Study summary · research use only
Evidence for the existence of a local activin follistatin negative feedback loop in the goldfish pituitary and its regulation by activin and gonadal steroids
Plain-language summary
Paraphrased from the published abstract below — not a verdict on whether anything works.
In this goldfish study, the authors examined a local activin-follistatin feedback loop in the pituitary. A full-length follistatin cDNA was cloned in goldfish, showing 74% amino acid identity with mammals. Recombinant goldfish follistatin expressed in Chinese hamster ovary cells blocked activin-induced F5-5 cell differentiation. Follistatin was expressed across tissues including brain, pituitary, ovary, and testis, and its pituitary mRNA expression was regulated by activin and gonadal steroids in vitro. Treatment with goldfish activin B for 48 h up-regulated follistatin expression, suggesting a closed feedback loop, while both human and goldfish follistatin down-regulated follistatin's own expression. Examination of FSHbeta and LHbeta expression supported roles in differential FSH/LH regulation. Estradiol and testosterone up-regulated follistatin in vitro. The authors suggest follistatin plays a regulatory role in the intra-pituitary activin system in teleosts.
Abstract
Activin is an important regulator of gonadotropin expression and production in the vertebrate pituitary, and its activity is fine-tuned by its binding protein follistatin. In the present study, a full-length cDNA for follistatin was cloned in the goldfish, which shows 74% amino acid sequence identity with that of mammals. Recombinant goldfish follistatin expressed in the Chinese hamster ovary cells significantly blocked activin-induced F5-5 cell differentiation. Goldfish follistatin is expressed in a wide range of tissues including the brain, pituitary, ovary, and testis. The expression of follistatin mRNA in the pituitary is regulated by both activin and gonadal steroids in vitro. Treatment with goldfish activin B for 48 h significantly up-regulated follistatin expression in cultured pituitary cells, suggesting a closed activin-follistatin feedback loop in the pituitary. In agreement with this, both human and goldfish follistatin down-regulated the expression of follistatin itself, probably due to the neutralization of endogenous activin. Examination of FSHbeta and LHbeta expression in the same samples supports the role of activin and follistatin in the differential regulation of FSH and LH as demonstrated previously. Since the expression level of activin beta(B) in the pituitary is rather stable both in vitro and in vivo, it is conceivable that follistatin may play a pivotal regulatory role in the intra-pituitary activin system. Both estradiol and testosterone up-regulated follistatin expression in vitro, suggesting a mediating role for follistatin in steroid feedback on pituitary hormones. These results provide clues to the potential physiological roles of activin-follistatin system in the regulation of gonadotropin biosynthesis in teleosts.
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