Abstract
Luteinizing hormone- (LH)-dependent ovarian follicle maturation has been recently described in two stages for teleost fishes. The oocyte's ability to respond to the steroidal maturation-inducing hormone (MIH), also known as oocyte maturational competence (OMC), is acquired during the first stage+ADs- whereas the MIH-dependent resumption of meiosis occurs during the second stage. However, studies directly addressing OMC have been performed with a limited number of species and therefore the general relevance of the two-stage model and its mechanisms remain uncertain. In this study, we examined the hormonal regulation of OMC and its basic transduction mechanisms in ovarian follicles of the sciaenid teleost, Nibe (Nibea mitsukurii). Exposure to MIH +AFs-17,20+ACY-bgr+ADs--dihydroxy-4-pregnen-3-one or 17,20+ACY-bgr+ADs-,21-trihydroxy-4-pregnen-3-one] stimulated germinal vesicle breakdown (index of meiotic resumption) in full-grown follicles primed with human chorionic gonadotropin (HCG, an LH-like gonadotropin) but not in those pre-cultured in plain incubation medium. The induction of OMC by HCG was mimicked by protein kinase A (PKA) activators (forskolin and dibutyryl cyclic AMP), and blocked by specific inhibitors of PKA (H89 and H8) as well as inhibitors of RNA (actinomycin D) and protein (cycloheximide) synthesis. Forskolin-induced OMC was also inhibited by actinomycin D and cycloheximide. A strong activator of protein kinase C, PMA, inhibited HCG-dependent OMC. In conclusion, OMC in Nibe ovarian follicles is gonadotropin-dependent and requires activation of the PKA pathway followed by gene transcription and translation events. These observations are consistent with the two-stage model of ovarian follicle maturation proposed for other teleosts, and suggest that Nibe can be used as new model species for mechanistic studies of ovarian follicle differentiation and maturation in fishes.
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REFERENCES
CerdĆ”, J.L., Petrino, T.R. and Wallace, R.A. 1993. Functional heterologous gap junctions in Fundulus ovarian follicles maintain meiotic arrest and permit hydration during oocyte maturation. Dev. Biol. 160: 228ā235.
Chang, X., PatiƱo, R., Thomas, P. and Yoshizaki, G. 1999. Developmental and protein kinase-dependent regulation of ovarian connexin mRNA and oocyte maturational competence in Atlantic croaker. Gen. Comp. Endocrinol. 114: 330ā339.
Haus-Seuffert, P. and Meisterernst, M. 2000. Mechanisms of transcriptional activation of cAMP-responsive element-binding protein CREB. Mol. Cell. Biochem. 212: 5ā9.
Ishikawa, H. 1977. Ecology of Nibe in Ibaraki prefecture-1, reproduction. Report of Ibaraki Prefectural Fish. Res. Institute 21: 43ā51.
Jalabert, B. and Fostier, A. 1984. The follicular sensitivity in vitro to maturation-inducing hormones in rainbow trout, Salmo gairdneri: role of oestradial-17β. Aquaculture 43: 1ā11.
Kagawa, H., Tanaka, H., Okuzawa, Y. and Hirose, K. 1994. Development of maturational competence of oocytes of red seabream, Pagrus major, after human chorionic gonadotropin treatment requires RNA and protein synthesis. Gen. Comp. Endocrinol. 94: 199ā206.
Nagahama, Y. 1987. Gonadotropin action on gametogenesis and steroidogenesis in teleost gonads. Zool. Sci. 4: 209ā222.
Nagahama, Y. 1997. 17β,20β-dihydroxy-4-pregnen-3-one, a maturation-inducing hormone in fish oocytes: mechanisms of synthesis and action. Steroids 62: 190ā196.
Nagahama, Y., Kagawa, H. and Tashiro, F. 1980. The in vitro effects of various gonadotropins and steroid hormones on oocyte maturation in amago salmon Oncorhynchus rhodurus and rainbow trout Salmo gairdneri. Bull. Japan. Soc. Sci. Fish. 46: 1097ā1102.
