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正常人皮肤来源的分散成纤维细胞对1,25 - 二羟基[3H]胆钙化醇的核摄取。

Nuclear uptake of 1,25-dihydroxy[3H]cholecalciferol in dispersed fibroblasts cultured from normal human skin.

作者信息

Eil C, Marx S J

出版信息

Proc Natl Acad Sci U S A. 1981 Apr;78(4):2562-6. doi: 10.1073/pnas.78.4.2562.

Abstract

Because of the relative inaccessibility of known calciferol target tissues (i.e., intestine and bone), we examined fibroblasts derived from normal human skin and grown in tissue culture as a means of evaluating the interaction of 1,25-dihydroxycholecalciferol [1,25(OH)2D3] and its effector system. When dispersed, intact cells were used, nuclear uptake of 1,25-dihydroxy[23,24(n)3-H]cholecalciferol [1,25(OH)2[3H]D3) was temperature-dependent, optimal at 45 min at 37 degrees C, and saturable. In competition experiments with other calciferols, the 1,25(OH)2[3H]D3 uptake showed specificity indistinguishable from that reported for 1,25(OH)2D3 receptors from calciferol target tissues. Analysis of 1,25(OH)2[3H]D3 nuclear uptake in fibroblast strains from six normal adults (four male, two female) yielded an average binding capacity (R0) of 10,600 +/- 2,000 (SEM) nuclear sites per cell and an apparent dissociation contant (Kd) of 0.50 +/- 0.07 (SEM) x 10(-9) M. Donor sex, donor age, or anatomic site of origin of the cell line did not affect the characteristics of uptake. Similar nuclear uptake was demonstrable with cultured MCF-7 cells (derived from human breast cancer) when assayed in the same fashion. When hypertonic extracts of nuclei obtained from skin fibroblasts incubated with 1,25(OH)2[3H]D3 were subjected to centrifugation on sucrose gradients, a single peak of radioactivity sedimented at approximately 3 S; when excess 1,25(OH)2D3 was coincubated during the cellular uptake phase, this 3S peak was not observed. Molybdate was an essential buffer component for receptor stabilization during cell fractionation and sedimentation analysis. In summary, by using fibroblasts cultured from normal human skin, we have identified a process of nuclear uptake of 1,25(OH)2[3H]D3 with the affinity, saturability, and specificity characteristics of a steroid hormone--receptor interaction. This method should be useful in studying 1,25(OH)2D3 recept physiology in cells from normal persons as well as in cells from patients who have disorders in the responsiveness of calciferol target tissues.

摘要

由于已知的维生素D靶组织(即肠道和骨骼)相对难以获取,我们检测了源自正常人类皮肤并在组织培养中生长的成纤维细胞,以此作为评估1,25 - 二羟胆钙化醇[1,25(OH)₂D₃]及其效应系统相互作用的一种手段。当使用分散的完整细胞时,1,25 - 二羟基[23,24(n)₃ - H]胆钙化醇[1,25(OH)₂[³H]D₃]的核摄取是温度依赖性的,在37℃下45分钟时达到最佳,且具有饱和性。在与其他维生素D的竞争实验中,1,25(OH)₂[³H]D₃的摄取显示出的特异性与报道的维生素D靶组织中1,25(OH)₂D₃受体的特异性无法区分。对来自六名正常成年人(四名男性,两名女性)的成纤维细胞系中1,25(OH)₂[³H]D₃核摄取的分析得出,每个细胞的平均结合能力(R₀)为10,600 ± 2,000(标准误)个核位点,表观解离常数(Kd)为0.50 ± 0.07(标准误)×10⁻⁹ M。供体性别、供体年龄或细胞系的起源解剖部位均不影响摄取特征。以同样方式检测时,培养的MCF - 7细胞(源自人类乳腺癌)也显示出类似的核摄取。当对用1,25(OH)₂[³H]D₃孵育的皮肤成纤维细胞核的高渗提取物进行蔗糖梯度离心时,一个单一的放射性峰在约3 S处沉降;当在细胞摄取阶段同时孵育过量的1,25(OH)₂D₃时,未观察到这个3S峰。钼酸盐是细胞分级分离和沉降分析过程中受体稳定的必需缓冲成分。总之,通过使用从正常人类皮肤培养的成纤维细胞,我们确定了1,25(OH)₂[³H]D₃的核摄取过程,其具有类固醇激素 - 受体相互作用的亲和力、饱和性和特异性特征。该方法对于研究正常人细胞以及维生素D靶组织反应性紊乱患者细胞中的1,25(OH)₂D₃受体生理学应该是有用的。

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