Mary Photini Stella, Chaiwangyen Wittaya, Weber Maja, Al-Kawlani Boodor, Favaro Rodolfo R, Jeschke Udo, Schleussner Ekkehard, Morales-Prieto Diana M, Markert Udo R
Placenta-Lab, Department of Obstetrics, Jena University Hospital, Am Klinikum 1, 07747 Jena, Germany.
Placenta-Lab, Department of Obstetrics, Jena University Hospital, Am Klinikum 1, 07747 Jena, Germany; School of Medical Sciences, University of Phayao, Phayao 56000, Thailand.
Exp Cell Res. 2017 Oct 1;359(1):275-283. doi: 10.1016/j.yexcr.2017.07.019. Epub 2017 Jul 18.
Proviral insertion in murine (PIM) lymphoma proteins are mainly regulated by the Janus Kinase/Signal Transducer Activator of Transcription (JAK/STAT) signaling pathway, which can be activated by members of the Interleukin-6 (IL-6) family, including Leukemia Inhibitory Factor (LIF). Aim of the study was to compare PIM1, PIM2 and PIM3 expression and potential cellular functions in human first and third trimester trophoblast cells, the immortalized first trimester extravillous trophoblast cell line HTR8/SVneo and the choriocarcinoma cell line JEG-3. Expression was analyzed by qPCR and immunochemical staining. Functions were evaluated by PIM inhibition followed by analysis of kinetics of cell viability as assessed by MTS assay, proliferation by BrdU assay, and apoptosis by Western blotting for BAD, BCL-XL, (cleaved) PARP, CASP3 and c-MYC. Apoptosis and necrosis were tested by flow cytometry (annexin V/propidium iodide staining). All analyzed PIM kinases are expressed in primary trophoblast cells and both cell lines and are regulated upon stimulation with LIF. Inhibition of PIM kinases significantly reduces viability and proliferation and induces apoptosis. Simultaneously, phosphorylation of c-MYC was reduced. These results demonstrate the involvement of PIM kinases in LIF-induced regulation in different trophoblastic cell lines which may indicate similar functions in primary cells.
鼠类原病毒插入淋巴瘤(PIM)蛋白主要由Janus激酶/信号转导子和转录激活子(JAK/STAT)信号通路调控,该通路可被白细胞介素-6(IL-6)家族成员激活,包括白血病抑制因子(LIF)。本研究的目的是比较PIM1、PIM2和PIM3在人早孕期和孕晚期滋养层细胞、永生化早孕期绒毛外滋养层细胞系HTR8/SVneo和绒毛膜癌细胞系JEG-3中的表达及潜在细胞功能。通过qPCR和免疫化学染色分析表达情况。通过抑制PIM后,用MTS法评估细胞活力动力学、用BrdU法评估增殖、用Western印迹法检测BAD、BCL-XL、(裂解的)PARP、CASP3和c-MYC来评估凋亡,从而评估其功能。通过流式细胞术(膜联蛋白V/碘化丙啶染色)检测凋亡和坏死情况。所有分析的PIM激酶均在原代滋养层细胞和两种细胞系中表达,并在LIF刺激下受到调控。抑制PIM激酶可显著降低细胞活力和增殖并诱导凋亡。同时,c-MYC的磷酸化水平降低。这些结果表明PIM激酶参与了LIF诱导的不同滋养层细胞系的调控,这可能表明其在原代细胞中具有相似功能。