Specific and extensive endometrial deregulation is present before conception in IVF/ICSI repeated implantation failures (IF) or recurrent miscarriages.
[en] The objective was to examine if IVF/ICSI repeated implantation failures (IF) or recurrent miscarriages (RM) could be related to preconceptional endometrial deregulations. IF was defined as the absence of pregnancy despite the transfer of at least ten IVF/ICSI good quality embryos, and RM as having at least three unexplained miscarriages. Fertile controls (FC) were women who had given birth at least once. Endometrial biopsy was performed in the mild luteal phase of a non-conceptual cycle (five women were selected in each group). Affymetrix chips (GeneChip Human Genome U133 Plus2.0 Array) were used for hybridization. Data were normalized by the gcRMA method, and raw p values adjusted by the Bonferroni procedure (1%). Differential expression of selected genes was analysed using real-time PCR. Gene networks and biological functions were explored using the Ingenuity Pathways Analysis software. Endometrial gene expression profiles at the time of uterine receptivity differ dramatically in the endometrium among FC, RM, and IF patients. Compared to FC, 2126 and 2477 genes are differentially expressed in IF and RM groups, respectively, and 2363 between IF and RM. In both conditions, differential gene expression referred mainly to DNA transcription and expression. Other main cellular functions deregulated in IF conditions correspond to cell morphology, cellular development, cell cycle, and cellular assembly, while in RM conditions, deregulated cellular functions relate to cell signalling (degradation of cyclic AMP and calcium metabolism) and cellular maintenance. In both conditions, there is an over-representation of deregulations related to the haematological system. In the IF condition, cell-mediated immune response and nervous system development and function are highly deregulated, while in RM patients, main deregulations are in organ and tissue development, humoral immune response, and muscular system development and function. Extensive endometrial deregulations are present before conception in patients who experienced IF or RM with both distinct and common deregulation.
Disciplines :
Reproductive medicine (gynecology, andrology, obstetrics)
Author, co-author :
Lédée, Nathalie
Munaut, Carine ; Université de Liège - ULiège > Département des sciences cliniques > Labo de biologie des tumeurs et du développement
Aubert, Julie
Sérazin, Valérie
Rahmati, Mona
Chaouat, Gérard
Sandra, Olivier
Foidart, Jean-Michel ; Université de Liège - ULiège > Département des sciences cliniques > Gynécologie - Obstétrique
Language :
English
Title :
Specific and extensive endometrial deregulation is present before conception in IVF/ICSI repeated implantation failures (IF) or recurrent miscarriages.
Publication date :
2011
Journal title :
Journal of Pathology
ISSN :
0022-3417
eISSN :
1096-9896
Publisher :
John Wiley & Sons, Inc, Chichester, United Kingdom
Psychoyos A,. Hormonal control of ovoimplantation. Vitam Horm 1973; 31: 201-256.
Bergh PA, Navot D,. The impact of embryonic development and endometrial maturity on the timing of implantation. Fertil Steril 1992; 58: 537-542.
Gellersen B, Brosens IA, Brosens JJ,. Decidualization of the human endometrium: mechanisms, functions, and clinical perspectives. Semin Reprod Med 2007; 25: 445-453.
Noyes RW, Hertig AT, Rock J,. Dating the endometrial biopsy. Am J Obstet Gynecol 1975; 122: 262-263.
Ledee N, Chaouat G, Serazin V, et al., Endometrial vascularity by three-dimensional power Doppler ultrasound and cytokines: a complementary approach to assess uterine receptivity. J Reprod Immunol 2008; 77: 57-62.
Vandesompele J, De Preter K, Pattyn F, et al., Accurate normalization of real-time quantitative RT-PCR data by geometric averaging of multiple internal control genes. Genome Biol 2002; 3:research0034.1-0034.11.
Irizarry RA, Hobbs B, Collin F, et al., Exploration, normalization, and summaries of high density oligonucleotide array probe level data. Biostatistics 2003; 4: 249-264.
Delmar P, Robin S, Daudin JJ,. VarMixt: efficient variance modelling for the differential analysis of replicated gene expression data. Bioinformatics 2005; 21: 502-508.
Salilew-Wondim D, Holker M, Rings F, et al., Bovine pretransfer endometrium and embryo transcriptome fingerprints as predictors of pregnancy success after embryo transfer. Physiol Genomics 2010; 42: 201-218.
Churchill GA,. Fundamentals of experimental design for cDNA microarrays. Nature Genet 2002; 32:(Suppl): 490-495.
Carson DD, Lagow E, Thathiah A, et al., Changes in gene expression during the early to mid-luteal (receptive phase) transition in human endometrium detected by high-density microarray screening. Mol Hum Reprod 2002; 8: 871-879.
Kao LC, Tulac S, Lobo S, et al., Global gene profiling in human endometrium during the window of implantation. Endocrinology 2002; 143: 2119-2138.
Borthwick JM, Charnock-Jones DS, Tom BD, et al., Determination of the transcript profile of human endometrium. Mol Hum Reprod 2003; 9: 19-33.
