Laboratory for Cell Biology, Institute of Biology and Ecology, Faculty of Science, PJ Šafárik University, 040 01 Košice, Slovak Republic.
Oncol Rep. 2012 Jul;28(1):141-6. doi: 10.3892/or.2012.1795. Epub 2012 Apr 30.
Erythropoietin (Epo) is a critical regulator of erythroid cell proliferation, differentiation and apoptosis. In the form of a recombinant protein, it is widely used to treat various forms of anemia, including that associated with cancer and with the myelosuppressive effects of chemotherapy. Studies of ovarian cancer cell lines have demonstrated the presence of the Epo receptor (EpoR), but there are disagreements regarding its localization and functionality in these cells. Using fluorescence microscopy, we were not able to identify the EpoR on the surface of A2780 cells, in contrast to the positive control K562 cells. Flow cytometry did reveal a weak surface EpoR signal in A2780 cells. Interestingly, most of the EpoR in A2780 cells was found in the cytoplasm, more abundantly as an intracellular membrane-associated protein than a soluble one. Silencing EpoR expression by lentiviral-mediated shRNA resulted in reduced A2780 proliferation as well as reduction in Epo-induced phosphorylation of Erk1/2. Our findings provide important insights into the biology of the EpoR in ovarian cancer cells.
促红细胞生成素(Epo)是红细胞增殖、分化和凋亡的关键调节因子。以重组蛋白的形式,它被广泛用于治疗各种形式的贫血,包括与癌症和化疗的骨髓抑制作用相关的贫血。对卵巢癌细胞系的研究表明存在促红细胞生成素受体(EpoR),但关于其在这些细胞中的定位和功能存在分歧。通过荧光显微镜,我们无法在 A2780 细胞表面识别出 EpoR,而 K562 细胞作为阳性对照则可以识别出 EpoR。流式细胞术确实显示 A2780 细胞表面存在微弱的 EpoR 信号。有趣的是,A2780 细胞中的大部分 EpoR 存在于细胞质中,作为细胞内膜相关蛋白的含量多于可溶性蛋白。通过慢病毒介导的 shRNA 沉默 EpoR 表达会导致 A2780 增殖减少,以及 Epo 诱导的 Erk1/2 磷酸化减少。我们的研究结果为卵巢癌细胞中 EpoR 的生物学特性提供了重要的见解。