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Mitogen-activated protein kinase phosphorylation patterns in pig oocytes and cumulus cells during gonadotrophin-induced resumption of meiosis in vitro

Published online by Cambridge University Press:  01 May 2007

S. Ebeling
Affiliation:
University of Veterinary Medicine, Hannover, Germany
C. Schuon
Affiliation:
University of Veterinary Medicine, Hannover, Germany
B. Meinecke*
Affiliation:
University of Veterinary Medicine, Hannover, Germany
*
All correspondence to: Burkhard Meinecke, Department of Reproductive Biology, University of Veterinary Medicine Hannover, Foundation, Buenteweg 2, D-30559 Hannover, Germany. Tel: +49 511 953 7181. Fax: +49 511 953 7150. e-mail: [email protected]

Summary

The present study investigated the phosphorylation pattern of mitogen-activated protein kinase (MAPK) in cumulus–oocyte complexes (COCs) during spontaneous and FSH/LH-induced in vitro maturation (IVM). Both isoforms of MAPK were unphosphorylated in oocytes recovered immediately after liberation from follicles and became phosphorylated following 25 h incubation, corresponding to the time of germinal vesicle breakdown (GVBD). In contrast, MAPK was already phosphorylated in minimal amounts in cumulus cells at the time of liberation from follicles and phosphorylation of MAPK increased after 0.5 h incubation. Supplementation of medium with gonadotrophins intensified phosphorylation at 0.5 h incubation, demonstrating the early and rapid action of FSH/LH on MAPK phosphorylation. Phosphorylation of MAPK in cumulus cells peaked after 21 h of incubation, whereas MAPK was almost completely dephosphorylated at the end of incubation (45 h). During subsequent incubation in the absence of added gonadotrophins, between 5 and 10 h exposure to FSH/LH-supplemented medium was required to induce resumption of meiosis in COCs. Phosphorylation of MAPK in oocytes was prevented by the MEK inhibitor U0126, but the inhibitor reduced phosphorylation of MAPK in cumulus cells only during the first 2 h of IVM. The data support the hypothesis that two different MAPK phosphorylation events occurred following gonadotrophin stimulation, one in cumulus cells and the other in oocytes. In cumulus cells, FSH/LH induced early and rapid U0126-insensitive phosphorylation of MAPK, whereas U0126-susceptible MAPK phosphorylation took place in the oocyte itself around the time of GVBD.

