Notch signaling in reproduction.

The Notch signaling pathways plays notable roles throughout the male reproductive system ( Key Figure 2 ). Notch1 and its ligand Jag2 are expressed in the rat testis during spermatocyte development[ 15 ]. N1ICD constitutive expression under a mouse mammary tumor virus long terminal repeat ( MMTV/Notch1 intraΔCys ) in male mice results in sterility[ 16 ]. The authors verified N1ICD transgene expression in the efferent ducts, epididymis, and vas deferens and total Notch1 was found in both the epididymis and the vas deferens[ 16 ]. There were no differences between MMTV/Notch1 intraΔCys expressing mice and their wild-type littermates at postnatal days 8 and 21, but adult mice at postnatal day 28 exhibited undifferentiated proximal epididymis, epithelial folding, and absence of spermatozoa in the epididymis, and hyperplasia in the vas deferens[ 16 ]. The authors concluded that constitutive expression of the N1ICD resulted blockage of the rete testis-efferent duct interface preventing the migration of sperm, inducing infertility[ 16 ]. While this study shows that constitutive activation of Notch signaling is detrimental to male murine fertility, inhibition of Notch signaling also compromises fertility. Treatment of adult male mice with DAPT, a γ-secretase complex inhibitor known to inhibit Notch signal propagation, for an entire cycle of spermatogenesis or for half of a spermatogenesis cycle resulted in abnormal germ cell morphology and increased germ cell apoptosis ultimately disrupting spermatogenesis and resulting in morphologically abnormal sperm, potentially compromising fertility[ 17 ]. It is important to note that DAPT, like other γ-secretase inhibitors, is an indirect inhibitor of Notch signaling and that the γ-secretase complex has many receptor targets including NOTCH receptors, amyloid-β precursor protein, ErbB4 and other type I membrane proteins indicating that these aberrations in spermatogenesis may result from the effect of these inhibitors on other signaling pathways ( Box 3 )[ 18 , 19 ]. Another study performed in a murine model showed that Notch receptors and ligands are expressed temporally in the testis specifically within the seminiferous tubules in multiple cell types including germ cells, Sertoli and Leydig cells indicating that Notch signaling is active during spermatogenesis, the process that results in the production of mature sperm[ 20 ]. In addition to localization within the seminiferous tubules, Notch1 , Notch2 , Notch3 , Dll4 , Jag1 , Hes1 , and Hes2 transcripts are highly expressed in the epididymis and Notch1 , Notch2 , and Hes5 transcripts are evident in the vas deferens[ 21 ]. Notch signaling is active as evidenced by nuclear localization of NICD, suggesting a role for Notch signaling in sperm maturation[ 21 ]. Together these studies indicate that careful regulation of Notch signaling is required for male fertility, and that Notch signaling contributes to male reproductive tract development and function and offers areas of future study to investigate the precise mechanisms by which Notch signaling regulates these critical processes. Notch signaling is critical for male reproductive function and plays equally important roles throughout the female reproductive system ( Key Figure 1 and Box 4 ). Notch signaling components are expressed throughout the female reproductive tract in rodents, baboons, and humans. In mice, Notch signaling components including Notch1-4, Jagged1-2 , and Dll4 and target genes Hes1, 2 , and 5 are all expressed in the oviduct and within the mouse uterus[ 6 ]. It is thought that the Notch signaling pathway contributes to cellular remodeling that occurs throughout the estrous cycle since this pathway functions through cell-to-cell contact and is differentially expressed throughout the estrous cycle[ 6 ]. We have shown that Notch1 protein expression varies throughout the menstrual cycle suggesting that Notch signaling may play distinct roles in primates[ 7 ]. Histological analyses of the human endometrium have shown a similar pattern of expression throughout the menstrual cycle[ 22 ]. The human endometrial glandular epithelium expresses NOTCH1 and NOTCH4 during the proliferative phase, and the glandular epithelium and stroma express NOTCH1, NOTCH4, and JAG1 during the secretory phase indicating that the Notch signaling pathway is most likely to be active during the secretory phase of the menstrual cycle[ 22 ]. The Notch signaling pathway is clearly active throughout the female reproductive tract but what are its specific roles in these diversely functioning