Skip to main content

Dynamics of Leydig Cell Regeneration After EDS

A Model for Postnatal Leydig Cell Development

  • Chapter
The Leydig Cell in Health and Disease

Part of the book series: Contemporary Endocrinology ((COE))

Abstract

Synthesis and secretion of androgens is the most important function of Leydig cells in the testis. The levels of androgens produced by these cells not only depend on their capacity to produce these steroids, but also on the number of Leydig cells present in the testis. Therefore, it is essential to understand how the formation of the Leydig cell population is regulated and to identify the factors, which play a role in this developmental process. However, the initial studies to investigate the regulation of Leydig cell development were not undertaken in the (pre)pubertal testis but in the adult testis. With the identification of ethane-1,2-dimethyl sulphonate (EDS) as a specific Leydig cell toxicant a large number of studies were initiated. The latter was because of the fact that following EDS administration a completely new Leydig cell population was formed. This chapter summarizes more than 20 yr of research on Leydig cell development in the adult testis using EDS as a model. The sensitivity of Leydig cells in different species for the cytotoxic action of EDS is discussed as well as the possible mechanism of action of this cytotoxic compound. A comparison is made between Leydig cell development in the (pre)pubertal testis and the adult testis during the regeneration process following EDS administration. Specific emphasis is paid to the regulatory role of the gonadotropins luteinizing hormone (LH) and folliclestimulating hormone (FSH) as well as other systemic and locally produced factors, such as thyroid hormone, insulinlike growth factor (IGF)-1, and transforming growth factors (TGF)-a and TGF-β, in this developmental process. It is concluded that there appear to be many similarities and hardly any discrepancies in the regulation of the development of precursor cells into mature adult-type Leydig cells during (pre)puberty and in the adult rat following EDS administration.

In the perinatal period when the stem cells become committed to lineage-specific differentiation, there are also differentiated Leydig cells present in the interstitium, namely, the fetal-type Leydig cells, which could influence the development of the adult-type Leydig cell population. Moreover, the intratesticular microenvironment of the (pre)pubertal testis is presumably rich in growth and differentiation inducing factors, whereas not only adult-type Leydig cells are developing but also other somatic cells are undergoing growth and differentiation. In contrast, following EDS administration in the adult animal, all differentiated Leydig cells are eliminated; the only undifferentiated cells left are presumably the stem cells/precursor cells. Taking into account the aforementioned, although EDS is a toxic compound which might influence the testicular microenvironment, the similarities between adult-type Leydig cell development in the (pre)pubertal testis and Leydig cell regeneration after EDS, make it tempting to speculate that the EDS-treated adult rat is better model for the study of the regulation of adult-type Leydig cell development than the (pre)pubertal testis. It is easier to follow cellular differentiation and ontogeny when no other mature cells are around.

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

Access this chapter

Chapter
USD 29.95
Price excludes VAT (USA)
  • Available as PDF
  • Read on any device
  • Instant download
  • Own it forever
eBook
USD 129.00
Price excludes VAT (USA)
  • Available as PDF
  • Read on any device
  • Instant download
  • Own it forever
Hardcover Book
USD 169.99
Price excludes VAT (USA)
  • Durable hardcover edition
  • Dispatched in 3 to 5 business days
  • Free shipping worldwide - see info

Tax calculation will be finalised at checkout

Purchases are for personal use only

Institutional subscriptions

Preview

Unable to display preview. Download preview PDF.

Unable to display preview. Download preview PDF.

References

  1. Kerr JB, Donachie K, Rommerts FFG. Selective destruction and regeneration of rat Leydig cells in vivo: A new method for the study of seminiferous tubular-interstitial tissue interaction. Cell Tissue Res 1985;242:145–156.

    Article  PubMed  CAS  Google Scholar 

  2. Molenaar R, de Rooij DG, Rommerts FFG, Reuvers PJ, van der Molen HJ. Specific destruction of Leydig cells in mature rats after in vivo administration of ethane dimethyl sulfonate. Biol Reprod 1985;33:1213–1222.

    Article  PubMed  CAS  Google Scholar 

  3. Morris ID, Phillips DM, Bardin CW. Ethylene dimethanesulfonate destroys Leydig cells in the rat testis. Endocrinology 1986;118:709–719.

    PubMed  CAS  Google Scholar 

  4. King SR, Rommerts FFG, Ford SL, Hutson JC, Orly J, Stocco DM. Ethane dimethane sulfonate and NNN′N′tetrakis-(2-pyridylmethyl) ethylenediamine inhibit steroidogenic acute regulatory (StAR) protein expression in MA-10 Leydig cells and rat Sertoli cells. Endocr Res 1998;24:469–478.

    Article  PubMed  CAS  Google Scholar 

  5. Tarka-Leeds DK, Suarez JD, Roberts NL, Rogers JM, Hardy MP, Klinefelter GR. Gestational exposure to ethane dimethanesulfonate permanently alters reproductive competence in the CD-1 mouse. Biol Reprod 2003;69:959–967.

    Article  PubMed  CAS  Google Scholar 

  6. Rommerts FFG, Kühne L, van Cappellen GWA, Stocco DM, King SR, Jankowska A. Specific dose-dependent effects of ethane 1,2-dimethanesulfonate in rat and mouse Leydig cells and non-steroidogenic cells on programmed cell death. J Endocrinol 2004;181:169–178.

    Article  PubMed  CAS  Google Scholar 

  7. Kerr JB, Knell CM, Abbott M, Donachie K. Ultrastructural analysis of the effect of ethane dimethanesulphonate on the testis of the rat, guinea pig, hamster and mouse. Cell Tissue Res 1987;249:451–457.

    PubMed  CAS  Google Scholar 

  8. Gray LE, Klinefelter G, Kelce G, Laskey J, Ostby J, Ewing L. Hamster Leydig cells are less sensitive to ethane dimethanesulfonate when compared to rat Leydig cells both in vivo and in vitro. Toxicol Appl Pharmacol 1995; 130:248–256.

    Article  PubMed  CAS  Google Scholar 

  9. Rao JN, Debeljuk L, Bartke A, Gao YP, Wilber JF, Feng P. The detection of thyrotropin-releasing hormone (TRH) and TRH receptor gene expression in Siberian hamster testes. Peptides 1997;18:1217–1222.

    Article  PubMed  CAS  Google Scholar 

  10. Sumathi R, Sriraman V, Kurkalli BS, Rommerts FFG, Rao AJ. Ethane dimethylsulphonate selectively destroys Leydig cells in the adult bonnet monkeys (Macaca radiata). Asian J Androl 1999;1:115–120.

    PubMed  CAS  Google Scholar 

  11. Laskey JW, Klinefelter GR, Kelce WR, Ewing LL. Effects of ethane dimethanesulfonate (EDS) on adult and immature rabbit Leydig cells: comparison with EDS-treated rat Leydig cells. Biol Reprod 1994;50:1151–1160.

    Article  PubMed  CAS  Google Scholar 

  12. Minucci D, De Rienzo G, Di Sena R, et al. Effects of multiple injections of ethane 1,2-dimethane sulphonate (EDS) on the frog, Rana esculenta, testicular activity. J Exp Zool 2000;287:384–393.

    Article  PubMed  CAS  Google Scholar 

  13. Palmiero C, Ferrara D, De Rienzo G, d’ Istria M, Minucci S. Ethane 1,2-dimethane sulphonate is a useful tool for studying cell-to-cell interactions in the testis of the frog, Rana esculenta. Gen Comp Endocrinol 2003;131:38–47.