PatiƱo, R., Chang, X., Yoshizaki, G., Thomas, P. and Kagawa, H. 2000. Role and regulation of gap junctions during oocyte maturation in teleosts. In: Proceedings of the Sixth International Symposium on the Reproductive Physiology of Fish. Pp. 292ā294. Edited by Norberg, B., Kjesbu, O.S., Taranger, G.L., Andersson, E. and Stefansson, S.O. Bergen: Institute of Marine Research and University of Bergen, Norway.
PatiƱo, R. and Thomas, P. 1990a. Effects of gonadotropin on ovarian intrafollicular processes during the development of oocyte maturational competence in a teleost, the Atlantic croaker: evidence for two distinct stages of gonadotropic control of final oocyte maturation. Biol. Reprod. 43: 818ā827.
PatiƱo, R. and Thomas, P. 1990b. Characterization of membrane receptor activity for 17β,20β,21-trihydroxy-4-pregnen-3-one in ovaries of spotted seatrout (Cynoscion nebulosus). Gen. Comp. Endocrinol. 78: 204ā217.
PatiƱo, R., Yoshizaki, G., Thomas, P. and Kagawa, H. 2001. Gonadotropic control of ovarian follicle maturation: the two-stage concept and its mechanisms. Comp. Biochem. Physiol. B, 129: 427ā439.
Steel, R.G.D. and Torrie, J. H. 1980. Principles and procedures of statistics. A biometrical approach. Second edition. pp. 633, McGraw-Hill, New York.
Thomas, P., Pinter, J. and Das, S. 2001. Upregulation of the maturation-inducing steroid membrane receptor in spotted seatrout ovaries by gonadotropin during maturation and its physiological significance. Biol. Reprod. 64: 21ā29.
Thomas, P. and PatiƱo, R. 1991. Changes in 17β,20β,21-trihydroxy-4-pregnen-3-one membrane receptor in ovaries of spotted seatrout during final oocyte maturation. In: Proceedings of the Fourth International Symposium of the Reproductive Biology of Fish. pp. 122ā124. Edited by Scott, A.P., Sumpter, J.P., Kime, D.E. and Rolfe, M.S. Sheffield: FishSymp 91, United Kingdom.
Van Der Kraak, G. 1992. Mechanisms by which calcium ionophore and phorbol ester modulate steroid production by goldfish preovulatory ovarian follicles. J. Exp. Zool. 262: 271ā278.
York, W.S., PatiƱo, R. and Thomas, P. 1993. Ultrastructural change in follicle cell-oocyte associations during development and maturation of the ovarian follicle in Atlantic croaker. Gen. Comp. Endocrinol. 92: 402ā418.
Yoshizaki, G., PatiƱo, R. and Thomas, P. 1994. Connexin messenger ribonucleic acids in the ovary of Atlantic croaker: molecular cloning and characterization, hormonal control, and correlation with appearance of oocyte maturational competence. Biol. Reprod. 51: 493ā503.
Yoshizaki, G., PatiƱo, R., Thomas, P., Bolamba, D. and Chang, X. 2001. Effects of maturation-inducing hormone and phorbol ester on heterologous gap junctional communication in Atlantic croaker. Gen. Comp. Endocrinol. 124: 359ā366.
Yoshizaki, G., Wei, J., PatiƱo, R., Thomas, P. and Janecek, L. 2000. Structural organization of the Atlantic croaker connexin 32.2 gene and its 5' flanking region. Mar. Biotechnol. 2: 154ā160.
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Yoshizaki, G., Shusa, M., Takeuchi, T. et al. Gonadotropin-dependent oocyte maturational competence requires activation of the protein kinase A pathway and synthesis of RNA and protein in ovarian follicles of Nibe, Nibea mitsukurii (Teleostei, Sciaenidae). Fish Physiology and Biochemistry 25, 201ā208 (2001). https://doi.org/10.1023/A:1022209710224
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DOI: https://doi.org/10.1023/A:1022209710224
- fish
- gonadotropin
- maturation
- ovarian follicle
- protein
- protein kinase A
- protein kinase C
- RNA
- steroid