Corneal Sensory Nerve Injury Disrupts Lacrimal Gland Function by Altering Circadian Rhythms in Mice.

IF 5 2区 医学 Q1 OPHTHALMOLOGY
Senmao Li, Jingbin Xie, Jiayan Xiang, Ruyu Yan, Jiangman Liu, Qiwei Fan, Liyuan Lu, Jiaxin Wu, Jun Liu, Yunxia Xue, Ting Fu, Zhijie Li
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Abstract

Purpose: To investigate the impact of corneal sensory nerve injury on lacrimal gland function, focusing on mechanisms involving the superior salivatory nucleus (SSN), circadian rhythm disruption, immune microenvironment alterations, and the potential for neural regeneration.

Methods: A murine model of corneal sensory nerve injury was used to assess lacrimal gland function, with tear secretion measured using the phenol red thread test. Transcriptomic analysis of lacrimal glands examined circadian rhythm and immune-related gene expression. Basic fibroblast growth factor (bFGF) was used to promote corneal nerve regeneration, and its effects on tear secretion and nerve repair were evaluated.

Results: Corneal nerve injury resulted in a 35% reduction in tear secretion and significantly impaired SSN activity, as evidenced by a 31% decrease in c-FOS-positive neurons in choline acetyltransferase (ChAT)-expressing neurons. Transcriptomic analysis revealed significant downregulation of immune-related pathways, including Toll-like receptor (TLR), NOD-like receptor (NLR), and T-cell receptor signaling. Circadian rhythm gene expression exhibited phase shifts, with a 2.13-hour delay in peak expression and a substantial change in the number and types of rhythmic genes, which were enriched in different signaling pathways. The bFGF treatment restored tear secretion by 22% and promoted nerve regeneration, although nerve fiber density remained 74% lower than that of controls.

Conclusions: Corneal sensory nerve injury disrupts both central and peripheral circadian clock functions in the lacrimal gland, leading to reduced tear secretion and immune dysregulation. These findings highlight the novel role of circadian rhythms and neural-immune interactions in lacrimal gland dysfunction. Neural regeneration strategies, such as bFGF, offer therapeutic potential for dry eye syndrome, providing new directions for clinical intervention.

角膜感觉神经损伤通过改变小鼠昼夜节律破坏泪腺功能。
目的:探讨角膜感觉神经损伤对泪腺功能的影响,重点探讨其机制包括上涎核(SSN)、昼夜节律紊乱、免疫微环境改变和神经再生的潜力。方法:采用小鼠角膜感觉神经损伤模型评价泪腺功能,采用酚红线法测定泪液分泌量。泪腺转录组学分析检测昼夜节律和免疫相关基因表达。应用碱性成纤维细胞生长因子(bFGF)促进角膜神经再生,并观察其对泪液分泌和神经修复的影响。结果:角膜神经损伤导致泪液分泌减少35%,SSN活性明显受损,胆碱乙酰转移酶(ChAT)表达神经元中c- fos阳性神经元减少31%。转录组学分析显示免疫相关通路显著下调,包括toll样受体(TLR)、nod样受体(NLR)和t细胞受体信号。昼夜节律基因的表达呈现相移,表达峰值延迟2.13 h,节律基因的数量和类型发生了实质性变化,这些基因在不同的信号通路中富集。尽管神经纤维密度仍比对照组低74%,但bFGF治疗使泪液分泌恢复22%,促进神经再生。结论:角膜感觉神经损伤破坏泪腺中枢和外周生物钟功能,导致泪液分泌减少和免疫失调。这些发现强调了昼夜节律和神经免疫相互作用在泪腺功能障碍中的新作用。以bFGF为代表的神经再生策略对干眼综合征具有治疗潜力,为临床干预提供了新的方向。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
6.90
自引率
4.50%
发文量
339
审稿时长
1 months
期刊介绍: Investigative Ophthalmology & Visual Science (IOVS), published as ready online, is a peer-reviewed academic journal of the Association for Research in Vision and Ophthalmology (ARVO). IOVS features original research, mostly pertaining to clinical and laboratory ophthalmology and vision research in general.
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