    Article  PubMed  CAS  Google Scholar 

  14. Minucci S, Fasano S, Marmorino C, Chieffi P, Pierantoni R. Ethane 1,2-dimethane sulfonate effects on the testis of the lizard, Podarcis s. sicula Raf: morphological and hormonal changes. Gen Comp Endocrinol 1995;97:273–282.

    Article  PubMed  CAS  Google Scholar 

  15. De Kretser DM, Kerr JB. The cytology of the testis. In: Knobil E, Neill JD. eds. The Physiology of Reproduction, 2nd edn. Vol. 1. Raven Press, New York, 1994; pp. 1177–1290.

    Google Scholar 

  16. Majdic G, Saunders PT, Teerds KJ. Immunoexpression of the steroidogenic enzymes 3-β hydroxysteroid dehydrogenase and 17-α-hydroxylase C17,20 lyase and the receptor for luteinizing hormone (LH) in the fetal rat testis suggests that the onset of Leydig cell steroid production is independent of LH action. Biol Reprod 1998;58:520–525.

    Article  PubMed  CAS  Google Scholar 

  17. O’Shaughnessy PJ, Baker P, Sohnius U, Haavisto AM, Charlton HM, Huhtaniemi I. Fetal development of Leydig cell activity in the mouse is independent of pituitary gonadotroph function. Endocrinology 1998; 139: 1141–1146.

    Article  PubMed  CAS  Google Scholar 

  18. Migrenne S, Pairault C, Racine C, Livera G, Geloso A, Habert R. Luteinizing hormone-dependent activity and luteinizing hormone-independent differentiation of rat fetal Leydig cells. Mol Cell Endocrinol 2001;172:193–202.

    Article  PubMed  CAS  Google Scholar 

  19. Mendis-Handagama SMLC, Risbridger GP, de Kretser DM. Morphometric analysis of the components of the neonatal and adult testis interstitium. Int J Androl 1987;10:525–534.

    PubMed  CAS  Google Scholar 

  20. Hardy MP, Zirkin BR, Ewing LL. Kinetic studies on the development of the adult population of Leydig cells in the testes of the pubertal rat. Endocrinology 1989;124: 762–770.

    PubMed  CAS  Google Scholar 

  21. Mendis-Handagama SMLC, Ariyaratne HBS. Differentiation of the adult Leydig cell population in the postnatal testis. Biol Reprod 2001;65:660–671.

    Article  PubMed  CAS  Google Scholar 

  22. Haider SG. Cell biology of Leydig cells in the testis. Int Rev Cytol 2004;233:181–241.

    PubMed  CAS  Google Scholar 

  23. Kerr JB, Knell CM. The fate of fetal Leydig cells during the development of the fetal and postnatal rat testis. Development 1988;103:535–544.

    PubMed  CAS  Google Scholar 

  24. Ge RS, Dong Q, Sottas CM, Papadopoulos V, Zirkin BR, Hardy MP. In search of rat stem Leydig cells: Identification, isolation and lineage specific development. Proc Natl Acad Sci USA 2006; 2719–2724.

    Google Scholar 

  25. Vergouwen RPFA, Jacobs SGPM, Huiskamp R, Davids JAG, de Rooij DG. Proliferative activity of gonocytes, Sertoli cells and interstitial cells during testicular development in mice. J Reprod Fertil 1991;93:233–243.

    Article  PubMed  CAS  Google Scholar 

  26. Teerds KJ, de Rooij DG, de Jong FH, van Haaster LH. Development of the adult-type Leydig cell population in the rat is affected by neonatal thyroid hormone levels. Biol Reprod 1998;59:344–350.

    Article  PubMed  CAS  Google Scholar 

  27. Teerds KJ, Veldhuizen-Tsoerkan MB, Rommerts FFG, de Rooij DG, Dorrington JH. Proliferation and differentiation of testiscular cells: aspects of Leydig cell development in the prepubertal and adult testis. In: Verhoeven G, Habenicht U, eds. Molecular and Cellular Endocrinology of the Testis. Springer Verlag, Berlin, 1994; pp. 37–65.

    Google Scholar 

  28. Ge RS, Dong Q, Sottas CM, Chen H, Zirkin BR, Hardy MP. Gene expression in rat Leydig cells during development from the progenitor to adult stage: a cluster analysis. Biol Reprod 2005;72:1405–1415.

    Article  PubMed  CAS  Google Scholar 

  29. O’Shaughnessy PJ, Baker PJ, Heikkilä M, Vainio S, McMahon AP. Localization of 17beta-hydroxysteroid dehydrogenase/17-ketosteroid reductase isoform expression in the developing mouse testis-androstenedione is the major androgen secreted by fetal/neonatal Leydig cells. Endocrinology 2000;141:2631–2637.

    Article  PubMed  CAS  Google Scholar 

  30. O’Shaughnessy PJ, Willerton L, Baker PJ. Changes in Leydig cell gene expression during development in the mouse. Biol Reprod 2002;66:966–975.

    Article  PubMed  CAS  Google Scholar 

  31. Ketelslegers JM, Hetzel WD, Sherins RJ, Catt KJ. Developmental changes in testicular gonadotropin receptors: plasma gonadotropins and plasma testosterone in the rat. Endocrinology 1978;103:212–222.

    PubMed  CAS  Google Scholar 

  32. Chemes HE, Gottlieb SE, Pasqualini T, Domenichini E, Rivarola MA, Bergada C. Response to acute hCG stimulation and steroidogenic potential of Leydig cell fibroblastic precursors in humans. J Androl 1985;6:102–112.

    PubMed  CAS  Google Scholar 

  33. Chemes HE, Cigorraga S, Bergada C, Schteingart H, Rey R, Pellizzari E. Isolation of human Leydig cell mesenchymal precursors from patients with the androgen insensitivity syndrome: testosterone production and response to human chorionic gonadotropin stimulation in culture. Biol Reprod 1992;46:793–801.

    Article  PubMed  CAS  Google Scholar 

  34. Kerr JB, Sharpe RM. Stimulatory effect of follicle-stimulating hormone on rat Leydig cells. A morphometric and ultrastructural study. Cell Tissue Res 1985;239:405–445.

    Article  PubMed  CAS  Google Scholar 

  35. Kerr JB, Sharpe RM. Follicle-stimulating hormone induction of Leydig cell maturation. Endocrinology 1985;116: 2592–2604.

    PubMed  CAS  Google Scholar 

  36. Teerds KJ, Closset J, Rommerts FFG, et al. Effects of pure FSH and LH preparations on the number and function of Leydig cells in immature hypophysectomized rats. J Endocrinol 1989;120:97–106.

    PubMed  CAS  Google Scholar 

  37. Vihko KK, Nishimori K, LaPolt PS, Hsueh AJW. Stimulatory effects of recombinant follicle-stimulating hormone on Leydig cell function and spermatogenesis in immature hypophysectomized rats. Endocrinology 1991;129:1926–1932.

    PubMed  CAS  Google Scholar 

  38. Baker PJ, O’Shaughnessy PJ. Role of the gonadotrophins in regulating numbers of Leydig and Sertoli cells during fetal and postnatal development in mice. Reproduction 2001; 122: 227–234.

    Article  PubMed  CAS  Google Scholar 

  39. Zhang FP, Poutanen M, Wilbertz J, Huhtaniemi I. Normal prenatal but arrested postnatal sexual development of luteinizing hormone receptor knockout (LuRKO) mice. Mol Endocrinol 2001;15:172–183.

