Development of the foetal and neonatal testis
V. Rouiller-Fabre
Fonctionnal Differentiation of Gonads Laboratory, Gametogenesis and Genotoxicity Unit, INSERM U 566 – CEA, Université Paris, Paris, France
Search for more papers by this authorC. Levacher
Fonctionnal Differentiation of Gonads Laboratory, Gametogenesis and Genotoxicity Unit, INSERM U 566 – CEA, Université Paris, Paris, France
Search for more papers by this authorC. Pairault
Fonctionnal Differentiation of Gonads Laboratory, Gametogenesis and Genotoxicity Unit, INSERM U 566 – CEA, Université Paris, Paris, France
Search for more papers by this authorC. Racine
Fonctionnal Differentiation of Gonads Laboratory, Gametogenesis and Genotoxicity Unit, INSERM U 566 – CEA, Université Paris, Paris, France
Search for more papers by this authorE. Moreau
Fonctionnal Differentiation of Gonads Laboratory, Gametogenesis and Genotoxicity Unit, INSERM U 566 – CEA, Université Paris, Paris, France
Search for more papers by this authorR. Olaso
Fonctionnal Differentiation of Gonads Laboratory, Gametogenesis and Genotoxicity Unit, INSERM U 566 – CEA, Université Paris, Paris, France
Search for more papers by this authorG. Livera
Fonctionnal Differentiation of Gonads Laboratory, Gametogenesis and Genotoxicity Unit, INSERM U 566 – CEA, Université Paris, Paris, France
Search for more papers by this authorS. Migrenne
Fonctionnal Differentiation of Gonads Laboratory, Gametogenesis and Genotoxicity Unit, INSERM U 566 – CEA, Université Paris, Paris, France
Search for more papers by this authorG. Delbes
Fonctionnal Differentiation of Gonads Laboratory, Gametogenesis and Genotoxicity Unit, INSERM U 566 – CEA, Université Paris, Paris, France
Search for more papers by this authorR. Habert
Fonctionnal Differentiation of Gonads Laboratory, Gametogenesis and Genotoxicity Unit, INSERM U 566 – CEA, Université Paris, Paris, France
Search for more papers by this authorV. Rouiller-Fabre
Fonctionnal Differentiation of Gonads Laboratory, Gametogenesis and Genotoxicity Unit, INSERM U 566 – CEA, Université Paris, Paris, France
Search for more papers by this authorC. Levacher
Fonctionnal Differentiation of Gonads Laboratory, Gametogenesis and Genotoxicity Unit, INSERM U 566 – CEA, Université Paris, Paris, France
Search for more papers by this authorC. Pairault
Fonctionnal Differentiation of Gonads Laboratory, Gametogenesis and Genotoxicity Unit, INSERM U 566 – CEA, Université Paris, Paris, France
Search for more papers by this authorC. Racine
Fonctionnal Differentiation of Gonads Laboratory, Gametogenesis and Genotoxicity Unit, INSERM U 566 – CEA, Université Paris, Paris, France
Search for more papers by this authorE. Moreau
Fonctionnal Differentiation of Gonads Laboratory, Gametogenesis and Genotoxicity Unit, INSERM U 566 – CEA, Université Paris, Paris, France
Search for more papers by this authorR. Olaso
Fonctionnal Differentiation of Gonads Laboratory, Gametogenesis and Genotoxicity Unit, INSERM U 566 – CEA, Université Paris, Paris, France
Search for more papers by this authorG. Livera
Fonctionnal Differentiation of Gonads Laboratory, Gametogenesis and Genotoxicity Unit, INSERM U 566 – CEA, Université Paris, Paris, France
Search for more papers by this authorS. Migrenne
Fonctionnal Differentiation of Gonads Laboratory, Gametogenesis and Genotoxicity Unit, INSERM U 566 – CEA, Université Paris, Paris, France
Search for more papers by this authorG. Delbes
Fonctionnal Differentiation of Gonads Laboratory, Gametogenesis and Genotoxicity Unit, INSERM U 566 – CEA, Université Paris, Paris, France
Search for more papers by this authorR. Habert
Fonctionnal Differentiation of Gonads Laboratory, Gametogenesis and Genotoxicity Unit, INSERM U 566 – CEA, Université Paris, Paris, France
Search for more papers by this authorSummary.
The foetal testis originates from a proliferation of the mesonephric and the coelomic epithelia which are colonized by the primordial germ cells. In the foetal testis, the development and functions of the three main cell type precursors (Leydig, Sertoli and germ cells) do not depend upon gonadotropins. Numerous intra- and extra-testicular factors are candidates for the control of its development and functions. To study the potential involvement of these factors, we developed an organotypic culture system. In absence of any growth factors or hormone, this system allows a development of the three main cell types which mimics that observed in vivo. The effects of different regulators (gonadotropin-releasing hormone, follicle-stimulating hormone, transforming growth factor-β, insulin-like growth factor-I, anti-Mullerian hormone, retinoic acid, oestrogens) were tested in this system. Whether or not some of the effects observed in vitro have a physiological relevance was evaluated using appropriate transgenic mice. It is concluded that the foetal testis cannot be considered as an adult mini-testis since it has a specific physiology which largely differs from that of the immature or adult testis.
References
- Boulogne B, Olaso R, Levacher C, Durand P, Habert R (1999) Apoptosis and mitosis in the gonocytes of the rat testis during fetal and neonatal development. Int J Androl 22: 356 – 365.
- Capel B (2000) The battle of sexes. Mech. Dev 15: 89 – 103.
