Signaling Modalities During Oogenesis in Mammals

Current Topics in Developmental Biology

Volumn 102, Issue , 2013, Pages 227-242

  McGinnis, Lynda K ^a   Limback, S Darlene ^a   Albertini, David F ^a  

^a UNIVERSITY OF KANSAS SCHOOL OF MEDICINE   (United States)

Author keywords

Epidermal growth factor; Follicles; Gap junctions; Growth; Growth differentiation factor 9; Growth factors; Maturation; Oocytes; Receptor tyrosine kinases; Transzonal projections

Indexed keywords

EID: 84871776460     PISSN: 00702153     EISSN: None     Source Type: Book Series    
DOI: 10.1016/B978-0-12-416024-8.00008-8     Document Type: Chapter

References (53)

1. Acevedo N., Ding J., Smith G.D. Insulin signaling in mouse oocytes. Biology of Reproduction 2007, 77:872-879.
2. Albertini D.F., Combelles C.M., Benecchi E., Carabatsos M.J. Cellular basis for paracrine regulation of ovarian follicle development. Reproduction 2001, 121:647-653.
3. Allworth A.E., Albertini D.F. Meiotic maturation in cultured bovine oocytes is accompanied by remodeling of the cumulus cell cytoskeleton. Developmental Biology 1993, 158:101-112.
4. Ben-Haroush A., Abir R., Ao A., Jin S., Kessler-Icekson G., Feldberg D., et al. Expression of basic fibroblast growth factor and its receptors in human ovarian follicles from adults and fetuses. Fertility and Sterility 2005, 84(Suppl. 2):1257-1268.
5. Borggrefe T., Liefke R. Fine-tuning of the intracellular canonical Notch signaling pathway. Cell Cycle 2012, 11:264-276.
6. Bray S.J. Notch signalling: A simple pathway becomes complex. Nature Reviews Molecular Cell Biology 2006, 7:678-689.
7. Carabatsos M.J., Elvin J., Matzuk M.M., Albertini D.F. Characterization of oocyte and follicle development in growth differentiation factor-9-deficient mice. Developmental Biology 1998, 204:373-384.
8. Childs A.J., Bayne R.A., Murray A.A., Martins Da Silva S.J., Collins C.S., Spears N., et al. Differential expression and regulation by activin of the neurotrophins BDNF and NT4 during human and mouse ovarian development. Developmental Dynamics 2010, 239:1211-1219.
9. Choi Y., Rajkovic A. Genetics of early mammalian folliculogenesis. Cellular and Molecular Life Sciences: CMLS 2006, 63:579-590.
10. Combelles C.M.H., Carabatsos M.J., Kumar T.R., Matzuk M.M., Albertini D.F. Hormonal control of somatic cell oocyte interactions during ovarian follicle development. Molecular Reproduction and Development 2004, 69:347-355.
11. Conti M., Hsieh M., Park J.Y., Su Y.Q. Role of the epidermal growth factor network in ovarian follicles. Molecular Endocrinology 2006, 20:715-723.
12. de Matos D.G., Furnus C.C., Moses D.F. Glutathione synthesis during in vitro maturation of bovine oocytes: Role of cumulus cells. Biology of Reproduction 1997, 57:1420-1425.
13. Dole G., Nilsson E.E., Skinner M.K. Glial-derived neurotrophic factor promotes ovarian primordial follicle development and cell-cell interactions during folliculogenesis. Reproduction 2008, 135:671-682.
14. Dong J., Albertini D.F., Nishimori K., Kumar T.R., Lu N., Matzuk M.M. Growth differentiation factor-9 is required during early ovarian folliculogenesis. Nature 1996, 383:531.
15. Eppig J.J. Oocyte control of ovarian follicular development and function in mammals. Reproduction 2001, 122:829-838.
16. Gridley T. Notch signaling in the vasculature. Current Topics in Developmental Biology 2010, 92:277-309.
17. Guo M., Zhang H., Bian F., Li G., Mu X., Wen J., et al. P4 down-regulates Jagged2 and Notch1 expression during primordial folliculogenesis. Frontiers in Bioscience (Elite Edition) 2012, 4:2731-2744.