Type
Research Articles
Copyright
Copyright © Cambridge University Press 2007

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References

Ainsworth, L., Tsang, B.K., Downey, B.R., Marcus, G.J. & Armstrong, D.T. (1980). Interrelationships between follicular fluid steroid levels, gonadotropic stimuli, and oocyte maturation during preovulatory development of porcine follicles. Biol. Reprod. 23, 621–7.CrossRefGoogle ScholarPubMed
Black, J.L. & Erickson, B.H. (1968). Oogenesis and ovarian development in the prenatal pig. Anat. Rec. 161, 4556.CrossRefGoogle ScholarPubMed
Cameron, M.R., Foster, J.S., Bukovsky, A. & Wimalasena, J. (1996). Activation of mitogen-activated protein kinases by gonadotrophins and cyclic adenosine 5′-monophosphates in porcine granulosa cells. Biol. Reprod. 55, 111–9.CrossRefGoogle Scholar
Campbell, J.S., Seger, R., Graves, J.D., Graves, L.M., Jensen, A.M. & Krebs, E.G. (1995). The MAP kinase cascade. Recent Prog. Horm. Res. 50, 131–59.Google ScholarPubMed
Colledge, W.H., Carlton, M.B.L., Udy, G.B. & Evans, M.J. (1994). Disruption of c-mos causes parthenogenetic development of unfertilized mouse eggs. Nature 370, 65–7.CrossRefGoogle ScholarPubMed
Dedieu, T., Gall, L., Crozet, N., Sevellec, C. & Ruffini, S. (1996). Mitogen-activated protein kinase activity during goat oocyte maturation and the acquisition of meiotic competence. Mol. Reprod. Dev. 45, 351–8.3.0.CO;2-1>CrossRefGoogle ScholarPubMed
Edwards, R.G. (1965). Maturation in vitro of mouse, sheep, cow, pig, rhesus monkey and human ovarian oocytes. Nature 208, 349–51.CrossRefGoogle ScholarPubMed
Fan, H.Y. & Sun, Q.Y. (2004). Involvement of MAPK cascade during oocyte maturation and fertilization in mammals. Biol. Reprod. 70, 535–47.CrossRefGoogle ScholarPubMed
Fan, H.Y., Tong, C., Lian, L., Li, S.W., Gao, W.X., Cheng, Y., Chen, D.Y., Schatten, H. & Sun, Q.Y. (2003). Characterization of ribosomal S6 protein kinase p90rsk during meiotic maturation and fertilization in pig oocytes: mitogen-activated protein kinase-associated activation and localization. Biol. Reprod. 68, 968–77.CrossRefGoogle ScholarPubMed
Favata, M.F., Horiuchi, K.Y., Manos, E.J., Daulerio, A.J., Stradley, D.A., Feeser, W.S., Van Dyk, D.E., Pitts, W.J., Earl, R.A., Hobbs, F., Copeland, R.A., Magola, R.L., Scherle, P.A. & Trzaskos, J.M. (1998). Identification of a novel inhibitor of mitogen-activated protein kinase kinase. J. Biol. Chem. 273, 18623–32.CrossRefGoogle ScholarPubMed
Fissore, R.A., He, C.L. & Van de Woude, G.F. (1996). Potential role of mitogen-activated protein kinase during meiosis resumption in bovine oocytes. Biol. Reprod. 55, 1261–70.CrossRefGoogle ScholarPubMed
Fulka, J. Jr., Motlik, J., Fulka, J. & Jilek, F. (1986). Effect of cycloheximide on nuclear maturation of pig and mouse oocytes. J. Reprod. Fertil. 77, 281–5.CrossRefGoogle ScholarPubMed
Gotoh, Y., Nishida, E., Matsuda, S., Shina, X., Kosaka, H., Shiokawa, K., Akiyama, T., Ohta, K. & Sakai, H. (1991). In vitro effects on microtubule dynamics of purified Xenopus M phase-activated MAP kinase. Nature 349, 251–4.CrossRefGoogle ScholarPubMed
Goudet, G., Belin, F., Bézard, J. & Gérad, N. (1998). Maturation-promoting factor (MPF) and mitogen-activated protein kinase (MAPK) expression in relation to oocyte competence for in vitro maturation in the mare. Mol. Hum. Reprod. 4, 563–70.CrossRefGoogle ScholarPubMed
Hashimoto, N., Watanabe, N., Furuta, Y., Tamemoto, H., Sagata, N., Yokoyama, M., Okazaki, K., Nagayoshi, M., Takeda, N. & Ikawa, Y. (1994). Parthenogenetic activation of oocytes in c-mos-deficient mice. Nature 370, 6871.CrossRefGoogle ScholarPubMed
Inoue, M., Naito, K., Aoki, F., Toyoda, Y. & Sato, E. (1995). Activation of mitogen-activated protein kinase during meiotic maturation in porcine oocytes. Zygote 3, 265–71.CrossRefGoogle ScholarPubMed
Inoue, M., Naito, K., Nakayama, T. & Sato, E. (1998). Mitogen-activated protein kinase translocates into the germinal vesicle and induces germinal vesicle breakdown in porcine oocytes. Biol. Reprod 58, 130–6.CrossRefGoogle ScholarPubMed
Kagii, H., Naito, K., Sugiura, K., Iwamori, N., Ohashi, S., Goto, S., Yamanouchi, K. & Tojo, H. (2000). Requirement of mitogen-activated protein kinase activation for the meiotic resumption of porcine oocytes. J. Reprod. Develop. 46, 249–56.CrossRefGoogle Scholar
Kanayama, N, Miyano, T, & Lee, J. (2002) Acquisition of meiotic competence in growing pig oocytes correlates with their ability to activate Cdc2 kinase and MAP kinase. Zygote 10, 261–70.CrossRefGoogle ScholarPubMed
Lämmli, U.K. (1970). Cleavage of structural proteins during the assembly of the head of bacteriophage T4. Nature 227, 680–5.CrossRefGoogle Scholar