    Article  PubMed  CAS  Google Scholar 

  40. Jackson H, Craig AW. Effects of alkylating chemicals on reproductive cells. Ann NY Acad Sci 1969;160:215–227.

    Article  PubMed  CAS  Google Scholar 

  41. Delic JL, Hendry JH, Morris ID, Shalet SM. Dose and time relationships in the endocrine response of the irradiated adult rat testis. J Androl 1986;7:32–41.

    PubMed  CAS  Google Scholar 

  42. Delic JL, Schlappack OK, Harwood JR, Stanley JA. Comparative effects of X-irradiation on the testes of adult Sprague-Dawley and Wistar rats. Radiat Res 1987;112:99–104.

    Article  PubMed  CAS  Google Scholar 

  43. Edwards G, Jackson H, Morris ID. Testicular endocrine effects of alkane methanesulphonates related to the Leydig cell cytotoxic compound EDS. Cancer Chemother Pharmacol 1990;26:19–25.

    PubMed  CAS  Google Scholar 

  44. Cooper ERA, Jackson H. Comparative effects of methylene, ethylene and propylene dimethanesulphonates on the male rat reproductive system. J Reprod Fertil 1970;23:103–108.

    Article  PubMed  CAS  Google Scholar 

  45. Jackson H. The effects of alkylating agents on fertility. Br Med Bull 1964;20:107–114.

    PubMed  CAS  Google Scholar 

  46. Klinefelter GR, Laskey JW, Roberts NL. In vitro/in vivo effects of ethane dimethanesulfonate on Leydig cells of adult rats. Toxicol Appl Pharmacol 1991;107:460–471.

    Article  PubMed  CAS  Google Scholar 

  47. Bu’Lock DE, Jackson CM. Suppression of testicular androgen synthesis in the rat by ethane 1,2 dimethanesulphonate. J Steroid Biochem 1975;6:1181–1185.

    Article  CAS  Google Scholar 

  48. Jackson CM, Morris ID. Gonadotrophin levels in male rats following impairment of Leydig cell function by ethylene dimethanesulphonate. Andrologia 1977;9:29–35.

    Article  PubMed  CAS  Google Scholar 

  49. Morris ID, McCluckie JA. Temporal changes in serum androgen after temporary impairment of Leydig cell function by ethane-l,2-dimethane sulphonate. J Steroid Biochem 1979;10: 467–469.

    Article  PubMed  CAS  Google Scholar 

  50. Bu’Lock DE, Jones P. Effect of ethane 1,2-dimethane sulphonate on the cyclic AMP response in rat testis to stimulation by HCG. J Reprod Fertil 1976;47:151–153.

    CAS  Google Scholar 

  51. Morris AJ, Taylor MF, Morris ID. Leydig cell apoptosis in response to ethane dimethanesulphonate after both in vivo and in vitro treatment. J Androl 1997;18:274–280.

    PubMed  CAS  Google Scholar 

  52. Taylor MF, Woolveridge I, Metcalfe AD, Streuli CH, Hickman JA, Morris ID. Leydig cell apoptosis in the rat testes after administration of the cytotoxin ethane dimethanesulphonate: role of the Bcl-2 family members. J Endocrinol 1998;157:317–326.

    Article  PubMed  CAS  Google Scholar 

  53. Taylor MF, de Boer-Brouwer M, Woolveridge I, Teerds KJ, Morris ID. Leydig cell apoptosis after the administration of ethane dimethanesulfonate to the adult male rat is a Fasmediated process. Endocrinology 1999;140:3797–3804.

    Article  PubMed  CAS  Google Scholar 

  54. Kim JM, Luo L, Zirkin BR. Caspase-3 activation is required for Leydig cell apoptosis induced by ethane dimethanesulfonate. Endocrinology 2000;141:1846–1853.

    Article  PubMed  CAS  Google Scholar 

  55. Woolveridge I, Taylor MF, Rommerts FFG, Morris ID. Apoptosis related gene products in differentiated and tumorigenic rat Leydig cells and following regression induced by the cytotoxin ethane dimethanesulphonate. Int J Androl 2001;24:56–64.

    Article  PubMed  CAS  Google Scholar 

  56. Ariyaratne HBS, Mills N, Mason JL. Mendis-Handagama SMLC. Effects of thyroid hormone on Leydig cell regeneration in the adult rat following ethane dimethane sulphonate treatment. Biol Reprod 2000;63:1115–1123.

    Article  PubMed  CAS  Google Scholar 

  57. Bakalska M, Koeva I, Atanassova N, Angelova P, Nikolov B, Davidoff M. Steroidogenic and structural differentiation of new Leydig cell population following exposure of adult rats to ethane dimethanesulphonate. Folia Biol 2002;48:205–209.

    CAS  Google Scholar 

  58. Bartlett JMS, Kerr JB, Sharpe RM. The effect of selective destruction and regeneration of rat Leydig cells on the intratesticular distribution of testosterone and morphology of the seminiferous epithelium. J Androl 1986; 7:240–253.

    PubMed  CAS  Google Scholar 

  59. Jackson AE, O’Leary PC, Ayers MM, de Kretser DM. The effects of ethylene dimethane sulphonate (EDS) on rat Leydig cells: evidence to support a connective tissue origin of Leydig cells. Biol Reprod 1986;35:425–437.

    Article  PubMed  CAS  Google Scholar 

  60. Kerr JB, Donachie K. Regeneration of Leydig cells in unilateral cryptorchid rats: evidence for stimulation by local testicular factors. Cell Tissue Res 1986;245:649–655.

    PubMed  CAS  Google Scholar 

  61. Kerr JB, Bartlett JMS, Donachie K. Acute response of testicular interstitial tissue in rats to the cytotoxic drug ethane dimethanesulphonate. Cell Tissue Res 1986;245:649–655.

    PubMed  CAS  Google Scholar 

  62. Kerr JB, Bartlett JMS, Donachie K, Sharpe RM. Origin of regenerating Leydig cells in the testis of the adult rat. An ultrastructural, morphometric and hormonal assay study. Cell Tissue Res 1987;249:367–377.

    PubMed  CAS  Google Scholar 

  63. Kerr JB, Knell CM. The regenerative capacity of testicular interstitial cells: A recurrent pattern of experimental destruction and regeneration of rat Leydig cells. Roux’s Arch Dev Biol 1987;196:467–471.

    Article  Google Scholar 

  64. Molenaar R, de Rooij DG, Rommerts FFG, van der Molen HJ. Repopulation of Leydig cells in mature rats after selective destruction of the existent Leydig cells with ethylene dimethane sulfonate is dependent on luteinizing hormone and not follicle-stimulating hormone. Endocrinology 1986;118: 2546–2554.

    PubMed  CAS  Google Scholar 

  65. O’Leary PC, Jackson AE, Averill S, de Kretser DM. The effects of ethane dimethane sulphonate (EDS) on bilaterally cryptorchid rat testes. Mol Cell Endocrinol 1986;45:183–190.

    Article  PubMed  CAS  Google Scholar 

  66. O’Leary PC, Jackson AE, de Kretser DM. Evaluation of testicular hCG binding in unilateral cryptorchid rats following administration of ethane dimethane sulphonate (EDS). Mol Cell Endocrinol 1986;48:51–58.

    Article  PubMed  CAS  Google Scholar 

  67. Teerds KJ, de Rooij DG, Molenaar R, Rommerts FFG, Wensing CJG. Specific cytotoxic effects of ethane dimethyl sulfonate (EDS) and repopulation of Leydig cells after depletion. In: Stefanini M, Conti M, Geremia R, Ziparo E, eds. Molecular and Cellular Endocrinology of the Testis. Elsevier Science Pub BV, Amsterdam, 1986;173–183.

