2013
DOI: 10.1093/humrep/det058
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Preimplantation human blastocysts release factors that differentially alter human endometrial epithelial cell adhesion and gene expression relative to IVF success

Abstract: This study was supported by the National Health and Medical Research Council of Australia (Fellowship support #550905, #611827) and project grants by Monash IVF, Australia. There are no conflicts of interest to be declared.

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Cited by 47 publications
(48 citation statements)
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“…Both ligands strongly localize to the endometrial glandular and luminal epithelium, with very little to no expression in the stroma. Jagged1 mRNA and protein are highest during the mid-secretory phase compared with the proliferative phase (Cobellis et al 2008, Cuman et al 2013. Whilst DLL4 mRNA expression is highest during the early secretory phase (Mazella et al 2008), DLL4 protein shows no significant changes across the cycle (Mitsuhashi et al 2012).…”
Section: Notch Signalling In the Endometriummentioning
confidence: 90%
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“…Both ligands strongly localize to the endometrial glandular and luminal epithelium, with very little to no expression in the stroma. Jagged1 mRNA and protein are highest during the mid-secretory phase compared with the proliferative phase (Cobellis et al 2008, Cuman et al 2013. Whilst DLL4 mRNA expression is highest during the early secretory phase (Mazella et al 2008), DLL4 protein shows no significant changes across the cycle (Mitsuhashi et al 2012).…”
Section: Notch Signalling In the Endometriummentioning
confidence: 90%
“…To date, however, no studies have investigated the role of Notch in endometrial receptivity or blastocyst attachment in humans. However, there is reduced or absent immunostaining of Jagged1 in the mid-secretory luminal epithelium of women with primary infertility (Cuman et al 2013), suggesting that this ligand may be important for blastocyst-epithelial attachment. Furthermore, microarray analysis demonstrates that blastocyst-conditioned media regulates the endometrial epithelial expression of Notch1 and Jagged1 in vitro (Cuman et al 2013); thus, blastocysts may facilitate endometrial Notch expression, and possibly endometrial receptivity, via soluble mediators.…”
Section: Function Of Notch Signalling In Blastocyst-maternal Interactmentioning
confidence: 99%
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“…The profile of ECM proteins is remodelled and the expression of immune cells changes, giving rise to a priority of macrophages and uterine natural killer (NK) cells (13,14). When conception occurred and the blastocyst arrives into the uterus, it releases hormones, cytokines, integrins, growth factors, and other peptides that induce and facilitate endometrial receptivity (7,15,16). Embryo-endometrial interactions allow obtaining not only a receptive endometrium but also a competent blastocyst.…”
Section: Mechanisms Regulating the Embryo Endometrial Cross-talkmentioning
confidence: 99%
“…IL-6 is a well-established potent regulator of the host innate and humoral immune responses and has been shown to be up-regulated during a variety of viral infections including CMV [8,26,42]. IL-6 and its signalling molecules are also secreted by the endometrial and tubal cells of several species including human and have been described as major regulators of endometrial receptivity and blastocyst implantation [7,11,20]. Furthermore, abnormal expression of IL-6 by the endometrium has been associated with implantation failure, abortion and poor reproductive outcomes [13,20].…”
Section: Introductionmentioning
confidence: 99%