Carsia R V, Weber H
Department of Animal Sciences, Rutgers State University, New Brunswick, New Jersey 08903.
Endocrinology. 1988 Feb;122(2):681-8. doi: 10.1210/endo-122-2-681.
Our previous work suggests that persistent protein malnutrition in immature domestic fowl (Gallus gallus domesticus) alters ACTH-adrenocortical cell interaction, possibly including ACTH receptors. To investigate this possibility, we measured some ACTH receptor parameters in isolated adrenocortical cells from normal and dietary protein-restricted domestic fowl. White Leghorn cockerels (2 weeks old) were fed isocaloric semipurified diets containing either 8% [low (L)] or 20% [normal (N)] soy protein for 4 weeks ad libitum. Cockerels were quickly killed by decapitation and exsanguination, and adrenal glands were removed and prepared for cell isolation. Highly enriched (greater than 80% pure) adrenocortical cells (collagenase isolated, followed by separation on a Percoll continuous density gradient) were evaluated for ACTH receptors using pharmacological and radioligand approaches. In a pharmacological approach, we measured the influence of the complete, competitive antagonist, human (h) ACTH-(7-38) on hACTH-(7-39)-induced corticosterone production by adrenocortical cells from L and N cockerels. Inhibitor constants of hACTH-(7-38), calculated from Schild plots, were 3.16 X 10(-7) and 9.82 X 10(-7) M for L and N cockerel cells, respectively, thus suggesting differences in ACTH receptor function between the two treatment groups. To characterize ACTH receptors directly, we measured the binding of a monoiodinated ACTH analog [125I-Tyr23]hACTH-(1-39) to domestic fowl adrenocortical cells. Binding was linear with cell concentration, highly specific (only ACTH peptides caused significant displacement), rapid (maximal binding by 1 h), reversible (half-time of dissociation, approximately 40 min), and saturable. Curvilinear Scatchard plots were obtained, and vectorial analysis resolved both high and low affinity sites. The concentrations (femtomoles per 50 micrograms DNA) and dissociation constants (Kd) of both classes of sites were different between N and L bird cells. Values of these receptor parameters for N and L cockerel cells were, respectively, as follows: concentrations of low affinity sites, 7.45 and 11.60; concentrations of high affinity sites, 3.16 and 5.50; Kd of low affinity sites, 2.05 X 10(-8) and 2.58 X 10(-9) M; Kd of high affinity sites, 1.01 X 10(-9) and 1.27 X 10(-10) M. Thus, the overall binding capacity of L bird cells was 65% greater than that of N bird cells. In addition, the overall affinity (1/Kd) of sites of L bird cells was 9 times that of sites of N bird cells. These data indicate that persistent protein malnutrition in the domestic fowl increased both the number and affinity of adrenocortical cell ACTH receptors.
我们之前的研究表明,未成熟家禽(家鸡)长期蛋白质营养不良会改变促肾上腺皮质激素(ACTH)与肾上腺皮质细胞的相互作用,可能还包括ACTH受体。为了探究这种可能性,我们测定了正常饮食和蛋白质限制饮食的家禽分离肾上腺皮质细胞中的一些ACTH受体参数。将白色来航公鸡(2周龄)随意喂食含8%[低蛋白(L)]或20%[正常蛋白(N)]大豆蛋白的等热量半纯化日粮4周。通过断头放血快速处死公鸡,取出肾上腺并准备进行细胞分离。使用药理学和放射性配体方法评估高度富集(纯度大于80%)的肾上腺皮质细胞(经胶原酶分离,然后在Percoll连续密度梯度上分离)的ACTH受体。在药理学方法中,我们测定了完全竞争性拮抗剂人(h)ACTH-(7 - 38)对L组和N组公鸡肾上腺皮质细胞中hACTH-(7 - 39)诱导的皮质酮生成的影响。根据Schild图计算,hACTH-(7 - 38)对L组和N组公鸡细胞的抑制常数分别为3.16×10⁻⁷和9.82×10⁻⁷ M,这表明两个处理组之间ACTH受体功能存在差异。为了直接表征ACTH受体,我们测定了单碘化ACTH类似物[¹²⁵I-Tyr²³]hACTH-(1 - 39)与家禽肾上腺皮质细胞的结合。结合与细胞浓度呈线性关系,具有高度特异性(只有ACTH肽能引起显著的置换),快速(1小时达到最大结合),可逆(解离半衰期约40分钟)且可饱和。得到了曲线型Scatchard图,矢量分析解析出高亲和力和低亲和力位点。N组和L组禽类细胞中这两类位点的浓度(每50微克DNA的飞摩尔数)和解离常数(Kd)均不同。N组和L组公鸡细胞这些受体参数的值分别如下:低亲和力位点浓度,7.45和11.60;高亲和力位点浓度,3.16和5.50;低亲和力位点Kd,2.05×10⁻⁸和2.58×10⁻⁹ M;高亲和力位点Kd,1.01×10⁻⁹和