    Google Scholar 

  68. Teerds KJ, de Rooij DG, Rommerts FFG, Wensing CJG. The regulation of the proliferation and differentiation of rat Leydig cell precursor cells after EDS administration or daily HCG treatment. J Androl 1988;9:343–351.

    PubMed  CAS  Google Scholar 

  69. Teerds KJ, de Rooij DG, Rommerts FFG, van den Hurk R, Wensing CJG. Proliferation and differentiation of possible Leydig cell precursors after destruction of the existing Leydig cells with ethane dimethyl sulphonate: the role of LH/human chorionic gonadotrophin. J Endocrinol 1989;122: 689–696.

    PubMed  CAS  Google Scholar 

  70. Teerds KJ, de Rooij DG, Rommerts FFG, van den Hurk R, Wensing CJG. Stimulation of the proliferation and differentiation of Leydig cell precursors after destruction of existing Leydig cells with ethane dimethyl sulphonate (EDS) can take place in the absence of LH. J Androl 1989;10:472–477.

    PubMed  CAS  Google Scholar 

  71. Teerds KJ, de Rooij DG, Rommerts FFG, Wensing CJG. Development of a new Leydig cell population after the destruction of existing Leydig cells by ethane dimethane sulphonate in rats: an autoradiographic study. J Endocrinol 1990;126:229–236.

    PubMed  CAS  Google Scholar 

  72. Teerds KJ, de Boer-Brouwer M, Dorrington JH, Baivers M, Ivell R. Identification of markers for precursor and Leydig cell differentiation in the adult rat testis following ethane dimethyl sulphonate administration. Biol Reprod 1999;60:1437–1445.

    Article  PubMed  CAS  Google Scholar 

  73. Edwards G, Robertson WR, Morris ID. Characterization of the regenerated Leydig cell population of the rat after destruction by ethylene-l,2-dimethanesulphonate. J Endocrinol 1988;117:11–18.

    PubMed  CAS  Google Scholar 

  74. Myers RB, Abney TO. Interstitial cell proliferation in the testis of the ethylene dimethane sulfonate-treated rat. Steroids 1991;56:91–96.

    Article  PubMed  CAS  Google Scholar 

  75. Naka Y, Inui T, Okada H, et al. Rapid recovery of Leydig cell population in rat cryptorchid testis after ethanedimethanesulfonate injury: immunohistochemical studies. Acta Histochem Cytochem 1991; 24:257–265.

    Google Scholar 

  76. Gaytan F, Aceitero J, Lucena C, et al. Simultaneous proliferation and differentiation of mast cells and Leydig cells in the rat testis. Are common regulatory factors involved? J Androl 1992;13:387–397.

    PubMed  CAS  Google Scholar 

  77. Chen H, Huhtaniemi I, Zirkin BR. Depletion and repopulation of Leydig cells in the testes of aging brown Norway rats. Endocrinology 1996; 137:3447–3452.

    Article  PubMed  CAS  Google Scholar 

  78. Tena-Sempere M, Rannikko A, Kero J, Zhang FP, Huhtaniemi IT. Molecular mechanisms of reappearance of luteinizing hormone receptor expression and function in rat testis after selective Leydig cell destruction by ethylene dimethane sulfonate. Endocrinology 1997; 138:3340–3348.

    Article  PubMed  CAS  Google Scholar 

  79. Ariyaratne S, Kim I, Mills N, Mason I, Mendis-Handagama C. Effects of ethane dimethane sulfonate on the functional structure of the adult rat testis. Arch Androl 2003;49:313–326.

    Article  PubMed  CAS  Google Scholar 

  80. Sprando RL, Santulli R, Awoniyi CA, Ewing LL, Zirkin BR. Does ethane 1,2-dimethanesulphonate (EDS) have a direct cytotoxic effect on the seminiferous epithelium of the rat testis? J Androl 1990;1l:344–352.

    Google Scholar 

  81. Klinefelter GR, Lasky JW, Roberts NR, Slott V, Suarez JD. Multiple effects of ethane dimethanesulfonate on the epididiymis of adult rats. Toxicol Appl Pharmacol 1990; 105: 271–287.

    Article  PubMed  CAS  Google Scholar 

  82. Morris ID, Lendon RG, Waters C, Naylor G, Jones N. Thymic regression and apoptosis in the rat after treatment with the Leydig cell cytotoxin ethylene dimethanesulphonate (EDS). Toxicology 1997; 120:19–27.

    Article  PubMed  CAS  Google Scholar 

  83. Plecas B, Glavaski A, Savic V, Hristic M, Duric D, Solarovic T. Effects of ethane dimethanesulfonate on the structure of adult male rat adrenale cortex. Pharmacol Res 1997;35: 541–546.

    Article  PubMed  CAS  Google Scholar 

  84. Smart JL, Massey RF, Lendon RG, Morris ID. Growth and development of male and female rats treated with the Leydig cell cytotoxin ethane dimethane sulphonate during the sucking period. Food Chem Toxicol 1990;28:121–128.

    Article  PubMed  CAS  Google Scholar 

  85. Rommerts FFG, Teerds KJ, Hoogerbrugge JW. In vitro effects of ethylene-dimethane sulfonate (EDS) on Leydig cells: inhibition of steroid production and cytotoxic effects are dependent on species and age of rat. Mol Cell Endocrinol 1988;55:87–94.

    Article  PubMed  CAS  Google Scholar 

  86. Morii S, Naka Y, Inui T, Shintani H. Necrotizing effect of ethanedimethanesulphonate on spontaneously occurring Leydig cell tumors in old F344 rats. Cancer Res 1988;48:4395–4398.

    PubMed  CAS  Google Scholar 

  87. Teerds KJ, de Rooij DG, de Jong FH, Rommerts FFG. Rapid development of Leydig cell tumors in a Wistar substrain. J Androl 1991;12:171–179.

    PubMed  CAS  Google Scholar 

  88. Kelce WR, Zirkin BR, Ewing LL. Immature rat Leydig cells are intrinsically less sensitive than adult Leydig cells to ethane dimethanesulfonate. Toxicol Appl Pharmacol 1991;111: 189–200.

    Article  PubMed  CAS  Google Scholar 

  89. Morris ID. Leydig cell resistance to the cytotoxic effect of ethylene dimethanesulphonate in the adult rat testis. J Endocrinol 1985;105:311–316.

    PubMed  CAS  Google Scholar 

  90. Rommerts FFG, Grootenhuis AJ, Hoogerbrugge JW, van der Molen HJ. Ethane dimethane sulphonate (EDS) specifically inhibits LH stimulated steroidogenesis in Leydig cells isolated from mature rats but not in cells from immature rats. Mol Cell Endocrinol 1985;42:105–111.

    Article  PubMed  CAS  Google Scholar 

  91. Edwards G, Lendon R, Morris ID. Leydig cell recovery following a second challenge with ethane-1,2-dimethanesulphonate is enhanced by short intervals between cytotoxin administration to rats. J Endocrinol 1989;123:197–203.

    PubMed  CAS  Google Scholar 

  92. Vreeburg JTM, Ooms MP, Rommerts FFG, Teerds KJ. Functional properties of developing rat Leydig cells after treatment with ethylene dimethanesulphonate (EDS). J Reprod Fertil 1988;84:63–69.

    PubMed  CAS  Google Scholar 

  93. Kerr JB, Risbridger GP, Knell CM. Stimulation of interstitial cell growth after selective destruction of foetal Leydig cells in the testis of postnatal rats. Cell Tissue Res 1988;252: 89–98.

