GDF9 and BMP15 induce development of antrum-like structures by bovine granulosa cells without oocytes

The role of oocytes in follicular antrum formation is not well understood. We examined the effect of oocyte-derived growth factors, growth differentiation factor 9 (GDF9) and bone morphogenetic protein 15 (BMP15), on the formation of antrum-like structures by cultured bovine oocyte-granulosa cell complexes (OGCs). OGCs containing growing oocytes (105‒115 µm in diameter) were collected from early antral follicles (1.2‒1.8 mm) and used to prepare oocytectomized complexes (OXCs) and granulosa cell complexes (GCs). The mRNAs of GDF9 and BMP15 were expressed in the oocytes, but not in the granulosa cells. The complexes were cultured for five days with or without GDF9 and BMP15 either alone or in combination. The OGCs maintained their complex integrity and developed antrum-like structure, whereas OXCs and GCs neither maintained their integrity nor developed any antrum-like structure without growth factors. GDF9 or BMP15 alone increased the integrity of these complexes and induced antrum-like structures in OXCs and GCs. Moreover, the combination of GDF9 and BMP15 was more potent for both phenomena in all types of complexes. In OXCs and GCs cultured without GDF9 and BMP15 or with BMP15 alone, outgrowing granulosa cells differentiated into fibroblast-like cells. The combination of GDF9 and BMP15 suppressed the appearance of fibroblast-like cells in OXCs and GCs during incubation. Instead, the granulosa cells appeared rhomboid and pebble-like in shape, similar to those in OGCs cultured without supplementation of GDF9 and BMP15. These results suggest that oocytes maintain complex integrity by preventing granulosa cell differentiation and participate in follicular antrum formation via GDF9 and BMP15.

[1]  T. Miyano,et al.  Inhibition of PDE3A sustains meiotic arrest and gap junction of bovine growing oocytes in in vitro growth culture. , 2018, Theriogenology.

[2]  H. Clarke,et al.  Mammalian Oocytes Locally Remodel Follicular Architecture to Provide the Foundation for Germline-Soma Communication , 2018, Current Biology.

[3]  T. Miyano,et al.  The fertilization ability and developmental competence of bovine oocytes grown in vitro , 2016, The Journal of reproduction and development.

[4]  T. Mueller,et al.  Cumulin, an Oocyte-secreted Heterodimer of the Transforming Growth Factor-β Family, Is a Potent Activator of Granulosa Cells and Improves Oocyte Quality* , 2015, The Journal of Biological Chemistry.

[5]  T. Miyano,et al.  Steroid hormones promote bovine oocyte growth and connection with granulosa cells. , 2014, Theriogenology.

[6]  R. Gilchrist,et al.  Bone Morphogenetic Protein 15 in the Pro-Mature Complex Form Enhances Bovine Oocyte Developmental Competence , 2014, PloS one.

[7]  K. Sugiura,et al.  Role of oocyte-derived paracrine factors in follicular development , 2014, Animal science journal = Nihon chikusan Gakkaiho.

[8]  M. Matzuk,et al.  Growth differentiation factor 9:bone morphogenetic protein 15 heterodimers are potent regulators of ovarian functions , 2013, Proceedings of the National Academy of Sciences.

[9]  R. Gilchrist,et al.  Signalling pathways mediating specific synergistic interactions between GDF9 and BMP15. , 2012, Molecular human reproduction.

[10]  K. Sugiura,et al.  Estrogen promotes the development of mouse cumulus cells in coordination with oocyte-derived GDF9 and BMP15. , 2010, Molecular endocrinology.

[11]  R. Rodgers,et al.  Formation of the Ovarian Follicular Antrum and Follicular Fluid1 , 2010, Biology of reproduction.

[12]  J. Juengel,et al.  Effects of active immunization against growth differentiation factor 9 and/or bone morphogenetic protein 15 on ovarian function in cattle. , 2009, Reproduction.

[13]  K. Wigglesworth,et al.  Oocytes determine cumulus cell lineage in mouse ovarian follicles , 2007, Journal of Cell Science.

[14]  D. Mottershead,et al.  Bone morphogenetic protein 15 and growth differentiation factor 9 co-operate to regulate granulosa cell function in ruminants. , 2005, Reproduction.

