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dc.contributor.authorCrespo, Diego
dc.contributor.authorAssis, Luiz H. C.
dc.contributor.authorZhang, Yu Ting
dc.contributor.authorSafian, Diego
dc.contributor.authorFurmanek, Tomasz
dc.contributor.authorSkaftnesmo, Kai Ove
dc.contributor.authorNorberg, Birgitta
dc.contributor.authorGe, Wei
dc.contributor.authorChoi, Yung-Ching
dc.contributor.authorden Broeder, Marjo J.
dc.contributor.authorLegler, Juliette
dc.contributor.authorBogerd, Jan
dc.contributor.authorSchulz, Rüdiger W
dc.date.accessioned2021-10-22T12:44:30Z
dc.date.available2021-10-22T12:44:30Z
dc.date.created2021-08-24T16:43:03Z
dc.date.issued2021
dc.identifier.citationCommunications Biology. 2021, 4 (1), 1-13.en_US
dc.identifier.issn2399-3642
dc.identifier.urihttps://hdl.handle.net/11250/2825042
dc.description.abstractPituitary hormones can use local signaling molecules to regulate target tissue functions. In adult zebrafish testes, follicle-stimulating hormone (Fsh) strongly increases the production of insulin-like 3 (Insl3), a Leydig cell-derived growth factor found in all vertebrates. Little information is available regarding Insl3 function in adult spermatogenesis. The Insl3 receptors Rxfp2a and 2b were expressed by type A spermatogonia and Sertoli and myoid cells, respectively, in zebrafish testis tissue. Loss of insl3 increased germ cell apoptosis in males starting at 9 months of age, but spermatogenesis appeared normal in fully fertile, younger adults. Insl3 changed the expression of 409 testicular genes. Among others, retinoic acid (RA) signaling was up- and peroxisome proliferator-activated receptor gamma (Pparg) signaling was down-regulated. Follow-up studies showed that RA and Pparg signaling mediated Insl3 effects, resulting in the increased production of differentiating spermatogonia. This suggests that Insl3 recruits two locally active nuclear receptor pathways to implement pituitary (Fsh) stimulation of spermatogenesis.en_US
dc.language.isoengen_US
dc.titleInsulin-like 3 affects zebrafish spermatogenic cells directly and via Sertoli cellsen_US
dc.typePeer revieweden_US
dc.typeJournal articleen_US
dc.description.versionpublishedVersionen_US
dc.source.pagenumber1-13en_US
dc.source.volume4en_US
dc.source.journalCommunications Biologyen_US
dc.source.issue1en_US
dc.identifier.doi10.1038/s42003-021-01708-y
dc.identifier.cristin1928445
dc.relation.projectNorges forskningsråd: 226221en_US
dc.relation.projectNorges forskningsråd: 221648en_US
cristin.ispublishedtrue
cristin.fulltextoriginal
cristin.qualitycode1


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