Riesewijk A, Martin J, van Os R, et al., Gene expression profiling of human endometrial receptivity on days LH + 2 versus LH + 7 by microarray technology. Mol Hum Reprod 2003; 9: 253-264.
Haouzi D, Assou S, Mahmoud K, et al., Gene expression profile of human endometrial receptivity: comparison between natural and stimulated cycles for the same patients. Hum Reprod 2009; 24: 1436-1445.
Mirkin S, Nikas G, Hsiu JG, et al., Gene expression profiles and structural/functional features of the peri-implantation endometrium in natural and gonadotropin-stimulated cycles. J Clin Endocrinol Metab 2004; 89: 5742-5752.
Eyster KM, Boles AL, Brannian JD, et al., DNA microarray analysis of gene expression markers of endometriosis. Fertil Steril 2002; 77: 38-42.
Horcajadas JA, Sharkey AM, Catalano RD, et al., Effect of an intrauterine device on the gene expression profile of the endometrium. J Clin Endocrinol Metab 2006; 91: 3199-3207.
Chaouat G, Ledee-Bataille N, Dubanchet S, et al., Reproductive immunology 2003: reassessing the Th1/Th2 paradigm? Immunol Lett 2004; 92: 207-214.
Saito S, Nakashima A, Shima T, et al., Th1/Th2/Th17 and regulatory T-cell paradigm in pregnancy. Am J Reprod Immunol 2010; 63: 601-610.
Blois SM, Kammerer U, Alba Soto C, et al., Dendritic cells: key to fetal tolerance? Biol Reprod 2007; 77: 590-598.
Merce LT, Barco MJ, Bau S, et al., Are endometrial parameters by three-dimensional ultrasound and power Doppler angiography related to in vitro fertilization/embryo transfer outcome? Fertil Steril 2008; 89: 111-117.
Ng EH, Chan CC, Tang OS, et al., Changes in endometrial and subendometrial blood flow in IVF. Reprod Biomed Online 2009; 18: 269-275.
Rees MC, Bicknell R,. Angiogenesis in the endometrium. Angiogenesis 1998; 2: 29-35.
Fujimoto J, Toyoki H, Jahan I, et al., Sex steroid-dependent angiogenesis in uterine endometrial cancers. J Steroid Biochem Mol Biol 2005; 93: 161-165.
Osuga Y, Toyoshima H, Mitsuhashi N, et al., The presence of platelet-derived endothelial cell growth factor in human endometrium and its characteristic expression during the menstrual cycle and early gestational period. Hum Reprod 1995; 10: 989-993.
Al-Jefout M, Dezarnaulds G, Cooper M, et al., Diagnosis of endometriosis by detection of nerve fibres in an endometrial biopsy: a double blind study. Hum Reprod 2009; 3019-3024.
Kammerer U, Kruse A, Barrientos G, et al., Role of dendritic cells in the regulation of maternal immune responses to the fetus during mammalian gestation. Immunol Invest 2008; 37: 499-533.
Brosens I, Derwig I, Brosens J, et al., The enigmatic uterine junctional zone: the missing link between reproductive disorders and major obstetrical disorders? Hum Reprod 2010; 25: 569-574.
Mansouri-Attia N, Sandra O, Aubert J, et al., Endometrium as an early sensor of in vitro embryo manipulation technologies. Proc Natl Acad Sci U S A 2009; 106: 5687-5692.
Bauersachs S, Ulbrich SE, Zakhartchenko V, et al., The endometrium responds differently to cloned versus fertilized embryos. Proc Natl Acad Sci U S A 2009; 106: 5681-5686.
Salker M, Teklenburg G, Molokhia M, et al., Natural selection of human embryos: impaired decidualization of endometrium disables embryo-maternal interactions and causes recurrent pregnancy loss. PLoS One 2010; 5: e10287.
Ledee N, Lombroso R, Lombardelli L, et al., Cytokines and chemokines in follicular fluids and potential of the corresponding embryo: the role of granulocyte colony-stimulating factor. Hum Reprod 2008; 23: 2001-2009.
Ledee N, Munaut C, Serazin V, et al., Performance evaluation of microbead and ELISA assays for follicular G-CSF: a non-invasive biomarker of oocyte developmental competence for embryo implantation. J Reprod Immunol 2010; 86: 126-132.
Ledee N, Frydman R, Osipova A, et al., Levels of follicular G-CSF and interleukin-15 appear as noninvasive biomarkers of subsequent successful birth in modified natural in vitro fertilization/intracytoplasmic sperm injection cycles. Fertil Steril 2011; 95: 94-98.
Robertson SA,. GM-CSF regulation of embryo development and pregnancy. Cytokine Growth Factor Rev 2007; 18: 287-298.
Scarpellini F, Sbracia M,. Use of granulocyte colony-stimulating factor for the treatment of unexplained recurrent miscarriage: a randomised controlled trial. Hum Reprod 2009; 24: 2703-2708.
Guillemin Y, Lalle P, Gillet G, et al., Oocytes and early embryos selectively express the survival factor BCL2L10. J Mol Med 2009; 87: 923-940.