tissues? The ovary contains maturing follicles that are surrounded by granulosa cells, extracellular matrix, and a layer of theca cells. After ovulation, the remaining granulosa and theca cells transform into the luteal cells of the corpus luteum, which provides hormonal support in early pregnancy[ 23 ]. Within the ovarian environment, Notch signaling has been shown to play roles in granulosa cell differentiation, luteal cell function, and ovarian steroid hormone production[ 24 ]. During embryonic ovarian development, Jag1 , Jag2, Notch2 and targets Hes1 and Hey2 are highly expressed in the prenatal ovary[ 25 ]. Our understanding of the roles of Notch signaling in the developing murine ovary has evolved from research conducted utilizing conditional knockout mouse lines. Two such models include the Vasa cre/+ Jagged1 Fl/+ mice that contain a conditional deletion of the Notch ligand Jag1 in their germ line, and Amhr2 cre/+ Notch2 Fl/+ , which conditionally deletes Notch2 in the developing ovary[ 25 ]. These models are temporally specific and have allowed researchers to determine the importance of Notch signaling in specific cell types at critical developmental timepoints. The ovaries from both transgenic models contain multioocytic follicles indicating a failure to form correct follicle units prenatally[ 25 ]. Additionally, the postnatal follicles in these mice display decreased granulosa cell proliferation and increased apoptosis indicating that Notch signaling is required for granulosa cell survival[ 25 ]. Notably, the Jag1 knockout mice are subfertile, and both knockout models show premature reproductive aging suggesting that Notch signaling is the prenatal ovary is required for proper ovary function[ 25 ]. Postnatal studies in the ovary conducted in the presence of hCG resulted in increased Jag1 and Notch2 expression indicating that Notch signaling is hormonally regulated in the ovary[ 26 ]. Further studies utilizing DAPT, a γ-secretase inhibitor, in organ-cultured ovaries resulted in degenerating oocytes, decreased primordial follicles which were negative for Ki-67, a marker of proliferation, signifying that Notch signaling is integral to oocyte survival and proliferation[ 27 ]. Although Notch signaling is most likely an important pathway in the ovary, the γ-secretase complex cleaves many proteins that regulate proliferation. Therefore, these results may also indicate a role for other pathways that promote oocyte survival and proliferation ( Box 3 )[ 18 ]. More recently, evidence of lateral crosstalk of the Notch signaling pathway amongst multiple cell types in the ovary has surfaced[ 28 ]. In this study the authors determine that Jag1 in the oocyte activates Notch2 or Notch3 in granulosa cells showing that different cell types communicate via Notch signaling[ 28 ]. These studies support that the Notch signaling pathway is integral to maintaining fertility at the level of the ovary through developmental regulation and granulosa cell function. The endometrium is the primary site of female reproductive function and cyclically responds to ovarian hormones and the presence of an embryo, ultimately providing a hospitable and nourishing environment for an embryo and fetus ( Box 4 ). The endometrium is composed of four major cell types, the epithelium that forms the lumen and branching glands, stromal cells that provide support in the endometrium, various immune cells that regulate maternal-fetal interactions and repair within the endometrium, and endothelial cells that line the spiral arteries, which serve to support the embryo during implantation and in utero development[ 5 ]. The cells that make up the endometrium participate in significant crosstalk to encourage reproductive success ( Box 4 ). The cyclical changes of the menstrual cycle, decidualization, implantation, and uterine repair are all processes that are in part regulated by Notch signaling. Decidualization is the terminal differentiation of endometrial stromal cells that begins during the latter part of the menstrual cycle in humans and non-human primates, and at the time of implantation in mice ( Box 4 ). Decidualization is an important process for the success of pregnancy. Decidualized stromal cells function throughout pregnancy in the maternal decidua, a tissue which forms as the maternal side of the placenta. Notch1 regulates decidualization in mice, nonhuman primates, and humans[ 7 , 29 , 30 ]. Extensive studies in our laboratory provide a role for Notch signaling in endometrial stromal cell decidualization. In HuF cells, knockdown of the NOTCH1 receptor compromises the