ABSTRACT
The objective of this study was to establish a protocol for the characterization, isolation, and culture of type A spermatogonia using specific molecular markers for these cells in fish. To this end, adult Prochilodus lineatus testes were collected and digested enzymatically and the resulting testicular suspension was separated using a discontinuous Percoll gradient, followed by differential plating. The cell cultures obtained were monitored for 15 days and analyzed using the immunofluorescence method with anti-Vasa, anti-GFRα1, and anti-OCT4 antibodies. Spermatogonial enrichment was also performed using flow cytometry. Although discontinuous Percoll gradient centrifugation followed by differential plating enabled the removal of differentiated germ cells and somatic cells, enriching the pool of type A spermatogonia, the enrichment of type A spermatogonia through flow cytometry of samples without Percoll proved to be more efficient. Prominent cell agglomerates that were characterized according to different stem cell markers as type A spermatogonia were observed during the 15 days of the cell culture. The use of immunoperoxidase and western blot analysis methods confirmed the specificity of the markers for type A spermatogonia of P. lineatus. When combined with specific cell culture conditions, the positive characterization of these molecular markers clarified certain aspects of spermatogonial regulation, such as survival and proliferation. Finally, understanding the regulation of the in vitro germ cell maintenance process may contribute to the enhancement of in vivo and in vitro reproduction techniques of endangered or aquaculture fish species.
ABSTRACT
Gonadotropin-releasing hormone (GnRH) is a key molecule in the initiation of the hypothalamic-pituitary-gonadal axis. Thus, knowledge about GnRH may contribute to the effectiveness of species reproduction. Using a Neotropical tetra Astyanax altiparanae as a fish model species, the GnRH forms were characterized at the molecular level and the role of injected GnRHs in vivo was evaluated. The full-length complementary DNA (cDNA) sequences of preproGnRH2 (612 bp) and preproGnRH3 (407 bp) of A. altiparanae were obtained, and the GnRH1 form was not detected. The cDNA sequences of preproGnRH2 and preproGnRH3 were found to be conserved, but a change in the amino acid at position 8 of the GnRH3 decapeptide of A. altiparanae was observed. All the injected GnRHs stimulated lhß messenger RNA (mRNA) expression but not fshß mRNA expression, and only GnRH2 was able to increase maturation-inducing steroid (MIS) levels and possibly stimulate oocyte release. Furthermore, only GnRH2 was able to start the entire reproductive hormonal cascade and induce spawning.
Subject(s)
Characidae , Gonadotropin-Releasing Hormone/genetics , Gonadotropin-Releasing Hormone/pharmacology , Reproduction/drug effects , Animals , Characidae/genetics , Characidae/metabolism , Characidae/physiology , Characiformes/genetics , Characiformes/metabolism , Cloning, Molecular , Female , Gonadotropin-Releasing Hormone/metabolism , Protein Precursors/genetics , Protein Precursors/metabolism , Pyrrolidonecarboxylic Acid/analogs & derivatives , Pyrrolidonecarboxylic Acid/metabolism , Reproduction/genetics , Sequence Analysis, DNA/veterinaryABSTRACT
The pituitary gonadotropins, Fsh (follicle-stimulating hormone) and Lh (luteinizing hormone), regulate testicular development and functions in all vertebrates. At the pituitary, different signaling systems regulate the synthesis and secretion of the gonadotropins, such as the hypothalamic neuropeptides GnRH (gonadotropin-releasing hormone) and GnIH (gonadotropin-inhibitory hormone). While GnRH exerts stimulatory roles, the actions of GnIH remain controversial for many teleost species. Therefore, the aim of this study was to evaluate the in vitro effects of chicken GnRH2 (cGnRH2) and zebrafish GnIH-3 (zGnIH-3) on the male gonadotropin and GnRH system expression using pituitary explants and brain slices from a neotropical species with economical and ecological relevance, Astyanax altiparanae. Our results showed that in males, cGnRH2 increased fshb and lhb mRNA levels in the pituitary explants. Interestingly, zGnIH-3 has no effect on basal gonadotropin expression, however zGnIH-3 decreased the cGnRH2-induced fshb and lhb transcripts in male pituitary explants. In the male brain slices, zGnIH-3 showed stimulatory effects, increasing gnrh2 mRNA levels. Overall, our results suggested that GnIH seems to have dual regulatory actions on gonadotropin and GnRH2 expression of A. altiparanae males. This study provided basic information on endocrine regulation of A. altiparanae reproduction, and the obtained results will expand our knowledge, improving the reproductive management of this economically important freshwater species.
Subject(s)
Brain/metabolism , Characidae/metabolism , Gonadotropin-Releasing Hormone/pharmacology , Neuropeptides/pharmacology , Pituitary Gland/metabolism , Animals , Brain/drug effects , Characidae/genetics , Chickens , Female , Male , Models, Biological , Pituitary Gland/anatomy & histology , Pituitary Gland/drug effects , RNA, Messenger/genetics , Reference Standards , Time Factors , ZebrafishABSTRACT
O desenvolvimento embrionário dos peixes é de grande importância para a piscicultura e na reintrodução de espécies ameaçadas de extinção em seus ambientes, e seu conhecimento constitui uma importante maneira para minimizar doenças e mortalidades dessas espécies. Com o auxílio de técnicas como a Microscopia Eletrônica de Varredura (MEV) e a imuno-histoquimica para identificar proteínas ósseas, foi possível avaliar as fases de desenvolvimento com mais riqueza de detalhes, facilitando a compreensão de hábitos e da biologia da espécie. Neste trabalho pudemos observar a ontogenia e osteogênese da Piapara (Leporinus elongatus), desde a fecundação até a fase juvenil, sendo evidenciadas estruturas importantes como o tamanho do vitelo, essencial para a nutrição do embrião; o fechamento do blastóporo, evento principal da embriogênese, que indica as taxas de fertilização; a metamorfose, que indica a formação dos primeiros e principais órgãos do animal e a formação de sua estrutura óssea. As Proteínas Ósseas Morfogenéticas (BMP-2 e BMP-4), moléculas essenciais reguladoras no desenvolvimento embrionário e na formação óssea, foram observadas apenas no estádio larval até o período juvenil, não sendo evidenciadas nos estágios anteriores. Os resultados desse trabalho trouxeram novas informações quanto à biologia do desenvolvimento dessa espécie, que certamente poderão auxiliar no aprimoramento de técnicas reprodutivas visando uma melhora na sua produção seja para fins comerciais ou de repovoamento.(AU)
The embryonic development of fishes has great importance in fish culture and on reintroduction of species at risk of extinction into their environment; its knowledge constitutes an important way to minimize diseases and mortality of these species. By using techniques like electron microscopy and immunohistochemistry for bone markers identification, it was possible to evaluate the developmental stages of Leporinus elongatus in more details, helping to clarify the habits and biology of this species. Results showed the ontogeny and ostheogenesis of of Leporinus elongatus this species from fecundation to juvenile, evidencing important structures as size of the yolk, essential to embryo nutrition, the blastopores closure, important event in embryogenesis because it indicates fertilization indexes, and the metamorphosis, which shows the main organs' development including bones. Bone morphogenetic markers 1 and 4, essential regulatory molecules for bone development, had their expression restricted from larva to fry stages, and were not observed in their previous stages. In sum, these results provided new data that may improve reproductive techniques for L. elongatus, and will support commercial and repopulation purposes.(AU)
