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Granulosa Transcriptome

Inside the granulosa transcriptome

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Pages 951-956 | Received 06 Jul 2016, Accepted 08 Aug 2016, Published online: 18 Oct 2016

References

  • Hutt KJ, McLaughlin EA, Holland MK. Kit ligand and c-Kit have diverse roles during mammalian oogenesis and folliculogenesis. Mol Hum Reprod 2006;12:61–9
  • McNatty KP, Smith P, Moore LG, et al. Oocyte-expressed genes affecting ovulation rate. Mol Cell Endocrinol 2005;234:57–66
  • Su YQ, Wu X, O’Brien MJ, et al. Synergistic roles of BMP15 and GDF9 in the development and function of the oocyte-cumulus cell complex in mice: genetic evidence for an oocyte-granulosa cell regulatory loop. Dev Biol 2004;276:64–73
  • Jagarlamudi K, Rajkovic A. Oogenesis: transcriptional regulators and mouse models. Mol Cell Endocrinol 2012;356:31–9
  • Cohen PE, Holloway JK. “Predicting gene networks in human oocyte meiosis”. Biol Reprod 2010;82:469–72
  • Monget P, Bobe J, Gougeon A, et al. The ovarian reserve in mammals: a functional and evolutionary perspective. Mol Cell Endocrinol 2012;356:2–12
  • Gilchrist RB, Lane M, Thompson JG. Oocyte-secreted factors: regulators of cumulus cell function and oocyte quality. Hum Reprod Update 2008;14:159–77
  • Kaivo-oja N, Jeffery LA, Ritvos O, Mottershead DG. “Smad signalling in the ovarysignalling in the ovary.,”. Reprod Biol Endocrinol 2006;4:21
  • Joyce IM, Clark AT, Pendola FL, Eppig JJ. “Comparison of recombinant growth differentiation factor-9 and oocyte regulation of KIT ligand messenger ribonucleic acid expression in mouse ovarian follicles”. Biol Reprod 2000;63:1669–75
  • Otsuka F, Shimasaki S. “A negative feedback system between oocyte bone morphogenetic protein 15 and granulosa cell kit ligand: its role in regulating granulosa cell mitosis”. Proc Natl Acad Sci USA 2002;99:8060–5
  • Driancourt M. Roles of KIT and KIT LIGAND in ovarian function. Rev Reprod Sep 2000;5:143–52
  • Thomas FH, Ismail RS, Jiang JY, Vanderhyden BC. Kit ligand 2 promotes murine oocyte growth in vitro. Biol Reprod 2008;78:167–75
  • Brown C, LaRocca J, Pietruska J, et al. Subfertility caused by altered follicular development and oocyte growth in female mice lacking PKB alpha/Akt1. Biol Reprod 2010;82:246–56
  • Liu K, Rajareddy S, Liu L, et al. Control of mammalian oocyte growth and early follicular development by the oocyte PI3 kinase pathway: new roles for an old timer. Dev Biol 2006;299:1–11
  • Ezzati MM, Baker MD, Saatcioglu HD, et al. Regulation of FOXO3 subcellular localization by Kit ligand in the neonatal mouse ovary. J Assist Reprod Genet 2015;32:1741–7
  • Zhang X, Zhang H, Gao Q, et al. Sohlh2 inhibits the apoptosis of mouse primordial follicle oocytes via C-kit/PI3K/Akt/Foxo3a signalling pathway. Reprod Biomed Online 2015;30:514–21
  • Reddy P, Liu L, Adhikari D, et al. Oocyte-specific deletion of Pten causes premature activation of the primordial follicle pool. Science 2008;319:611–13
  • Pangas SA, Choi Y, Ballow DJ, et al. Oogenesis requires germ cell-specific transcriptional regulators Sohlh1 and Lhx8. Proc Natl Acad Sci USA 2006;103:8090–5
  • Banerjee AA, Mahale SD. Role of the Extracellular and Intracellular Loops of Follicle-Stimulating Hormone Receptor in Its Function. Front Endocrinol (Lausanne) 2015;6:110
  • Gershtein E, Kushlinskii N. Clinical prospects of IGF-signaling system components study in ovarian cancer patients. Drug Metab Pers Ther 2015;30:75–85
  • Jones RL, Pepling ME. KIT signaling regulates primordial follicle formation in the neonatal mouse ovary. Dev Biol 2013;382:186–97
  • Gittens JEI, Barr KJ, Vanderhyden BC, Kidder GM. Interplay between paracrine signaling and gap junctional communication in ovarian follicles. J Cell Sci 2005;118:113–22
  • Tong D, Gittens JEI, Kidder GM, Bai D. Patch-clamp study reveals that the importance of connexin43-mediated gap junctional communication for ovarian folliculogenesis is strain specific in the mouse. Am J Physiol Cell Physiol 2006;290:C290–7
  • Hennet ML, Combelles CMH. The antral follicle: a microenvironment for oocyte differentiation. Int J Dev Biol 2012;56:819–31
  • Mattioli M, Barboni B. Signal transduction mechanism for LH in the cumulus-oocyte complex. Mol Cell Endocrinol 2000;161:19–23
  • Sánchez F, Smitz J. Molecular control of oogenesis. Biochim Biophys Acta 2012;1822:1896–912
