Li Bo, Suzuki-Kerr Haruna, Martis Renita M, Lim Christopher J J, Wang Zhou-Ai, Nguyen Tai X, Donaldson Paul J, Poulsen Raewyn C, Lim Julie C
Department of Physiology, School of Medical Sciences, University of Auckland, Auckland, New Zealand.
New Zealand National Eye Centre, University of Auckland, Auckland, New Zealand.
Front Ophthalmol (Lausanne). 2024 Aug 15;4:1407582. doi: 10.3389/fopht.2024.1407582. eCollection 2024.
Evidence in non-ocular tissues indicate that the antioxidant glutathione (GSH) may be regulated in a circadian manner leading to the idea that GSH levels in the lens may also be controlled in a circadian manner to anticipate periods of oxidative stress.
Male rat Wistar lenses (6 weeks) were collected every 4 hours over a 24-hour period at 6am, 10am, 2pm, 6pm, 10pm and 2am and quantitative-PCR, western blotting and immunohistochemistry performed to examine the expression of core clock genes and proteins (BMAL1, CLOCK, CRY1-2, PER 1-3) and their subcellular localisation over a 24-hour period. Western blotting of lenses was also performed to examine the expression of NRF2, a transcription factor involved in regulating genes involved in GSH homeostasis and GSH related enzymes (GCLC, GS and GR) over the 24-hour period. Finally, HLPC was used to measure GSH levels in the aqueous humour and lenses every 4 hours over a 24-hour period.
The rat lens contains the core molecular components of a circadian clock with the expression of core clock proteins, NRF2 and GSH related enzymes fluctuating over a 24-hour period. BMAL1 expression was highest during the day, with BMAL1 localised to the nuclei at 10am. NRF2 expression remained constant over the 24-hour period, although appeared to move in and out of the nuclei every 4 hours. GSH related enzyme expression tended to peak at the start of night which correlated with high levels of GSH in the lens and lower levels of GSH in the aqueous humour.
The lens contains the key components of a circadian clock, and time-of-day differences exist in the expression of GSH and GSH related enzymes involved in maintaining GSH homeostasis. GSH levels in the rat lens were highest at the start of night which represents the active phase of the rat when high GSH levels may be required to counteract oxidative stress induced by cellular metabolism. Future work to directly link the clock to regulation of GSH levels in the lens will be important in determining whether the clock can be used to help restore GSH levels in the lens.
非眼部组织中的证据表明,抗氧化剂谷胱甘肽(GSH)可能受昼夜节律调控,这引发了一种观点,即晶状体中的GSH水平也可能以昼夜节律的方式得到控制,以应对氧化应激期。
在上午6点、10点、下午2点、6点、晚上10点和凌晨2点的24小时内,每隔4小时收集雄性Wistar大鼠(6周龄)的晶状体,并进行定量PCR、蛋白质印迹和免疫组织化学,以检测核心生物钟基因和蛋白质(BMAL1、CLOCK、CRY1 - 2、PER 1 - 3)在24小时内的表达及其亚细胞定位。还对晶状体进行蛋白质印迹,以检测NRF2(一种参与调节与GSH稳态相关基因的转录因子)以及GSH相关酶(GCLC、GS和GR)在24小时内的表达。最后,在24小时内每隔4小时使用高效液相色谱法测量房水和晶状体中的GSH水平。
大鼠晶状体含有昼夜节律钟的核心分子成分,核心生物钟蛋白、NRF2和GSH相关酶的表达在24小时内波动。BMAL1表达在白天最高,上午10点时BMAL1定位于细胞核。NRF2表达在24小时内保持恒定,尽管似乎每隔4小时进出细胞核一次。GSH相关酶的表达往往在夜间开始时达到峰值,这与晶状体中高水平的GSH和房水中较低水平的GSH相关。
晶状体含有昼夜节律钟的关键成分,参与维持GSH稳态的GSH和GSH相关酶的表达存在昼夜差异。大鼠晶状体中的GSH水平在夜间开始时最高,这代表大鼠的活跃期,此时可能需要高水平的GSH来抵消细胞代谢诱导的氧化应激。未来直接将生物钟与晶状体中GSH水平调节联系起来的工作,对于确定生物钟是否可用于帮助恢复晶状体中的GSH水平至关重要。