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9 - Differential gene expression mediated by oocyte–granulosa cell communication

from Section 3 - Developmental biology

Published online by Cambridge University Press:  05 October 2013

Saiichi Furukawa
Affiliation:
University of Tokyo, Tokyo, Japan
Koji Sugiura
Affiliation:
University of Tokyo, Tokyo, Japan
Alan Trounson
Affiliation:
California Institute for Regenerative Medicine
Roger Gosden
Affiliation:
Center for Reproductive Medicine and Infertility, Cornell University, New York
Ursula Eichenlaub-Ritter
Affiliation:
Universität Bielefeld, Germany
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Biology and Pathology of the Oocyte
Role in Fertility, Medicine and Nuclear Reprograming
, pp. 99 - 108
Publisher: Cambridge University Press
Print publication year: 2013

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References

Eppig, JJ, Pendola, FL, Wigglesworth, K, Pendola, JK. Mouse oocytes regulate metabolic cooperativity between granulosa cells and oocytes: amino acid transport. Biol Reprod 2005; 73(2): 351–7.CrossRefGoogle ScholarPubMed
Sugiura, K, Pendola, FL, Eppig, JJ.Oocyte control of metabolic cooperativity between oocytes and companion granulosa cells: energy metabolism. Dev Biol 2005; 279(1): 20–30.CrossRefGoogle ScholarPubMed
Colonna, R, Mangia, F.Mechanisms of amino acid uptake in cumulus-enclosed mouse oocytes. Biol Reprod 1983; 28(4): 797–803.CrossRefGoogle ScholarPubMed
Haghighat, N, Van Winkle, LJ.Developmental change in follicular cell-enhanced amino acid uptake into mouse oocytes that depends on intact gap junctions and transport system Gly. J Exp Zool 1990; 253(1): 71–82.CrossRefGoogle ScholarPubMed
Donahue, RP, Stern, S.Follicular cell support of oocyte maturation: production of pyruvate in vitro. J Reprod Fertil 1968; 17(2): 395–8.CrossRefGoogle ScholarPubMed
Leese, HJ, Barton, AM.Production of pyruvate by isolated mouse cumulus cells. J Exp Zool 1985; 234(2): 231–6.CrossRefGoogle ScholarPubMed
Zlotkin, T, Farkash, Y, Orly, J.Cell-specific expression of immunoreactive cholesterol side-chain cleavage cytochrome P-450 during follicular development in the rat ovary. Endocrinology 1986; 119(6): 2809–20.CrossRefGoogle ScholarPubMed
Whitelaw, PF, Smyth, CD, Howles, CM, Hillier, SG.Cell-specific expression of aromatase and LH receptor mRNAs in rat ovary. J Mol Endocrinol 1992; 9(3): 309–12.CrossRefGoogle ScholarPubMed
Camp, TA, Rahal, JO, Mayo, KE.Cellular localization and hormonal regulation of follicle-stimulating hormone and luteinizing hormone receptor messenger RNAs in the rat ovary. Mol Endocrinol 1991; 5(10): 1405–17.CrossRefGoogle ScholarPubMed
Peng, XR, Hsueh, AJ, LaPolt, PS, Bjersing, L, Ny, T.Localization of luteinizing hormone receptor messenger ribonucleic acid expression in ovarian cell types during follicle development and ovulation. Endocrinology 1991; 129(6): 3200–7.CrossRefGoogle ScholarPubMed
Chen, L, Russell, PT, Larsen, WJ.Functional significance of cumulus expansion in the mouse: roles for the preovulatory synthesis of hyaluronic acid within the cumulus mass. Mol Reprod Dev 1993; 34(1): 87–93.CrossRefGoogle ScholarPubMed
Eppig, JJ, Wigglesworth, K, Pendola, F, Hirao, Y.Murine oocytes suppress expression of luteinizing hormone receptor messenger ribonucleic acid by granulosa cells. Biol Reprod 1997; 56(4): 976–84.CrossRefGoogle ScholarPubMed
