Effect of bone morphogenetic protein-4 on in vitro growth, steroidogenesis and subsequent developmental competence of the oocyte-granulosa cell complex derived from bovine early antral follicles

详细信息    查看全文

• 作者：Yinghua Yang ; Chihiro Kanno ; Weiping Huang…
• 关键词：BMP ; 4 ; Developmental competence ; Early antral follicle ; In vitro growth ; Progesterone
• 刊名：Reproductive Biology and Endocrinology
• 出版年：2016
• 出版时间：December 2016
• 年：2016
• 卷：14
• 期：1
• 全文大小：535 KB
• 参考文献：1.Neglia G, Gasparrini B, Di Brienza VC, Di Palo R, Campanile G, Presicce GA, et al. Bovine and buffalo in vitro embryo production using oocytes derived from abattoir ovaries or collected by transvaginal follicle aspiration. Theriogenology. 2003;59(5–6):1123–30.PubMed CrossRef
  2.Lonergan P, Fair T. In vitro-produced bovine embryos-Dealing with the warts. Theriogenology. 2008;69(1):17–22. doi:10.​1016/​j.​theriogenology.​2007.​09.​007 .PubMed CrossRef
  3.Eppig JJ, O’Brien MJ. Development in vitro of mouse oocytes from primordial follicles. Biol Reprod. 1996;54(1):197–207.PubMed CrossRef
  4.O’Brien MJ, Pendola JK, Eppig JJ. A revised protocol for in vitro development of mouse oocytes from primordial follicles dramatically improves their developmental competence. Biol Reprod. 2003;68(5):1682–6. doi:10.​1095/​biolreprod.​102.​013029 .PubMed CrossRef
  5.Yamamoto K, Otoi T, Koyama N, Horikita N, Tachikawa S, Miyano T. Development to live young from bovine small oocytes after growth, maturation and fertilization in vitro. Theriogenology. 1999;52(1):81–9.PubMed CrossRef
  6.Senbon S, Miyano T. Bovine oocytes in early antral follicles grow in serum-free media: effect of hypoxanthine on follicular morphology and oocyte growth. Zygote. 2002;10(4):301–9.PubMed CrossRef
  7.Huang W, Kang SS, Nagai K, Yanagawa Y, Takahashi Y, Nagano M. Mitochondrial activity during pre-maturational culture in in vitro-grown bovine oocytes is related to maturational and developmental competences. Reprod Fertil Dev. 2014. doi:10.​1071/​RD14023 .
  8.Hirao Y, Itoh T, Shimizu M, Iga K, Aoyagi K, Kobayashi M, et al. In vitro growth and development of bovine oocyte-granulosa cell complexes on the flat substratum: effects of high polyvinylpyrrolidone concentration in culture medium. Biol Reprod. 2004;70(1):83–91. doi:10.​1095/​biolreprod.​103.​021238 .PubMed CrossRef
  9.Young JM, McNeilly AS. Theca: the forgotten cell of the ovarian follicle. Reproduction. 2010;140(4):489–504. doi:10.​1530/​REP-10-0094 .PubMed CrossRef
  10.Kayamori T, Kosaka N, Miyamoto A, Shimizu T. The differential pathways of bone morphogenetic protein (BMP)-4 and–7 in the suppression of the bovine granulosa cell apoptosis. Mol Cell Biochem. 2009;323(1–2):161–8. doi:10.​1007/​s11010-008-9976-1 .PubMed CrossRef
  11.Knight PG, Glister C. Local roles of TGF-beta superfamily members in the control of ovarian follicle development. Anim Reprod Sci. 2003;78(3–4):165–83.PubMed CrossRef
  12.Erickson GF, Shimasaki S. The spatiotemporal expression pattern of the bone morphogenetic protein family in rat ovary cell types during the estrous cycle. Reprod Biol Endocrinol. 2003;1:9.PubMed PubMedCentral CrossRef
  13.Yamashita H, Murayama C, Takasugi R, Miyamoto A, Shimizu T. BMP-4 suppresses progesterone production by inhibiting histone H3 acetylation of StAR in bovine granulosa cells in vitro. Mol Cell Biochem. 2011;348(1–2):183–90. doi:10.​1007/​s11010-010-0653-9 .PubMed CrossRef
