Decidualization is an absolutely essential process for the successful establishment of pregnancy in primates and rodents. The decidual process is associated with a morphological transformation of fibroblast cells to highly secretory epitheloid-like cells coupled with a biochemical reprogramming of the endometrial stromal cells. As a consequence of this differentiation process, decidualized stromal cells acquire the unique ability to regulate trophoblast invasion, resist inflammatory and oxidative insults and dampen local maternal immune responses. However, the early events that permit these cells to initiate their differentiation cascade have yet to be elucidated. The understanding of these mechanisms is critical since impaired decidualization is associated with numerous gynecological malignancies in women with a broad range of etiologies from infertility to early pregnancy loss. During the previous funding period we demonstrated that the early primate embryonic signal, chorionic gonadotropin (CG), coupled with progesterone, directly modulates endometrial gene expression and alters the cytoskeletal architecture of uterine stromal fibroblasts. These cytoskeletal changes are necessary to prevent the stromal cells from undergoing apoptosis in a conceptual cycle and allow for cellular restructuring during decidual transformation. Our data also demonstrated for the first time that the evolutionary conserved Notch1 protein, which plays a critical role in cell fate decisions, is regulated by CG and progesterone in endometrial stromal cells in vivo and in vitro. The importance of Notch1 in the decidualization process was evident in a genetically modified mouse model that failed to decidualize when Notch1 was specifically ablated in the uterus. Based on these studies three specific aims are proposed in this application to elucidate the role of Notch1 in inhibiting stromal cell apoptosis and initiating the decidualization process.
In Specific Aim 1 we will test the hypothesis that the induction and activation of Notch1 by CG and progesterone is required to induce -smooth muscle actin (SMA) in uterine stromal fibroblasts. The proposed studies will focus on the transcriptional regulation of SMA expression by Notch1 in stromal fibroblasts and whether this in turn prevents the cells from undergoing apoptosis.
Specific Aim 2 will test the hypothesis that the Notch1 mediated decrease in FOXO3a and Notch1 mediated increase in IL-11 is a necessary prerequisite for the initiation of decidualization. FOXO3a is suppressed during decidualization and another Notch1 targert, IL-11, is an earlier initiator of the decidualization process. Studies proposed in these two aims will utilize human uterine fibroblast cells (HuF cells).
In Specific Aim 3 we will use the PRCre/+Notch1flox/flox bigenic mouse mouse that we have generated. This model demonstrates a significant decidualization failure and provides an in vivo model to identify the molecular and cellular targets of Notch1 that are required for the decidualization response. It is anticipated that these studies will provide critical information on the decidualization process and translate to therapeutic potentials of Notch1 for women with decidual defects. We believe a better understanding of the molecular mechanisms responsible for decidualization and implantation will improve clinician's ability to detect, diagnose and treat early pregnancy loss.

Public Health Relevance

Understating the mechanisms that govern decidualization is critical to the successful establishment of pregnancy. Several disease conditions such as endometriosis and endometrial cancer are associated with impaired decidualization. The proposal studies will focus on the role of Notch 1 in stromal cell differentiation. Although implicated in the developmental regulation of cell fate and multiple malignancies its physiological role in uterine biology has never been studied. Thus, given its current clinical potential these studies may provide insight into new therapeutic targets for decidualization failure.

National Institute of Health (NIH)
Eunice Kennedy Shriver National Institute of Child Health & Human Development (NICHD)
Research Project (R01)
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Study Section
Pregnancy and Neonatology Study Section (PN)
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Yoshinaga, Koji
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Michigan State University
Obstetrics & Gynecology
Schools of Medicine
East Lansing
United States
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Strug, Michael R; Su, Ren-Wei; Kim, Tae Hoon et al. (2018) RBPJ mediates uterine repair in the mouse and is reduced in women with recurrent pregnancy loss. FASEB J 32:2452-2466
Godbole, Geeta; Suman, Pankaj; Malik, Ankita et al. (2017) Decrease in Expression of HOXA10 in the Decidua After Embryo Implantation Promotes Trophoblast Invasion. Endocrinology 158:2618-2633
Olson, Mark R; Su, Renwei; Flaws, Jodi A et al. (2017) Bisphenol A impairs decidualization of human uterine stromal fibroblasts. Reprod Toxicol 73:339-344
Su, Ren-Wei; Strug, Michael R; Jeong, Jae-Wook et al. (2016) Aberrant activation of canonical Notch1 signaling in the mouse uterus decreases progesterone receptor by hypermethylation and leads to infertility. Proc Natl Acad Sci U S A 113:2300-5
Strug, Michael R; Su, Renwei; Young, James E et al. (2016) Intrauterine human chorionic gonadotropin infusion in oocyte donors promotes endometrial synchrony and induction of early decidual markers for stromal survival: a randomized clinical trial. Hum Reprod 31:1552-61
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Su, Ren-Wei; Strug, Michael R; Joshi, Niraj R et al. (2015) Decreased Notch pathway signaling in the endometrium of women with endometriosis impairs decidualization. J Clin Endocrinol Metab 100:E433-42
Su, Ren-Wei; Fazleabas, Asgerally T (2015) Implantation and Establishment of Pregnancy in Human and Nonhuman Primates. Adv Anat Embryol Cell Biol 216:189-213
Devi, Y Sangeeta; DeVine, Majesta; DeKuiper, Justin et al. (2015) Inhibition of IL-6 signaling pathway by curcumin in uterine decidual cells. PLoS One 10:e0125627
Yoshinaga, Koji; PrabhuDas, Mercy; Davies, Christopher et al. (2014) Interdisciplinary collaborative team for blastocyst implantation research: inception and perspectives. Am J Reprod Immunol 71:1-11

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