Buccione, R, Vanderhyden, BC, Caron, PJ, Eppig, JJ.FSH-induced expansion of the mouse cumulus oophorus in vitro is dependent upon a specific factor(s) secreted by the oocyte. Dev Biol 1990; 138(1): 16–25.CrossRefGoogle ScholarPubMed
Dong, J, Albertini, DF, Nishimori, K, et al. Growth differentiation factor-9 is required during early ovarian folliculogenesis. Nature 1996; 383(6600): 531–5.CrossRefGoogle ScholarPubMed
Vitt, UA, McGee, EA, Hayashi, M, Hsueh, AJ.In vivo treatment with GDF-9 stimulates primordial and primary follicle progression and theca cell marker CYP17 in ovaries of immature rats. Endocrinology 2000; 141(10): 3814–20.CrossRefGoogle ScholarPubMed
Nilsson, EE, Skinner, MK.Growth and differentiation factor-9 stimulates progression of early primary but not primordial rat ovarian follicle development. Biol Reprod 2002; 67(3): 1018–24.CrossRefGoogle Scholar
Hreinsson, JG, Scott, JE, Rasmussen, C, et al. Growth differentiation factor-9 promotes the growth, development, and survival of human ovarian follicles in organ culture. J Clin Endocrinol Metab 2002; 87(1): 316–21.CrossRefGoogle ScholarPubMed
Wu, X, Chen, L, Brown, CA, Yan, C, Matzuk, MM.Interrelationship of growth differentiation factor 9 and inhibin in early folliculogenesis and ovarian tumorigenesis in mice. Mol Endocrinol 2004; 18(6): 1509–19.CrossRefGoogle ScholarPubMed
Elvin, JA, Clark, AT, Wang, P, Wolfman, NM, Matzuk, MM.Paracrine actions of growth differentiation factor-9 in the mammalian ovary. Mol Endocrinol 1999; 13(6): 1035–48.CrossRefGoogle ScholarPubMed
Yeo, CX, Gilchrist, RB, Thompson, JG, Lane, M.Exogenous growth differentiation factor 9 in oocyte maturation media enhances subsequent embryo development and fetal viability in mice. Hum Reprod 2008; 23(1): 67–73.CrossRefGoogle ScholarPubMed
Yeo, CX, Gilchrist, RB, Lane, M.Disruption of bidirectional oocyte-cumulus paracrine signaling during in vitro maturation reduces subsequent mouse oocyte developmental competence. Biol Reprod 2009; 80(5): 1072–80.CrossRefGoogle ScholarPubMed
Galloway, SM, McNatty, KP, Cambridge, LM, et al. Mutations in an oocyte-derived growth factor gene (BMP15) cause increased ovulation rate and infertility in a dosage-sensitive manner. Nat Genet 2000; 25(3): 279–83.CrossRefGoogle Scholar
Yan, C, Wang, P, DeMayo, J, et al. Synergistic roles of bone morphogenetic protein 15 and growth differentiation factor 9 in ovarian function. Mol Endocrinol 2001; 15(6): 854–66.CrossRefGoogle ScholarPubMed
Elvin, JA, Yan, C, Matzuk, MM.Oocyte-expressed TGF-beta superfamily members in female fertility. Mol Cell Endocrinol 2000; 159(1–2): 1–5.CrossRefGoogle ScholarPubMed
Sugiura, K, Su, YQ, Eppig, JJ.Does bone morphogenetic protein 6 (BMP6) affect female fertility in the mouse?Biol Reprod 2010; 83: 997–1004.CrossRefGoogle ScholarPubMed
Hashimoto, O, Moore, RK, Shimasaki, S.Posttranslational processing of mouse and human BMP-15: potential implication in the determination of ovulation quota. Proc Natl Acad Sci USA 2005; 102(15): 5426–31.CrossRefGoogle ScholarPubMed
Yi, SE, LaPolt, PS, Yoon, BS, et al. The type I BMP receptor BmprIB is essential for female reproductive function. Proc Natl Acad Sci USA 2001; 98(14): 7994–9.CrossRefGoogle ScholarPubMed
Pangas, SA, Li, X, Umans, L, et al. Conditional deletion of Smad1 and Smad5 in somatic cells of male and female gonads leads to metastatic tumor development in mice. Mol Cell Biol 2008; 28(1): 248–57.CrossRefGoogle ScholarPubMed
