[en] Activin was originally isolated from follicular fluid as a factor stimulating FSH from the pituitary. Recent studies also suggest a local role for activin in the development of preantral and early antral follicles. In the present study, activin and activin receptor immunoreactivity are shown in oocyte and granulosa cells of bovine preantal follicles. In addition, activin immunoreactivity was observed in the theca of secondary follicles. In addition, activin preantral follicles, activin increased follicular growth and granulosa cell proliferation in a dose-dependent manner. This increase was further stimulated by addition of FSH. In conclusion, activin and its receptor are present on bovine follicles, and additional activin stimulates development of those follicles.
Disciplines :
Veterinary medicine & animal health
Author, co-author :
Hulshof, S. C. J.; University of Utrecht - Netherlands > Dept of Functional Morphology Heard Health and Reproduction
Figueiredo, J. R.; Université de Liège - ULiège - ULG > Dept of animal endocrinology
Beckers, Jean-François ; Université de Liège - ULiège > Département de sciences fonctionnelles > Physiologie de la reproduction
Bevers, M. M.; University of Utrecht - Netherlands > Dept of Functional Morphology Herd Health and Reproduction
Vanderstichele, H.; Inogenetics - Ghent Belgium
Language :
English
Title :
Bovine preantral follicles and activin: immunohistochemistry for activin and activin receptor and the effect of bovine activin A in vitro
Adashi EY. The intraovarian insulin-like growth factor system. In: Adashi EY and Leung PCK (eds), The Ovary. New York, Raven Press: 1993;319-337.
De Jong FH. Inhibin. Phys Rev 1988; 68:555-607.
De Winter JP. Activins and activin receptors in the rat testis. Ph.D. dissertation, Erasmus University, Rotterdam, The Netherlands, 1994.
De Winter JP, Vanderstichele HMJ, Verhoeven G, Timmerman MA, Wesseling JG, de Jong FH. Peritubular myoid cells from immature rat testis secrete activin-A and express activin receptor type II in vitro. Endocrinology 1994; 135:759-767.
Dieleman SJ, Kruip TAM, Fontijne P, De Jong WHR, Van der Weyden GC. Changes in oestradiol, progesteron and testosterone concentration in follicular fluid and in the micromorphology of preovulatory bovine follicles relative to the peak of luteinizing hormone. J Endocrinol 1983; 97:31-42.
Findlay JK, Xiao S, Shukovski L, Michel U. Novel peptides in ovarian physiology: inhibin, activin, and follistatin. In: Adashi EY, Leung PCK (eds), The Ovary. New York, Raven Press: 1993;413-433.
Figueiredo JR, Hulshof SCJ, Van den Hurk R, Ectors FJ, Fontes RJ, Nusgens B, Bevers MM, Beckers JF. Development of a new mechanical and enzymatic method for the isolation of intact preantral follicles from fetal, calf and adult bovine ovaries. Theriogenology 1993; 40:789-799.
Figueiredo JR, Hulshof SCJ, Van den Hurk R, Nusgens B, Bevers MM, Ectors FJ, Beckers JF. Preservation of oocyte and granulosa cell morphology in bovine preantral follicles cultured in vitro. Theriogenology 1994; 41:1333-1346.
Greenwald GS, Roy SK. Follicular development and its control. In: Knobil E, Neill JD (eds), Physiology of Reproduction. New York: Raven Press, 1994;629-725.
Hillier SG, Yong EL, Illingworth PJ, Baird DT, Schwall RH, Mason AJ. Effect of recombinant activin on androgen synthesis in cultured human thecal cells. J Clin Endocrinol Metab 1991;72:1206-1211.
Hulshof SCJ, Figueiredo JR, Beckers JF, Bevers MM, Van der Donk HA, Van den Hurk. Effects of fetal bovine serum, FSH and 17ß-estradiol on the culture of bovine preantral follicles. Theriogenology 1995; 44:217-226.
Hopko-Ireland JL, Ireland JJ. Changes in expression of inhibin/activin α, ßA and ßB-subunit messenger ribonucleic acids following increases in size and during different stages of differentiation or atresia of non-ovulatory follicles in cows. Biol Reprod 1994; 50: 492-501.
Hsueh AJW, Dahl KD, Vaughan J, Tucker E, Rivier J, Bardin CW, Vale W. Heterodimers and homodimers of inhibin subunits have different paracrine action in the modulation of luteinizing hormone-stimulated androgen biosynthesis. Proc Natl Acad Sci USA 1987; 84:5082-5086.
Hutchinson LA, Findlay JK, de Vos FL, Robertson DM. Effect of bovine inhibin, transforming growth factor-ß and bovine activin-A on granulosa cell differentiation. Biochem Biophys Res Commun 1987; 146:1405-1412.
Koika E, Adashi EY. Potential roles of cytokines in ovarian physiology: the case for interleukin-1. In: Adashi EY, Leung PCK (eds), The Ovary. New York, Raven Press: 1993;383-395.
LaPolt PS, Soto D, Su JG, Campen CA, Vaughan J, Vale W, Hsueh AJW. Activin stimulation of inhibin secretion and messenger RNA levels in cultured granulosa cells. Mol Endocrinol 1989; 3:1666-1673.
Li R, Phillips DM, Mather P. Activin promotes ovarian follicle development in vitro. Endocrinology 1995; 136:849-856.
Ling N, Ying S-Y, Ueno N, Shimasaki S, Esch F, Hotta M, Guillemin R. Pituitary FSH is released by a heterodimer of the ß-subunits from the two forms of inhibin. Nature 1986; 321:779-782.
Mathews LS, Vale W. Expression cloning of an activin receptor, a predicted transmembrane serine kinase. Cell 1991; 65:973-982.
