Manteniotis S, Wojcik S, Göthert J R, Dürig J, Dührsen U, Gisselmann G, Hatt H
Department of Cell Physiology, Ruhr-University Bochum , Bochum, Germany.
Department of Hematology, University Hospital Essen , Essen, Germany.
Cell Death Discov. 2016 May 9;2:16010. doi: 10.1038/cddiscovery.2016.10. eCollection 2016.
The ectopic expression of olfactory receptors (ORs) in the human body has been of major interest in the past decade. Several studies have reported the expression of ORs not only in healthy tissues such as heart, sperm or skin cells, but also in cancerous tissues of the liver, prostate or intestine. In the present study, we detected the expression of OR51B5 in the chronic myelogenous leukemia (CML) cell line K562 and in white blood cell samples of clinically diagnosed acute myelogenous leukemia (AML) patients by reverse transcription-PCR and immunocytochemical staining. The known OR51B5 ligand isononyl alcohol increased the levels of intracellular Ca(2+) in both AML patient blood cells and K562 cells. With calcium imaging experiments, we characterized in greater detail the OR51B5-mediated signaling pathway. Here, we observed an involvement of adenylate cyclase and the downstream L-type and T-type calcium channels. In addition, the activation of OR51B5 leads to an inhibition of cell proliferation in K562 cells. In western blot experiments, we found that incubation with isononyl alcohol led to a reduction in p38-MAPK (mitogen-activated protein kinase) phosphorylation that might be responsible for the decreased cell proliferation. In the present study, we characterized the OR51B5-mediated signaling pathway downstream of the activation with isononyl alcohol, which leads to reduced proliferation and therefore provide a novel pharmacological target for CML and AML, the latter of which remains difficult to treat.
在过去十年中,人体中嗅觉受体(ORs)的异位表达一直是主要研究热点。多项研究报告称,ORs不仅在心脏、精子或皮肤细胞等健康组织中表达,还在肝脏、前列腺或肠道的癌组织中表达。在本研究中,我们通过逆转录聚合酶链反应(RT-PCR)和免疫细胞化学染色,检测了慢性粒细胞白血病(CML)细胞系K562以及临床诊断的急性髓性白血病(AML)患者白细胞样本中OR51B5的表达。已知的OR51B5配体异壬醇可提高AML患者血细胞和K562细胞内Ca(2+)的水平。通过钙成像实验,我们更详细地描述了OR51B5介导的信号通路。在此,我们观察到腺苷酸环化酶以及下游的L型和T型钙通道参与其中。此外,OR51B5的激活导致K562细胞的细胞增殖受到抑制。在蛋白质印迹实验中,我们发现用异壬醇孵育会导致p38丝裂原活化蛋白激酶(p38-MAPK)磷酸化水平降低,这可能是细胞增殖减少的原因。在本研究中,我们描述了异壬醇激活后OR51B5介导的信号通路,该通路导致增殖减少,因此为CML和AML提供了一个新的药理学靶点,其中AML仍然难以治疗。