Su, YQ, Sugiura, K, Wigglesworth, K, et al. Oocyte regulation of metabolic cooperativity between mouse cumulus cells and oocytes: BMP15 and GDF9 control cholesterol biosynthesis in cumulus cells. Development 2008; 135(1): 111–21.CrossRefGoogle ScholarPubMed
Valve, E, Penttila, TL, Paranko, J, Harkonen, P. FGF-8 is expressed during specific phases of rodent oocyte and spermatogonium development. Biochem Biophys Res Commun 1997; 232(1): 173–7.CrossRefGoogle ScholarPubMed
Sugiura, K, Su, YQ, Diaz, FJ, et al. Oocyte-derived BMP15 and FGFs cooperate to promote glycolysis in cumulus cells. Development 2007; 134(14): 2593–603.CrossRefGoogle ScholarPubMed
Sugiura, K, Su, YQ, Li, Q, et al. Fibroblast growth factors and epidermal growth factor cooperate with oocyte-derived members of the TGFbeta superfamily to regulate Spry2 mRNA levels in mouse cumulus cells. Biol Reprod 2009; 81(5): 833–41.CrossRefGoogle ScholarPubMed
Paladino, G.I ponti intercellulari fra l'uovo ovarico e le cellule follicolari, et la formazione della zona pellucida. Anat Anz 1890; 15: 254–9.Google Scholar
Biggers, JD, Whittingham, DG, Donahue, RP.The pattern of energy metabolism in the mouse oocyte and zygote. Proc Natl Acad Sci USA 1967; 58(2): 560–7.CrossRefGoogle ScholarPubMed
Eppig, JJ.Analysis of mouse oogenesis in vitro. Oocyte isolation and the utilization of exogenous energy sources by growing oocytes. J Exp Zool 1976; 198(3): 375–82.CrossRefGoogle ScholarPubMed
Sugiura, K, Eppig, JJ.Society for Reproductive Biology Founders’ Lecture 2005. Control of metabolic cooperativity between oocytes and their companion granulosa cells by mouse oocytes. Reprod Fertil Dev 2005; 17(7): 667–74.CrossRefGoogle ScholarPubMed
Su, YQ, Sugiura, K, Eppig, JJ.Mouse oocyte control of granulosa cell development and function: paracrine regulation of cumulus cell metabolism. Semin Reprod Med 2009; 27(1): 32–42.CrossRefGoogle ScholarPubMed
Pincus, G, Enzmann, EV.The comparative behavior of mammalian eggs in vivo and in vitro: I. The activation of ovarian eggs. J Exp Med 1935; 62(5): 665–75.CrossRefGoogle ScholarPubMed
Edwards, RG.Maturation in vitro of mouse, sheep, cow, pig, rhesus monkey and human ovarian oocytes. Nature 1965; 208(5008): 349–51.CrossRefGoogle ScholarPubMed
Tsafriri, A, Pomerantz, SH.Regulation of the development of meiotic competence and of the resumption of oocyte maturation in the rat. Symp Soc Exp Biol 1984; 38: 25–43.Google ScholarPubMed
Zhang, M, Su, YQ, Sugiura, K, Eppig, JJ.Granulosa cell ligand NPPC and its receptor NPR2 maintain meiotic arrest in mouse oocytes. Science 2010; 330: 366–9.CrossRefGoogle ScholarPubMed
Kawamura, K, Cheng, Y, Kawamura, N, et al. Pre-ovulatory LH/hCG surge decreases C-type natriuretic peptide secretion by ovarian granulosa cells to promote meiotic resumption of pre-ovulatory oocytes. Hum Reprod 2011; 26(11): 3094–101.CrossRefGoogle ScholarPubMed
Zhang, M, Su, YQ, Sugiura, K, et al. Estradiol promotes and maintains cumulus cell expression of natriuretic peptide receptor 2 (NPR2) and meiotic arrest in mouse oocytes in vitro. Endocrinology 2011; 152(11): 4377–85.CrossRefGoogle ScholarPubMed
Diaz, FJ, O’Brien, MJ, Wigglesworth, K, Eppig, JJ.The preantral granulosa cell to cumulus cell transition in the mouse ovary: development of competence to undergo expansion. Dev Biol 2006; 299(1): 91–104.CrossRefGoogle ScholarPubMed
