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Follicle-stimulating hormone increases gap junction communication in sertoli cells from immature rat testis in primary culture

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Abstract

The gap junction communication in Sertoli cells from immature rat testes, cultured either in absence or in presence of follicle-stimulating hormone (FSH), was studied by microinjection of a fluorescent dye and by Fluorescence Recovery After Photobleaching (gapFRAP).

The cells cultured for 2–4 days in the absence of FSH showed a flattened “epithelial-like” appearance. They were poorly coupled, as judged by the low frequency of cell-to-cell spread of microinjected Lucifer Yellow, and by the value of the rate constant of dye transfer (k) estimated in gapFRAP experiments. However, when two different subpopulations of cells were separately analyzed, namely the cells forming small groups contacting over part of their circumference (“adjoining cells”), and the cells arranged in tight clusters, we found that the value of k in the latter group was much higher, reaching about 75% of that obtained in the presence of FSH.

The cells cultured for two days in a medium containing ovine FSH underwent striking morphological changes and presented a rounded, “fibroblast-like” appearance. They were arranged in networks or in clusters. The frequency of cell-to-cell dye diffusion after microinjection and the rate constant of dye transfer were rapidly increased to the same final level by FSH, although they were initially different in these two groups. A concentration dependence of k, in the range 0.05 to 3 ng/ml, was observed in the cells in networks, contrasting with an all-or-none increase in the cells in clusters.

Two days after FSH withdrawal, the dye transfer constant returned to prestimulation control values in the cells in clusters, but not in the cells in networks, which maintained a stable degree of coupling comparable to that of the unstimulated cells in clusters. This observation suggests (i) that an initial promoting effect of FSH already exists in the immature rat testis, which is preserved after enzymatic treatment in the cell clusters, but not in the more dispersed cells, and (ii) that the decreased junctional coupling is re-established in the dispersed cells by FSH, through a synthesis or a membrane insertion of connexin.

The effects of FSH were mimicked by a brief exposure to 1 m m dibutyryl-cyclicAMP, but not to 10 n m human chorionic gonadotropin (hCG), indicating that the gap junction communication in Sertoli cells is upregulated by FSH through a specific membrane receptor, with cyclicAMP acting as a second messenger.

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References

  • Amsterdam, A., Knecht, M., Catt, K.J. 1981. Hormonal regulation of cytodifferentiation and intercellular communication in cultured granulosa cells. Proc. Natl. Acad. Sci. USA 78:3000–3004

    Google Scholar 

  • Anders, J.J., Salopek, M. 1989. Meningeal cells increase in vitro astrocytic gap junctional communication as measured by fluorescence recovery after laser photobleaching. J. Neurocytol. 18:257–264

    Google Scholar 

  • Barrows, G.H., Sisken, J.E., Allegra, J.C., Grasch, S.D. 1984. Measurement of fluorescence using digital integration of video images. J. Histochem. Cytochem. 32:741–746

    Google Scholar 

  • Bernier, M., Saez, J.M. 1985. Evidence de 2 mécanismes impliqués dans le phénomène de la régulation négative des récepteurs à l'hCG-LH. In: Développements récents de l'endocrinologie du testicule. INSERM 1984 123:239–244

    Google Scholar 

  • Beyer, E.C., Paul, D.L., Goodenough, D.A. 1987. Connexin43: a protein from rat heart homologous to a gap junction protein from liver. J. Cell Biol. 105:2621–2629

    Google Scholar 

  • Burt, J.M., Spray, D.C. 1988. Inotropic agents modulate gap junctional conductance between cardiac myocytes. Amer. J. Physiol. 254: H1206-H1210

    Google Scholar 

  • Cole, W.C., Garfield, R.E. 1986. Evidence for physiological regulation of myometrial gap junction permeability. Am. J. Physiol. 251:C411-C420

    Google Scholar 

  • D'Agostino, A., Menè, P., Stefanini, M. 1992. Voltage-gated calcium channels in rat Sertoli cells. Biol. Reprod. 46:414–418

    Google Scholar 

  • De Mello, W.C. 1988. Increase in junctional conductance caused by isoproterenol in heart cell pairs is suppressed by cAMP-dependent protein-kinase inhibitor. Biochem. Biophys. Res. Commun. 154: 509–514

    Google Scholar 

  • Djakiew, D., Hadley, M.A., Byers, S.W., Dym, M. 1986. Transferrin-mediated transcellular transport of 59Fe across confluent epithelial sheets of Sertoli cells grown in bicameral cell culture chambers. J. Androl. 7:355–366

    Google Scholar 

  • Dorrington, J.H., Roller, N.F., Fritz, I.B. 1975 Effects of follicle-stimulating hormone on cultures of Sertoli cell preparations. Mol. Cell. Endocrinol. 3:57–70

