Norton J N, Skinner M K
Department of Pharmacology, Vanderbilt University School of Medicine, Nashville, Tennessee 37232.
Endocrinology. 1989 Jun;124(6):2711-9. doi: 10.1210/endo-124-6-2711.
The current study was designed to investigate the actions of the testicular paracrine factor P-Mod-S on Sertoli cell function and differentiation. Transferrin production by Sertoli cells was stimulated by P-Mod-S to a greater extent than any individual regulatory agent and in a manner similar to a combination of FSH, insulin, retinol, and testosterone (FIRT). P-Mod-S had an additive response in combination with FIRT. The increase in transferrin production with a combination of P-Mod-S and FIRT is the highest level of stimulation (up to 8-fold) observed. These profound effects of P-Mod-S on Sertoli cell function implied a potential unique mechanism of action for the paracrine factor. FSH and FIRT significantly stimulated cAMP levels with both 60-min and 72-h treatments. In contrast, P-Mod-S had no effect on cAMP levels with a 60-min treatment and only a small increase with a 72-h treatment. Interestingly, P-Mod-S stimulated cGMP levels that remained above basal levels up to 72 h of treatment. FSH had no effect on cGMP levels. P-Mod-S did not affect inositol phosphate hydrolysis with treatments between 15 and 60 min. The actions of P-Mod-S on cGMP levels influenced Sertoli cell function on a molecular level. Northern blot analysis indicated that P-Mod-S and FIRT both stimulated the apparent levels of the 2.6-kilobase transcript of transferrin and the 1.7-kilobase transcript of androgen-binding protein. A solution hybridization procedure was used to quantitate the influence of P-Mod-S on Sertoli cell gene expression. P-Mod-S stimulated steady state levels of both transferrin and androgen-binding protein message approximately 2-fold, similar to the effects of FIRT. Both forms of P-Mod-S had similar biological activities and mechanisms of action. P-Mod-S (A) and P-Mod-S (B) both stimulated cGMP, altered Sertoli cell gene expression, and had profound effects on transferrin production. Although slightly different biochemically, both forms of P-Mod-S appear to be functionally similar. Combined observations indicate that the paracrine factor produced by peritubular cells, P-Mod-S, acts on Sertoli cells in part through a cGMP-mediated response to influence the expression of specific genes which subsequently have profound effects on Sertoli cell function and differentiation.
本研究旨在探究睾丸旁分泌因子P-Mod-S对支持细胞功能及分化的作用。与任何单一调节因子相比,P-Mod-S对支持细胞转铁蛋白生成的刺激作用更强,且其作用方式与促卵泡激素(FSH)、胰岛素、视黄醇和睾酮的组合(FIRT)相似。P-Mod-S与FIRT联合使用时具有相加效应。P-Mod-S与FIRT联合使用时转铁蛋白生成的增加是所观察到的最高刺激水平(高达8倍)。P-Mod-S对支持细胞功能的这些深远影响暗示了旁分泌因子潜在的独特作用机制。FSH和FIRT在60分钟和72小时的处理中均显著刺激了环磷酸腺苷(cAMP)水平。相比之下,P-Mod-S在60分钟处理时对cAMP水平无影响,在72小时处理时仅略有增加。有趣的是,P-Mod-S刺激了环磷酸鸟苷(cGMP)水平,在长达72小时的处理中cGMP水平一直高于基础水平。FSH对cGMP水平无影响。在15至60分钟的处理中,P-Mod-S不影响肌醇磷酸水解。P-Mod-S对cGMP水平的作用在分子水平上影响了支持细胞功能。Northern印迹分析表明,P-Mod-S和FIRT均刺激了转铁蛋白2.6千碱基转录本和雄激素结合蛋白1.7千碱基转录本的表观水平。采用溶液杂交程序来定量P-Mod-S对支持细胞基因表达的影响。P-Mod-S刺激了转铁蛋白和雄激素结合蛋白信息的稳态水平约2倍,与FIRT的作用效果相似。两种形式的P-Mod-S具有相似的生物学活性和作用机制。P-Mod-S(A)和P-Mod-S(B)均刺激了cGMP,改变了支持细胞基因表达,并对转铁蛋白生成有深远影响。尽管在生化方面略有不同,但两种形式的P-Mod-S在功能上似乎相似。综合观察表明,由睾丸周细胞产生的旁分泌因子P-Mod-S部分通过cGMP介导的反应作用于支持细胞,以影响特定基因的表达,进而对支持细胞功能和分化产生深远影响。