Emmen, JM, Couse, JF, Elmore, SA, et al. In vitro growth and ovulation of follicles from ovaries of estrogen receptor (ER)α and ERβ null mice indicate a role for ERβ in follicular maturation. Endocrinology 2005; 146(6): 2817–26.CrossRefGoogle ScholarPubMed
Couse, JF, Yates, MM, Deroo, BJ, Korach, KS.Estrogen receptor-beta is critical to granulosa cell differentiation and the ovulatory response to gonadotropins. Endocrinology 2005; 146(8): 3247–62.CrossRefGoogle ScholarPubMed
Dupont, S, Krust, A, Gansmuller, A, et al. Effect of single and compound knockouts of estrogen receptors alpha (ERalpha) and beta (ERbeta) on mouse reproductive phenotypes. Development 2000; 127(19): 4277–91.Google ScholarPubMed
Sugiura, K, Su, YQ, Li, Q, et al. Estrogen promotes the development of mouse cumulus cells in coordination with oocyte-derived GDF9 and BMP15. Mol Endocrinol 2010; 24: 2303–14.CrossRefGoogle ScholarPubMed
Augereau, P, Badia, E, Balaguer, P, et al. Negative regulation of hormone signaling by RIP140. J Steroid Biochem Mol Biol 2006; 102(1–5): 51–9.CrossRefGoogle ScholarPubMed
Augereau, P, Badia, E, Carascossa, S, et al. The nuclear receptor transcriptional coregulator RIP140. Nucl Recept Signal 2006; 4: e024.Google ScholarPubMed
White, R, Leonardsson, G, Rosewell, I, et al. The nuclear receptor co-repressor nrip1 (RIP140) is essential for female fertility. Nat Med 2000; 6(12): 1368–74.CrossRefGoogle ScholarPubMed
Tullet, JM, Pocock, V, Steel, JH, et al. Multiple signaling defects in the absence of RIP140 impair both cumulus expansion and follicle rupture. Endocrinology 2005; 146(9): 4127–37.CrossRefGoogle ScholarPubMed
Davis, BJ, Lennard, DE, Lee, CA, et al. Anovulation in cyclooxygenase-2-deficient mice is restored by prostaglandin E2 and interleukin-1beta. Endocrinology 1999; 140(6): 2685–95.CrossRefGoogle ScholarPubMed
Varani, S, Elvin, JA, Yan, C, et al. Knockout of pentraxin 3, a downstream target of growth differentiation factor-9, causes female subfertility. Mol Endocrinol 2002; 16(6): 1154–67.CrossRefGoogle ScholarPubMed
Ochsner, SA, Day, AJ, Rugg, MS, et al. Disrupted function of tumor necrosis factor-alpha-stimulated gene 6 blocks cumulus cell-oocyte complex expansion. Endocrinology 2003; 144(10): 4376–84.CrossRefGoogle ScholarPubMed
Fulop, C, Szanto, S, Mukhopadhyay, D, et al. Impaired cumulus mucification and female sterility in tumor necrosis factor-induced protein-6 deficient mice. Development 2003; 130(10): 2253–61.CrossRefGoogle ScholarPubMed
Sugiura, K, Su, YQ, Eppig, JJ.Targeted suppression of Has2 mRNA in mouse cumulus cell-oocyte complexes by adenovirus-mediated short-hairpin RNA expression. Mol Reprod Dev 2009; 76(6): 537–47.CrossRefGoogle ScholarPubMed
Park, JY, Su, YQ, Ariga, M, et al. EGF-like growth factors as mediators of LH action in the ovulatory follicle. Science 2004; 303(5658): 682–4.CrossRefGoogle ScholarPubMed
Su, YQ, Wigglesworth, K, Pendola, FL, O’Brien, MJ, Eppig, JJ.Mitogen-activated protein kinase activity in cumulus cells is essential for gonadotropin-induced oocyte meiotic resumption and cumulus expansion in the mouse. Endocrinology 2002; 143(6): 2221–32.CrossRefGoogle ScholarPubMed
Fan, HY, Liu, Z, Shimada, M, et al. MAPK3/1 (ERK1/2) in ovarian granulosa cells are essential for female fertility. Science 2009; 324(5929): 938–41.CrossRefGoogle ScholarPubMed