    Google Scholar 

  • Dym, M., Fawcett, D.W. 1970. The blood-testis barrier in the rat and the physiological compartmentation of the seminiferous epithelium. Biol. Reprod. 3:308–326

    Google Scholar 

  • Eusebi, F., Grassi, F., Fratamico, G., Dolci, S., Conti, M., Stefanini, M. 1985. Cell-to-cell communication in cultured Sertoli cells. Pfluegers Arch. 404:382–384

    Google Scholar 

  • Eusebi, F., Ziparo, E., Fratamico, G., Russo, M.A., Stefanini, M. 1983. Intercellular communication in rat seminiferous tubules. Dev. Biol. 10:249–255

    Google Scholar 

  • Flagg-Newton, J.L., Dahl. G., Loewenstein, W.R. 1981. Cell junction and cyclic AMP: I. Upregulation of junctional membrane permeability and junctional membrane particles by administration of cyclic nucleotide or phosphodiesterase inhibitor. J. Membrane Biol. 63:105–121

    Google Scholar 

  • Gilula, N.B., Fawcett, D.W., Aoki, A. 1976. The Sertoli cell occluding junctions and gap junctions in mature and developing mammalian testis. Dev. Biol. 50:142–168

    Google Scholar 

  • Gorczynska, E., Handelsman, D.J. 1991. The role of calcium in follicle-stimulating hormone signal. Transduction in Sertoli cells. J. Biol. Chem. 266:23739–23744

    Google Scholar 

  • Grassi, F., Monaco, L., Fratamico, G., Dolci, S., Iannini, E., Conti, M., Eusebi, F., Stefanini, M. 1986. Putative second messengers affect cell coupling in the seminiferous tubules. Cell. Biol. Int. Rep. 10:631–639

    Google Scholar 

  • Grasso, P., Joseph, M.P., Reichert, L.E. 1991. A new role for follicle-stimulating hormone in the regulation of calcium influx in Sertoli cells: inhibition of Na+/Ca++ exchange. Endocrinology 128:158–164

    Google Scholar 

  • Grasso, P., Reichert, L.E. 1989. Follicle-stimulating hormone receptor-mediated uptake of 45Ca2+ by proteoliposomes and cultured rat Sertoli cells: evidence for involvement of voltage-activated and voltage-independent calcium channels. Endocrinology 125: 3029–3036

    Google Scholar 

  • Grasso, P., Reichert, L.E. 1990. Follicle-stimulating hormone receptor-mediated uptake of toxinor pertussis toxin-sensitive guanine nucleotide binding proteins or adenylate cyclase. Endocrinology 127:949–956

    Google Scholar 

  • Grasso, P., Santa-Coloma, T.A., Reichert, L.E. 1991. Synthetic peptides corresponding to human (hFSH)-β-(1–15) and (hFSH)-β(51–65) induce uptake of 45Ca2+ by liposomes: evidence for calcium-conducting trans-membrane channel formation. Endocrinology 128:2745–2751

    Google Scholar 

  • Hadley, M.A., Byers, S.W., Suarez-Quian, C., Kleinman, H.K., Dym, M. 1985. Extracellular matrix regulates Sertoli cell differentiation, testicular cord formation, and germ cell development in vitro. J. Cell. Biol. 101:1511–1522

    Google Scholar 

  • Hertzberg, E.L., Lawrence, T.S., Gilula, N.B. 1981. Gap junctional communication. Annu. Rev. Physiol. 43:479–491

    Google Scholar 

  • Hutson, J.C. 1978. The effects of various hormones on the surface morphology of testicular cells in culture. Am. J. Anat. 151:55–69

    Google Scholar 

  • Hutson, J.C., Garner, C.W., Stocco, D.M. 1980. Effects of serum components on the morphology of Sertoli cells in culture. Anat. Rec. 197:205–211

    Google Scholar 

  • Iwatsuki, N., Petersen, O.H. 1978. Pancreatic acinar cells: acetylcholine-evoked electrical uncoupling and its ionic dependency. J. Physiol. 274:81–86

    Google Scholar 

  • Janecki, A., Steinberger, A. 1987. Bipolar secretion of androgenbinding protein and transferrin by Sertoli cells cultured in a twocompartment culture chamber. Endocrinology 120:291–298

    Google Scholar 

  • Janecki, A., Jakubowiak, A., Steinberger, A. 1991a. Effects of cyclic AMP and phorbol ester on transepithelial electrical resistance of Sertoli cell monolayer in two-compartment culture. Mol. Cell. Endocrinol. 82:61–69

    Google Scholar 

  • Janecki, A., Jakubowiak, A., Steinberger, A. 1991b. Regulation of transepithelial electrical resistance in two-compartment Sertoli cell cultures: in vitro model of the blood-testis barrier. Endocrinology 129:1489–1496

