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从激素反应性和激素抵抗性乳腺癌细胞中鉴定潜在的肿瘤分化因子(TDF)受体。

Identification of potential tumor differentiation factor (TDF) receptor from steroid-responsive and steroid-resistant breast cancer cells.

机构信息

Department of Chemistry and Biomolecular Science, Biochemistry and Proteomics Group, Clarkson University, Potsdam, New York 13699-5810, USA.

出版信息

J Biol Chem. 2012 Jan 13;287(3):1719-33. doi: 10.1074/jbc.M111.284091. Epub 2011 Nov 30.

Abstract

Tumor differentiation factor (TDF) is a recently discovered protein, produced by the pituitary gland and secreted into the bloodstream. TDF and TDF-P1, a 20-amino acid peptide selected from the open reading frame of TDF, induce differentiation in human breast and prostate cancer cells but not in other cells. TDF protein has no identified site of action or receptor, and its mechanism of action is unknown. Here, we used TDF-P1 to purify and identify potential TDF receptor (TDF-R) candidates from MCF7 steroid-responsive breast cancer cells and non-breast HeLa cancerous cells using affinity purification chromatography (AP), and mass spectrometry (MS). We identified four candidate proteins from the 70-kDa heat shock protein (HSP70) family in MCF7 cells. Experiments in non-breast HeLa cancerous cells did not identify any TDF-R candidates. AP and MS experiments were validated by AP and Western blotting (WB). We additionally looked for TDF-R in steroid-resistant BT-549 cells and human dermal fibroblasts (HDF-a) using AP and WB. TDF-P1 interacts with potential TDF-R candidates from MCF7 and BT-549 breast cells but not from HeLa or HDF-a cells. Immunofluorescence (IF) experiments identified GRP78, a TDF-R candidate, at the cell surface of MCF7, BT-549 breast cells, and HeLa cells but not HDF-a cells. IF of other HSP70 proteins demonstrated labeling on all four cell types. These results point toward GRP78 and HSP70 proteins as strong TDF-R candidates and suggest that TDF interacts with its receptor, exclusively on breast cells, through a steroid-independent pathway.

摘要

肿瘤分化因子 (TDF) 是一种新发现的蛋白质,由垂体分泌并分泌到血液中。TDF 和 TDF-P1,一种从 TDF 开放阅读框中选择的 20 个氨基酸肽,可诱导人乳腺癌和前列腺癌细胞分化,但不诱导其他细胞分化。TDF 蛋白没有确定的作用部位或受体,其作用机制尚不清楚。在这里,我们使用 TDF-P1 通过亲和纯化色谱 (AP) 和质谱 (MS) 从 MCF7 甾体反应性乳腺癌细胞和非乳腺 HeLa 癌细胞中纯化和鉴定潜在的 TDF 受体 (TDF-R) 候选物。我们从 MCF7 细胞中的 70kDa 热休克蛋白 (HSP70) 家族中鉴定出四个候选蛋白。非乳腺 HeLa 癌细胞中的实验未鉴定出任何 TDF-R 候选物。AP 和 MS 实验通过 AP 和 Western blot (WB) 进行了验证。我们还使用 AP 和 WB 在甾体耐药 BT-549 细胞和人真皮成纤维细胞 (HDF-a) 中寻找 TDF-R。TDF-P1 与 MCF7 和 BT-549 乳腺癌细胞中的潜在 TDF-R 候选物相互作用,但与 HeLa 或 HDF-a 细胞不相互作用。免疫荧光 (IF) 实验在 MCF7、BT-549 乳腺癌细胞和 HeLa 细胞的细胞表面鉴定出 TDF-R 候选物 GRP78,但在 HDF-a 细胞中未鉴定出。其他 HSP70 蛋白的 IF 实验表明在所有四种细胞类型上均有标记。这些结果表明 GRP78 和 HSP70 蛋白是强有力的 TDF-R 候选物,并表明 TDF 通过一种与甾体无关的途径与其受体在乳腺细胞上特异性相互作用。

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