Gui, LM, Joyce, IM.RNA interference evidence that growth differentiation factor-9 mediates oocyte regulation of cumulus expansion in mice. Biol Reprod 2005; 72(1): 195–9.CrossRefGoogle ScholarPubMed
Roh, JS, Bondestam, J, Mazerbourg, S, et al. Growth differentiation factor-9 stimulates inhibin production and activates Smad2 in cultured rat granulosa cells. Endocrinology 2003; 144(1): 172–8.CrossRefGoogle ScholarPubMed
Diaz, FJ, Wigglesworth, K, Eppig, JJ.Oocytes determine cumulus cell lineage in mouse ovarian follicles. J Cell Sci 2007; 120(Pt 8): 1330–40.CrossRefGoogle ScholarPubMed
Li, Q, Pangas, SA, Jorgez, CJ, et al. Redundant roles of SMAD2 and SMAD3 in ovarian granulosa cells in vivo. Mol Cell Biol 2008; 28(23): 7001–11.CrossRefGoogle ScholarPubMed
Elvin, JA, Yan, C, Wang, P, Nishimori, K, Matzuk, MM.Molecular characterization of the follicle defects in the growth differentiation factor 9-deficient ovary. Mol Endocrinol 1999; 13(6): 1018–34.CrossRefGoogle ScholarPubMed
Joyce, IM, Pendola, FL, O’Brien, M, Eppig, JJ.Regulation of prostaglandin-endoperoxide synthase 2 messenger ribonucleic acid expression in mouse granulosa cells during ovulation. Endocrinology 2001; 142(7): 3187–97.CrossRefGoogle ScholarPubMed
Fulop, C, Salustri, A, Hascall, VC.Coding sequence of a hyaluronan synthase homolog expressed during expansion of the mouse cumulus-oocyte complex. Arch Biochem Biophys 1997; 337(2): 261–6.CrossRefGoogle Scholar
Su, YQ, Denegre, JM, Wigglesworth, K, et al. Oocyte-dependent activation of mitogen-activated protein kinase (ERK1/2) in cumulus cells is required for the maturation of the mouse oocyte-cumulus cell complex. Dev Biol 2003; 263(1): 126–38.CrossRefGoogle ScholarPubMed
Reizel, Y, Elbaz, J, Dekel, N.Sustained activity of the EGF receptor is an absolute requisite for LH-induced oocyte maturation and cumulus expansion. Mol Endocrinol 2010; 24(2): 402–11.CrossRefGoogle ScholarPubMed
Wong, ES, Fong, CW, Lim, J, et al. Sprouty2 attenuates epidermal growth factor receptor ubiquitylation and endocytosis, and consequently enhances Ras/ERK signalling. EMBO J 2002; 21(18): 4796–808.CrossRefGoogle ScholarPubMed
Egan, JE, Hall, AB, Yatsula, BA, Bar-Sagi, D.The bimodal regulation of epidermal growth factor signaling by human Sprouty proteins. Proc Natl Acad Sci USA 2002; 99(9): 6041–6.CrossRefGoogle ScholarPubMed
Rubin, C, Litvak, V, Medvedovsky, H, et al. Sprouty fine-tunes EGF signaling through interlinked positive and negative feedback loops. Curr Biol 2003; 13(4): 297–307.CrossRefGoogle ScholarPubMed
Eppig, JJ, Wigglesworth, K, Pendola, FL.The mammalian oocyte orchestrates the rate of ovarian follicular development. Proc Natl Acad Sci USA 2002; 99(5): 2890–4.CrossRefGoogle ScholarPubMed
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(12): 8060–5.CrossRefGoogle ScholarPubMed
Miyoshi, T, Otsuka, F, Nakamura, E, et al. Regulatory role of kit ligand-c-kit interaction and oocyte factors in steroidogenesis by rat granulosa cells. Mol Cell Endocrinol 2012; 358(1): 18–26.CrossRefGoogle ScholarPubMed
Joyce, IM, Pendola, FL, Wigglesworth, K, Epping, JJ.Oocyte regulation of kit ligand expression in mouse ovarian follicles. Dev Biol 1999; 214(1): 342–53.CrossRefGoogle ScholarPubMed
Salmon, NA, Handyside, AH, Joyce, IM.Oocyte regulation of anti-Mullerian hormone expression in granulosa cells during ovarian follicle development in mice. Dev Biol 2004; 266(1): 201–8.CrossRefGoogle ScholarPubMed

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