  14.Glister C, Kemp CF, Knight PG. Bone morphogenetic protein (BMP) ligands and receptors in bovine ovarian follicle cells: actions of BMP-4,–6 and–7 on granulosa cells and differential modulation of Smad-1 phosphorylation by follistatin. Reproduction. 2004;127(2):239–54. doi:10.​1530/​rep.​1.​00090 .PubMed CrossRef
  15.Ireland J, Ward F, Jimenez-Krassel F, Ireland JLH, Smith GW, Lonergan P, et al. Follicle numbers are highly repeatable within individual animals but are inversely correlated with FSH concentrations and the proportion of good-quality embryos after ovarian stimulation in cattle. Hum Reprod. 2007;22(6):1687–95. doi:10.​1093/​humrep/​dem071 .PubMed CrossRef
  16.Rosen MP, Johnstone E, Addauan-Andersen C, Cedars MI. A lower antral follicle count is associated with infertility. Fertil Steril. 2011;95(6):1950–U107. doi:10.​1016/​j.​fertnstert.​2011.​01.​151 .PubMed PubMedCentral CrossRef
  17.Modina S, Borromeo V, Luciano AM, Lodde V, Franciosi F, Secchi C. Relationship between growth hormone concentrations in bovine oocytes and follicular fluid and oocyte developmental competence. Eur J Histochem. 2007;51(3):173–80.PubMed
  18.Huang W, Nagano M, Kang SS, Yanagawa Y, Takahashi Y. Effects of in vitro growth culture duration and prematuration culture on maturational and developmental competences of bovine oocytes derived from early antral follicles. Theriogenology. 2013;80(7):793–9. doi:10.​1016/​j.​theriogenology.​2013.​07.​004 .PubMed CrossRef
  19.Yanagawa Y, Matsuura Y, Suzuki M, Saga S, Okuyama H, Fukui D, et al. Accessory corpora lutea formation in pregnant Hokkaido sika deer (Cervus nippon yesoensis) investigated by examination of ovarian dynamics and steroid hormone concentrations. J Reprod Dev. 2015;61(1):61–6. doi:10.​1262/​jrd.​2014-076 .PubMed PubMedCentral CrossRef
  20.Takahashi Y, Hishinuma M, Matsui M, Tanaka H, Kanagawa H. Development of in vitro matured/fertilized bovine embryos in a chemically defined medium: influence of oxygen concentration in the gas atmosphere. J Vet Med Sci. 1996;58(9):897–902.PubMed CrossRef
  21.Nagano M, Kang SS, Koyama K, Huang WP, Yanagawa Y, Takahashi Y. In vitro maturation system for individual culture of bovine oocytes using micro-volume multi-well plate. Jpn J Vet Res. 2013;61(4):149–54.PubMed
  22.Takahashi Y, Kanagawa H. Effect of oxygen concentration in the gas atmosphere during in vitro insemination of bovine oocytes on the subsequent embryonic development in vitro. J Vet Med Sci. 1998;60(3):365–7.PubMed CrossRef
  23.Takahashi Y, First NL. In vitro development of bovine one-cell embryos: Influence of glucose, lactate, pyruvate, amino acids and vitamins. Theriogenology. 1992;37(5):963–78.PubMed CrossRef
  24.Murphy BD. Models of luteinization. Biol Reprod. 2000;63(1):2–11.PubMed CrossRef
  25.O’Shea JD, Rodgers RJ, D’Occhio MJ. Cellular composition of the cyclic corpus luteum of the cow. J Reprod Fertil. 1989;85(2):483–7.PubMed CrossRef
  26.Meidan R, Girsh E, Blum O, Aberdam E. In vitro differentiation of bovine theca and granulosa cells into small and large luteal-like cells: morphological and functional characteristics. Biol Reprod. 1990;43(6):913–21.PubMed CrossRef
  27.Jolly PD, Tisdall DJ, Heath DA, Lun S, Mcnatty KP. Apoptosis in Bovine Granulosa-Cells in Relation to Steroid-Synthesis, Cyclic Adenosine-3′,5′-Monophosphate Response to Follicle-Stimulating-Hormone and Luteinizing-Hormone, and Follicular Atresia. Biol Reprod. 1994;51(5):934–44. doi:10.​1095/​biolreprod51.​5.​934 .PubMed CrossRef