decidualization response when these cells are treated with decidualization stimuli: E2, the progesterone analogue medroxyprogesterone acetate (MPA), and cAMP (EPC)[ 7 ]. In a conditional Notch1 knockout mouse model in the uterus ( Pgr cre/+ Notch1 Fl/Fl ), we noted a decreased decidualization response as measured by uterine wet weight and mRNA expression of decidualization markers Bmp2 and Wnt4 [ 29 ] and a smaller litter size in the first pregnancy[ 31 ]. While these data suggest that Notch1 is required for an appropriate decidualization response both in vitro and in vivo , we sought to investigate the specific mechanisms of these interactions. We generated a uterine N1ICD overexpression mouse model ( Pgr cre/+ Rosa26 N1ICD/+ ) to ascertain whether constitutive activation of the Notch1 signaling pathway would affect the decidualization response. We observed that constitutive activation of the Notch1 signaling pathway through N1ICD overexpression compromises decidualization and implantation[ 32 ]. We also sought to determine if Rbpj, the transcriptional effector for all four Notch receptors, plays an independent role in the uterus. In an Rbpj conditional knockout mouse model in the uterus ( Pgr cre/+ Rbpj Fl/Fl ), we observed a severely compromised decidualization response, as measured by uterine wet weight and mRNA levels of Bmp2 and Wnt4 , and compromised uterine repair that resulted in a recurrent pregnancy loss phenotype[ 33 ]. In this model, we determined that the decidualization failure occurred as a result of decreased progesterone receptor expression and signaling as well as reduced Slc2a1 expression, a glucose transporter important for stromal cell differentiation[ 33 ]. We further characterized the roles of Notch signaling in vitro through Notch1 knockdown in HuF cells followed by EPC treatment to induce decidualization[ 30 ]. These data indicate that NOTCH1 knockdown prior to the initiation of decidualization compromises the decidualization response, but if the decidualization reaction has already begun, NOTCH1 knockdown has no effect[ 30 ]. These studies indicate that NOTCH1 is an early regulator of decidualization in endometrial stromal cells. Another Notch receptor is also implicated in endometrial stromal cell decidualization. In primary human decidual stromal cells (HDSCs) of early pregnancy, NOTCH2 is the most abundant receptor as determined by immunofluorescence of decidual tissue[ 34 ]. The authors then treated isolated HDSCs in vitro with cAMP, E2 and P4; and EPC treatment. There were no alterations in NOTCH2 protein or mRNA expression after 3 and 6 days of treatment but increases in ligands DLL1 and DLL4 were induced with cAMP and EPC treatment showing that Notch ligand availability is decidualization dependent[ 34 ]. Furthermore, inhibition of Notch2 expression or activation treatment of HDSCs with subsequent EPC treatment compromised decidualization suggesting that NOTCH2 expression and signaling activation are required for decidualization in HDSCs[ 34 ]. While we and others have established a clear role for Notch signaling in the decidualization process, the question that remains is what regulates Notch signaling during decidualization and how is Notch signaling mediating the decidualization response? This remains an open area of research, but one study shows that post-translational modification of the Notch1 receptor may be one mechanism. Fucosylation of Notch1 by poFUT1 increased receptor-ligand binding since we know from previous studies that Notch receptors contain EGF repeats that are glycosylated to promote receptor-ligand interactions[ 35 ]. This mechanism permits increased Notch1 signaling activation in endometrial stromal cells, but when poFUT1 is inhibited, fucosylation of Notch1 is decreased leading to a compromised decidualization response[ 35 ]. This suggests that fucosylation is an active mechanism of Notch1 signaling regulation in decidualizing endometrial stromal cells[ 35 ]. Future directions for the field include discerning mechanisms, either hormonal or otherwise, that are regulating the Notch signaling pathway during the decidualization process and how the Notch signaling mediates the decidualization response. Implantation is the process whereby a developing embryo enters the uterine cavity and attaches to the endometrium following fertilization ( Box 4 ). Notch signaling and target gene expression play a role throughout the implantation process. During the peri-implantation period, Notch signaling is active in the endothelial cells of the uterus[ 36 ]. Endothelial cells within the uterus typically