Soni Upendra Kumar, Chadchan Sangappa Basanna, Joshi Anubha, Kumar Vijay, Maurya Vineet Kumar, Verma Raj Kumar, Jha Rajesh Kumar
Female Reproductive Biology Laboratory, Endocrinology Division, CSIR-Central Drug Research Institute, B.S. 10/1, Sector-10, Jankipuram Extension, Sitapur Road, Lucknow, 226031, India.
Female Reproductive Biology Laboratory, Endocrinology Division, CSIR-Central Drug Research Institute, B.S. 10/1, Sector-10, Jankipuram Extension, Sitapur Road, Lucknow, 226031, India.
Mol Cell Endocrinol. 2020 Dec 1;518:110946. doi: 10.1016/j.mce.2020.110946. Epub 2020 Jul 15.
Embryo implantation is a very complex process and several factors play important roles. Using a mouse model, we investigated the functions of PARP-2 and caspase-8 during endometrial receptivity for blastocyst implantation. We found that PARP-2 was upregulated at the receptive stage's implantation region and predominantly expressed in the endometrial stromal region, but downregulated during pregnancy failure and pseudopregnancy. To reinforce the necessity of PARP-2 for embryo implantation, we pharmacologically inhibited PARP-2 'before' & 'after' embryo arrival and observed a reduction in blastocyst implantation. Conversely, elevated caspase-8 expression and activity during pseudopregnancy, delayed implantation, and embryo implantation failure conditions and decreased levels in the decidualization exhibited an inverse pattern with PARP-2, suggesting caspase-8 as a negative regulator for embryo implantation. In vitro caspase-8 downregulates the PARP-2 activity in the mouse endometrial epithelial and stromal cells. These data suggest that PARP-2 and its negative regulation by caspase-8 constitute a crucial step in embryo implantation.
胚胎着床是一个非常复杂的过程,有几个因素起着重要作用。我们使用小鼠模型,研究了PARP - 2和半胱天冬酶 - 8在子宫内膜对囊胚着床的接受性中的功能。我们发现,PARP - 2在接受期的着床区域上调,主要在内膜基质区域表达,但在妊娠失败和假孕期间下调。为了强化PARP - 2对胚胎着床的必要性,我们在胚胎到达“之前”和“之后”用药物抑制PARP - 2,并观察到囊胚着床减少。相反,在假孕、着床延迟和胚胎着床失败情况下,半胱天冬酶 - 8的表达和活性升高,而在蜕膜化过程中水平降低,呈现出与PARP - 2相反的模式,表明半胱天冬酶 - 8是胚胎着床的负调节因子。在体外,半胱天冬酶 - 8下调小鼠子宫内膜上皮和基质细胞中的PARP - 2活性。这些数据表明,PARP - 2及其被半胱天冬酶 - 8的负调节是胚胎着床的关键步骤。