  • Chronowska E. High-throughput analysis of ovarian granulosa cell transcriptome. Biomed Res Int 2014;2014:213570
  • Munakata Y, Kawahara-Miki R, Shiratsuki S, et al. Gene expression patterns in granulosa cells and oocytes at various stages of follicle development as well as in in vitro grown oocyte-and-granulosa cell complexes. J Reprod Dev 2016. [Epub ahead of print]
  • Huang X, Hao C, Shen X, et al. RUNX2, GPX3 and PTX3 gene expression profiling in cumulus cells are reflective oocyte/embryo competence and potentially reliable predictors of embryo developmental competence in PCOS patients. Reprod Biol Endocrinol 2013;11:109
  • Cillo F, Brevini TAL, Antonini S, et al. Association between human oocyte developmental competence and expression levels of some cumulus genes. Reproduction 2007;134:645–50
  • McKenzie LJ, Pangas SA, Carson SA, et al. Human cumulus granulosa cell gene expression: a predictor of fertilization and embryo selection in women undergoing IVF. Hum Reprod 2004;19:2869–74
  • Fragouli E, Lalioti MD, Wells D. The transcriptome of follicular cells: biological insights and clinical implications for the treatment of infertility. Hum Reprod Update 2014;20:1–11
  • Borup R, Thuesen LL, Andersen CY, et al. Competence Classification of Cumulus and Granulosa Cell Transcriptome in Embryos Matched by Morphology and Female Age. PLoS One 2016;11:e0153562
  • Fragouli E, Wells D, Iager AE, et al. Alteration of gene expression in human cumulus cells as a potential indicator of oocyte aneuploidy.. Hum Reprod 2012;27:2559–68
  • Assou S, Haouzi D, Dechaud H, et al. Comparative gene expression profiling in human cumulus cells according to ovarian gonadotropin treatments. Biomed Res. Int 2013;2013:354582
  • Russell DL, Salustri A. Extracellular matrix of the cumulus-oocyte complex. Semin Reprod Med 2006;24:217–27
  • Dunning KR, Watson LN, Sharkey DJ, et al. Molecular filtration properties of the mouse expanded cumulus matrix: controlled supply of metabolites and extracellular signals to cumulus cells and the oocyte. Biol Reprod 2012;87:89
  • Childs AJ, Kinnell HL, He J, Anderson RA. LIN28 is selectively expressed by primordial and pre-meiotic germ cells in the human fetal ovary. Stem Cells Dev 2012;21:2343–9
  • Tong XH, Xu B, Zhang YW, et al. Research resources: comparative microRNA profiles in human corona radiata cells and cumulus oophorus cells detected by next-generation small RNA sequencing. PLoS One 2014;9:e106706
  • Yang X, Zhou Y, Peng S, et al. Differentially expressed plasma microRNAs in premature ovarian failure patients and the potential regulatory function of mir-23a in granulosa cell apoptosis. Reproduction 2012;144:235–44
  • Hennebold JD. Preventing granulosa cell apoptosis through the action of a single microRNA. Biol Reprod 2010;83:165–7
  • Zhang Q, Wang HY, Liu X, et al. IL-2R common gamma-chain is epigenetically silenced by nucleophosphin-anaplastic lymphoma kinase (NPM-ALK) and acts as a tumor suppressor by targeting NPM-ALK. Proc Natl Acad Sci USA 2011;108:11977–82
  • Devjak R, Fon Tacer K, Juvan P, et al. Cumulus cells gene expression profiling in terms of oocyte maturity in controlled ovarian hyperstimulation using GnRH agonist or GnRH antagonist. PLoS One 2012;7:e47106
  • Brannian J, Eyster K, Mueller BA, et al. Differential gene expression in human granulosa cells from recombinant FSH versus human menopausal gonadotropin ovarian stimulation protocols. Reprod Biol Endocrinol 2010;8:25
  • Grøndahl ML, Borup R, Lee YB, et al. Differences in gene expression of granulosa cells from women undergoing controlled ovarian hyperstimulation with either recombinant follicle-stimulating hormone or highly purified human menopausal gonadotropin. Fertil Steril 2009;91:1820–30
  • Gurgan T, Montjean D, Demirol A, Menezo YJR. Sequential (hFSH + recFSH) vs homogenous (hFSH or recFSH alone) stimulation: clinical and biochemical (cumulus cell gene expression) aspects. J Assist Reprod Genet 2014;31:657–65
  • Gatta V, Tatone C, Ciriminna R, et al. Gene expression profiles of cumulus cells obtained from women treated with recombinant human luteinizing hormone + recombinant human follicle-stimulating hormone or highly purified human menopausal gonadotropin versus recombinant human follicle-stimulatin. Fertil Steril 2013;99:2000–8.e1
