Haksar A, Maudsley D V, Péron F G, Bedigian E
J Cell Biol. 1976 Jan;68(1):142-53. doi: 10.1083/jcb.68.1.142.
Lanthanum (La+++) is a well-known Ca++ antagonist in a number of biological systems. It was used in the present study to examine the role of Ca++ in the regulation of adenyl cyclase of the adrenal cortex by ACTH. In micromolar concentrations, .La+++ inhibited both cyclic AMP and corticosterone response of isolated adrenal cortex cells to ACTH. However, a number of intracellular processes were not affected by La+++. These include the stimulation of steroidogenesis by dibutyryl cyclic AMP, conversion of several steroid precursors into corticosterone, and stimulation of the latter by glucose. Thus, inhibition of steroidogenesis by La+++ appears to be solely due to an inhibition of ACTH-stimulated cyclic AMP formation. Electron microscope examination showed that La+++ was localized on plasma membrane of the cells and did not appear to penetrate beyond this region. Since La+++ is believed to replace Ca++ at superficial binding sites on the cell membrane, it is proposed that Ca++ at these sites plays an important role in the regulation of adenyl cyclase by ACTH. Similarities in the role of Ca++ in "excitation-contraction" coupling and in the ACTH-adenyl cyclase system raise the possibility that a contractile protein may be involved in the regulation of adenyl cyclase by those hormones which are known to require Ca++ in the process.
镧(La+++)在许多生物系统中是一种著名的钙离子拮抗剂。在本研究中,它被用于检验钙离子在促肾上腺皮质激素(ACTH)对肾上腺皮质腺苷酸环化酶调节中的作用。在微摩尔浓度下,La+++抑制了分离的肾上腺皮质细胞对ACTH的环磷酸腺苷(cAMP)和皮质酮反应。然而,一些细胞内过程不受La+++影响。这些过程包括二丁酰环磷酸腺苷对类固醇生成的刺激、几种类固醇前体向皮质酮的转化以及葡萄糖对皮质酮生成的刺激。因此,La+++对类固醇生成的抑制似乎完全是由于对ACTH刺激的环磷酸腺苷形成的抑制。电子显微镜检查显示,La+++定位于细胞的质膜上,似乎没有穿透该区域之外。由于人们认为La+++在细胞膜表面结合位点取代了钙离子,因此有人提出这些位点的钙离子在ACTH对腺苷酸环化酶的调节中起重要作用。钙离子在“兴奋-收缩”偶联和ACTH-腺苷酸环化酶系统中的作用相似,这增加了一种可能性,即一种收缩蛋白可能参与了那些在该过程中需要钙离子的激素对腺苷酸环化酶的调节。