form the vasculature and are critical for nutrient delivery through the uterus to the fetus. In addition, decidualization, implantation, placental development and pregnancy maintenance are all dependent on angiogenesis or the formation of new blood vessels[ 36 ]. Notch and vascular endothelial growth factor signaling are well known players in angiogenesis but have only recently been associated with decidual angiogenesis[ 36 ]. Notch1, 2, and 4 as well as ligands Dll4 and Jag1 are expressed in murine endothelial cells during the peri-implantation period and there is limited expression of Notch3 and Jag1 in pericytes, vascular peripheral cells, prior to implantation[ 36 ]. In addition, Notch1, 4, Dll4 and Jag1 are expressed in decidual endothelial cells after implantation suggesting a role for Notch signaling in pre- and post-implantation angiogenesis[ 36 ]. An endothelial post-implantation, pre-placentation Jag1 deletion mouse model exhibits increased Notch1 signaling and increased Dll4 expression, suggesting that Jag1 is not an essential Notch ligand in post-implantation, pre-placentation angiogenesis[ 37 ]. Early studies focused on identifying expression of Notch signaling member expression in angiogenesis, therefore functional analyses of Notch signaling in post-implantation angiogenesis are lacking. Notch signaling also plays direct roles in the endometrium during the implantation process. Notch1 receptor and ligands, DLL4 and Jagged1, are expressed on the apical surface of luminal epithelial cells of the mid-secretory endometrium indicating that Notch signaling may aid in blastocyst implantation[ 38 ]. Cuman et al reported that blastocyst-conditioned media influences Notch1 and Jag1 expression in epithelial cells in vitro suggesting that blastocysts may modulate uterine receptivity and implantation through mechanisms that alter Notch signaling[ 39 ]. In the peri-implantation uterus, Rbpj is expressed in stromal cells in the primary and secondary decidual zones[ 40 ]. In an Rbpj uterine conditional deletion mouse model ( Pgr cre/+ Rbpj Fl/Fl ), deletion of Rbpj results in altered embryo implantation orientation producing a high rate of miscarriage as evident by many resorbing implantation sites[ 40 ]. The deletion of Rbpj also results in increased E2 responsiveness in the endometrial stroma and increased epithelial cell proliferation[ 40 ]. The authors noted that Rbpj directly interacts with estrogen receptor α (ER) in a Notch independent manner suggesting that Rbpj may act to regulate E2 signaling in the endometrium[ 40 ]. These studies show expression and function of Notch signaling components within the processes of implantation, implantation associated angiogenesis, and maternal-fetal crosstalk of endometrial receptivity. In addition to the Notch signaling pathway’s role in the uterus throughout the menstrual cycle and in the establishment of pregnancy, the Notch signaling pathway is implicated in placentation[ 41 ]. During the initiation of decidualization, Notch signaling is active in endothelial cells of the decidua and in nonvascular decidual cells at embryonic day 8.5 in a mouse model[ 41 ]. In the mature murine placenta on embryonic day 12.5, Notch receptors and ligands are expressed in the decidua, junctional zone, and labyrinth in multiple cell types indicating that the Notch signaling components are available during placental development and function[ 41 ]. Notch1 signaling is active in proximal cell column trophoblasts and promotes proliferation and cell survival in the mature placenta[ 42 ]. In conjunction, Notch2 is the active receptor in the distal cell column of placental villi and functions to promote endovascular invasion and remodeling[ 42 ]. Another functional study established the role of Rbpj, the primary NOTCH signaling transcriptional effector, in placental morphogenesis[ 43 ]. Lu et al generated several Rbpj systemic, and conditional knockout mouse models that revealed that RBPJ deletion in the placenta compromises chorioallantoic branching and trophoblast differentiation in the ectoplacental zone[ 43 ]. These results combined with their other observations indicate that allantoic Rbpj expression targets Vcam1 to aid chorioallantoic fusion which is critical for fetal vessel development in the chorion. In addition, Rbpj is essential for specification of trophoblast cells as it functions with Mash2 to induce trophoblast specific protein α expression[ 43 ]. These diverse roles of Rbpj show the ubiquitous importance of Notch signaling and independent action of Rbpj as drivers of placental structure and function.