Liang, C.G., Li-Jun, H., Zhong, Z.S., Chen, D.Y., Schatten, H. & Sun, Q.Y. (2005). cAMP-dependent activation of MAPK in cumulus cells is essential for germinal vesicle breakdown of porcine cumulus-enclosed oocytes. Endocrinology 146, 4437–44.CrossRefGoogle Scholar
Mattioli, M., Galeati, G., Bacci, M.L. & Barboni, B. (1991). Changes in maturation-promoting activity in the cytoplasm of pig oocytes throughout maturation. Mol. Reprod. Dev. 30, 119–25.CrossRefGoogle ScholarPubMed
Mauléon, P.T. & Mariana, J.C. (1977). Oogenesis and folliculogenesis. In Reproduction in Domestic Animals, 3rd edn (eds Cole, H.H. & Cupps, P.T.), pp. 175202. New York, San Francisco, London: Academic Press.Google Scholar
Meinecke, B. & Krischek, C. (2003). MAPK/ERK kinase (MEK) signalling is required for resumption of meiosis in cultured cumulus-enclosed pig oocytes. Zygote 11, 716.CrossRefGoogle ScholarPubMed
Motlik, J. & Fulka, J. (1976). Breakdown of the germinal vesicle in pig oocytes in vivo and in vitro. J. Exp. Zool. 198, 155–62.CrossRefGoogle ScholarPubMed
Motlik, J., Nagai, T. & Kikuchi, K. (1991). Resumption of meiosis in pig oocytes cultured with cumulus and parietal granulosa cells: the effect of protein synthesis inhibition. J Exp Zool. 259, 386–91.CrossRefGoogle ScholarPubMed
Motlik, J., Pavlok, A., Kubelka, M., Kalous, J. & Kalab, P. (1998). Interplay between CDC2 kinase and MAP kinase pathway during maturation of mammalian oocytes. Theriogenology 49, 461–9.CrossRefGoogle ScholarPubMed
Ohashi, S., Naito, K., Sugiura, K., Iwamori, N., Goto, S., Naruoka, H. & Tojo, H. (2003). Analyses of mitogen-activated protein kinase function in the maturation of porcine oocytes. Biol. Reprod. 68, 604–9.CrossRefGoogle ScholarPubMed
Shimada, M., Maeda, T. & Terada, T. (2001). Dynamic changes of connexin-43, gap junctional protein, in outer layers of cumulus cells are regulated by PKC and PI3-kinase during meiotic resumption in porcine oocytes. Biol. Reprod. 64, 1255–63.CrossRefGoogle ScholarPubMed
Sobajima, T., Aoki, F. & Kohmoto, K. (1993). Activation of mitogen-activated protein kinase during meiotic maturation in mouse oocytes. J. Reprod. Fertil. 97, 389–94.CrossRefGoogle ScholarPubMed
Su, Y.Q., Denegre, J.M., Wigglesworth, K., Pendola, F.L., O'Brien, M.J. & Eppig, J.J. (2003). 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. 263, 126–38.CrossRefGoogle ScholarPubMed
Su, Y.Q., Rubinstein, S., Luria, A., Lax, Y. & Breitbart, H. (2001). Involvement of MEK–mitogen-activated protein kinase pathway in follicle-stimulating hormone-induced but not spontaneous meiotic resumption of mouse oocytes. Biol. Reprod. 65, 358–65.CrossRefGoogle Scholar
Su, Y.Q., Wigglesworth, K., Pendola, F.L., O'Brien, M.J. & Eppig, J.J. (2002). Mitogen-activated protein kinase activity in cumulus cells is essential for gonadotrophin-induced oocyte meiotic resumption and cumulus expansion in the mouse. Endocrinology 143, 2221–32.CrossRefGoogle Scholar
Sun, Q.Y., Breitbart, H. & Schatten, H. (1999a). Role of the MAPK cascade in mammalian germ cells. Reprod. Fertil. Dev. 11, 443–50.CrossRefGoogle ScholarPubMed
Sun, Q.Y., Blumenfeld, Z., Rubinstein, S., Goldman, S., Gonen, Y. & Breitbart, H. (1999b). Mitogen-activated protein kinase in human eggs. Zygote 7, 181–5.CrossRefGoogle ScholarPubMed
Tong, C., Fan, H.Y., Chen, D.Y., Song, X.F., Schatten, H. & Sun, Q.Y. (2003). Effects of MEK inhibitor U0126 on meiotic progression in mouse oocytes: microtubule organization, asymmetric division and metaphase II arrest. Cell Res. 13, 375–85.CrossRefGoogle ScholarPubMed
Verlhac, M.H., Pennart, H.D., Maro, B., Cobb, M.H. & Clarke, H.J. (1993). MAP kinase becomes stably activated at metaphase and is associated with microtubule-organizing centers during meiotic maturation of mouse oocytes. Dev. Biol. 158, 330–40.CrossRefGoogle ScholarPubMed
Wehrend, A. & Meinecke, B. (2001). Kinetics of meiotic progression, M-phase promoting factor (MPF) and mitogen-activated protein kinase (MAP kinase) activities during in vitro maturation of porcine and bovine oocytes: species specific differences in the length of the meiotic stages. Anim. Reprod. Sci. 66, 175–84.CrossRefGoogle ScholarPubMed
Ye, J., Flint, A.P., Luck, M.R. & Campbell, K.H. (2003). Independent activation of MAP kinase and MPF during the initiation of meiotic maturation in pig oocytes. Reproduction 125, 645–56.CrossRefGoogle ScholarPubMed
Zernicka-Goetz, M., Verlhac, M-H., Géraud, G. & Kubiak, J.Z. (1997). Protein phosphatases control MAP kinase activation and microtubule organization during rat oocyte maturation. Eur. J. Cell Biol. 72, 30–8.Google ScholarPubMed