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MCF7乳腺癌细胞和SaOS-2骨肉瘤细胞中配体与甲状旁腺激素/甲状旁腺激素相关肽受体结合的特性研究。

Characterisation of ligand binding to the parathyroid hormone/parathyroid hormone-related peptide receptor in MCF7 breast cancer cells and SaOS-2 osteosarcoma cells.

作者信息

Alokail Majed S, Peddie Margaret J

机构信息

Department of Biochemistry, College of Science, King Saud University, Riyadh, Saudi Arabia.

出版信息

Cell Biochem Funct. 2007 Mar-Apr;25(2):139-47. doi: 10.1002/cbf.1280.

Abstract

Parathyroid hormone-related peptide (PTHrP) and parathyroid hormone (PTH)/PTHrP-receptor, PTH/PTHrP-R, are frequently expressed in mammary carcinomas as well as in bone cells. In this study we compared the ligand binding characteristics of the PTH/PTHrP-R in SaOS-2 human osteosarcoma cells with those in MCF7 breast cancer cells. We used both Scatchard analysis of saturation kinetics for iodinated ligand and the level of expressed receptor protein by visualising the single radio-labelled receptor-ligand complex from isolated membrane preparations from the two cell lines. In MCF7 cells, ligand binding, (receptor number) was increased by prior exposure of the cultured cells to epidermal growth factor (EGF), estradiol (E2), or dexamethasone (DEX), and decreased following calcitriol (1,25 DHCC). In contrast in the SaOS-2 cells, PTH/PTHrP-R number was increased by exposure to E2 and 1,25DHCC and decreased by DEX while EGF had no effect. These data were confirmed when the PTH/PTHrP-R was cross linked with (125)I-PTHrP-1-34(Tyr), and extended by visualising the intensity of the isolated radiolabelled receptor complex by autoradiography following SDS-PAGE at several time points during the treatment.

摘要

甲状旁腺激素相关肽(PTHrP)和甲状旁腺激素(PTH)/PTHrP受体(PTH/PTHrP-R)在乳腺癌以及骨细胞中经常表达。在本研究中,我们比较了人骨肉瘤SaOS-2细胞和乳腺癌MCF7细胞中PTH/PTHrP-R的配体结合特性。我们通过对碘化配体的饱和动力学进行Scatchard分析以及通过可视化来自两种细胞系分离膜制剂的单一放射性标记受体-配体复合物来检测表达的受体蛋白水平。在MCF7细胞中,将培养的细胞预先暴露于表皮生长因子(EGF)、雌二醇(E2)或地塞米松(DEX)后,配体结合(受体数量)增加,而在骨化三醇(1,25-二羟胆钙化醇,1,25 DHCC)作用后减少。相比之下,在SaOS-2细胞中,PTH/PTHrP-R数量在暴露于E2和1,25 DHCC后增加,在DEX作用下减少,而EGF没有影响。当PTH/PTHrP-R与(125)I-PTHrP-1-34(Tyr)交联时,这些数据得到证实,并通过在处理过程中的几个时间点进行SDS-PAGE后放射自显影来可视化分离的放射性标记受体复合物的强度进行扩展。

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