    Article  PubMed  CAS  Google Scholar 

  94. Morris ID, Lendon RG, Zaidi A. Inhibition of testicular and somatic cell development after treatment of the postnatal rat with the Leydig cell cytotoxic ethylene dimethanesulphonate. J Endocrinol 1988; 119:467–474.

    PubMed  CAS  Google Scholar 

  95. Risbridger G, Kerr J, de Kretser DM. Differential effects of the destruction of Leydig cells by administration of ethane dimethane sulphonate to postnatal rats. Biol Reprod 1989;40: 801–809.

    Article  PubMed  CAS  Google Scholar 

  96. Zaidi A, Lendon RG, Dixon JS, Morris ID. Abnormal development of the testis after administration of the Leydig cell cytotoxic ethylene-1,2-dimethanesulphonate to the immature rat. J Reprod Fertil 1988;82:381–392.

    Article  PubMed  CAS  Google Scholar 

  97. Jackson CM, Jackson H. Comparative protective actions of gonadotrophins and testosterone against the antispermatogenic action of ethane dimethanesulphonate. J Reprod Fertil 1984;71:393–401.

    Article  PubMed  CAS  Google Scholar 

  98. Teerds KJ, de Rooij DG, Wensing CJG, Rommerts FFG. Hormone-induced resistance of rat Leydig cells to the cytotoxic effects of ethane-l,2-dimethane sulphonate. J Endocrinol 1992;134:85–90.

    PubMed  CAS  Google Scholar 

  99. Onyango DW, Wang EO, Oduor-Okelo D, Werner G. Early testicular response to intraperitoneal administration of ethane dimethylsulphonate (EDS) in the goat (Capra hircus). J Submicrosc Cytol Pathol 2001;33:117–124.

    PubMed  CAS  Google Scholar 

  100. Minucci S, Fasano S, di Matteo L, Chieffi Boccari G, Pierantoni R. Morphological and hormonal changes in the frog, Rana esculenta, testis after administration of ethane dimethane sulfonate. Gen Comp Endocrinol 1990;79:335–345.

    Article  PubMed  CAS  Google Scholar 

  101. Minucci S, di Matteo L, Fasano S, Chieffi Baccari G, Pierantoni R. Regeneration of the testicular interstitial compartment after ethane dimethane sulfonate treatment in the hypophysectomized frog, Rana esculenta: independence of pituitary control. Gen Comp Endocrinol 1994;95:84–91.

    Article  PubMed  CAS  Google Scholar 

  102. Ferrara D, Palmiero C, Branno M, Pierantoni R, Minucci S. Testicular activity of Mos in the frog, Rana esculenta: a new role in spermatogonial proliferation. Biol Reprod 2004;70: 1782–1789.

    Article  PubMed  CAS  Google Scholar 

  103. Minucci S, Chieffi Baccari G, di Mateo L, et al. Resumption of testicular activity in Gobus paganellus after administration of ethanel,2-dimethane sulfonate (EDS). Comp Biochem Physiol 1992;102:319–323.

    Article  CAS  Google Scholar 

  104. Flinterman JF, Nooter K, Rommerts FFG. Activation of programmed cell death in rat Leydig cells by EDS. In: Verhoeven G ed. Book of Miniposters 8th European Workshop on Molecular and Cellular Endocrinology of the Testis. De Panne, 1994; Miniposter 18.

    Google Scholar 

  105. Clark BJ, Wells J, King SR, Stocco DM. The purification, cloning and expression of a novel luteinizing hormoneinduced mitochondrial protein in MA-10 mouse Leydig tumor cells. Characterization of the steroidogenic acute regulatory protein StAR. J Biol Chem 1994;269:28,314–28,322.

    CAS  Google Scholar 

  106. Lin D, Sugawara T, Strauss JF, 3rd, et al. Role of steroidogenic acute regulatory protein in adrenal and gonadal steroidogenesis. Science 1995;267:1828–1831.

    Article  PubMed  CAS  Google Scholar 

  107. Stocco DM, Clark BJ. Regulation of the acute production of steroids in steroidogenic cells. Endocr Rev 1996;17:221–244.

    Article  PubMed  CAS  Google Scholar 

  108. Kelce WR, Zirkin BR. Mechanism by which ethane dimethanesulfonate kills adult rat Leydig cells: involvement of intracellular glutathione. Toxicol Appl Pharmacol 1993; 120: 80–88.

    Article  PubMed  CAS  Google Scholar 

  109. Kelce WR. Buthionine sulfoximine protects the viability of adult rat Leydig cells exposed to ethane dimethanesulfonate. Toxicol Appl Pharmacol 1994;125:237–246.

    Article  PubMed  CAS  Google Scholar 

  110. Chemes HE, Rivarola MA, Bergada C. Effect of hCG on the interstitial cells and androgen production in the immature rat testis. J Reprod Fertil 1976;46:279–282.

    PubMed  CAS  Google Scholar 

  111. Christensen AK, Peacock KC. Increase in Leydig cell number in the testes of adult rats treated chronically with an excess of human chorionic gondotropin. Biol Reprod 1980;22: 383–391.

    PubMed  CAS  Google Scholar 

  112. Savage GN, Kerr JB. Effect of seminiferous tubule size on hCG-induced regeneration of peritubular Leydig cells in hypophysectomized, EDS-treated rats. Int J Androl 1995; 18: 35–45.

    PubMed  CAS  Google Scholar 

  113. Sriraman V, Sairam MR, Rao AJ. Evaluation of relative roles of LH and FSH in regulation of differentiation of Leydig cells using an ethane 1,2-dimethanesulfonate-treated adult rat model. J Endocrinol 2003;176:151–161.

    Article  PubMed  CAS  Google Scholar 

  114. Abney TO, Myers RB. 17beta-estradiol inhibition of Leydig cell regeneration in the ethane dimethylsulfonate treated mature rat. J Androl 1991;12:295–304.

    PubMed  CAS  Google Scholar 

  115. Dhar JD, Setty BS. Epididymal response to exogenous testosterone in rats sterilized neonatally by estrogen. Endokrinol 1976;68:14–21.

    CAS  Google Scholar 

  116. Zhai J, Lanclos KD, Abney TO. Estrogen receptor messenger ribonucleic acid changes during Leydig cell development. Biol Reprod 1996;55:782–788.

    Article  PubMed  CAS  Google Scholar 

  117. Canick JA, Makris A, Gunsalus GL, Ryan KJ. Testicular aromatization in immature rats: localization and stimulation after gonadotropin administration in vivo. Endocrinology 1979;102:285–288.

    Google Scholar 

  118. Wang J, Wreford NGM, Lan HY, Atkins R, Hedger MP. Leukocyte populations in the adult rat testis following removal of the Leydig cells by treatment with ethane dimethane sulfonate and subcutaneous testosterone implants. Biol Reprod 1994;51:551–561.

    Article  PubMed  CAS  Google Scholar 

  119. Gaytan F, Bellido C, Morales C, Reymundo C, Aguilar E, van Rooijen N. Effects of macrophage depletion at different times after treatment with ethylene dimethane sulfonate (EDS) on the regeneration of Leydig cells in the adult rat. J Androl 1994;15:558–564.

    PubMed  CAS  Google Scholar 

  120. Gaytan F, Bellido C, Morales C, Reymundo C, Aguilar E, van Rooijen N. Selective depletion of testicular macrophages and prevention of Leydig cell repopulation after treatment with ethylene dimethane sulfonate in rats. J Reprod Fertil 1994;101:175–182.

    Article  PubMed  CAS  Google Scholar 

  121. Gaytan F, Bellido C, Morales C, Reymundo C, Aguilar E, van Rooijen N. Response to Leydig cell apoptosis in the absence of testicular macrophages. J Reprod Immunol 1995;29:81–94.

