Xue Yunxia, Liu Peng, Wang Hanqing, Xiao Chengju, Lin Cuipei, Liu Jun, Dong Dong, Fu Ting, Yang Yabing, Wang Zhaorui, Pan Hongwei, Chen Jiansu, Li Yangqiu, Cai Dongqing, Li Zhijie
International Ocular Surface Research Center and Institute of Ophthalmology, Jinan University, Guangzhou, China.
Key Laboratory for Regenerative Medicine, Ministry of Education, Jinan University, Guangzhou, China.
Invest Ophthalmol Vis Sci. 2017 Mar 1;58(3):1865-1874. doi: 10.1167/iovs.16-21154.
In mammalian corneal epithelium, mitosis shows a distinct circadian pattern. However, how this circadian pattern is maintained, and how it or its disruption influence renewal and regeneration remain unclear.
C57BL/6 mice were maintained under 12-hour light/12-hour dark (LD), 12-hour light/12-hour light (LL), 12-hour dark/12-hour dark (DD), or reversed LD (DL, 12-hour dark/12-hour light; jet-lag defined as a shift of 12 hours) conditions. Mitotic cells in corneal epithelium were enumerated and analyzed via immunofluorescence at different zeitgeber times (ZTs). Expression of core clock genes (Clock, Bmal1, Period2, Cry1, and Rev-erbα) was qualified via quantitative RT-PCR. The rate and quality of healing at different ZT times and after administration of two small-molecule modifiers of the circadian clock, KL001 and SR8278, was evaluated.
In this study, photic cues were found to influence the 24-hour rhythm of corneal clock gene expression and epithelial cell mitosis in mice. Disruption of the circadian clock by exposure to constant light, constant dark, or jet-lag conditions modified the normal 24-hour patterns of corneal epithelial mitosis and corneal clock gene expression. The time of day of wound occurrence affected the rate and quality of corneal healing, with both of these parameters peaking during the more mitotically active hours of the morning. The two small-molecule modifiers of the circadian clock, KL001 and SR8278, had negative and positive effects on corneal wound healing, respectively.
Circadian rhythms significantly influence corneal epithelium renewal and repair in mice. Our findings reveal possible opportunities for biological rhythm-based interventional strategies to control corneal healing and restore corneal homeostasis.
在哺乳动物角膜上皮中,有丝分裂呈现出明显的昼夜节律模式。然而,这种昼夜节律模式是如何维持的,以及它或其破坏如何影响更新和再生仍不清楚。
将C57BL/6小鼠饲养在12小时光照/12小时黑暗(LD)、12小时光照/12小时光照(LL)、12小时黑暗/12小时黑暗(DD)或反向LD(DL,12小时黑暗/12小时光照;时差定义为12小时的偏移)条件下。在不同的授时因子时间(ZT)通过免疫荧光对角膜上皮中的有丝分裂细胞进行计数和分析。通过定量RT-PCR对核心生物钟基因(Clock、Bmal1、Period2、Cry1和Rev-erbα)的表达进行定量。评估在不同ZT时间以及在给予两种昼夜节律小分子调节剂KL001和SR8278后伤口愈合的速率和质量。
在本研究中,发现光信号会影响小鼠角膜生物钟基因表达和上皮细胞有丝分裂的24小时节律。通过持续光照、持续黑暗或时差条件破坏昼夜节律会改变角膜上皮有丝分裂和角膜生物钟基因表达的正常24小时模式。伤口发生的时间会影响角膜愈合的速率和质量,这两个参数在早晨有丝分裂更活跃的时段达到峰值。两种昼夜节律小分子调节剂KL001和SR8278分别对角膜伤口愈合有负面和正面影响。
昼夜节律显著影响小鼠角膜上皮的更新和修复。我们的研究结果揭示了基于生物节律的干预策略在控制角膜愈合和恢复角膜稳态方面的潜在机会。