Skip to main content

Advertisement

Log in

Development of an in vitro system for functional studies of ovarian follicular cells in European sea bass (Dicentrarchus labrax)

  • Original Research
  • Published:
Cytotechnology Aims and scope Submit manuscript

Abstract

The layers of follicular cells surrounding the oocyte and the interactions among them and the germ cells are critical for the successful maintenance of the ovarian functions. We have set up the isolation procedure and culture conditions of sea bass ovarian follicular cells. Their behaviour at three different physiological temperatures (25, 18 and 15 °C) was evaluated by verifying their steroidogenic capacity along time together with the expression of follicular specific genes (cyp19a1, fshr, lhr and star). These characteristics revealed this culture as a good in vitro alternative to short term in vivo studies at the level of the ovarian follicle. Moreover, to evaluate the suitability of this system for gene function studies conditions for transient transfection of plasmid DNA were optimized. Finally, the characteristics of the follicular culture were not affected by freezing and thawing cycles what facilitates the performance of experiments independently of the reproductive season. In conclusion, we have developed an in vitro homologous system that enables functional and gene expression studies and resembles the in vivo situation in the ovarian follicle.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Fig. 1
Fig. 2
Fig. 3
Fig. 4
Fig. 5

Similar content being viewed by others

References

  • Ahne W (1979) Fish cell culture: a fibroblastic line (PG) from ovaries of juvenile pike (Esox lucius). In Vitro 15:839–840. doi:10.1007/BF02618036

    Article  Google Scholar 

  • Alvariño JMR, Carrillo M, Zanuy S, Prat F, Mañanós E (1992) Pattern of sea bass oocyte development after ovarian stimulation by LHRHa. J Fish Biol 41:965–970. doi:10.1111/j.1095-8649.1992.tb02723.x

    Article  Google Scholar 

  • Anderson E, Little B, Lee GS (1987) Androgen-induced changes in rat ovarian granulosa cells in vitro. Tissue Cell 19:217–234. doi:10.1016/0040-8166(87)90007-3

    Article  CAS  Google Scholar 

  • Andersson E, Nijenhuis W, Male R, Swanson P, Bogerd J, Taranger GL, Schulz RW (2009) Pharmacological characterization, localization and quantification of expression of gonadotropin receptors in Atlantic salmon (Salmo salar L.) ovaries. Gen Comp Endocrinol 163:329–339. doi:10.1016/j.ygcen.2009.05.001

    Article  CAS  Google Scholar 

  • Asturiano JF, Sorbera LA, Ramos J, Kime DE, Carrillo M, Zanuy S (2000) Hormonal regulation of the European sea bass reproductive cycle: an individualized female approach. J Fish Biol 56:1155–1172. doi:10.1111/j.1095-8649.2000.tb02131.x

    Article  CAS  Google Scholar 

  • Benninghoff AD, Thomas P (2006) Gonadotropin regulation of testosterone production by primary cultured theca and granulosa cells of Atlantic croaker: I. Novel role of CaMKs and interactions between calcium- and adenylyl cyclase-dependent pathways. Gen Comp Endocrinol 147:276–287. doi:10.1016/j.ygcen.2006.01.014

    Article  CAS  Google Scholar 

  • Bowser PR, Plumb JA (1980) Fish cell lines: establishment of a line from ovaries of channel catfish. In Vitro 16:365–368. doi:10.1007/BF02618357

    Article  CAS  Google Scholar 

  • Camp TA, Rahal JO, Mayo KE (1991) Cellular localization and hormonal regulation of follicle-stimulating hormone and luteinizing hormone receptor messenger RNAs in the rat ovary. Mol Endocrinol 5:1405–1417. doi:10.1210/mend-5-10-1405

    Article  CAS  Google Scholar 

  • Carlone DL, Richards JS (1997) Functional interactions, phosphorylation, and levels of 3′,5′-cyclic adenosine monophosphate-regulatory element binding protein and steroidogenic factor-1 mediate hormone-regulated and constitutive expression of aromatase in gonadal cells. Mol Endocrinol 11:292–304. doi:10.1210/me.11.3.292