    Article  PubMed  CAS  Google Scholar 

  122. Takao T, Culp SG, de Souza EB. Reciprocal modulation of interleukin-1β (IL-1β) and IL-1 receptors by lipopolysaccharide (endotoxin) treatment in the mouse brain-endocrineimmune axis. Endocrinology 1993;132:1497–1504.

    Article  PubMed  CAS  Google Scholar 

  123. Khan SA, Khan SJ, Dorrington JH. Interleukin-1 stimulates deoxyribonucleic acid synthesis in immature rat Leydig cells in vitro. Endocrinology 1992;131:1853–1857.

    Article  PubMed  CAS  Google Scholar 

  124. Yan W, Kero J, Huhtaniemi I, Toppari J. Stem cell factor functions as a survival factor for mature Leydig cells and a growth factor for precursor Leydig cells after ethylene dimethane sulfonate treatment: implication of a role of the stem cell factor/c-kit system in Leydig cell development. Dev Biol 2000;227:169–182.

    Article  PubMed  CAS  Google Scholar 

  125. Tsuchida J, Dohmae K, Kitamura Y, Nishimune Y The role of the c-kit receptor in the regenerative differentiation of rat Leydig cells. Int J Androl 2003;26:121–125.

    Article  PubMed  CAS  Google Scholar 

  126. Salva A, Hardy MP, Wu XF, et al. Müllerian-inhibiting substance inhibits Leydig cell regeneration after ethylene dimethansulphonate ablation. Biol Reprod 2004;70:600–607.

    Article  PubMed  CAS  Google Scholar 

  127. Buzzard JJ, Morrison JR, O’Bryan MK, Song Q, Wreford NG. Developmental expression of thyroid hormone receptors in the rat testis. Biol Reprod 2000;62:664–669.

    Article  PubMed  CAS  Google Scholar 

  128. Palmero S, Maggiani S, Fugassa E. Nuclear triiodothyronine receptors in rat Sertoli cells. Mol Cell Endocrinol 1988;58: 253–256.

    Article  PubMed  CAS  Google Scholar 

  129. Mendis-Handagama SM, Ariyaratne HB, Teunissen van Manen KR, Haupt RL. Differentiation of adult Leydig cells in the neonatal rat testis is arrested by hypothyroidism. Biol Reprod 1998;59:351–357.

    Article  PubMed  CAS  Google Scholar 

  130. McFarland KC, Sprengel R, Phillips HS, et al. Lutropinchoriogonadotropin receptor: an unusual member of the G protein-coupled receptor family. Science 1989;245:494–499.

    Article  PubMed  CAS  Google Scholar 

  131. Pakarinen P, Vihko KK, Voutilainen R, Huhtaniemi I. Differential response of luteinizing hormone receptor and steroidogenic enzyme gene expression to human chorionic gonadotropin stimulation in the neonatal and adult rat testis. Endocrinology 1990;127:2469–2474.

    PubMed  CAS  Google Scholar 

  132. LaPolt PS, Jia XC, Sincich C, Hsueh AJW. Ligand-induced down-regulation of testicular and ovarian luteinizing hormone (LH) receptors is preceded by tissue specific inhibition of alternatively processed LH receptor transcripts. Mol Endocrinol 1991;5:397–403.

    PubMed  CAS  Google Scholar 

  133. Shan LX, Hardy MP. Developmental changes in levels of luteinizing hormone receptor and androgen receptor in rat Leydig cells. Endocrinology 1992;131:1107–1114.

    Article  PubMed  CAS  Google Scholar 

  134. Vihko KK, Nishimori K, LaPolt PS, Hsueh AJW. Expression of testicular ribonucleic acid for luteinizing hormone receptor in the rat: developmental regulation of multiple transcripts during postnatal life. Biol Reprod 1992;46:1016–1020.

    Article  PubMed  CAS  Google Scholar 

  135. Veldhuizen-Tsoerkan MB, Ivell R, Teerds KJ. hCG-induced changes in LH/hCG receptor mRNA transcript levels in the testis of adult hypophysectomized, ethane dimethyl sulphonatetreated rats. Mol Cell Endocrinol 1994;105:37–44.

    Article  PubMed  CAS  Google Scholar 

  136. Tena-Sempere M, Zhang FP, Huhtaniemi I. Persistent expression of a truncated form of the luteinizing hormone receptor messenger ribonucleic acid in the rat testis after selective Leydig cell destruction by ethylene dimethane sulfonate. Endocrinology 1994;135:1018–1024.

    Article  PubMed  CAS  Google Scholar 

  137. Abney TO, Zhai J. Gene expression of luteinizing hormone receptor and steroidogenic enzymes during Leydig cell development. J Mol Endocrinol 1998;20:119–127.

    Article  PubMed  CAS  Google Scholar 

  138. Tena-Sempere M, Kero J, Rannikko A, Huhtaniemi I. Experimental cryptorchidism induces a change in the pattern of expression of LH receptor mRNA in rat testis after selective Leydig cell destruction by ethylene dimethane sulfonate. J Endocrinol 1999;161:131–141.

    Article  PubMed  CAS  Google Scholar 

  139. Koo YB, Ji I, Ji TH. Characterization of different sizes of rat luteinizing hormone/chorionic gonadotropin receptor messenger ribonucleic acids. Endocrinology 1994;134:19–26.

    Article  PubMed  CAS  Google Scholar 

  140. Jackson NC, Jackson H, Shanks JH, Dixon JS, Lendon RG. Study using in vivo binding of 125I-labeled hCG, light and electron microscopy of the repopulation of rat Leydig cells after destruction due to administration of ethylene-1, 2-dimethanesulphonate. J Reprod Fertil 1986;76:1–10.

    Article  PubMed  CAS  Google Scholar 

  141. Risbridger GP, Davies A. Isolation of rat Leydig cells and precursors forms after administration of ethane dimethane sulfonate. Am J Physiol 1994;266:E975–E979.

    Google Scholar 

  142. Indrapichate K, Meehan D, Lane TA, et al. Biological actions of monoclonal luteinizing hormone/human chorionic gonadotropin receptor antibodies. Biol Reprod 1992;46: 265–278.

    Article  PubMed  CAS  Google Scholar 

  143. Dohler KD, Wuttke W. Changes with age in levels of serum gonadotropins, prolactin and gonadal steroids in prepubertal male and female rats. Endocrinology 1975;97:898–907.

    PubMed  CAS  Google Scholar 

  144. Odell WD, Swerdloff RS. Etiologies of sexual maturation: a model system based on the sexually maturing rat. Recent Prog Horm Res 1976;432:245–288.

    Google Scholar 

  145. Khan SA, Teerds K, Dorrington J. Growth factor requirements for DNA synthesis by Leydig cells from the immature rat. Biol Reprod 1992;46:335–341.

    Article  PubMed  CAS  Google Scholar 

  146. Khan SA, Teerds K, Dorrington J. Regulation of DNA synthesis in Leydig cells. In: Bartke A, ed. Function of Somatic Cells in the Testis. Springer Verlag, New York, 1994: pp. 151–166.

    Google Scholar 

  147. Ge RS, Hardy MP. Decreased cyclin A2 and increased cyclin Gl levels coincide with loss of proliferative capacity of rat Leydig cells during pubertal development. Endocrinology 1997;138:3719–3726.

    Article  PubMed  CAS  Google Scholar 

  148. Wang G, Hardy MP. Development of Leydig cells in the insulin-like growth factor-1 (IGF-1) knockout mouse: effects of IGF-1 replacement and gonadotropic stimulation. Biol Reprod 2004;70:632–639.