Polycystic ovary syndrome (PCOS) affects approximately 10–20% of reproductive aged women and is characterized by hormonal dysregulation accompanied by enlarged ovaries with an accumulation of ovarian follicles creating a cyst-like appearance on the surface of the ovary[ 44 ]. Notch receptor and ligand expression is aberrant in patients with PCOS including decreased NOTCH1, JAG1, JAG2 , and increased NOTCH3 mRNA expression during the window of implantation in endometrial samples ( Figure 3 ) [ 45 ]. Protein expression of JAG1 and JAG2 is also decreased in the endometrium of PCOS patients[ 45 ]. In addition to altered endometrial expression, Notch signaling is enriched in granulosa cells of patients with PCOS as identified by microarray analysis, and members of this pathway are suggested as potential biomarkers of PCOS[ 46 ]. Together these data suggest that Notch signaling may contribute to PCOS pathology and could be utilized to identify patients with PCOS. Endometriosis is an E2 dependent disease characterized by endometrial-like tissue found at ectopic sites, most commonly in the peritoneal cavity[ 47 ]. This disease is associated with idiopathic infertility and is a major cause of pelvic pain in women of reproductive age[ 47 ]. We have shown that NOTCH1 expression as well as ligands JAG2 and DLL4 and NOTCH1 gene targets NOTCH4 , HES5 , and HEY1 are significantly decreased in the eutopic (Eu) endometrium (E) of women with endometriosis[ 30 ]. In addition, stromal cells isolated from women with endometriosis have reduced NOTCH1 and ligand expression as well as a reduced decidualization response in vitro [ 30 ]. We hypothesized based on gene expression profiling, that the reduced Notch1 signaling contributes to a decidualization defect in women with endometriosis by downregulating FOXO1 , a molecule that is critical for many reproductive functions including decidualization[ 30 , 48 – 51 ]. Another study has corroborated the decrease in NOTCH1 and ligand expression in the EuE of women with endometriosis[ 45 ]. In addition, during the window of receptivity the endometrium from women with endometriosis exhibits reduced NOTCH3 expression[ 45 ]. Additional histological studies determined the localization of NOTCH receptors and ligands in the endometrium of women with and without endometriosis[ 52 ]. In addition to the EuE, the Notch signaling pathways is integral in endometriotic lesion pathogenesis. Angiogenesis or establishing a blood supply for growth is essential to ectopic lesions and Notch signaling plays a major role in this process in other contexts. Korbel et al found that the γ-secretase inhibitor DAPT increased angiogenic sprouts in lesions[ 53 ]. They postulated this increase could lead to a reduction in lesion size and decreased function based on similar results in tumor studies[ 53 ]. Significant differences in NOTCH1 expression and activation have been identified in ectopic (Ec) and EuE, including increased N1ICD expression that is associated with increased proliferation measured by Ki-67 expression, ER expression, and decreased PR expression in EcE[ 54 ]. Given these data, the authors suggest that increased Notch1 signaling in Ec may contribute to P4 resistance since inhibition of Notch signaling with DAPT helped to sensitize immortalized uterine fibroblasts, HESCs, to P4[ 54 ]. Additionally, Notch signaling is linked with oxidative stress and severity of disease in endometriosis. A study of peritoneal fluid and stromal cells isolated from eutopic and ectopic endometrium from women with deep infiltrating endometriosis showed higher ADAM17 expression and activity, higher Notch signaling activation, and that these changes are associated with increased oxidative stress and lesion fibrosis[ 55 ]. Notch signaling is also activated by immune modulation in many other contexts, as well as in EcE. In our study of ectopic tissue, we identified increased NOTCH1 expression in humans and in our baboon model of endometriosis[ 56 ]. In addition to these alterations in expression, we elucidated a potential mechanism of Notch1 signaling regulation in the epithelium of lesions where IL-6 regulates P38/MAPK signaling to induce NOTCH1 promoter occupancy of E2A/HEB[ 56 ]. Notch signaling is altered in Ec and EuE of women with endometriosis providing potential therapeutic targets for future studies to identify to combat this pathology ( Figure 3 ). Adenomyosis is a disease characterized by endometrial tissue found within the myometrium resulting in dysmenorrhea, dyspareunia, abnormal uterine bleeding, and infertility[ 57 ]. A histological study performed on endometria from fertile women and women with adenomyosis revealed increased NOTCH1 expression in ectopic endometria of women with adenomyosis[ 58 ]. Expression of an inhibitory regulator of Notch signaling, NUMB, is