Department of Ophthalmology, Gavin Herbert Eye Institute, University of California Irvine, Irvine, CA, 92697, USA.
Department of Ophthalmology, Gavin Herbert Eye Institute, University of California Irvine, Irvine, CA, 92697, USA; Department of Pediatrics, All India Institute of Medical Sciences, New Delhi, India.
Exp Eye Res. 2022 Jan;214:108857. doi: 10.1016/j.exer.2021.108857. Epub 2021 Nov 29.
Our goal was to explore the detrimental impacts of ciprofloxacin (CPFX) and tetracycline (TETRA) on human retinal Müller (MIO-M1) cells in vitro. Cells were exposed to 30, 60 and 120 μg/ml of CPFX and TETRA. The cellular metabolism was measured with the MTT assay. The JC-1 and CM-H2DCFDA assays were used to evaluate the levels of mitochondrial membrane potential (MMP) and ROS (reactive oxygen species), respectively. Mitochondrial DNA (mtDNA) copy number, along with gene expression levels associated with apoptotic (BAX, BCL2-L13, BCL2, CASP-3 and CASP-9), inflammatory (IL-6, IL-1β, TGF-α, TGF-β1 and TGF-β2) and antioxidant pathways (SOD2, SOD3, GPX3 and NOX4) were analyzed via Quantitative Real-Time PCR (qRT-PCR). Bioenergetic profiles were measured using the Seahorse® XF Flux Analyzer. Cells exposed 24 h to 120 μg/ml TETRA demonstrated higher cellular metabolism compared to vehicle-treated cells. At each time points, (i) all TETRA concentrations reduced MMP levels and (ii) ROS levels were reduced by TETRA 120 μg/ml treatment. TETRA caused (i) higher expression of CASP-3, CASP-9, TGF-α, IL-1B, GPX3 and SOD3 but (ii) decreased levels of TGF-B2 and SOD2. ATP production and spare respiratory capacity declined with TETRA treatment. Cellular metabolism was reduced with CPFX 120 μg/ml in all cultures and 60 μg/ml after 72 h. The CPFX 120 μg/ml reduced MMP in all cultures and ROS levels (72 h). CPFX treatment (i) increased expression of CASP-3, CASP-9, and BCL2-L13, (ii) elevated the basal oxygen consumption rate, and (iii) lowered the mtDNA copy numbers and expression levels of TGF-B2, IL-6 and IL-1B compared to vehicle-control cells. We conclude that clinically relevant dosages of bactericidal and bacteriostatic antibiotics can have negative effects on the cellular metabolism and mitochondrial membrane potential of the retinal MIO-M1 cells in vitro. It is noteworthy to mention that apoptotic and inflammatory pathways in exposed cells were affected significantly This is the first study showing the negative impact of fluoroquinolones and tetracyclines on mitochondrial behavior of human retinal MIO-M1 cells.
我们的目的是探究环丙沙星(CPFX)和四环素(TETRA)对体外人视网膜 Müller(MIO-M1)细胞的有害影响。将细胞暴露于 30、60 和 120μg/ml 的 CPFX 和 TETRA 中。通过 MTT 测定法测量细胞代谢。使用 JC-1 和 CM-H2DCFDA 测定法分别评估线粒体膜电位(MMP)和 ROS(活性氧)的水平。通过定量实时 PCR(qRT-PCR)分析线粒体 DNA(mtDNA)拷贝数以及与凋亡(BAX、BCL2-L13、BCL2、CASP-3 和 CASP-9)、炎症(IL-6、IL-1β、TGF-α、TGF-β1 和 TGF-β2)和抗氧化途径(SOD2、SOD3、GPX3 和 NOX4)相关的基因表达水平。使用 Seahorse® XF 通量分析仪测量生物能量谱。与对照组相比,暴露于 120μg/ml TETRA 的细胞在 24 小时时显示出更高的细胞代谢水平。在每个时间点,(i)所有 TETRA 浓度均降低了 MMP 水平,(ii)TETRA 120μg/ml 处理降低了 ROS 水平。TETRA 导致(i)CASP-3、CASP-9、TGF-α、IL-1β、GPX3 和 SOD3 的表达增加,但(ii)TGF-B2 和 SOD2 的水平降低。TETRA 处理后,ATP 产生和备用呼吸能力下降。在所有培养物中,CPFX 120μg/ml 降低了细胞代谢,72 小时后 CPFX 60μg/ml 降低了细胞代谢。CPFX 120μg/ml 在所有培养物中降低了 MMP 和 ROS 水平(72 小时)。CPFX 处理(i)增加了 CASP-3、CASP-9 和 BCL2-L13 的表达,(ii)提高了基础耗氧率,(iii)降低了 mtDNA 拷贝数和 TGF-B2、IL-6 和 IL-1B 的表达水平与对照组相比。我们得出结论,临床相关剂量的杀菌和抑菌抗生素可能对体外人视网膜 MIO-M1 细胞的细胞代谢和线粒体膜电位产生负面影响。值得注意的是,暴露细胞中的凋亡和炎症途径受到显著影响。这是第一项表明氟喹诺酮类和四环素类药物对人视网膜 MIO-M1 细胞线粒体行为产生负面影响的研究。