18. Hahn K.L., Johnson J., Beres B.J., Howard S., Wilson-Rawls J. Lunatic fringe null female mice are infertile due to defects in meiotic maturation. Development (Cambridge, England) 2005, 132:817-828.
19. Hutt K.J., Albertini D.F. An oocentric view of folliculogenesis and embryogenesis. Reproductive Biomedicine Online 2007, 14:758-764.
20. Hutt K.J., McLaughlin E.A., Holland M.K. KIT/KIT Ligand in mammalian oogenesis and folliculogenesis: Roles in rabbit and murine ovarian follicle activation and oocyte growth. Biology of Reproduction 2006, 75:421-433.
21. Johnson J., Espinoza T., McGaughey R.W., Rawls A., Wilson-Rawls J. Notch pathway genes are expressed in mammalian ovarian follicles. Mechanisms of Development 2001, 109:355-361.
22. Kerr B., Garcia-Rudaz C., Dorfman M., Paredes A., Ojeda S.R. NTRK1 and NTRK2 receptors facilitate follicle assembly and early follicular development in the mouse ovary. Reproduction 2009, 138:131-140.
23. Kezele P.R., Ague J.M., Nilsson E., Skinner M.K. Alterations in the ovarian transcriptome during primordial follicle assembly and development. Biology of Reproduction 2005, 72:241-255.
24. Knight P.G., Glister C. TGF-{beta} superfamily members and ovarian follicle development. Reproduction 2006, 132:191-206.
25. Li Q., Rajanahally S., Edson M.A., Matzuk M.M. Stable expression and characterization of N-terminal tagged recombinant human bone morphogenetic protein 15. Molecular Human Reproduction 2009, 15:779-788.
26. Liu K., Rajareddy S., Liu L., Jagarlamudi K., Boman K., Selstam G., et al. Control of mammalian oocyte growth and early follicular development by the oocyte PI3 kinase pathway: New roles for an old timer. Developmental Biology 2006, 299:1-11.
27. Luo J., McGinnis L.K., Kinsey W.H. Fyn kinase activity is required for normal organization and functional polarity of the mouse oocyte cortex. Molecular Reproduction and Development 2009, 76:819-831.
28. Matzuk M.M., Burns K.H., Viveiros M.M., Eppig J.J. Intercellular communication in the mammalian ovary: Oocytes carry the conversation. Science 2002, 296:2178-2180.
29. Mazerbourg S., Klein C., Roh J., Kaivo-Oja N., Mottershead D.G., Korchynskyi O., et al. Growth differentiation factor-9 signaling is mediated by the type I receptor, activin receptor-like kinase 5. Molecular Endocrinology 2004, 18:653-665.
30. McGinnis L.K., Albertini D.F. Dynamics of protein phosphorylation during meiotic maturation. Journal of Assisted Reproduction and Genetics 2010, 27:169-182.
31. McGinnis L.K., Carroll D.J., Kinsey W.H. Protein tyrosine kinase signaling during oocyte maturation and fertilization. Molecular Reproduction and Development 2011, 78:831-845.
32. McLaren A. The developmental history of female germ cells in mammals. Oxford Reviews of Reproductive Biology 1988, 10:162-179.
33. McNatty K.P., Juengel J.L., Reader K.L., Lun S., Myllymaa S., Lawrence S.B., et al. Bone morphogenetic protein 15 and growth differentiation factor 9 co-operate to regulate granulosa cell function in ruminants. Reproduction 2005, 129:481-487.
34. Miyoshi T., Otsuka F., Nakamura E., Inagaki K., Ogura-Ochi K., Tsukamoto N., et al. Regulatory role of kit ligand-c-kit interaction and oocyte factors in steroidogenesis by rat granulosa cells. Molecular and Cellular Endocrinology 2012, 358:18-26.
35. Moore R.K., Otsuka F., Shimasaki S. Molecular basis of bone morphogenetic protein-15 signaling in granulosa cells. The Journal of Biological Chemistry 2003, 278:304-310.