decreased in adenomyosis lesions within the myometrium[ 58 ]. Decreased NUMB expression may explain the increased NOTCH1 expression noted in adenomyosis lesions. Functional analyses revealed that adenomyosis lesions exhibit increased Slug and Snail, known markers of epithelial to mesenchymal transition (EMT), transcriptional expression that is mediated by NOTCH1 signaling activation thereby inducing EMT that contributes to the pathogenesis of adenomyosis[ 58 ]. The etiology and pathophysiology of adenomyosis remain significant areas of study, but these results suggest that the Notch signaling pathway may be an important contributor to the disease warranting future investigation of the role of Notch signaling in adenomyosis. Pre-eclampsia is a pregnancy disorder that is characterized by hypertension and proteinuria in the mother. This disease affects 3–5% of pregnancies and can result in significant health risks for both mother and fetus including death[ 59 ]. NOTCH1 and NOTCH4 are decreased in pre-eclamptic placentas compared to normal control placentas suggesting that defective Notch signaling may contribute to the etiology of this disease[ 60 ]. A study performed in vitro indicates that inhibition of Notch signaling resulted in reduced trophoblast invasion suggesting a role for Notch signaling in placental invasion[ 61 ]. In addition, the authors also noted that NOTCH2 deletion resulted in placental development defects, which resulted in offspring lethality[ 61 ]. The study also suggests that decreased JAG1 expression combined with the role of Notch signaling in vascular development could contribute to pre-eclampsia[ 61 ]. Several studies provide a role for Notch signaling in infertility and uterine repair. We utilized a murine model to constitutively activate Notch1 signaling through overexpression of the Notch1 intracellular domain ( Pgr cre/+ Rosa26 N1ICD/+ )[ 32 ]. This constitutive activation of Notch1 signaling resulted in a glandless phenotype that resulted in infertility suggesting that Notch1 signaling is critical for glandular development in mice[ 32 ]. In addition to being infertile, these mice fail to respond to decidualization stimuli and display decreased P4 responsiveness highlighting the importance of Notch signaling in regulating and responding to hormonal signals[ 32 ]. Further investigation uncovered that N1ICD overexpression results in hypermethylation of the progesterone receptor through activation of a PU.1/Dnmt3b complex and this reduction allowed for an increase in estrogen signaling compromising decidualization and implantation[ 32 ]. We also generated Pgr cre/+ Rbpj Fl/Fl mice to conditionally delete all Notch signaling in the mouse uterus[ 62 ]. These mice display a recurrent pregnancy loss (RPL) phenotype where mice give birth to a normal sized first litter, but subsequent litters decrease in size, and these mice show a reduced decidualization response compared to controls[ 62 ]. We noted postpartum nodules following parturition in these mice that did not regress normally and an abnormal inflammatory environment that compromised implantation in future pregnancies[ 62 ]. Furthermore, in this study we found that women with recurrent pregnancy loss also exhibited reduced RBPJ expression suggesting that women exhibiting recurrent pregnancy loss may have dysregulated uterine repair mechanisms contributing to their pathology[ 62 ]. In addition, endometria from infertile women exhibit decreased NOTCH1 and DLL1 expression and increased NUMB expression by histological analysis[ 52 ]. These results indicate that Notch signaling as well as the Notch transcriptional effector, Rbpj may significantly contribute to infertility. Endometrial cancer encompasses two subtypes of endometrial carcinoma: Type I endometroid endometrial cancer (EEC) and Type II serous endometrial cancer (SEC). EEC is the more common type of endometrial cancer where the endometrium is hyperplastic, and tumors are ER and PR positive. In SEC, the endometrium is atrophic and tumors are ER independent[ 63 ]. Alterations in NOTCH receptor, ligand, and target gene expression are associated with the endometrium of endometrial carcinoma patients. A NOTCH4 decrease was originally identified in endometrial cancer cells and later validated by immunohistochemical analysis in endometrial carcinoma tissue [ 22 , 64 ]. Conversely, NOTCH1 expression is increased in endometrial cancer and is associated with a poor prognosis[ 63 ]. Mixed data also indicate both increases and decreases in JAG1, JAG2, and NOTCH3, while data for other Notch receptor and ligand expression is currently lacking[ 63 ]. Aberrations in Notch signaling component expression are present in both non-malignant and malignant gynecologic disorders, suggesting diverse roles for this pathway in reproductive tract abnormalities.

