Manukyan G, Petrek M, Navratilova Z, Margaryan S, Boyajyan A
Department of Pathological Physiology, Faculty of Medicine and Dentistry, Palacky University, Olomouc, Czech Republic.
Group of Molecular and Cellular Immunology, Institute of Molecular Biology, National Academy of Sciences, Yerevan, Armenia.
J Biol Regul Homeost Agents. 2015 Jan-Mar;29(1):125-30.
Colchicine is an antimitotic drug which binds to tubulin and at high doses results in cytoskeleton disruption. Colchicine is believed to be an anti-inflammatory agent, though its modulatory effects on the level and transcriptional activity of genes is still a matter of debate. There is growing evidence that alterations in the cytoskeleton exert specific effects on the expression of various genes. This study was undertaken to analyze whether disrupting the microtubule cytoskeleton by colchicine modulates transcriptional levels of MEFV, NF-κB p65, NLRP3, HMGB1, and caspase-3 in neutrophils from patients with familial Mediterranean fever (FMF) and healthy subjects. In the present study, colchicine caused increased expression of NLRP3 (p=0.007) and MEFV (p=0.03), but had no effect on caspase-3, NF-κB p65 and HMGB1 genes in healthy neutrophils. FMF neutrophils were less responsive to the drug treatment. This study supports the hypothesis that, being an anti-inflammatory agent, colchicine at relatively high concentrations might lead to the activation of pro-inflammatory signalling pathways in neutrophils.
秋水仙碱是一种抗有丝分裂药物,它与微管蛋白结合,高剂量时会导致细胞骨架破坏。秋水仙碱被认为是一种抗炎剂,但其对基因水平和转录活性的调节作用仍存在争议。越来越多的证据表明,细胞骨架的改变对各种基因的表达产生特定影响。本研究旨在分析秋水仙碱破坏微管细胞骨架是否会调节家族性地中海热(FMF)患者和健康受试者中性粒细胞中MEFV、NF-κB p65、NLRP3、HMGB1和caspase-3的转录水平。在本研究中,秋水仙碱导致健康中性粒细胞中NLRP3(p = 0.007)和MEFV(p = 0.03)的表达增加,但对caspase-3、NF-κB p65和HMGB1基因没有影响。FMF中性粒细胞对药物治疗的反应较小。本研究支持这样的假设,即作为一种抗炎剂,相对高浓度的秋水仙碱可能会导致中性粒细胞中促炎信号通路的激活。