Moghadam Kenneth K, Kessler Cherie A, Schroeder Jennifer K, Buckley Arthur R, Brar Anoop K, Handwerger Stuart
Division of Endocrinology, Cincinnati Children's Hospital Medical Center, 3333 Burnet Avenue, Cincinnati, OH 45229-3039, USA.
Mol Cell Endocrinol. 2005 Jan 14;229(1-2):65-74. doi: 10.1016/j.mce.2004.09.007.
The role of cannabinoid receptor I (CBR-1) in the induction of decidualization was examined using decidual fibroblasts and human endometrial stromal cells as model systems. Decidual fibroblasts decidualized in vitro for 3 and 6 days in the presence of the CBR-1 agonist R(+)-WIN 55,212-2 mesylate (WIN, 0.1-10 microM) expressed less of the decidualization-specific markers prolactin, CBR-1, forkhead (FKHR), TIMP-3, laminin, endometrial bleeding associated factor (EBAF), decorin and insulin-like growth factor binding protein-1 (IGFBP-1) mRNA levels compared to control cells. The maximal decrease for each transcript was in the range of 50-99%. In contrast, cells exposed to the CBR-1 inhibitor AM-251 (1 microM) expressed about two-fold higher levels of the decidualization-specific marker gene mRNAs. The WIN-exposed cells showed a marked decrease in intracellular cAMP levels and a progressive, concentration-dependent increase in DNA fragmentation (TUNEL assay) and caspase 3 levels during decidualization compared to control cells. These studies strongly suggest that activation of CBR-1 inhibits human decidualization and stimulates apoptosis by a cAMP-dependent mechanism.
使用蜕膜成纤维细胞和人子宫内膜基质细胞作为模型系统,研究了大麻素受体I(CBR-1)在诱导蜕膜化中的作用。在CBR-1激动剂R(+)-WIN 55,212-2甲磺酸盐(WIN,0.1 - 10 microM)存在下,体外蜕膜化3天和6天的蜕膜成纤维细胞,与对照细胞相比,蜕膜化特异性标志物催乳素、CBR-1、叉头蛋白(FKHR)、金属蛋白酶组织抑制因子-3(TIMP-3)、层粘连蛋白、子宫内膜出血相关因子(EBAF)、核心蛋白聚糖和胰岛素样生长因子结合蛋白-1(IGFBP-1)的mRNA水平表达较低。每个转录本的最大减少幅度在50 - 99%范围内。相反,暴露于CBR-1抑制剂AM-251(1 microM)的细胞,蜕膜化特异性标志物基因mRNA水平表达约高两倍。与对照细胞相比,暴露于WIN的细胞在蜕膜化过程中细胞内cAMP水平显著降低,DNA片段化(TUNEL检测)和半胱天冬酶3水平呈浓度依赖性逐渐增加。这些研究强烈表明,CBR-1的激活通过cAMP依赖性机制抑制人蜕膜化并刺激细胞凋亡。