Despite the physiological importance of Notch signaling, there remain significant gaps in our knowledge regarding its regulation and functional diversity ( Box 2 ). Major gaps currently include factors upstream of receptor and ligand presentation as well as tissue-specific signaling mechanisms. The governing hormones within the female reproductive tract are estradiol (E2), progesterone (P4), and human chorionic gonadotropin (hCG). These hormones regulate processes that are integral to fertility maintenance, like ovarian and uterine development, and the ovarian and menstrual cycles ( Box 4 ). Thus, the Notch signaling pathway, which we suggest is an arbiter of reproductive function, could be regulated by these essential hormones. In mice, Notch signaling activation mimics P4 levels throughout the estrous cycle indicating that P4 signaling may contribute to cycle specific regulation of Notch signaling activation[ 6 ]. Transcriptional levels of receptors: Notch1-4, ligands: Dll4, Jagged 1 and 2, and target genes: Hes1, Hes5, and Nrarp increase in the mouse uterus throughout the estrous cycle indicating that the Notch signaling pathway activity may increase as the estrous cycle progresses[ 6 ]. In the Olive baboon, Papio anubis , Notch1 expression is low in the endometrium during the proliferative phase of the menstrual cycle ( Box 4 ) followed by an increase in glandular expression of Notch1 during the secretory phase[ 7 ]. In addition, Notch1 expression is positively regulated by hCG[ 7 , 8 ]. Following administration of hCG, Notch1 increases in the stromal compartment of the endometrium providing a role for embryonic signal-mediated regulation of Notch signaling[ 7 ]. Additionally, hCG induces NOTCH1 expression in human stromal cells in vitro [ 7 ]. In a clinical trial to determine the effect of hCG infusion on the human endometrium during the period of implantation, increased glandular and stromal protein levels of NOTCH1 were noted without observable changes in mRNA expression, suggesting that hCG may induce post-translational modification of NOTCH[ 9 ]. To further investigate how hCG regulates Notch1 in the endometrial environment, human uterine fibroblasts (HuFs) were treated with P4 and hCG, which resulted in cleavage of NOTCH1 at the primary γ-secretase cleavage site, valine residue 1744, suggesting that hCG acts to induce NOTCH1 signaling activation in stromal cells[ 7 ]. E2 also significantly affects Notch signaling in several systems. Treatment of human umbilical vein endothelial cells with E2 leads to increased activation of NOTCH1 and NOTCH4 and decreased NOTCH2 expression showing that E2 modulates Notch signaling activation in some cellular contexts[ 10 ]. Conversely, in breast cancer cell lines, E2 treatment reduces Notch signaling activation by causing accumulations of full-length membrane bound NOTCH1[ 11 ]. Additionally, N1ICD can stimulate estrogen receptor α (ER) dependent transcription in the absence of estradiol in breast cancer cells by recruiting coactivators to ER-responsive elements[ 12 ]. E2-regulated NOTCH signaling has also been described in various tissues throughout the reproductive tract. Ishikawa cells, an endometrial carcinoma cell line, exhibit increased availability of NOTCH1 protein and mRNA with E2 administration[ 13 ]. In addition, an in vitro study of human fallopian tube epithelial cells showed that E2 and P4 induced an increase in mRNA expression of a NOTCH target gene, Hes1[ 14 ]. These studies collectively indicate that there may be tissue specific and even cell type specific hormonal regulation of Notch signaling at multiple levels.

Regulation of Notch signaling is an underexplored area of research in the context of reproduction. Due to the importance of this signaling pathway in reproductive tract development, function, and disease, it warrants increased investigation. Current areas of investigation include hormonal regulation of Notch signaling by hCG, E2, and P4, but these mechanisms and interactions are not well understood. It is possible that these hormones may be regulating Notch signaling at the level of ligand presentation, receptor activation, cleavage enzyme activation, or by interacting with the Notch transcriptional activator RBPJ. Other evidence also suggests that Notch may interact with epigenetic modifiers, such as members of the SWI/SNF family, to alter chromatin accessibility, but this has not been thoroughly investigated in the context of reproductive physiology[ 32 , 65 ]. In addition, dysregulation of Notch signaling has been shown to play a role in developmental defects, reproductive diseases, and cancer. The Notch signaling pathway may be an integral pathway in many different disease etiologies, especially in pathologies of the reproductive tract such as endometriosis, PCOS, pre-eclampsia, adenomyosis, and infertility. Targeting Notch signaling could also provide novel and beneficial therapeutics to advance patient treatment for reproductive pathologies and infertility. Therefore, there are multiple avenues open for further investigation and evidence suggests that Notch signaling, and regulation may differ within the different organs of the reproductive tract.