- Carr EE, Chin WW (1985) Absence of detectable chorionic gonadotropin subunit messenger ribonucleic acids in the rat placenta throughout gestation. Endocrinology 116: 1151 – 1157.
- Creasy RK, Jost A (1966) Multiplication des cellules germinales dans le testicule du fœtus de rat hypophysectomisé par décapitation. Arch Anat Microsc Morph Exp 55: 561 – 570.
-
Dieckmann KP,
Skakkebaek NE (1999) Carcinoma in situ of the testis: review of biological and clinical features.
Int J Cancer
83: 815
–
822.
10.1002/(SICI)1097-0215(19991210)83:6<815::AID-IJC21>3.0.CO;2-Z CAS PubMed Web of Science® Google Scholar
- Gautier C, Levacher C, Saez JM, Habert R (1997) Transforming growth factor β1 inhibits steroidogenesis in dispersed fetal testicular cells in culture. Molec Cell Endocrinol 131: 21 – 30.
- Habert R (1992) Effects of decapitation and chronic in vivo treatment with a gonadotropin releasing hormone agonist on testicular steroidogenesis in the rat fetus. J Endocrinol 133: 245 – 251.
- Habert R, Devif I, Gangnerau MN, Lecerf L (1991) Ontogenesis of the in vitro response of rat testis to gonadotropin releasing hormone. Mol Cell Endocrinol 82: 199 – 206.
- Habert R, Lejeune H, Saez JM (2001) Ontogenesis of Leydig cells and regulation of their functions. Mol Cell Endocrinol 179: 47 – 74.
- Habert R, Picon R (1982) Control of testicular steroidogenesis in fetal rat: effect of decapitation on testosterone and plasma luteinizing hormone-like activity. Acta Endocrinol 99: 466 – 473.
- Habert R, Picon R (1990) Attempts for identification of a chorionic gonadotrophin-like bioactivity in the rat placenta which stimulates the testosterone secretion of the fetal testis in vitro. Biol Neonate 58: 24 – 31.
- Jost A, Vigier B, Prepin J, Perchellet J (1973) Studies on sex differentiation in mammals. Recent Prog Horm Res 29: 1 – 41.
- Lecerf L, Rouiller-Fabre V, Levacher C, Gautier C, Saez JM, Habert R (1993) Stimulatory effects of Follicle stimulating hormone on basal and LH-stimulated testosterone secretion by the fetal rat testis in vitro. Endocrinology 133: 2313 – 2318.
- Livera G, Rouiller-Fabre V, Durand P, Habert R (2000) Multiple effects of retinoids on the development of Sertoli, germ and Leydig cells of fetal and neonatal rat testis in culture. Biol Reprod 62: 1303 – 1314.
- Livera G, Rouiller-Fabre V, Habert R (2001) Retinoid acid receptors involved in the effects of retinoic acid on rat testis development. Biol Reprod 64: 1307 – 1314.
- Lufkin T, Lohnes D, Mark M, Dierich A, Gorry P, Gaub MP, Le Meur M, Chambon P (1993) High postnatal lethality and testis degeneration in retinoic acid receptor α mutant mice. Dev Biol 90: 7225 – 7229.
- Magre S, Jost A (1991) Sertoli cells and testicular differentiation in the rat fetus. J Electron Microsc Tech 19: 172 – 188.
- McLachlan JA (2001) Environmental signalling: what embryos and evolution teach us about endocrine disrupting chemicals. Endocr Rev 22: 319 – 341.
- McLaren (1999) Signalling for germ cells. Genes Dev 13: 373 – 376.
- Migrenne S, Pairault C, Racine C, Livera G, Géloso A, Habert R (2001) LH dependent activity and LH-independent differentiation of rat fetal Leydig cells. Mol Cell Endocrinol 172: 193 – 202.
- Olaso R, Habert R (2000) Genetic and cellular analysis of male germ cell development. J Androl 21: 497 – 511.
- Olaso R, Pairault C, Boulogne B, Durand P, Habert R (1998) Transforming growth factor β1 and β2 reduce the number of gonocytes by increasing apoptosis. Endocrinology 139: 733 – 740.
- Orth JM (1984) The role of follicle stimulating hormone in controlling Sertoli cell proliferation in testes of fetal rats. Endocrinology 115: 1248 – 1255.
- Picon R, Habert R (1981) A sensitive bioassay for LH-like activity applied to systemic plasma of fetal rat. Acta Endocrinol 97: 176 – 180.
- Rouiller-Fabre V, Lecerf L, Gautier C, Saez JM, Habert R (1998) Expression and effect of IGF-I in the rat fetal testis. Endocrinology 139: 2226 – 2234.
- Saez JM (1994) Leydig cells: endocrine, paracrine, and autocrine regulation. Endocr Rev 15: 574 – 626.
- Toppari J, Larsen JC, Christiansen P, Giwercman A, Grandjean P, Guillette LJ, Jegou B, Jensen TK, Jouannet P, Keiding N, Leffers H, McLachlan JA, Meyer O, Muller J, Rajpert-De Meyts E, Scheike T, Sharpe RM, Sumpter J, Skakkebaek NE (1996) Male reproductive health and environmental xenoestrogens. Environ Health Perspect 104: 741 – 803.
- Tougard C, Picart R, Tixier-Vidal A (1977) Cytogenesis of immunoreactive gonadotropic cells in the fetal rat pituitary at light and electron microscopic levels. Dev Biol 58: 148 – 163.