    Article  CAS  Google Scholar 

  • Carrillo M, Zanuy S, Prat F, Cerdá J, Ramos J, Mañanós E, Bromage N (1995) Sea Bass (Dicentrarchus labrax). In: Bromage N, Roberts R (eds) Broodstock management and egg and larval quality. Black Science, Oxford, pp 138–168

    Google Scholar 

  • Chen S, Kou G (1988) Establishment, characterization and application of 14 cell lines from warm-water fish. In: Kuroda Y, Kurstak E, Maramorosch K (eds) Invertebrate and fish tissue culture. Tokyo: Japan Sci Soc, pp 218–277

  • Chen C, Okayama H (1987) High-efficiency transformation of mammalian cells by plasmid DNA. Mol Cell Biol 7:2745–2752

    CAS  Google Scholar 

  • Chen SN, Chi SC, Ueno Y, Kou GH (1983) A cell line derived from tilapia ovary. Fish Pathol 18:13–18

    Article  Google Scholar 

  • Crisponi L, Deiana M, Loi A, Chiappe F, Uda M, Amati P, Bisceglia L, Zelante L, Nagaraja R, Porcu S, Ristaldi MS, Marzella R, Rocchi M, Nicolino M, Lienhardt-Roussie A, Nivelon A, Verloes A, Schlessinger D, Gasparini P, Bonneau D, Cao A, Pilia G (2001) The putative forkhead transcription factor FOXL2 is mutated in blepharophimosis/ptosis/epicanthus inversus syndrome. Nat Genet 27:159–166. doi:10.1038/84781

    Article  CAS  Google Scholar 

  • Dressing GE, Pang Y, Dong J, Thomas P (2010) Progestin signaling through mPRalpha in Atlantic croaker granulosa/theca cell cocultures and its involvement in progestin inhibition of apoptosis. Endocrinology 151:5916–5926. doi:10.1210/en.2010-0165

    Article  CAS  Google Scholar 

  • Epler P, Galas J, Stoklosowa S (1997) Steroidogenic activity of carp ovarian follicular and interstitial cells at the pre-spawning and resting time: a tissue culture approach. Comp Biochem Physiol C: Pharmacol Toxicol Endocrinol 116:167–170. doi:10.1016/S0742-8413(96)00149-1

    Article  Google Scholar 

  • Fernandez RD, Yoshimizu M, Kimura T, Ezura Y, Inouye K, Takami I (1993) Characterization of three continuous cell lines from marine fish. J Aquat Anim Health 5:127–136

    Article  Google Scholar 

  • Fryer JL, Lannan CN (1994) Three decades of fish cell culture: a current listing of cell lines derived from fishes. Methods Cell Sci 16:87–94. doi:10.1007/BF01404816

    Google Scholar 

  • Galas J, Epler P, Stoklosowa S (1999) Seasonal response of carp (Cyprinus carpio) ovarian cells to stimulation by various hormones as measured by steroid secretion: tissue culture approach. Endocr Regu 33:125–132

    CAS  Google Scholar 

  • García-López A, Sánchez-Amaya MI, Tyler CR, Prat F (2011) Mechanisms of oocyte development in European sea bass (Dicentrarchus labrax L.): investigations via application of unilateral ovariectomy. Reproduction 142:243–253. doi:10.1530/REP-11-0040

    Article  Google Scholar 

  • Halm S, Martínez-Rodríguez G, Rodríguez L, Prat F, Mylonas CC, Carrillo M, Zanuy S (2004) Cloning, characterisation, and expression of three oestrogen receptors (ERalpha, ERbeta1 and ERbeta2) in the European sea bass, Dicentrarchus labrax. Mol Cell Endocrinol 223:63–75. doi:10.1016/j.mce.2004.05.009

