Hainan Eye Hospital and Key Laboratory of Ophthalmology, Zhongshan Ophthalmic Center, Sun Yat-Sen University, No.19 Xiuhua Road, Xiuying District, Haikou, 570311, Hainan, China.
Sci Rep. 2024 Aug 21;14(1):19353. doi: 10.1038/s41598-024-69964-6.
Infectious endophthalmitis (IE) poses a significant threat to vision. This study aimed to explore the impact of microRNA (miR)-27a-3p on inflammation in IE. A rat model was developed through intravitreal injection of lipopolysaccharide. Clinical and demographic data were collected for 54 participants: 31 diagnosed with IE and 23 non-infectious patients with idiopathic macular holes. Expression levels of miR-27a-3p and inflammatory genes were quantified via reverse transcription quantitative polymerase chain reaction. Concentrations of inflammatory cytokines in human vitreous samples were measured using enzyme-linked immunosorbent assay. In vitro studies were conducted to explore the target gene of miR-27a-3p. The final animal experiments further verified the role of miR-27a-3p and tuberous sclerosis complex (TSC)1 in inflammatory responses. Results showed that miR-27a-3p was elevated in LPS-treated rats and IE patients. Thirty-one IE patients were divided into the High (n = 15) and Low (n = 16) groups according to the expression of miR-27a-3p. No significant differences were observed in baseline clinical and demographic characteristics between the control and IE patient groups. Pro-inflammatory cytokine mRNA levels and concentrations were notably increased in both LPS-treated rats and the High group of patients. Besides, results showed that TSC1 is a target gene of miR-27a-3p. Moreover, TSC1 inhibition promoted inflammation in rat vitreous samples. In summary, our findings suggested that miR-27a-3p exacerbated inflammatory responses in IE though targeting TSC1, offering novel insights for potential therapeutic strategies targeting miR-27a-3p in the clinical management of IE.
感染性眼内炎(IE)对视力构成重大威胁。本研究旨在探讨 microRNA(miR)-27a-3p 对 IE 炎症的影响。通过玻璃体内注射脂多糖建立大鼠模型。对 54 名参与者收集临床和人口统计学数据:31 名诊断为 IE,23 名非传染性特发性黄斑裂孔患者。通过逆转录定量聚合酶链反应定量检测 miR-27a-3p 和炎症基因的表达水平。使用酶联免疫吸附试验测量人玻璃体样本中炎症细胞因子的浓度。进行体外研究以探讨 miR-27a-3p 的靶基因。最后的动物实验进一步验证了 miR-27a-3p 和结节性硬化复合物(TSC)1 在炎症反应中的作用。结果表明,miR-27a-3p 在 LPS 处理的大鼠和 IE 患者中升高。根据 miR-27a-3p 的表达,31 名 IE 患者分为高(n=15)和低(n=16)组。对照组和 IE 患者组之间在基线临床和人口统计学特征方面无显著差异。LPS 处理的大鼠和 High 组患者的促炎细胞因子 mRNA 水平和浓度均明显增加。此外,结果表明 TSC1 是 miR-27a-3p 的靶基因。此外,TSC1 抑制促进了大鼠玻璃体样本中的炎症。总之,我们的研究结果表明,miR-27a-3p 通过靶向 TSC1 加重 IE 中的炎症反应,为 miR-27a-3p 在 IE 的临床管理中作为潜在治疗策略提供了新的见解。