Insulin-like growth factor-I and -II binding and action on DNA synthesis in rainbow trout spermatogonia and spermatocytes
| Autor: | Loir, Maurice, Le Gac, Florence |
|---|---|
| Přispěvatelé: | Station de physiologie des poissons, Institut National de la Recherche Agronomique (INRA) |
| Rok vydání: | 1994 |
| Předmět: |
Male
gamète biosynthèse Tritium reproduction Iodine Radioisotopes poisson spermatogonie Insulin-Like Growth Factor II Spermatocytes facteur de croissance Biologie de la reproduction somatomédine Animals Insulin Insulin-Like Growth Factor I Cells Cultured fish trout Reproductive Biology Dose-Response Relationship Drug growth factor spermatogonia spermatocyte adn contrôle hormonal [SDV.BDLR]Life Sciences [q-bio]/Reproductive Biology DNA facteur de croissance igf 1 facteur de croissance igf 2 Spermatogonia Insulin-Like Growth Factor Binding Proteins Bromodeoxyuridine Oncorhynchus mykiss testicule Carrier Proteins acide nucléique récepteur truite arc en ciel Thymidine |
| Zdroj: | Biology of Reproduction (51), 1154-1163. (1994) Biology of Reproduction Biology of Reproduction, Society for the Study of Reproduction, 1994, 51, pp.1154-1163. ⟨10.1095/biolreprod51.6.1154⟩ |
| ISSN: | 0006-3363 1529-7268 |
| DOI: | 10.1095/biolreprod51.6.1154⟩ |
| Popis: | International audience; Radio-labeled recombinant human insulin-like growth factor (I-125-rhIGF-I) bound specifically to total testicular cells and to spermatogonia plus primary spermatocytes (Go+Cl) that had been prepared from trout testes at various maturation stages by centrifugal elutriation and then cleared of somatic cells by preculture in the presence of 2% Ultroser G. Binding sites showed high affinity (Ka = 0.5 +/- 0.2 x 10(10) M(-1)) and low capacity (1.1 +/- 0.8 fmol/10(6) testicular cells) for I-125-IGF-I. (Gln(3), Ala(4), Tyr(15) Leu(16))IGF-I ([QAYL]IGF-I) was equipotent to IGF-I in competing with I-125-IGF-I for site occupancy on Go+Cl. Insulin-like growth factor-II (IGF-II) was 3- to 10-fold less potent than IGF-I or (QAYL)IGF-I, while bovine insulin competed only at about 300-fold higher concentrations. Go+Cl were cultured for 3 days in the presence or absence of mammalian IGF-I, IGF-II, (QAYL)IGF-I, and salmon or bovine insulin. All these molecules stimulated the incorporation of [H-3]thymidine (added during the last 24 h in culture) by Go+Cl in a dose-dependent manner. The mean ED(50), independent of testicular maturation stage, was 5.9 +/- 4.9 ng/ml and 29.1 +/- 15.8 ng/ml for IGF-I and IGF-II, respectively. (QAYL)IGF-I was as potent as IGF-I. Concentrations of salmon or bovine insulin 100- to 300-fold higher were required to produce effects similar to those of IGF-I. While recombinant human IGF binding protein (IGFBP-3) had no effect by itself on basal [H-3]thymidine incorporation, it inhibited the effect of IGF-I in a dose-dependent manner; however, it had no effect on the stimulation by (QAYL)IGF-I. Although combinations of low concentrations of IGF-I and IGF-II or salmon insulin had additive effects, combinations of maximum concentrations did not. We conclude that, in vitro, IGFs stimulate DNA synthesis of trout male germ cells by interacting directly with these cells through one IGF receptor. |
| Databáze: | OpenAIRE |
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