    Google Scholar 

  • Jégou, B. 1992. The Sertoli cell. Baillière's Clin. Endocrinol. Metab. 6:273–311

    Google Scholar 

  • Joffre, M., Roche, A. 1988. Follicle-stimulating hormone induces hyperpolarization of immature rat Sertoli cells in monolayer culture. J. Physiol. 400:481–499

    Google Scholar 

  • Johnson, M.H. 1970. The pituitary and the blood-testis barrier. J. Reprod. Fert. 22:181–186

    Google Scholar 

  • Lasater, E.M. 1987. Retinal horizontal cell gap junctional conductance is modulated by dopamine through a cyclic AMP-dependent protein kinase. Proc. Natl. Acad. Sci. USA. 84:7319–7323

    Google Scholar 

  • Loewenstein, W.R. 1981. Junctional intercellular communication: the cell-to-cell membrane channel. Physiol. Rev. 61:829–913

    Google Scholar 

  • Loewenstein, W.R. 1986. Cell-to-cell communication. Permeability, regulation, formation and functions of the cell-cell membrane channel in cell junctions. In: Physiology of Membrane Disorders. T.E. Andreoli, D.D. Fanestil, S.G. Schultz, editors. pp.329–343. Plenum, New York

    Google Scholar 

  • Loewenstein, W.R., Rose, B. 1992. The cell-cell channel in the control of growth. Semin. Cell Biol. 3:59–79

    Google Scholar 

  • Means, A.R., Dedman, J.R., Tash, J.S., Tindall, D.J., van Sickle, M., Welsh, M.J. 1980. Regulation of the testis Sertoli cell by follicle stimulating hormone. Annu. Rev. Physiol. 42:403–423

    Google Scholar 

  • Meda, P., Bosco, D., Chanson, M., Giordano, E., Vallar, L., Wollheim, C., Orci, L. 1990. Rapid and reversible secretion changes during uncoupling of rat insulin-producing cells. J. Clin. Inves. 86:759–768

    Google Scholar 

  • Meda, P., Michels, R.L., Halban, P.A., Orci, L.O., Sheridan, J.D. 1983. In vivo modulation of gap junctions and dye coupling between β-cells of the intact pancreatic islet. Diabetes 32:858–868

    Google Scholar 

  • Meyer, R., Posalaky, Z., McGinley, D. 1977. Intercellular junction development in maturing rat seminiferous tubules. J. Ultrastruct. Res. 61:271–283

    Google Scholar 

  • Munari-Silem, Y., Audebert, C., Rousset, B. 1991. Hormonal control of cell to cell communication: regulation by thyrotropin of the gap junction-mediated dye transfer between thyroid cells. Endocrinology 128:3299–3309

    Google Scholar 

  • Neyton, J., Trautmann, A. 1986. Acetylcholine modulation of the conductance of intercellular junctions between rat lacrimal cells. J. Physiol. 377:283–295

    Google Scholar 

  • Peters, R. 1983. Nuclear envelope permeability measured by fluorescence microphotolysis of single liver cell nuclei. J. Biol. Chem. 258:11427–11429

    Google Scholar 

  • Piccolino, M., Neyton, J., Gerschenfeld, H.M. 1984. Decrease of gap junction permeability induced by dopamine and cyclic adenosine 3′∶5-mono-phosphate in horizontal cells of the turtle retina. J. Neurosci. 4:2477–2488

    Google Scholar 

  • Pluciennik, F., Joffre, M., Délèze, J. 1991. Increase by FSH hormone and depression by testosterone of the diffusional coupling between Sertoli cells from immature rat testis in primary culture. C.R. Acad. Sci. III. 312:623–628

    Google Scholar 

  • Pluciennik, F., Joffre, M., Délèze, J. 1992. Sexual steroid esters might interfere with diffusional coupling promoted by FSH in primary cultures of immature Sertoli cells from rat testis. Arch. Int. Physiol. Biochim. Biophys. 100:A119

    Google Scholar 

  • Posalaky, Z., Meyer, R., McGinley, D. 1981. The effects of folliclestimulating hormone (FSH) on Sertoli cell junctions in vitro: a freeze-fracture study. J. Ultrastruct. Res. 74:241–254

    Google Scholar 

  • Redmer, D.A., Grazul-Bilska, A.T., Reynolds, L.P. 1991. Contact-dependent intercellular communication of bovine luteal cells in culture. Endocrinology 129:2757–2766

    Google Scholar 

  • Rich, K.A., Bardin, C.W., Gunsalus, G.L., Mather, J.P. 1983. Agedependent pattern of androgen-binding protein secretion from rat Sertoli cells in primary culture. Endocrinology 113:2284–2293

    Google Scholar 

  • Risek, B., Guthrie, S., Kumar, N., Gilula, N.B. 1990. Modulation of gap junction transcript and protein expression during pregnancy in the rat. J. Cell Biol. 110:269–282