    Article  CAS  Google Scholar 

  • Halm S, Rocha A, Miura T, Prat F, Zanuy S (2007) Anti-Mullerian hormone (AMH/AMH) in the European sea bass: its gene structure, regulatory elements, and the expression of alternatively-spliced isoforms. Gene 388:148–158. doi:10.1016/j.gene.2006.10.018

    Article  CAS  Google Scholar 

  • Havelock JC, Rainey WE, Carr BR (2004) Ovarian granulosa cell lines. Mol Cell Endocrinol 228:67–78. doi:10.1016/j.mce.2004.04.018

    Article  CAS  Google Scholar 

  • Hsu SY, Kubo M, Chun SY, Haluska FG, Housman DE, Hsueh AJ (1995) Wilms’ tumor protein WT1 as an ovarian transcription factor: decreases in expression during follicle development and repression of inhibin-alpha gene promoter. Mol Endocrinol 9:1356–1366. doi:10.1210/me.9.10.1356

    Article  CAS  Google Scholar 

  • Johnson AL, Langer JS, Bridgham JT (2002) Survivin as a cell cycle-related and antiapoptotic protein in granulosa cells. Endocrinology 143:3405–3413. doi:10.1210/en.2002-220107

    Article  CAS  Google Scholar 

  • Kananen K, Markkula M, Rainio E, Su JGJ, Hsueh AJW, Huhtaniemi IT (1995) Gonadal tumorigenesis in transgenic mice bearing the mouse inhibin alpha-subunit promoter simian-virus T-antigen fusion gene—characterization of ovarian-tumors and establishment of gonadotropin-responsive granulosa-cell lines. Mol Endocrinol 9:616–627. doi:10.1210/me.9.5.616

    Article  CAS  Google Scholar 

  • Kiriakidou M, McAllister JM, Sugawara T, Strauss JF III (1996) Expression of steroidogenic acute regulatory protein (StAR) in the human ovary. J Clin Endocrinol Metab 81:4122–4128. doi:10.1210/jc.81.11.4122

    Article  CAS  Google Scholar 

  • Kleppe L (2009) Quantification and localization of StAR expression in Atlantic cod ovaries. Dissertation, Universitetet i Bergen (UiB)

  • Kobayashi Y, Horiguchi R, Nozu R, Nakamura M (2010) Expression and localization of forkhead transcriptional factor 2 (Foxl2) in the gonads of protogynous wrasse, Halichoeres trimaculatus. Biol Sex Differ 1:3. doi:10.1186/2042-6410-1-3

    Article  CAS  Google Scholar 

  • Lakra WS, Swaminathan TR, Joy KP (2011) Development, characterization, conservation and storage of fish cell lines: a review. Fish Physiol Biochem 37:1–20. doi:10.1007/s10695-010-9411-x

    Article  CAS  Google Scholar 

  • Lannan C, Winton J, Fryer J (1984) Fish cell lines: establishment and characterization of nine cell lines from salmonids. In Vitro 20:671–676. doi:10.1007/bf02618871

    Article  CAS  Google Scholar 

  • Leung PC, Armstrong DT (1980) Interactions of steroids and gonadotropins in the control of steroidogenesis in the ovarian follicle. Annu Rev Physiol 42:71–82. doi:10.1146/annurev.ph.42.030180.000443

    Article  CAS  Google Scholar 

  • Lundgren E, Roos G (1978) Vacuolization in cultured cells induced by amphotericin B. Antimicrob Agents Chemother 14:267–269. doi:10.1128/AAC.14.2.267

    Article  CAS  Google Scholar 

  • Maestro MA, Planas JV, Moriyama S, Gutiérrez J, Planas J, Swanson P (1997) Ovarian receptors for insulin and insulin-like growth factor I (IGF-I) and effects of IGF-I on steroid production by isolated follicular layers of the preovulatory coho salmon ovarian follicle. Gen Comp Endocrinol 106:189–201. doi:10.1006/gcen.1996.6863

    Article  CAS  Google Scholar 

  • Manna PR, Dyson MT, Stocco DM (2009) Regulation of the steroidogenic acute regulatory protein gene expression: present and future perspectives. Mol Hum Reprod 15:321–333. doi:10.1093/molehr/gap025

