Massart S, Ban A M, Renaville R, Van Eenaeme C, Sneyers M, Falaki M, Istasse L, Clinquart A, Devolder A, Burny A, Portetelle D
Molecular Biology and Animal Physiology Department, Faculty of Agronomy, Gembloux, Belgium.
Domest Anim Endocrinol. 1996 Jan;13(1):47-57. doi: 10.1016/0739-7240(95)00043-7.
The purpose of this study was to characterize circulating growth hormone-binding proteins (GHBP) and prolactin-binding proteins (PRLBP) in cattle blood plasma. In particular, the 24-hr profile of these molecules was investigated. The preincubation of bull plasma with iodinated bovine growth hormone (bGH) or bovine prolactin (bPRL), followed by gel filtration chromatography (Superdex 200; 1.6 x 60 cm column), resulted in the formation of essentially two complexes. The majority of [125I]bPRL eluted with the first one (M(r) approximately 600 kDa), whereas [125I]bGH mainly appeared in the second one (M(r) approximately 70 kDa). The fractions corresponding to these two peaks were analyzed by western ligand blotting (WLB), under reducing conditions. WLB revealed, respectively, 190-, 56-, 52-, and 28-kDa bands for the first peak and only 52- and 28-kDa bands for the second one. The nature of the 600-kDa peak is at present undetermined, but the 70-kDa one was previously identified as high-affinity GHBP. Displacement studies demonstrated that bGH and bPRL were both able to bind to this GHBP, because the bGH- and bPRL-binding activities of this protein could be saturated by an excess of either of these two hormones. This was indirectly confirmed by the close correlation (r = 0.615; P = 0.0001; n = 155) observed between plasma bGH- and bPRL-binding activities, because this correlation could suggest that both ligands are bound to the same proteins. The temporal concentrations of plasma GHBP were measured in samples collected at 20-min intervals for 24 hr from 8 young bulls. The evaluation of GHBP was realized by WLB, followed by densitometric analysis. Some fluctuations were observed, but these were not correlated with bGH release, even with a +/- 2-hr lag period. In summary, we found that bovine high-affinity GHBP binds not only bGH, but also bPRL. A second type of protein, of higher molecular weight, also binds these two hormones, but further investigations are needed to determine its nature. Finally, GHBP concentrations in cattle blood plasma apparently show fluctuations over a 24-hr period, but no correlation was found between these fluctuations and plasma growth hormone concentrations.
本研究的目的是对牛血浆中循环生长激素结合蛋白(GHBP)和催乳素结合蛋白(PRLBP)进行特性分析。特别地,对这些分子的24小时变化情况进行了研究。将公牛血浆与碘化牛生长激素(bGH)或牛催乳素(bPRL)预孵育,然后进行凝胶过滤色谱分析(Superdex 200;1.6×60 cm柱),结果基本上形成了两种复合物。大部分[125I]bPRL随第一种复合物洗脱(相对分子质量约为600 kDa),而[125I]bGH主要出现在第二种复合物中(相对分子质量约为70 kDa)。在还原条件下,通过western配体印迹法(WLB)对对应于这两个峰的组分进行分析。WLB分别在第一个峰中检测到190 kDa、56 kDa、52 kDa和28 kDa的条带,在第二个峰中仅检测到52 kDa和28 kDa的条带。600 kDa峰的性质目前尚不确定,但70 kDa的峰先前已被鉴定为高亲和力GHBP。置换研究表明bGH和bPRL都能够与这种GHBP结合,因为该蛋白的bGH和bPRL结合活性都可以被这两种激素中的任何一种过量饱和。血浆bGH和bPRL结合活性之间存在密切相关性(r = 0.615;P = 0.0001;n = 155),这间接证实了上述结论,因为这种相关性可能表明两种配体都与相同的蛋白质结合。从8头年轻公牛身上每隔20分钟采集一次样本,共采集24小时,测定血浆中GHBP的时间浓度。通过WLB进行GHBP评估,随后进行光密度分析。观察到了一些波动,但即使有±2小时的延迟期,这些波动也与bGH释放无关。总之,我们发现牛高亲和力GHBP不仅能结合bGH,还能结合bPRL。另一种分子量更高的蛋白质也能结合这两种激素,但需要进一步研究来确定其性质。最后,牛血浆中GHBP浓度在24小时内显然呈现波动,但未发现这些波动与血浆生长激素浓度之间存在相关性。