1996
DOI: 10.1002/(sici)1097-010x(19960501)275:1<45::aid-jez7>3.0.co;2-a
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Pigment dispersion by prolactin in cultured xanthophores and erythrophores of some fish species

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Cited by 30 publications
(25 citation statements)
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“…In this case, a higher affinity for PRL 188 was observed and a correspondingly lower concentration of hormone was required to activate the Jak2/Stat5 pathway (Sohm et al, 1998). In addition, different potencies were reported for the two prolactins with regard to their effect on pigment dispersion in cultured xanthophores and erythrophores (Oshima et al, 1996). Pigment dispersion was affected by nanomolar concentrations of tilapia PRL 177 but only by micromolar concentrations of tilapia PRL 188 .…”
Section: Both Tilapia Prolactin Receptors Are Widely Expressed and Rementioning
confidence: 90%
“…In this case, a higher affinity for PRL 188 was observed and a correspondingly lower concentration of hormone was required to activate the Jak2/Stat5 pathway (Sohm et al, 1998). In addition, different potencies were reported for the two prolactins with regard to their effect on pigment dispersion in cultured xanthophores and erythrophores (Oshima et al, 1996). Pigment dispersion was affected by nanomolar concentrations of tilapia PRL 177 but only by micromolar concentrations of tilapia PRL 188 .…”
Section: Both Tilapia Prolactin Receptors Are Widely Expressed and Rementioning
confidence: 90%
“…In addition to GH, the tilapia pituitary secretes two forms of prolactin (tPRL177 and tPRL188), one of which contain 177 amino acid residues, and the other, 188 amino acid residues. These two prolactins, to which unique functions have been ascribed (Rubin & Specker 1992, Oshima et al 1996, are encoded by separate genes and share only 69% sequence identity (Specker et al 1985, Rentier-Delrue et al 1989, Yamaguchi et al 1991. In this study, we report the effects of KP-102 treatment on circulating GH and PRL(s) levels in a cichlid teleost.…”
Section: Introductionmentioning
confidence: 99%
“…The amino acid sequence identity of the two prolactins is only 69%, with each form being encoded by separate genes (Yamaguchi et al 1988, Rentier-Delrue et al 1989. Given these differences, studies have aimed at determining their unique physiological functions in ion and water balance (Specker et al 1985, Young et al 1988, Specker et al 1989, Auperin et al 1994, 1995, Flik et al 1994, growth (Shepherd et al 1997b), reproduction (Rubin & Specker 1992, Oshima et al 1996 and pigmentation (Kitta et al 1993, Oshima et al 1996. Both forms of PRL are colocalized within the same cells of the rostral pars distalis (RPD) of the pituitary , Specker et al 1993, but when the ratio of the two prolactins (tPRL 188 :tPRL 177 ) is examined, it becomes evident that they are differentially regulated during development (Ayson et al 1994), and by changes in environmental salinity (Borski et al 1992, Auperin et al 1994, Yada et al 1994, Yoshikawa-Ebesu et al 1995 and nutrition (Vijayan et al 1996, Shepherd et al 1997a.…”
Section: Introductionmentioning
confidence: 99%