36. Mora J.M., Fenwick M.A., Castle L., Baithun M., Ryder T.A., Mobberley M., et al. Characterization and significance of adhesion and junction-related proteins in mouse ovarian follicles. Biology of Reproduction 2012, 86:153.
37. Mottershead D.G., Ritter L.J., Gilchrist R.B. Signalling pathways mediating specific synergistic interactions between GDF9 and BMP15. Molecular Human Reproduction 2012, 18:121-128.
38. Nilsson E.E., Detzel C., Skinner M.K. Platelet-derived growth factor modulates the primordial to primary follicle transition. Reproduction 2006, 131:1007-1015.
39. Nilsson E., Dole G., Skinner M.K. Neurotrophin NT3 promotes ovarian primordial to primary follicle transition. Reproduction 2009, 138:697-707.
40. Nilsson E.E., Skinner M.K. Kit ligand and basic fibroblast growth factor interactions in the induction of ovarian primordial to primary follicle transition. Molecular and Cellular Endocrinology 2004, 214:19-25.
41. Otsuka F., McTavish K.J., Shimasaki S. Integral role of GDF-9 and BMP-15 in ovarian function. Molecular Reproduction and Development 2011, 78:9-21.
42. Purcell S.H., Chi M.M., Moley K.H. Insulin-stimulated glucose uptake occurs in specialized cells within the cumulus oocyte complex. Endocrinology 2012, 153:2444-2454.
43. Rodrigues P., Limback D., McGinnis L.K., Plancha C.E., Albertini D.F. Oogenesis: Prospects and challenges for the future. Journal of Cellular Physiology 2008, 216:355-365.
44. Schindler R., Nilsson E., Skinner M.K. Induction of ovarian primordial follicle assembly by connective tissue growth factor CTGF. PLoS One 2010, 5:e12979.
45. Sheldon H., Heikamp E., Turley H., Dragovic R., Thomas P., Oon C.E., et al. New mechanism for Notch signaling to endothelium at a distance by Delta-like 4 incorporation into exosomes. Blood 2010, 116:2385-2394.
46. Skinner M.K. Regulation of primordial follicle assembly and development. Human Reproduction Update 2005, 11:461-471.
47. Su Y.Q., Sugiura K., Li Q., Wigglesworth K., Matzuk M.M., Eppig J.J. Mouse oocytes enable LH-induced maturation of the cumulus-oocyte complex via promoting EGF receptor-dependent signaling. Molecular Endocrinology 2010, 24:1230-1239.
48. Su Y.Q., Sugiura K., Wigglesworth K., O'Brien M.J., Affourtit J.P., Pangas S.A., et al. Oocyte regulation of metabolic cooperativity between mouse cumulus cells and oocytes: BMP15 and GDF9 control cholesterol biosynthesis in cumulus cells. Development (Cambridge, England) 2008, 135:111-121.
49. Sugiura K., Eppig J.J. Society for Reproductive Biology Founders Lecture 2005. Control of metabolic cooperativity between oocytes and their companion granulosa cells by mouse oocytes. Reproduction, Fertility, and Development 2005, 17:667-674.
50. Sugiura K., Pendola F.L., Eppig J.J. Oocyte control of metabolic cooperativity between oocytes and companion granulosa cells: Energy metabolism. Developmental Biology 2005, 279:20-30.
51. Sugiura K., Su Y.-Q., Diaz F.J., Pangas S.A., Sharma S., Wigglesworth K., et al. Oocyte-derived BMP15 and FGFs cooperate to promote glycolysis in cumulus cells. Development (Cambridge, England) 2007, 134:2593-2603.
52. Tingen C., Kim A., Woodruff T.K. The primordial pool of follicles and nest breakdown in mammalian ovaries. Molecular Human Reproduction 2009, 15:795-803.
53. Valve E., Penttila T.L., Paranko J., Harkonen P. FGF-8 is expressed during specific phases of rodent oocyte and spermatogonium development. Biochemical and Biophysical Research Communications 1997, 232:173-177.