Immunocytochemical identification of GtH1 and GtH2 cells during the temperature-sensitive period for sex determination in pejerrey, Odontesthes bonariensis.

The ontogeny of gonadotropin 1 (GtH1) and 2 (GtH2) cells and its possible link to gonadal sex differentiation were studied in pejerrey, Odontesthes bonariensis, by immunocytochemistry using anti-chum salmon beta-GtH1 and beta-GtH2 antisera. In adults, GtH1 cells were found in the proximalis pars distalls (PPD) close to the neurohypophysis, whereas GtH2 cells were identified surrounding GtH1 cells, at the external layer of the PPD and in the pars intermedia. Essentially the same distribution was observed in larvae. In pejerrey, the phenotypic sex is governed by the temperature during the critical period of sex determination (temperature-dependent sex determination, TSD). Female proportions vary gradually from 100% at 15-19 degrees to 0% at 29 degrees, and the critical time of TSD has been estimated to be 3-5, 2-4, and 1-4 weeks after hatching at 17, 19, and 27 degrees, respectively. Thus, the expression of both GtHs was examined weekly in larvae reared from hatching to week 11, at 17, 24, and 29 degrees. The proportion of females at 17, 24, and 29 degrees was, 100%, 78%, and 0%, respectively. Histological ovarian differentiation was noticed at 7 and 4 weeks at 17 and 24 degrees, whereas testicular differentiation occurred at 7 and 4 weeks at 24 and 29 degrees. GtH1 cells were first observed at week 3 at 29 degrees and at week 4 at 17 and 24 degrees. These cells increased in number until week 4 and then decreased, disappearing after week 6 at all temperature regimes. GtH2 cells appeared at week 2 at 24 and 29 degrees and at week 3 at 17 degrees. GtH2 cell number increased until week 3 at 29 degrees and until week 4 at 17 and 24 degrees and then temporarily decreased, thereafter increasing again. These results strongly suggest that GtH1 and GtH2 are expressed by different cells. The fact that GtH1 and GtH2 cells appear just before histological gonadal differentiation at all temperatures, together with the peak of GtH1 and GtH2 cell number during the temperature-sensitive period, suggests that GtHs are related to sex differentiation or TSD in O. bonariensis.

[1]  S. Abe,et al.  Aromatase inhibitor and 17α‐methyltestosterone cause sex‐reversal from genetical females to phenotypic males and suppression of P450 aromatase gene expression in Japanese flounder (Paralichthys olivaceus) , 2000, Molecular reproduction and development.

[2]  S. Abe,et al.  Suppression of P450 aromatase gene expression in sex-reversed males produced by rearing genetically female larvae at a high water temperature during a period of sex differentiation in the Japanese flounder (Paralichthys olivaceus). , 1999, Journal of molecular endocrinology.

[3]  Y. Guiguen,et al.  Endocrine and environmental aspects of sex differentiation in fish , 1999, Cellular and Molecular Life Sciences CMLS.

[4]  K. Aida,et al.  Duality of gonadotropin in a primitive teleost, Japanese eel (Anguilla japonica). , 1999, General and comparative endocrinology.

[5]  M. Govoroun,et al.  GTH I and GTH II secretion profiles during the reproductive cycle in female rainbow trout: relationship with pituitary responsiveness to GnRH-A stimulation. , 1998, General and comparative endocrinology.

[6]  H. Kagawa,et al.  Immunocytochemical identification of two distinct gonadotropic cells (GTH I and GTH II) in the pituitary of bluefin tuna, Thunnus thynnus. , 1998, General and comparative endocrinology.

[7]  J. D. Neill,et al.  Encyclopedia of reproduction , 1998 .

[8]  C. A. Strüssmann,et al.  Thermal thresholds and critical period of thermolabile sex determination in two atherinid fishes, Odontesthes bonariensis and Patagonina hatcheri , 1997 .

[9]  H. Kawauchi,et al.  Isolation and characterization of two distinct gonadotropins from the pituitary gland of Mediterranean yellowtail, Seriola dumerilii (Risso, 1810). , 1997, General and comparative endocrinology.