Meunier H, Cajandar SB, Roberts VJ, Rivier C, Sawchenko PE, Hsueh AJW, Vale W. Rapid changes in the expression of inhibin α-, ßA-, and ßB-subunits in ovarian cell types during the rat estrous cycle. Mol Endocrinol 1988; 2:1352-1363.
Mulheron GW, Schomberg DW. The intraovarian transforming growth factor system. In: Adashi EY, Leung PCK (eds), The Ovary. New York, Raven Press: 1993;337-363.
Nakamura M, Sugino K, Kurosawa N, Sawai M, Takio K, Eto Y, Iwashita S, Muramatsu M Tikani K, Sugino H. Isolation and characterization of activin receptor from mouse embryonal carcinoma cells. J Biol Chem 1992; 267:18924-18928.
Rabinovici J, Spencer SJ, Doldi N, Goldsmith PC, Schwall R, Jaffe RB. Activin-A as an intraovarian modulator: actions, localization, and regulation of the intact dimer in human ovarian cells. J Clin Invest 1992; 89:1528-1536.
Roberts VJ, Barth S, El-Roeiy A, Yen SSC. Expression of inhibin/activin subunits and follistatin messenger ribonucleic acids and proteins in ovarian follicles and the corpus luteum during the human menstrual cycle. J Clin Endocrinol Metab 1993; 77:1402-1410.
Roy SK. Epidermal growth factor and transforming growth factor-ß modulation of follicle-stimulating hormone-induced deoxyribonucleic acid synthesis in hamster preantral and early antral follicles. Biol Reprod 1993; 48:552-557.
Roy SK. Transforming growth factor-ß potentiation of follicle-stimulating hormone-induced deoxyribonucleic acid synthesis in hamster preantral follicles is mediated by a latent induction of epidermal growth factor. Biol Reprod 1993; 48:558-563.
Schwall RH, Mason AJ, Wilcox JN, Bassett SG, Zeleznik AJ. Localization of inhibin/activin subunit mRNAs within the primate ovary. Mol Endocrinol 1990; 4:75-79.
Sugino H, Nakamura T, Hasegawa Y, Miyamoto K, Igarashi M, Eto Y, Shibai H,Tikani K. Identification of a specific receptor for erythroid differentiation factor on follicular granulosa cell. J Biol Chem 1988; 263:15249-15252.
Torney AH, Hodgson YM, Forage R, de Kretser. Cellular localization of inhibin mRNA in the bovine ovary by in-situ hybridisation. J Reprod Fertil 1989; 86:391-399.
Vale W, Rivier J, Vaughan J, McClintock RM, Corrigan A, Woo W, Karr D, Spiess J. Purification and characterization of an FSH releasing protein from porcine follicular fluid. Nature 1986; 321:776-779.
Van der Beek EM, Pool CW, Van Eerdenburg FJCM, Sluiter AA, Van der Donk HA, Van den Hurk R, Wiegant VM. Fc-mediated nonspecific staining of the porcine brain with rabbit antisera in immunocytochemistry is prevented by pre-incubation of the sera with proteins A and G. J Histochem Cytochem 1992; 41:1731-1739.
Van den Hurk R, Dijkstra G. An immunohistochemical study of bovine antral follicles, with special attention to non-atretic follicles with and without atypical granulosa cells. Vet Quart 1992; 14:148-151.
Vanderstichele H, Delaey B, de Winter J, de Jong FH, Rombauts L, Verhoeven G, Dello C, Van de Voorde A, Briers T. Secretion of steroids, growth factors and cytokines by immortalized mouse granulosa cell lines. Biol Reprod 1994; 50:1190-1202.
Verschueren K, Dewulf N, Goumans M-J, Lonnoy O, Feijen A, Grimsby S, VandeSpiegle K, ten Dijke P, Moren A, Vanscheeuwijck P, Heldin C-H, Miyazono K, Mummery C, Van Den Eijnden-Van Raaij J, Huylebroeck D. Expression of type I and type IB receptors for activin in midgestation mouse embryos suggests distinct functions in organogenesis. Mech Dev 1995; 52:109-123.
Woodruff TK, D'Agostino J, Schwartz NB, Mayo KE. Dynamic changes in inhibin messenger RNAs in rat ovarian follicles during the reproductive cycle. Science 1988; 239:1296-1299.
Woodruff TK, Lyon RJ, Hansen SE, Rice GC, Mather JP. Inhibin and activin locally regulate rat ovarian folliculogenesis. Endocrinology 1990; 127:3196-3205.
Xiao S, Findlay JK. Interactions between activin and follicle-stimulating hormone-suppressing protein and their mechanisms of action on cultured rat granulosa cells. Mol Cell Endocrinol 1991; 79:99-107.
Xiao S, Findlay JK, Robertson DM. The effect of bovine activin and follicle-stimulating hormone (FSH) suppressing protein/follistatin on FSH induced differentiation of rat granulosa cells in vitro. Mol Cell Endocrinol 1990; 69:1-8.
Xiao S, Robertson DM, Findlay JK. Effects of activin and FSH-suppressing protein/follistatin on FSH receptors and differentiation of cultured rat granulosa cells. Endocrinology 1992; 131:1009-1016.
Yamoto M, Minami S, Nakano R, Kobayashi M. Immunohistochemical localization of inhibin/activin subunits in human ovarian follicles during the menstrual cycle. J Clin Endocrinol Metab 1992; 77:1402-1410.
Yamashita H, ten Dijke P, Huylebroeck D, Sampath TK, Andries M, Smith JC, Heldin C-H, Miyazono K. Osteogenic protein-1 binds to activin type II receptors and induces certain activin-like effects. J Cell Biol 1995; 130:217-226.