Lussier J G, Carruthers T D, Murphy B D
Université de Montréal, Faculté de Médecine Vétérinaire, Centre de Recherche en Reproduction Animale, St-Hyacinthe, Quebec, Canada.
Reprod Nutr Dev. 1993;33(2):109-19. doi: 10.1051/rnd:19930203.
We have established a dispersed bovine pituitary cell culture system to study the effects of charcoal-extracted bovine follicular fluid (BFF) or bovine inhibin, partially purified by immunoaffinity chromatography (IPI), on the spontaneous release of follicle-stimulating hormone (FSH) and luteinizing hormone (LH). Pituitary cells were plated at 0.25, 0.5 or 1 x 10(6) viable cells/well (c/w) and incubated for 48 h. The medium was replaced and BFF (0, 0.54, 2.7, 13.7, 68.7 or 343.5 micrograms protein) or IPI (0, 0.01, 0.06, 0.29, 1.45 or 7.25 micrograms protein) added to the cultures and the incubation was continued for 48 h. Concentrations of FSH and LH in spent medium were determined by RIA and data analyzed by ANOVA with means compared by Student-Neuman-Keuls (SNK) test. We have shown an increase in spontaneous FSH and LH release attributable to both number of bovine pituitary cells plated and to the length of incubation. The addition of BFF reduced spontaneous FSH release over 48 h incubation. The dose-dependent inhibition curves observed in culture in which different numbers of cells were plated, indicates that inhibition was greater when 1 x 10(6) c/w were plated compared to 0.25 or 0.5 x 10(6) c/w. Bovine follicular fluid at 0.45 micrograms of protein (equivalent to 0.01 microliters of BFF) incubated with 1 x 10(6) c/w, suppressed FSH release by 10.6% compare to control. Maximal suppression of 34.1% was obtained with 50 micrograms (equivalent to 1.56 microliters of BFF). Immunopurified bovine inhibin at 1.45 micrograms tended to suppress FSH release and at 7.25 micrograms significantly reduced FSH release. Neither BFF nor IPI had a measurable effect on LH release. We conclude that BFF and IPI suppress the spontaneous release of FSH from bovine pituitary cells in culture in a dose-dependent manner, without concomitant suppression of LH release.
我们建立了一种分散的牛垂体细胞培养系统,以研究经活性炭处理的牛卵泡液(BFF)或经免疫亲和层析部分纯化的牛抑制素(IPI)对促卵泡激素(FSH)和促黄体生成素(LH)自发释放的影响。将垂体细胞以0.25、0.5或1×10⁶个活细胞/孔(c/w)接种,孵育48小时。更换培养基,向培养物中添加BFF(0、0.54、2.7、13.7、68.7或343.5微克蛋白质)或IPI(0、0.01、0.06、0.29、1.45或7.25微克蛋白质),并继续孵育48小时。通过放射免疫分析法(RIA)测定用过的培养基中FSH和LH的浓度,并采用方差分析(ANOVA)分析数据,均值通过Student-Neuman-Keuls(SNK)检验进行比较。我们已经表明,接种的牛垂体细胞数量和孵育时间均会导致FSH和LH的自发释放增加。添加BFF可在48小时孵育期间减少FSH的自发释放。在接种不同数量细胞的培养物中观察到的剂量依赖性抑制曲线表明,与接种0.25或0.5×10⁶ c/w相比,接种1×10⁶ c/w时抑制作用更强。与对照组相比,用0.45微克蛋白质(相当于0.01微升BFF)的牛卵泡液与1×10⁶ c/w一起孵育,可使FSH释放抑制10.6%。使用50微克(相当于1.56微升BFF)可获得34.1%的最大抑制率。1.45微克的免疫纯化牛抑制素倾向于抑制FSH释放,而7.25微克则显著降低FSH释放。BFF和IPI对LH释放均无明显影响。我们得出结论,BFF和IPI以剂量依赖性方式抑制培养的牛垂体细胞中FSH的自发释放,而不会同时抑制LH释放。