    Article  CAS  Google Scholar 

  • Miwa S, Yan L, Swanson P (1994) Localization of two gonadotropin receptors in the salmon gonad by in vitro ligand autoradiography. Biol Reprod 50:629–642. doi:10.1095/biolreprod50.3.629

    Article  CAS  Google Scholar 

  • Molés G, Gómez A, Rocha A, Carrillo M, Zanuy S (2008) Purification and characterization of follicle-stimulating hormone from pituitary glands of sea bass (Dicentrarchus labrax). Gen Comp Endocrinol 158:68–76. doi:10.1016/j.ygcen.2008.05.005

    Article  Google Scholar 

  • Molés G, Zanuy S, Muñoz I, Crespo B, Martínez I, Mañanós E, Gómez A (2011) Receptor specificity and functional comparison of recombinant sea bass (Dicentrarchus labrax) gonadotropins (Fsh and Lh) produced in different host systems. Biol Reprod 84:1171–1181. doi:10.1095/biolreprod.110.086470

    Article  Google Scholar 

  • Montserrat N, González A, Méndez E, Piferrer F, Planas JV (2004) Effects of follicle stimulating hormone on estradiol-17 beta production and P-450 aromatase (CYP19) activity and mRNA expression in brown trout vitellogenic ovarian follicles in vitro. Gen Comp Endocrinol 137:123–131. doi:10.1016/j.ygcen.2004.02.011

    Article  CAS  Google Scholar 

  • Moon YS, Duleba AJ (1982) Comparative studies of androgen metabolism in theca and granulosa cells of human follicles in vitro. Steroids 39:419–430

    Article  CAS  Google Scholar 

  • Nagahama Y (1987) Gonadotropin action on gametogenesis and steroidogenesis in teleost gonads. Zool Sci 4:209–222

    CAS  Google Scholar 

  • Nakamoto M, Matsuda M, Wang DS, Nagahama Y, Shibata N (2006) Molecular cloning and analysis of gonadal expression of Foxl2 in the medaka, Oryzias latipes. Biochem Biophys Res Commun 344:353–361. doi:10.1016/j.bbrc.2006.03.137

    Article  CAS  Google Scholar 

  • Nakamura S, Kurokawa H, Asakawa S, Shimizu N, Tanaka M (2009) Two distinct types of theca cells in the medaka gonad: germ cell-dependent maintenance of cyp19a1-expressing theca cells. Dev Dyn 238:2652–2657. doi:10.1002/dvdy.22068

    Article  CAS  Google Scholar 

  • Pala I, Schartl M, Thorsteinsdóttir S, Coelho MM (2009) Sex determination in the Squalius alburnoides complex: an initial characterization of sex cascade elements in the context of a hybrid polyploid genome. PLoS One 4:e6401. doi:10.1371/journal.pone.0006401

    Article  Google Scholar 

  • Paul S, Pramanick K, Kundu S, Kumar D, Mukherjee D (2010) Regulation of ovarian steroidogenesis in vitro by IGF-I and insulin in common carp, Cyprinus carpio: stimulation of aromatase activity and P450arom gene expression. Mol Cell Endorinol 315:95–103. doi:10.1016/j.mce.2009.10.014

    Article  CAS  Google Scholar 

  • Pelletier J, Schalling M, Buckler AJ, Rogers A, Haber DA, Housman D (1991) Expression of the Wilms’ tumor gene WT1 in the murine urogenital system. Genes Dev 5:1345–1356. doi:10.1101/gad.5.8.1345

    Article  CAS  Google Scholar 

  • Pregel P, Bollo E, Cannizzo FT, Rampazzo A, Appino S, Biolatti B (2007) Effect of anabolics on bovine granulosa-luteal cell primary cultures. Folia Histochem Cytobiol 45:265–271

