Zhang Qing, Su Jinxing, Chen Jing, Wu Sainan, Qi Xiaoxuan, Chu Min, Jiang Shangquan, He Kan
Department of Ophthalmology, The Second Hospital of Anhui Medical University, No. 678 Furong Road, Hefei, 230601, Anhui, People's Republic of China.
Center for Stem Cell and Translational Medicine, School of Life Sciences, Anhui University, Hefei, 230600, Anhui, People's Republic of China.
Int Ophthalmol. 2025 Jan 31;45(1):57. doi: 10.1007/s10792-025-03431-7.
To explore the regulatory mechanism of meibomian gland (MG) in hyperlipidemic mice under a diurnal rhythm by transcriptomic analysis based on high-throughput sequencing.
The mouse model of hyperlipidemia induced by four months of high-fat diet (HFD) feeding to a regular light-dark (LD) cycle for 2 weeks was used in this study. Phenotypic observation and RNA sequencing (RNA-seq) of MGs of the experimental mice were then performed to investigate transcriptional changes due to hyperlipidemia and the diurnal rhythm and their effects on meibomian gland dysfunction (MGD).
The expression levels of the identified dysregulated genes were then validated by qRT-PCR. Several significantly regulated genes and enriched pathways were identified as associated with MGD in hyperlipidemic mice under a diurnal rhythm; these genes included some core diurnal clock genes, e.g., Clock, Per2 and Per3. Phenotypic and histological analysis reveals abnormal morphology concomitantly with a modification of the transcriptional landscape of MG caused by HFD.
Our findings provide us with a deeper understanding of the diurnal rhythm regulation of MG in hyperlipidemic mice altered by daily nutritional challenge.
通过基于高通量测序的转录组分析,探索昼夜节律下高脂血症小鼠睑板腺(MG)的调控机制。
本研究采用给小鼠喂食四个月高脂饮食(HFD)并使其在正常昼夜(LD)循环下饲养2周来诱导高脂血症小鼠模型。然后对实验小鼠的睑板腺进行表型观察和RNA测序(RNA-seq),以研究高脂血症和昼夜节律引起的转录变化及其对睑板腺功能障碍(MGD)的影响。
通过qRT-PCR验证了所鉴定的失调基因的表达水平。在昼夜节律下,确定了几个与高脂血症小鼠MGD相关的显著调控基因和富集途径;这些基因包括一些核心昼夜节律基因,如Clock、Per2和Per3。表型和组织学分析显示,高脂饮食导致睑板腺形态异常,同时转录图谱也发生改变。
我们的研究结果使我们对日常营养挑战改变的高脂血症小鼠睑板腺昼夜节律调节有了更深入的了解。