    Google Scholar 

  • Risley, M.S., Ignatus, P.T., Roy, C., Saez, J.C. 1992. Cell-, ageand stage-dependent distribution of connexin 43 gap junctions in testes. J. Cell Sci. 103:81–96

    Google Scholar 

  • Roche, A., Joffre, M. 1989. Effect of uncoupling treatments on FSH-induced hyperpolarization of immature rat Sertoli cells from Sertoli cell-enriched cultures. J. Reprod. Fertil. 85:343–354

    Google Scholar 

  • Rotman, B., Papermaster, B.W. 1966. Membrane properties of living mammalian cells as studied by enzymatic hydrolysis of fluorogenic esters. Proc. Natl. Acad. Sci USA 55:134–141

    Google Scholar 

  • Saez, J.C., Gregory, W.A., Watanabe, T., Dermietzel, R., Hertzberg, E.L., Reid, L., Bennett, M.V.L., Spray, D.C. 1989. cAMP delays disappearance of gap junctions between pairs of rat hepatocytes in primary culture. Am. J. Physiol. 257:C1-C11

    Google Scholar 

  • Segaloff, D.L., Sprengel, R., Nikolics, K., Ascoli, M. 1990. Structure of the lutropin/choriogonadotropin receptor. Rec. Progr. Horm. Res. 46:261–303

    Google Scholar 

  • Socolar, S.J., Loewenstein, W.R. 1979. Methods for studying transmission through permeable cell-to-cell junctions. In: Methods in Membrane Biology. E.D. Korn, editor. Vol. 10, pp.123–179. Plenum, New York

    Google Scholar 

  • Solari, A.J., Fritz, I.B. 1978. The ultrastructure of immature Sertoli cells. Maturation-like changes during culture and the maintenance of mitotic potentiality. Biol. Reprod. 18:329–345

    Google Scholar 

  • Spray, D.C., Bennett, M.V.L. 1985. Physiology and pharmacology of gap junctions. Annu. Rev. Physiol. 47:281–303

    Google Scholar 

  • Spruill, W.A., White, M.G., Steiner, A.L., Tres, L.L., Kierszenbaum, A.L. 1981. Temporal sequence of cell shape changes in cultured rat Sertoli cells after experimental elevation of intracellular. cAMP. Exp. Cell. Res. 131:131–148

    Google Scholar 

  • Steinberger, A., Heindel, J.J., Lindsey, J.N., Elkington, J.S., Sanborn, B.M., Steinberger, E. 1975. Isolation and culture of FSH responsive Sertoli cells. Endocr. Res. Commun. 2:261–272

    Google Scholar 

  • Stewart, W.W. 1978. Functional connections between cells as revealed by dye-coupling with a highly fluorescent naphtalimide tracer. Cell 14:741–759

    Google Scholar 

  • Sugiura, H., Toyama, J., Tsuboi, N., Kamiya, K., Kodama, I. 1990. ATP directly affects junctional conductance between paired ventricular myocytes isolated from guinea pig heart. Circ. Res. 66:1095–1102

    Google Scholar 

  • Tung, P.S., Dorrington, J.H., Fritz, I. 1975. Structural changes induced by follicle-stimulating hormone or dibutyryl cyclic AMP on presumptive Sertoli cells in culture. Proc. Natl. Acad. Sci USA 72: 1838–1842

    Google Scholar 

  • Verhoeven, G., Dierickx, P., de Moor, P. 1979. Stimulation effect of neurotransmitters on the aromatization of testosterone by Sertoli cell-enriched cultures. Mol. Cell. Endocrinol. 13:241–253

    Google Scholar 

  • Vitale, R., Fawcett, D.W., Dym, M. 1973. The normal development of the blood-testis barrier and the effects of clomiphene and estrogen treatment. Anat. Rec. 176:331–344

    Google Scholar 

  • Wade, M.H., Trosko, J.E., Schindler, M. 1986. A fluorescence photobleaching assay of gap junction-mediated communication between human cells. Science 232:525–528

    Google Scholar 

  • Warner, A.E. 1988. The gap junction. J. Cell Sci. 89:1–7

    Google Scholar 

  • Welsh, M.J., Wiebe, J.P. 1975. Rat Sertoli cells: a rapid method for obtaining viable cells. Endocrinology 96:618–624

    Google Scholar 

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This work was supported by grants from the CNRS and the DRED du Ministère de l'Education Nationale, and the Fondation Langlois. Frédérique Pluciennik was a recipient of the Dufrenoy scholarship, given by l'Académie d'Agriculture de France.

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Pluciennik, F., Joffre, M. & Délèze, J. Follicle-stimulating hormone increases gap junction communication in sertoli cells from immature rat testis in primary culture. J. Membarin Biol. 139, 81–96 (1994). https://doi.org/10.1007/BF00232427

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