certain developing CL, whereas adjacent follicles did not express TIMP-3 mRNA. With continued luteal development, there was a homogenous, intense localization of TIMP-3 mRNA throughout the CL, which was unchanged during pseudopregnancy. To understand the induction of TIMP-3 mRNA in the developing CL, a series of experiments was performed to compare markers of follicular maturity with the presence of TIMP-3 mRNA. TIMP-3 mRNA appears to be switched on in granulosa cells of follicles destined to ovulate. The distinct pattern of expression of the three TIMPs suggests that each inhibitor may regulate either the site and extent of proteolytic action or specific matrix metalloproteinases at different periods of the luteal life span.
本研究确定了大鼠假孕期间金属蛋白酶组织抑制剂(TIMPs)mRNA在卵巢中的细胞定位。通过eCG/hCG刺激诱导假孕。在假孕第1天,观察到TIMP-1 mRNA在发育中的黄体(CL)周围有强烈反应产物,在颗粒黄体细胞中的表达较弱。随着黄体持续发育,围绕CL的TIMP-1 mRNA消失,尽管在CL内发现了低水平的表达。对于TIMP-2 mRNA,在发育中的CL周围观察到强烈反应产物,但与TIMP-1不同,它存在于颗粒黄体细胞中,在CL中心附近水平较高。TIMP-2 mRNA的定位模式在假孕后期保持不变。TIMP-3 mRNA的表达与其他TIMPs明显不同。在假孕第1天,在某些发育中的CL的颗粒黄体细胞中观察到TIMP-3 mRNA的强烈反应产物,而相邻卵泡不表达TIMP-3 mRNA。随着黄体持续发育,TIMP-3 mRNA在整个CL中呈现均匀、强烈的定位,在假孕期间保持不变。为了了解发育中的CL中TIMP-3 mRNA的诱导情况,进行了一系列实验,比较卵泡成熟标志物与TIMP-3 mRNA的存在情况。TIMP-3 mRNA似乎在注定要排卵的卵泡颗粒细胞中被开启。三种TIMPs不同的表达模式表明,每种抑制剂可能在黄体生命周期的不同阶段调节蛋白水解作用的位点和程度或特定的基质金属蛋白酶。