Japanese Eel Follicle-Stimulating Hormone (Fsh) and Luteinizing Hormone (Lh): Production of Biologically Active Recombinant Fsh and Lh by Drosophila S2 Cells and Their Differential Actions on the Reproductive Biology
Two gonadotropins (Gths), follicle-stimulating hormone (Fsh) and luteinizing hormone (Lh), control gonadal steroidogenesis and gametogenesis in vertebrates, including teleost fish. Here, we report on the production of biologically active recombinant Fsh (rec-Fsh) and Lh (rec-Lh) in Japanese eel usin...
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Veröffentlicht in: | Biology of reproduction 2008-11, Vol.79 (5), p.938-946 |
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Zusammenfassung: | Two gonadotropins (Gths), follicle-stimulating hormone (Fsh) and luteinizing hormone (Lh), control gonadal steroidogenesis
and gametogenesis in vertebrates, including teleost fish. Here, we report on the production of biologically active recombinant
Fsh (rec-Fsh) and Lh (rec-Lh) in Japanese eel using Drosophila S2 cells. The three subunits composing Gths, i.e., glycoprotein hormone, alpha polypeptide (Cga), follicle-stimulating hormone,
beta polypeptide (Fshb), and luteinizing hormone, beta polypeptide (Lhb), were at first independently produced and were proven
to be glycosylated and secreted as the mature peptides. Each beta subunit, along with its Cga, was simultaneously coexpressed
to produce heterodimeric rec-Fsh and rec-Lh that were subsequently highly purified. The biological activity of rec-Gths was
demonstrated in various in vitro assays. The rec-Gths differentially activated their receptors, which resulted in an increase
in 11-ketotestosterone (11KT) secretion, a differential alteration of gene expression of steroidogenic enzymes in immature
testis, and the induction of the complete process of spermatogenesis in vitro. The data strongly suggest that Fsh and Lh differentially
play important roles in the reproductive physiology of the Japanese eel. By contrast, these rec-Gths exhibited little activity
in the gonad when administered in vivo. This difference between in vitro and in vivo bioactivity is probably due to the qualitative
nature of glycosylation in S2 cells, which resulted in degradation of the recombinant protein in vivo. These differences in
the carbohydrate moieties need to be elucidated and ameliorated. . |
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ISSN: | 0006-3363 1529-7268 |
DOI: | 10.1095/biolreprod.108.070052 |