  • Papler TB, Bokal EV, Tacer KF, et al. Differences in cumulus cells gene expression between modified natural and stimulated in vitro fertilization cycles. J Assist Reprod Genet 2014;31:79–88
  • Karakaya C, Guzeloglu-Kayisli O, Uyar A, et al. Poor ovarian response in women undergoing in vitro fertilization is associated with altered microRNA expression in cumulus cells. Fertil Steril 2015;103:1469–76. e1–3
  • Fair T. The contribution of the maternal immune system to the establishment of pregnancy in cattle. Front Immunol 2015;6:7
  • Liu Z, de Matos DG, Fan HY, et al. Interleukin-6: an autocrine regulator of the mouse cumulus cell-oocyte complex expansion process. Endocrinology 2009;150:3360–8
  • Allegra A, Raimondo S, Volpes A, et al. The gene expression profile of cumulus cells reveals altered pathways in patients with endometriosis. J Assist Reprod Genet 2014;31:1277–85
  • Sanchez AM, Viganò P, Quattrone F, et al. The WNT/β-catenin signaling pathway and expression of survival promoting genes in luteinized granulosa cells: endometriosis as a paradigm for a dysregulated apoptosis pathway. Fertil Steril 2014;101:1688–96
  • Burney RO, Talbi S, Hamilton AE, et al. Gene expression analysis of endometrium reveals progesterone resistance and candidate susceptibility genes in women with endometriosis. Endocrinology 2007;148:3814–26
  • Smuc T, Hevir N, Ribic-Pucelj M, et al. Disturbed estrogen and progesterone action in ovarian endometriosis. Mol Cell Endocrinol 2009;301:59–64
  • Karita M, Yamashita Y, Hayashi A, et al. Does advanced-stage endometriosis affect the gene expression of estrogen and progesterone receptors in granulosa cells? Fertil Steril 2011;95:889–94
  • Osteen KG, Bruner-Tran KL, Eisenberg E. Reduced progesterone action during endometrial maturation: a potential risk factor for the development of endometriosis. Fertil Steril 2005;83:529–37
  • Barcelos IDES, Donabella FC, Ribas CP, et al. Down-regulation of the CYP19A1 gene in cumulus cells of infertile women with endometriosis. Reprod Biomed Online 2015;30:532–41
  • Pavone ME, Dyson M, Reirstad S, et al. Endometriosis expresses a molecular pattern consistent with decreased retinoid uptake, metabolism and action. Hum Reprod 2011;26:2157–64
  • Hsu AL, Townsend PM, Oehninger S, Castora FJ. Endometriosis may be associated with mitochondrial dysfunction in cumulus cells from subjects undergoing in vitro fertilization-intracytoplasmic sperm injection, as reflected by decreased adenosine triphosphate production. Fertil Steril 2015;103:347–52.e1
  • Au HK, Lin SH, Huang SY, et al. Deleted mitochondrial DNA in human luteinized granulosa cells. Ann NY Acad Sci 2005;1042:136–41
  • Tsai HD, Hsieh YY, Hsieh JN, et al. Mitochondria DNA deletion and copy numbers of cumulus cells associated with in vitro fertilization outcomes. J Reprod Med 2010;55:491–7
  • Yamashita Y, Asano M, Morishima S, et al. Mitochondrial gene expression in granulosa cells of severe endometriosis with in vitro fertilization and embryo transfer. Fertil Steril 2007;88:1703–5
  • Lin Y, Chen Y, Du J, et al. Mitochondrial D-loop Variations in Infertile Women Undergoing in Vitro Fertilization-Embryo Transfer. J Reprod Med 2015;60:383–8
  • Lin Y, Du J, Li L, et al. Mitochondrial D-loop variations in infertile women undergoing a long stimulation protocol. Eur J Obstet Gynecol Reprod Biol 2012;160:161–5
  • Ben-Meir A, Yahalomi S, Moshe B, et al. Coenzyme Q–dependent mitochondrial respiratory chain activity in granulosa cells is reduced with aging. Fertil Steril 2015;104:724–7
  • Xu B, Zhang YW, Tong XH, Liu YS. Characterization of microRNA profile in human cumulus granulosa cells: Identification of microRNAs that regulate Notch signaling and are associated with PCOS. Mol Cell Endocrinol 2015;404:26–36
  • Roth LW, McCallie B, Alvero R, et al. Altered microRNA and gene expression in the follicular fluid of women with polycystic ovary syndrome. J Assist Reprod Genet 2014;31:355–62
  • Li Q, McKenzie LJ, Matzuk MM. Revisiting oocyte-somatic cell interactions: in search of novel intrafollicular predictors and regulators of oocyte developmental competence. Mol Hum Reprod 2008;14:673–8
  • Regiani T, Cordeiro FB, do L, et al. Follicular fluid alterations in endometriosis: label-free proteomics by MS(E) as a functional tool for endometriosis. Syst Biol Reprod Med 2015;61:263–76

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