    Article  PubMed  CAS  Google Scholar 

  149. Teerds KJ, Rommerts FFG, Dorrington JH. Immunohistochemical detection of transforming growth factor-α in Leydig cells during development of the rat testis. Mol Cell Endocrinol 1990;69:R1–R6.

    Article  PubMed  CAS  Google Scholar 

  150. Mullaney BP, Skinner MK. Transforming growth factor-α and epidermal growth factor receptor gene expression and action during pubertal development of the seminiferous tubule. Mol Endocrinol 1992;6:2103–2113.

    Article  PubMed  CAS  Google Scholar 

  151. Skinner MK, Takacs K, Coffey RJ. Transforming growth factor-a gene expression and action in the seminiferous tubule: peritubular cell-Sertoli cell interactions. Endocrinology 1989;124:845–854.

    PubMed  CAS  Google Scholar 

  152. Cailleau J, Vermeire S, Verhoeven G. Independent control of the production of insulin-like growth factor I and its binding protein by cultured testicular cells. Mol Cell Endocrinol 1990;69:79–89.

    Article  PubMed  CAS  Google Scholar 

  153. Handelsman DJ, Spaliviero JA, Scott CD, Baxter RC. Identification of insulin-like growth factor-I and its receptors in the rat testis. Acta Endocrinol 1985;109:543–549.

    PubMed  CAS  Google Scholar 

  154. Tres LL, Smith EP, van Wyk JJ, Kierszenbaum AL. Immunoreactive sites and accumulation of somatomedin-C in rat Sertoli-spermatogenic cell co-cultures. Exp Cell Res 1986;162:33–50.

    Article  PubMed  CAS  Google Scholar 

  155. Smith EP, Svoboda ME, van Wyk JJ, Kierszenbaum AL, Tres LL. Partial characterization of a somatomedin-like peptide from the medium of cultured rat Sertoli cells. Endocrinology 1987;120:186–193.

    PubMed  CAS  Google Scholar 

  156. Suarez-Quian CA, Dai MZ, Onoda M, Kriss RM, Dym M. Epidermal growth factor receptor localization in the rat and monkey testes. Biol Reprod 1989;41:921–932.

    Article  PubMed  CAS  Google Scholar 

  157. Lin T, Haskell J, Vinson N, Terracio L. Characterization of insulin and insulin-like growth factor I receptors of purified Leydig cells and their role in steroidogenesis in primary culture: a comparative study. Endocrinology 1986;119:1641–1647.

    Article  PubMed  CAS  Google Scholar 

  158. Drummond AE, Risbridger GP, O’Leary PC, de Kretser DM. Alterations in mitogenic and steroidogenic activities in rat testicular interstitial fluid after administration of ethane dimethane sulphonate. J Reprod Fertil 1988;83:141–147.

    PubMed  CAS  Google Scholar 

  159. Takao T, Mitchell WM, Tracey DE, de Souza EB. Identification of interleukin-1 receptors in mouse testis. Endocrinology 1990;127:251–258.

    PubMed  CAS  Google Scholar 

  160. Lin T, Wang D, Nagpal ML. Human chorionic gonadotropin induces interleukin-1 gene expression in rat Leydig cells in vivo. Mol Cell Endocrinol 1993;95:139–145.

    Article  PubMed  CAS  Google Scholar 

  161. Cohen PF, Pollard JW. Normal sexual function in male mice lacking a functional type I interleukin-1 (IL-1) receptor. Endocrinology 1998;139:815–818.

    Article  PubMed  CAS  Google Scholar 

  162. Lee MM, Seah CC, Masiakos PT, et al. Müllerian-inhibiting substance type II receptor expression and function in purified rat Leydig cells. Endocrinology 1999;140:2819–2827.

    Article  PubMed  CAS  Google Scholar 

  163. Behringer RR, Finegold MJ, Cate RL. Müllerian-inhibiting substance function during mammalian sexual development. Cell 1994;79:415–425.

    Article  PubMed  CAS  Google Scholar 

  164. Behringer RR, Cate RL, Froelick GJ, Palmiter RD, Brinster RL. Abnormal sexual development in transgenic mice chronically expressing Müllerian inhibiting substance. Nature 990;345: 167–170.

    Google Scholar 

  165. Khan SA, Mirsafian M, Howdeshell K, Dorrington JH. Transforming growth factor-β inhibits DNA synthesis in immature rat Leydig cells in vitro. Mol Cell Endocrinol 1999;148:21–28.

    Article  PubMed  CAS  Google Scholar 

  166. Morera AM, Cochet C, Keramidas M, Chauvin MA, de Peretti E, Benahmed M. Direct regulating effects of transforming growth factor β on the Leydig cell steroidogenesis in primary culture. J Steroid Biochem 1988;30:443–447.

    Article  PubMed  CAS  Google Scholar 

  167. Le Magueresse-Battistoni B, Morera AM, Goddard I, Benahmed M. Expression of mRNAs for transforming growth factor-β receptors in the rat testis. Endocrinology 1995;136: 2788–2791.

    Article  PubMed  Google Scholar 

  168. Teerds KJ, Dorrington JH. Localization of transforming growth factor βl and β2 during testicular development in the rat. Biol Reprod 1993;48:40–45.

    Article  PubMed  CAS  Google Scholar 

  169. Gaytan F, Bellido C, Aceitero J, Aguilar E, Sanchez-Criado JE. Leydig cell involvement in the paracrine regulation of mast cells in the testicular interstitium of the rat. Biol Reprod 1990;43:665–671.

    Article  PubMed  CAS  Google Scholar 

  170. Myers RB, Abney TO. Testosterone and androstanediol production by regenerating Leydig cells in the ethylene dimethane sulphonate-treated mature rat. Int J Androl 1990;13:4–16.

    Article  PubMed  CAS  Google Scholar 

  171. O’Shaughnessy PJ, Murphy L. Steroidogenic enzyme activity in the rat testis following Leydig cell destruction by ethylene-1,2-dimethanesulphonate and subsequent Leydig cell regeneration. J Endocrinol 1991;131:451–457.

    PubMed  CAS  Google Scholar 

  172. Wiebe JP. Steroidogenesis in rat Leydig cells: changes in activity of 5-ane and 5-ene 3β-hydroxysteroid dehydrogenases during sexual maturation. Endocrinology 1976;98: 505–513.

    PubMed  CAS  Google Scholar 

  173. Shan LX, Phillips DM, Bardin CW, Hardy MP. Differential regulation of steroidogenic enzymes during differentiation optimizes testosterone production by adult rat Leydig cells. Endocrinology 1993;133:2277–2283.

    Article  PubMed  CAS  Google Scholar 

  174. Moger WH. Serum 5α-adrostane-3α, 17β-diol, androsterone, and testosterone concentrations in the male rat. Influence of age and gonadotropin stimulation. Endocrinology 1977;100: 1027–1032.

    PubMed  CAS  Google Scholar 

  175. Podesta EJ, Rivarola MA. Concentration of androgens in whole testes, seminiferous tubules and interstitial tissue of rats at different stages of development. Endocrinology 1974;95: 455–461.

    PubMed  CAS  Google Scholar 

  176. van der Molen HJ, Grootegoed JA, de Greef-Bijleveld MJ, Rommerts FFG, van der Vusse GJ. Distribution of steroids, steroid production and steroid metabolizing enzymes in the rat testis. In: French FS, Hansson V, Ritzen EM, Nayfeh SN, eds. Hormonal Regulation of Spermatogenesis. Plenum Press, New York, 1975; pp. 665–676.