[15]  J. Juengel,et al.  The role of proteins of the transforming growth factor-beta superfamily in the intraovarian regulation of follicular development. , 2005, Human reproduction update.

[16]  M. Matzuk,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. , 2004, Developmental biology.

[17]  M. Mullen,et al.  Mutations in the Genes for Oocyte-Derived Growth Factors GDF9 and BMP15 Are Associated with Both Increased Ovulation Rate and Sterility in Cambridge and Belclare Sheep (Ovis aries)1 , 2004, Biology of reproduction.

[18]  Martin M. Matzuk,et al.  Intercellular Communication in the Mammalian Ovary: Oocytes Carry the Conversation , 2002, Science.

[19]  M. Matzuk,et al.  Synergistic roles of bone morphogenetic protein 15 and growth differentiation factor 9 in ovarian function. , 2001, Molecular endocrinology.

[20]  S. Soyal,et al.  FIGalpha, a germ cell-specific transcription factor required for ovarian follicle formation. , 2000, Development.

[21]  M. Matzuk,et al.  Oocyte-expressed TGF-β superfamily members in female fertility , 2000, Molecular and Cellular Endocrinology.

[22]  C. Clay,et al.  Molecular cloning of the ovine Growth/Differentiation factor-9 gene and expression of growth/differentiation factor-9 in ovine and bovine ovaries. , 1999, Biology of reproduction.

[23]  T. Miyano,et al.  Promotion of follicular antrum formation by pig oocytes in vitro , 1998, Zygote.

[24]  T. Miyano,et al.  Bovine oocytes from early antral follicles grow to meiotic competence in vitro: effect of FSH and hypoxanthine. , 1997, Theriogenology.

[25]  David F. Albertini,et al.  Growth differentiation factor-9 is required during early ovarian folliculogenesis , 1996, Nature.

[26]  K. Wigglesworth,et al.  Mammalian oocyte growth and development in vitro , 1996, Molecular reproduction and development.

[27]  P. Motta,et al.  Oocyte follicle cells association during development of human ovarian follicle. A study by high resolution scanning and transmission electron microscopy. , 1994, Archives of histology and cytology.

[28]  T. Miyano,et al.  In vitro growth and maturation of pig oocytes. , 1994, Journal of reproduction and fertility.

[29]  S. Roy,et al.  Isolation and long-term culture of human preantral follicles. , 1993, Fertility and sterility.

[30]  P. Nayudu,et al.  Factors influencing the rate of preantral and antral growth of mouse ovarian follicles in vitro. , 1992, Journal of reproduction and fertility.

[31]  B. Vanderhyden,et al.  Mouse oocytes promote proliferation of granulosa cells from preantral and antral follicles in vitro. , 1992, Biology of reproduction.

[32]  J. Eppig Intercommunication between mammalian oocytes and companion somatic cells , 1991, BioEssays : news and reviews in molecular, cellular and developmental biology.

[33]  B. Vanderhyden,et al.  Developmental pattern of the secretion of cumulus expansion-enabling factor by mouse oocytes and the role of oocytes in promoting granulosa cell differentiation. , 1990, Developmental biology.

[34]  S. Daniel,et al.  Follicle-stimulating hormone and estradiol regulate antrum-like reorganization of granulosa cells in rat preantral follicle cultures. , 1990, Biology of reproduction.

[35]  R. Hunter,et al.  Physiological factors underlying the formation of ovarian follicular fluid. , 1988, Journal of reproduction and fertility.

[36]  M. Nekola,et al.  Morphological changes of rat follicular cells as influenced by oocytes. , 1971, Biology of reproduction.

[37]  Koji Sugiura,et al.  Transcriptomic Diversification of Developing Cumulus and Mural Granulosa Cells in Mouse Ovarian Follicles1 , 2015, Biology of reproduction.

[38]  N. Takenouchi,et al.  In Vitro Growth and Development of Bovine Oocyte-Granulosa Cell Complexes on the Flat Substratum: Effects of High Polyvinylpyrrolidone Concentration in Culture Medium1 , 2004, Biology of reproduction.

[39]  N. Horelli-Kuitunen,et al.  Human growth differentiation factor 9 (GDF-9) and its novel homolog GDF-9B are expressed in oocytes during early folliculogenesis. , 1999, The Journal of clinical endocrinology and metabolism.