Endocrine and paracrine regulation of zebrafish spermatogenesis: The Sertoli cell perspective

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MetadadosDescriçãoIdioma
Autor(es): dc.contributorUniversidade Estadual Paulista (UNESP)-
Autor(es): dc.creatorSchulz, R. W.-
Autor(es): dc.creatorNóbrega, R. H.-
Autor(es): dc.creatorMorais, R. D.V.S.-
Autor(es): dc.creatorDe Waal, P. P.-
Autor(es): dc.creatorFrança, L. R.-
Autor(es): dc.creatorBogerd, J.-
Data de aceite: dc.date.accessioned2021-03-11T00:27:54Z-
Data de disponibilização: dc.date.available2021-03-11T00:27:54Z-
Data de envio: dc.date.issued2018-12-11-
Data de envio: dc.date.issued2018-12-11-
Data de envio: dc.date.issued2015-01-01-
Fonte completa do material: dc.identifierhttp://hdl.handle.net/11449/167853-
Fonte: dc.identifier.urihttp://educapes.capes.gov.br/handle/11449/167853-
Descrição: dc.descriptionSpermatogonial stem cells (SSCs) either self-renew or differentiate into spermatogonia that further develop into spermatozoa. Self-renewal occurs when residing in a specific micro-environment (niche) while displacement from the niche would tip the signalling balance towards differentiation. Considering the cystic type of spermatogenesis in fish, the SSC candidates are single type A undifferentiated (A<inf>und</inf>) spermatogonia, enveloped by mostly one niche-forming Sertoli cell. When going through a self-renewal cell cycle, the resulting new single type A<inf>und</inf> spermatogonium would have to recruit another Sertoli cell to expand the niche space, while a differentiating germ cell cyle would result in a pair of spermatogonia that remain in contact with their cyst-forming Sertoli cells. In zebrafish, thyroid hormone stimulates the proliferation of Sertoli cells and of type A<inf>und</inf> spermatogonia, involving Igf3, a new member of the Igf family. In cystic spermatogenesis, type A<inf>und</inf> spermatogonia usually do not leave the niche, so that supposedly the signalling in the niche changes when switching from self-renewal to differentiation. Recombinant zebrafish (rz) Fsh down-regulated Sertoli cell anti-müllerian hormone (amh) mRNA levels, and rzAmh inhibited differentiation of type A<inf>und</inf> spermatogonia as well as Fsh-stimulated steroidogenesis. Thus, for Fsh to efficiently stimulate testis functions, Amh bioactivity should be dampened. We also discovered that Fsh increased Sertoli cell Igf3 gene and protein expression; rzIgf3 stimulated spermatogonial proliferation and Fsh-stimulated spermatogenesis was significantly impaired by inhibiting Igf receptor signaling. We propose that in zebrafish, Fsh is the major regulator of testis functions and, supported by other endocrine systems (e.g. thyroid hormone), regulates Leydig cell steroidogenesis as well as Sertoli cell number and growth factor production to promote spermatogenesis.-
Formato: dc.format81-87-
Idioma: dc.languageen-
Relação: dc.relationAnimal Reproduction-
Relação: dc.relation0,308-
Relação: dc.relation0,308-
Direitos: dc.rightsclosedAccess-
Palavras-chave: dc.subjectFollicle-stimulating hormone-
Palavras-chave: dc.subjectGrowth factors-
Palavras-chave: dc.subjectSertoli cells-
Palavras-chave: dc.subjectSex steroids-
Palavras-chave: dc.subjectSpermatogenesis-
Palavras-chave: dc.subjectSpermatogonial stem cells-
Palavras-chave: dc.subjectThyroid hormones-
Palavras-chave: dc.subjectZebrafish-
Título: dc.titleEndocrine and paracrine regulation of zebrafish spermatogenesis: The Sertoli cell perspective-
Tipo de arquivo: dc.typelivro digital-
Aparece nas coleções:Repositório Institucional - Unesp

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