    Google Scholar 

  177. Neumann A, Haider SG, Hilscher B. Temporal coincidence of the appearance of elongated spermatids and of histochemical reaction of 11β-hydroxysteroid dehydrogenase in rat Leydig cells. Andrologia 1993;25:263–269.

    Article  PubMed  CAS  Google Scholar 

  178. Phillips DM, Lakshmi V, Monder C. Cortiosteroid 11β-dehydrogenase in the rat testis. Endocrinology 1989;125:209–216.

    PubMed  CAS  Google Scholar 

  179. Ge RS, Hardy DO, Catteral JF, Hardy MP. Developmental changes in glucocorticoid receptor and 11β-hydroxysteroid dehydrogenase oxidative and reductive activities in rat Leydig cells. Endocrinology 1997;138:5089–5095.

    Article  PubMed  CAS  Google Scholar 

  180. Ge RS, Dong Q, Niu EM, et al. 11β-Hydroxysteroid dehydrogenase 2 in rat Leydig cells: its role in blunting glucocorticoid action at physiological levels of substrate. Endocrinology 2005;146:2657–2664.

    Article  PubMed  CAS  Google Scholar 

  181. Christensen AK. Leydig cells. In: Hamilton DW, Greep RO, eds. Handbook of Physiology, vol. 5. American Physiology Society, Washington, 1975;57–94.

    Google Scholar 

  182. Fouquet JP, Raynaud F. Renewal of Leydig cells in the neonatal and adult monkey: a radio autographic study. Biol Cell 1985;54:187–190.

    PubMed  CAS  Google Scholar 

  183. Fouquet JP, Kann MI. Mitotic activity in monkey and rat Leydig cells. Reprod Nutr Dev 1987;27:1053–1062.

    Article  PubMed  CAS  Google Scholar 

  184. Amat P, Paniagua R, Nistal M, Martin A. Mitosis in adult human Leydig cells. Cell Tissue Res 1986;243:219–221.

    Article  PubMed  CAS  Google Scholar 

  185. Teerds KJ, de Rooij DG, Rommerts FFG, van der Tweel I, Wensing CJG. Turnover time of rat Leydig cells and other interstitial cells in testes of adult rats. Arch Androl 1989;23:105–111.

    Article  PubMed  CAS  Google Scholar 

  186. Abney TO, Carswell LS. Gonadotropin regulation of Leydig cell DNA synthesis. Mol Cell Endocrinol 1986;45:157–165.

    Article  PubMed  CAS  Google Scholar 

  187. Abney TO. The potential role of estrogen in regulating Leydig cell development and function: a review. Steroids 1999;64: 610–617.

    Article  PubMed  CAS  Google Scholar 

  188. Saez JM, Haour F, Loras B, Sanchez P, Cathiard AM. Oestrogen induced Leydig cell refractoriness to gonadotrophin stimulation. Acta Endocrinol 1978;89:379–392.

    PubMed  CAS  Google Scholar 

  189. Chen H, Hardy MP, Huhtaniemi I, Zirkin BR. Age-related decreased Leydig cell testosterone production in the brown Norway rat. J. Androl 1994;15:551–557.

    PubMed  CAS  Google Scholar 

  190. Teerds KJ, Rommerts FFG, van de Kant HJG, de Rooij DG. Leydig cell number and function in the adult cynomolgus monkey (Macaca fascicularis) is stimulated by daily hCG treatment but not by daily FSH treatment. J Reprod Fertil 1989;87:141–146.

    Article  PubMed  CAS  Google Scholar 

  191. Sharpe RM. hCG-induced decrease in availability of rat testis receptors. Nature 1976;264:644–646.

    Article  PubMed  CAS  Google Scholar 

  192. Hsueh AJW, Dufau M, Catt KJ. Gonadotropin-induced regulation of luteinizing hormone receptors and desensitization of testicular 3′,5′-cyclic AMP and testosterone responses. Proc Natl Acad Sci USA 1977;74:592–595.

    Article  PubMed  CAS  Google Scholar 

  193. Nozu K, Matsuura S, Catt KJ, Dufau ML. Modulation of Leydig cell androgen biosynthesis and cytochrome P-450 levels during estrogen treatment and human chorionic gondadotropin-induced desensitization. J Biol Chem 1981; 256:10,012–10,017.

    CAS  Google Scholar 

  194. Calvo JC, Radicella JP, Pignataro OP, Charreau EH. Effect of a second injection of human chorion gonadotropin on the desensitized Leydig cells. Mol Cell Endocrinol 1984; 34:31–38.

    Article  PubMed  CAS  Google Scholar 

  195. Zhang FP, Pakarainen T, Zhu F, Poutanen M, Huhtaniemi I. Molecular characterization of postnatal development of testicular steroidogenesis in luteinizing hormone receptor knockout mice. Endocrinology 2004;145:1453–1463.

    Article  PubMed  CAS  Google Scholar 

  196. Clark AM, Garland KK, Russel LD. Desert hedgehog (Dhh) gene is required in the mouse testis for formation of adulttype Leydig cells and normal development of peritubular cells and seminiferous tubules. Biol Reprod 2000;63: 1825–1838.

    Article  PubMed  CAS  Google Scholar 

  197. Gnessi L, Basciani S, Mariani S, et al. Leydig cell loss and spermatogenic arrest in platelet-derived growth factor (PDGF)-A-deficient mice. J Cell Biol 2000;149: 1019–1025.

    Article  PubMed  CAS  Google Scholar 

  198. Huseby RA. Demonstration of a direct carcinogenic effect of estradiol on Leydig cells of the mouse. Cancer Res 1980;40: 1006–1013.

    PubMed  CAS  Google Scholar 

  199. Jurainsz RL, Huseby RA, Wilcox RB. Interactions of putative estrogens with the intracellular receptor complex in mouse Leydig cells: relationship to preneoplastic hyperplasia. Cancer Res 1988;48:14–18.

    Google Scholar 

  200. Kobrin MS, Asa SL, Samsoondar J, Kudlow JE. α-Transforming growth factor in the bovine anterior pituitary gland: secretion by dispersed cells and immunohistochemical localization. Endocrinology 1987;121:1412–1416.

    PubMed  CAS  Google Scholar 

  201. Kudlow JE, Kobrin MS, Purchio AF, et al. Ovarian transforming growth factor-α gene expression: immunohistochemical localization to the thecal-interstitial cells. Endocrinology 1987;121:1577–1579.

    PubMed  CAS  Google Scholar 

  202. Spiess AN, Balvers M, Tena-Sempere M, Huhtaniemi I, Parry L, Ivell R. Structure and expression of the rat relaxin-like factor (RLF) gene. Mol Reprod Dev 1999;54:319–325.

    Article  PubMed  CAS  Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Editor information

Editors and Affiliations

Rights and permissions

Reprints and permissions

Copyright information

© 2007 Humana Press Inc., Totowa, NJ

About this chapter

Cite this chapter

Teerds, K., Rijntjes, E. (2007). Dynamics of Leydig Cell Regeneration After EDS. In: Payne, A.H., Hardy, M.P. (eds) The Leydig Cell in Health and Disease. Contemporary Endocrinology. Humana Press. https://doi.org/10.1007/978-1-59745-453-7_6

Download citation

  • DOI: https://doi.org/10.1007/978-1-59745-453-7_6

  • Publisher Name: Humana Press

  • Print ISBN: 978-1-58829-754-9

  • Online ISBN: 978-1-59745-453-7

  • eBook Packages: MedicineMedicine (R0)

Publish with us

Policies and ethics