    CAS  Google Scholar 

  • Rocha A, Gómez A, Zanuy S, Cerda-Reverter JM, Carrillo M (2007) Molecular characterization of two sea bass gonadotropin receptors: cDNA cloning, expression analysis, and functional activity. Mol Cell Endocrinol 272:63–76. doi:10.1016/j.mce.2007.04.007

    Article  CAS  Google Scholar 

  • Rocha A, Zanuy S, Carrillo M, Gómez A (2009) Seasonal changes in gonadal expression of gonadotropin receptors, steroidogenic acute regulatory protein and steroidogenic enzymes in the European sea bass. Gen Comp Endocrinol 162:265–275. doi:10.1016/j.ygcen.2009.03.023

    Article  CAS  Google Scholar 

  • Rodríguez L, Begtashi I, Zanuy S, Carrillo M (2000) Development and validation of an enzyme immunoassay for testosterone: effects of photoperiod on plasma testosterone levels and gonadal development in male sea bass (Dicentrarchus labrax, L.) at puberty. Fish Physiol Biochem 23:141–150. doi:10.1023/A:1007871604795

    Article  Google Scholar 

  • Sekar N, Veldhuis JD (2001) Concerted transcriptional activation of the low density lipoprotein receptor gene by insulin and luteinizing hormone in cultured porcine granulosa-luteal cells: possible convergence of protein kinase a, phosphatidylinositol 3-kinase, and mitogen-activated protein kinase signalling pathways. Endocrinology 142:2921–2928. doi:10.1210/en.142.7.2921

    Article  CAS  Google Scholar 

  • Sharma RK, Bhardwaj JK (2009) In situ evaluation of granulosa cells during apoptosis in caprine ovary. Int J Integr Biol 5:58–61

    Article  Google Scholar 

  • Simione FP, Brown EM (1991) ATCC preservation methods: freezing and freeze-drying, 2nd edn. American Type Culture Collection, Rockville

    Google Scholar 

  • Stoklosowa S, Epler P (1985) The endocrine activity of isolated follicular cells of the carp ovary in primary culture. Gen Comp Endocrinol 58:386–393. doi:10.1016/0016-6480(85)90110-8

    Article  CAS  Google Scholar 

  • Stoklosowa S, Gregoraszczuk E, Channing CP (1982) Estrogen and progesterone secretion by isolated cultured porcine thecal and granulosa cells. Biol Reprod 26:943–952

    Article  CAS  Google Scholar 

  • Szoltys M, Stoklosowa S, Kasten FH (1982) Hormonal secretion of cultured rat ovarian follicles isolated at various hours of proestrus. In Vitro 18:463–468. doi:10.1007/BF02796474

    Article  CAS  Google Scholar 

  • Wang DS, Kobayashi T, Zhou LY, Paul-Prasanth B, Ijiri S, Sakai F, Okubo K, Morohashi K, Nagahama Y (2007) Foxl2 up-regulates aromatase gene transcription in a female-specific manner by binding to the promoter as well as interacting with ad4 binding protein/steroidogenic factor 1. Mol Endocrinol 21:712–725. doi:10.1210/me.2006-0248

    Article  CAS  Google Scholar 

  • Wolf K, Mann JA (1980) Poikilotherm vertebrate cell lines and viruses: a current listing for fishes. In Vitro 16:168–179. doi:10.1007/BF02831507

    Article  CAS  Google Scholar 

Download references

Acknowledgments

We thank especially to Soledad Ibáñez for excellent technical assistance with steroid analysis. This work was supported by the Spanish MICINN (AGL2008-02937, Aquagenomics CSD2007-00002), the GV (ACOMP2010/083) and CSIC (PIE-I3-2006 3 01 037).

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to A. Gómez.

Rights and permissions

Reprints and permissions

About this article

Cite this article

Crespo, B., Zanuy, S. & Gómez, A. Development of an in vitro system for functional studies of ovarian follicular cells in European sea bass (Dicentrarchus labrax). Cytotechnology 65, 273–286 (2013). https://doi.org/10.1007/s10616-012-9484-8

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s10616-012-9484-8

Keywords

Navigation