Wei Hai-Kun, Yang Si-Dong, Bai Zhi-Long, Zhang Xu, Yang Da-Long, Ding Wen-Yuan
Department of Spinal Surgery, The Third Hospital of Hebei Medical University Shijiazhuang 050051, China.
Department of Spinal Surgery, The Third Hospital of Hebei Medical UniversityShijiazhuang 050051, China; Hebei Provincial Key Laboratory of Orthopedic BiomechanicsShijiazhuang 050051, China.
Int J Clin Exp Med. 2015 Nov 15;8(11):20198-207. eCollection 2015.
Levofloxacin was previously reported to induce apoptosis of rat annulus fibrosus (AF) cells by upregulating active caspase-3 and matrix metalloproteinase (MMP)-3 expression in vitro. However, the effects of levofloxacin on rat AF cells, as well as the related mechanism, have not been revealed completely. The purpose of this study was to further explore the changes in extracellular matrix and MMPs of rat AF cells based on levofloxacin-induced apoptosis. AF cells isolated from rat AF regions were cultured in monolayers and treated with levofloxacin in a dose- and time-dependent manner. To determine the cytotoxic effects of levofloxacin, inverted phase-contrast microscopy was used to perform morphological observation of apoptotic cells. The mRNA expression levels of MMP-2, -9 and -13 were quantified by reverse transcription and real-time quantitative polymerase chain reaction (RT-qPCR). Protein level of MMP-2 and MMP-13 were determined by western blot. The results showed that levofloxacin induced marked AF cell apoptosis, which was observed by inverted phase-contrast microscopy, and indicated by the increased expression of active caspase-3. Both RT-qPCR and western blot revealed that MMP-2 and MMP-13 expression were upregulated by levofloxacin treatment in a time- and dose-dependent manner. Moreover, cellular binding to type I collagen was found to be decreased by levofloxacin. In conclusion, the results above suggest that the possible cytotoxic effects of levofloxacin on AF cells in vitro may be attributed to the decreased cell binding to type I collagen and up-regulated expression of MMP-2 and MMP-13.
先前有报道称,左氧氟沙星在体外可通过上调活性半胱天冬酶 -3和基质金属蛋白酶(MMP)-3的表达来诱导大鼠纤维环(AF)细胞凋亡。然而,左氧氟沙星对大鼠AF细胞的影响及其相关机制尚未完全阐明。本研究的目的是基于左氧氟沙星诱导的细胞凋亡,进一步探究大鼠AF细胞外基质和基质金属蛋白酶的变化。从大鼠AF区域分离的AF细胞进行单层培养,并用左氧氟沙星进行剂量和时间依赖性处理。为了确定左氧氟沙星的细胞毒性作用,使用倒置相差显微镜对凋亡细胞进行形态学观察。通过逆转录和实时定量聚合酶链反应(RT-qPCR)对MMP-2、-9和-13的mRNA表达水平进行定量。通过蛋白质印迹法测定MMP-2和MMP-13的蛋白水平。结果显示,左氧氟沙星诱导了明显的AF细胞凋亡,通过倒置相差显微镜观察到,并且活性半胱天冬酶-3表达增加表明了这一点。RT-qPCR和蛋白质印迹法均显示,左氧氟沙星处理以时间和剂量依赖性方式上调了MMP-2和MMP-13的表达。此外,发现左氧氟沙星降低了细胞与I型胶原的结合。总之,上述结果表明,左氧氟沙星在体外对AF细胞可能的细胞毒性作用可能归因于细胞与I型胶原结合的减少以及MMP-2和MMP-13表达的上调。