Rudraprasad Dhanwini, Nirmal Jayabalan, Mishra Dilip Kumar, Joseph Joveeta
Jhaveri Microbiology Centre, Brien Holden Eye Research Centre, L. V. Prasad Eye Institute, Hyderabad, Telangana, India.
Manipal Academy of Higher Education, Manipal, Karnataka, India.
Invest Ophthalmol Vis Sci. 2025 Apr 1;66(4):53. doi: 10.1167/iovs.66.4.53.
Extracellular vesicles (EVs) are critical mediators of cell-cell communication via transfer of molecular cargo including miRNAs and regulate transcription in various physiological and pathological conditions. This study aimed to investigate the role of EV-derived-microRNAs (EV-miRNAs) in bacterial endophthalmitis, focusing on their regulatory impact on inflammation and host immune responses.
C57BL/6 mice were infected with Pseudomonas aeruginosa (P. aeruginosa) and Staphylococcus aureus (S. aureus) to induce endophthalmitis. EVs were isolated and characterized followed by miRNA profiling to identify differentially expressed miRNAs. The miRNet platform was used to elucidate potential interactions between exosomal miRNA and retinal mRNA, followed by in vivo and in vitro validation of key miRNAs and their target genes. Additionally, EVs were extracted from vitreous fluid samples of patients with endophthalmitis, and miR-223-3p and NLRP3 expressions were assessed by qPCR.
Bacterial endophthalmitis led to pronounced neutrophil infiltration in the retina of mice. The miRNA profiling identified 651 differentially expressed miRNAs in P. aeruginosa and 29 in S. aureus, with 10 miRNAs shared between both infections. The miR-223-3p, miR-467a-3p, and miR-467d-3p emerged as major regulators of inflammatory pathways, targeting genes such as NLRP3, CXCL5, and IKKα. In patient vitreous samples, miR-223-3p was upregulated in culture-positive samples, correlating with reduced NLRP3 expression. The miRNAs, particularly miR-223-3p, play a critical role in modulating the immune response in bacterial endophthalmitis, largely through the regulation of the NLRP3 inflammasome.
The findings suggest that miR-223-3p could serve as biomarkers in culture-negative cases and therapeutic targets for managing inflammation in bacterial endophthalmitis, potentially guiding treatments aimed at preserving retinal integrity.
细胞外囊泡(EVs)是细胞间通讯的关键介质,通过转移包括微小RNA(miRNAs)在内的分子货物来实现,并在各种生理和病理条件下调节转录。本研究旨在探讨EV衍生的微小RNA(EV-miRNAs)在细菌性眼内炎中的作用,重点关注其对炎症和宿主免疫反应的调节影响。
用铜绿假单胞菌(P. aeruginosa)和金黄色葡萄球菌(S. aureus)感染C57BL/6小鼠以诱导眼内炎。分离并鉴定EVs,随后进行miRNA谱分析以鉴定差异表达的miRNAs。使用miRNet平台阐明外泌体miRNA与视网膜mRNA之间的潜在相互作用,随后在体内和体外验证关键miRNAs及其靶基因。此外,从眼内炎患者的玻璃体液样本中提取EVs,并通过qPCR评估miR-223-3p和NLRP3的表达。
细菌性眼内炎导致小鼠视网膜中明显的中性粒细胞浸润。miRNA谱分析在铜绿假单胞菌中鉴定出651个差异表达的miRNAs,在金黄色葡萄球菌中鉴定出29个,两种感染共有10个miRNAs。miR-223-3p、miR-467a-3p和miR-467d-3p成为炎症途径的主要调节因子,靶向NLRP3、CXCL5和IKKα等基因。在患者玻璃体样本中,miR-223-3p在培养阳性样本中上调,与NLRP3表达降低相关。这些miRNAs,尤其是miR-223-3p,在调节细菌性眼内炎的免疫反应中起关键作用,主要通过调节NLRP3炎性小体。
研究结果表明,miR-223-3p可作为培养阴性病例的生物标志物以及治疗细菌性眼内炎炎症的治疗靶点,可能为旨在保护视网膜完整性的治疗提供指导。