  28.Hsueh AJW, Billig H, Tsafriri A. Ovarian Follicle Atresia-a Hormonally Controlled Apoptotic Process. Endocr Rev. 1994;15(6):707–24. doi:10.​1210/​Er.​15.​6.​707 .PubMed
  29.Eppig JJ. Oocyte control of ovarian follicular development and function in mammals. Reproduction. 2001;122(6):829–38.PubMed CrossRef
  30.Gilchrist RB, Ritter LJ, Armstrong DT. Oocyte-somatic cell interactions during follicle development in mammals. Anim Reprod Sci. 2004;82–83:431–46. doi:10.​1016/​j.​anireprosci.​2004.​05.​017 .PubMed CrossRef
  31.Hussein TS, Froiland DA, Amato F, Thompson JG, Gilchrist RB. Oocytes prevent cumulus cell apoptosis by maintaining a morphogenic paracrine gradient of bone morphogenetic proteins. J Cell Sci. 2005;118(Pt 22):5257–68. doi:10.​1242/​jcs.​02644 .PubMed CrossRef
  32.Vanderhyden BC, Macdonald EA. Mouse oocytes regulate granulosa cell steroidogenesis throughout follicular development. Biol Reprod. 1998;59(6):1296–301. doi:10.​1095/​biolreprod59.​6.​1296 .PubMed CrossRef
  33.Mueller TD, Nickel J. Promiscuity and specificity in BMP receptor activation. FEBS Lett. 2012;586(14):1846–59. doi:10.​1016/​j.​febslet.​2012.​02.​043 .PubMed CrossRef
  34.Shimasaki S, Moore RK, Otsuka F, Erickson GF. The bone morphogenetic protein system in mammalian reproduction. Endocr Rev. 2004;25(1):72–101. doi:10.​1210/​er.​2003-0007 .PubMed CrossRef
  35.Pangas SA, Jorgez CJ, Matzuk MM. Growth differentiation factor 9 regulates expression of the bone morphogenetic protein antagonist gremlin. J Biol Chem. 2004;279(31):32281–6. doi:10.​1074/​jbc.​M403212200 .PubMed CrossRef
  36.Sudo S, Avsian-Kretchmer O, Wang LS, Hsueh AJ. Protein related to DAN and cerberus is a bone morphogenetic protein antagonist that participates in ovarian paracrine regulation. J Biol Chem. 2004;279(22):23134–41. doi:10.​1074/​jbc.​M402376200 .PubMed CrossRef
  37.Hirao Y, Naruse K, Kaneda M, Somfai T, Iga K, Shimizu M, et al. Production of fertile offspring from oocytes grown in vitro by nuclear transfer in cattle. Biol Reprod. 2013;89(3):57. doi:10.​1095/​biolreprod.​113.​109439 .PubMed CrossRef
  38.Fatehi AN, van den Hurk R, Colenbrander B, Daemen AJ, Van Tol HT, Monteiro RM, et al. Expression of bone morphogenetic protein2 (BMP2), BMP4 and BMP receptors in the bovine ovary but absence of effects of BMP2 and BMP4 during IVM on bovine oocyte nuclear maturation and subsequent embryo development. Theriogenology. 2005;63(3):872–89. doi:10.​1016/​j.​theriogenology.​2004.​05.​013 .PubMed CrossRef
  39.Hussein TS, Thompson JG, Gilchrist RB. Oocyte-secreted factors enhance oocyte developmental competence. Dev Biol. 2006;296(2):514–21. doi:10.​1016/​j.​ydbio.​2006.​06.​026 .PubMed CrossRef
  
• 作者单位：Yinghua Yang (1)
  Chihiro Kanno (1)
  Weiping Huang (1)
  Sung-Sik Kang (1)
  Yojiro Yanagawa (1)
  Masashi Nagano (1)
  
  1. Laboratory of Theriogenology, Department of Veterinary Clinical Sciences, Graduate School of Veterinary Medicine, Hokkaido University, Sapporo, 060-0818, Japan
  
• 刊物主题：Reproductive Medicine; Endocrinology;
• 出版者：BioMed Central
• ISSN：1477-7827

文摘

Background Bone morphogenetic proteins (BMPs) play important regulatory roles during folliculogenesis. Theca-derived BMP-4 may be beneficial to in vitro growth culture of early antral follicle-derived oocyte-granulosa cell complexes (OGCs), which is lacking in theca-derived products.