[10]  R. Patiño Manipulations of the Reproductive System of Fishes by Means of Exogenous Chemicals , 1997 .

[11]  C. A. Strüssmann,et al.  Structure and cell type distribution in the pituitary gland of pejerrey Odontesthes bonariensis , 1997 .

[12]  I. Parhar,et al.  GnRH neurons : gene to behavior , 1997 .

[13]  C. Schreck,et al.  Brain-pituitary-gonadal axis during early development and sexual differentiation in the rainbow trout, Oncorhynchus mykiss. , 1996, General and comparative endocrinology.

[14]  F. Takashima,et al.  Evidence of thermolabile sex determination in pejerrey , 1996 .

[15]  I. Huhtaniemi,et al.  Ontogeny of endocrine interactions of the rat hypothalamic–pituitary–gonadal axis , 1996 .

[16]  D. Crews Temperature-Dependent Sex Determination: The Interplay of Steroid Hormones and Temperature , 1996, Zoological science.

[17]  C. Pieau Temperature variation and sex determination in reptiles , 1996 .

[18]  C. A. Strüssmann,et al.  Sex differentiation and hormonal feminization in pejerrey Odontesthes bonariensis , 1996 .

[19]  L. Miranda,et al.  Immunocytochemical and morphometric study on the changes of TSH, PRL, GH and ACTH cells during the development of Bufo arenarum , 1995, Cell and Tissue Research.

[20]  D. Chourrout,et al.  Temperature and sex chromosomes govern sex ratios of the mouthbrooding Cichlid fish Oreochromis niloticus , 1995 .

[21]  H. Kawauchi,et al.  Purification and characterization of gonadotropin I and II from pituitary glands of tuna (Thunnus obesus) , 2009, International journal of peptide and protein research.

[22]  H. Kawauchi,et al.  Isolation and characterization of two distinct gonadotropins, GTHI and GTHII, from bonito (Katsuwonus plelamis) pituitary glands. , 2009, International journal of peptide & protein research.

[23]  M. Nozaki,et al.  Salmonid pituitary gonadotrophs. III. Chronological appearance of GTH I and other adenohypophysial hormones in the pituitary of the developing rainbow trout (Oncorhynchus mykiss irideus). , 1993, General and comparative endocrinology.

[24]  C. Schreck,et al.  In vitro steroid secretion during early development of mono-sex rainbow trout: sex differences, onset of pituitary control, and effects of dietary steroid treatment. , 1993, General and Comparative Endocrinology.

[25]  P. Thomas,et al.  Stimulation of in vitro steroidogenesis by pituitary hormones in a turtle (Trachemys scripta) within the temperature-sensitive period for sex determination. , 1992, Biology of reproduction.

[26]  R. Wallace,et al.  Fundulus heteroclitus gonadotropins. 3. Cloning and sequencing of gonadotropic hormone (GTH) I and II β-subunits using the polymerase chain reaction , 1992, Molecular and Cellular Endocrinology.

[27]  Richard C. Francis Sexual Lability in Teleosts: Developmental Factors , 1992, The Quarterly Review of Biology.

[28]  D. Nonclercq,et al.  Immunocytochemical study of cell type distribution in the pituitary of Barbus barbus (Teleostei, Cyprinidae). , 1991, General and comparative endocrinology.

[29]  H. Kawauchi,et al.  Isolation and characterization of two coho salmon gonadotropins, GTH I and GTH II. , 1991, Biology of reproduction.

[30]  M. Nozaki,et al.  Salmonid pituitary gonadotrophs. II. Ontogeny of GTH I and GTH II cells in the rainbow trout (Salmo gairdneri irideus). , 1990, General and comparative endocrinology.

[31]  M. Nozaki,et al.  Salmonid pituitary gonadotrophs. I. Distinct cellular distributions of two gonadotropins, GTH I and GTH II. , 1990, General and comparative endocrinology.

[32]  H. Kawauchi,et al.  Isolation and characterization of two distinct gonadotropins from chum salmon pituitary glands. , 1988, General and comparative endocrinology.

[33]  B. Kynard,et al.  Environmental sex determination: interaction of temperature and genotype in a fish. , 1981, Science.