Rosner W, Hryb D J, Khan M S, Singer C J, Nakhla A M
Department of Medicine, St. Luke's/Roosevelt Hospital Center, New York, New York 10019.
Ann N Y Acad Sci. 1988;538:137-45. doi: 10.1111/j.1749-6632.1988.tb48859.x.
Because it no longer seemed reasonable to us that the sole function of the steroid-binding proteins in plasma was to serve as a buffer reservoir for steroid hormones, we conducted experiments which sought out other possibilities. Both CBG and SHBG bind to cell membranes, and this interaction partakes of the general characteristics of peptide hormone-membrane receptor systems. Additionally, human CBG has the ability to cause an increase in the activity of membrane-bound adenylate cyclase in MCF-7 cells, and this, in turn, results in an increase in cellular cAMP content. Thus, CBG appears to be a protein hormone. As a first consideration, one might presume that because CBG's half-life is measured in days, it would be counted among the hormones which, for the most part, are tonic in their effects, e.g., thyroid hormone. However, two important considerations tend to believe this presumption: (1) CBG which is unoccupied by steroid is not hormonally active (Figure 5): (2) Depending upon the time of day, circulating CBG is approximately 0-60% occupied in normal humans. These observations result in a circumstance in which a substantial portion of circulating CBG is available for activation by bursts of cortisol secretion. It seems prudent to speculate that, because steroids are essential for CBG's activity, the hormonal role of CBG may be entwined with, or complementary to the steroids which it binds. Finally, we should comment on the impact that our model of CBG as a hormone has on the view that only unbound steroid can be hormonally active. First, it should be stated that we have not addressed this question experimentally. Although there is evidence that CBG may be required for cortisol action, we feel that an obligate role for it is not documented adequately. At this time, we believe that CBG's hormonal role is compatible with a hypothesis that encompasses the view that unbound steroid hormones can diffuse into cells in some tissues and that both free and bound steroid can enter cells in others. Obviously, the final word on these important topics, as always, awaits the proper experiments.
由于我们认为血浆中类固醇结合蛋白的唯一功能是作为类固醇激素的缓冲库,这似乎不再合理,因此我们进行了实验以探寻其他可能性。皮质类固醇结合球蛋白(CBG)和性激素结合球蛋白(SHBG)都能与细胞膜结合,这种相互作用具有肽类激素 - 膜受体系统的一般特征。此外,人CBG能够使MCF - 7细胞中膜结合型腺苷酸环化酶的活性增加,进而导致细胞内cAMP含量升高。因此,CBG似乎是一种蛋白质激素。首先可以推测,由于CBG的半衰期以天计算,它可能属于大多数情况下具有持续性作用的激素,例如甲状腺激素。然而,有两个重要因素使这种推测难以成立:(1)未被类固醇占据的CBG没有激素活性(图5);(2)根据一天中的不同时间,正常人体内循环中的CBG约有0 - 60%被占据。这些观察结果导致这样一种情况:循环中的CBG有很大一部分可因皮质醇分泌的突然增加而被激活。推测CBG的激素作用可能与其结合的类固醇相互交织或互补似乎是合理的,因为类固醇对CBG的活性至关重要。最后,我们应该谈谈我们将CBG视为一种激素的模型对只有未结合的类固醇才具有激素活性这一观点的影响。首先,应该说明我们尚未通过实验解决这个问题。尽管有证据表明皮质醇发挥作用可能需要CBG,但我们认为其必然作用尚未得到充分证明。目前,我们认为CBG的激素作用与一种假说相符,该假说认为未结合的类固醇激素可以扩散到某些组织的细胞中,而游离和结合的类固醇都可以进入其他组织的细胞。显然,一如既往,关于这些重要话题的最终定论仍有待进行适当的实验。