Intermittent fasting inhibits ferroptosis by modulating CD36 and its palmitoylation to alleviate diabetic dry eye.

IF 12.2 1区 生物学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY
Wenhui Wang, Jianwen Xue, Bing Xiao, Xiaobing Qian, Jing Li, Xingyan Lin, Ziyan Chen, Wei Wang, Lingyi Liang
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Abstract

BACKGROUND: Excessive lipid accumulation in the lacrimal glands under diabetic conditions can lead to lacrimal gland dysfunction and reduced tear secretion, subsequently resulting in ocular surface inflammation, dry eye syndrome, and corneal vulnerability, ultimately compromising the patient’s quality of life. There are limited and easily implemented intervention strategies to reduce excessive lipid accumulation. While intermittent fasting (IF) has emerged as a promising metabolic intervention, its mechanistic underpinnings and therapeutic potential in diabetes-associated lacrimal gland disorders require systematic elucidation. METHODS: Diabetic mice were divided into three groups for an 8-week dietary intervention: ad libitum, meal feeding, and every-other-day feeding. After dietary intervention, we assessed the damage to lacrimal glands and ocular surface, and elucidated lipid accumulation, ferroptosis, and functional changes in the lacrimal glands. Transcriptomic analysis was used to examine gene expression. CD36 and its palmitoylation were examined around three groups. In addition, damage to the ocular surface and lacrimal glands was assessed in vivo, after the mice were injected with the ferroptosis inhibitor Fer-1 and CD36 shRNA. RESULTS: In this study, we found that compared with caloric restriction, IF more effectively reduced lipid accumulation in the lacrimal glands of diabetic db/db mice, decreased lipid peroxidation and ferroptosis, and improved function. IF downregulated CD36 expression and its palmitoylation, potentially mediated by ZDHHC20. CD36 shRNA and ferroptosis inhibition (Fer-1) comparably restored lacrimal secretory function, yet only CD36 knockdown concurrently resolved lipidostasis and ferroptosis. CONCLUSIONS: This analysis identifies CD36 as a key regulator bridging lipotoxic stress and ferroptotic execution in diabetic lacrimal gland dysfunction. Importantly, our findings suggest that ferroptosis may serve as the critical effector mechanism converting metabolic overload to glandular dysfunction, suggesting potential therapeutic value in dual targeting of lipidostasis and cell death pathways. SIGNIFICANCE: Intermittent fasting, which appears more effective than that of caloric restriction, may be associated with reduced lipid absorption resulting from decreased CD36 expression and its palmitoylation on lacrimal gland cell membranes. These findings uncover a potential novel treatment strategy for diabetic dry eye.

间歇性禁食通过调节CD36及其棕榈酰化抑制铁下垂,缓解糖尿病性干眼症。
背景:糖尿病患者泪腺中过多的脂质积累可导致泪腺功能障碍和泪液分泌减少,进而导致眼表炎症、干眼综合征和角膜易损性,最终影响患者的生活质量。有有限的和容易实施的干预策略,以减少过度的脂质积累。虽然间歇性禁食(IF)已成为一种有前景的代谢干预手段,但其机制基础和治疗糖尿病相关泪腺疾病的潜力需要系统阐明。方法:将糖尿病小鼠分为三组,进行为期8周的饮食干预:随意喂养、膳食喂养和每隔一天喂养。在饮食干预后,我们评估了泪腺和眼表的损伤,并阐明了泪腺的脂质积累、铁下垂和功能变化。转录组学分析用于检测基因表达。在三组周围检测CD36及其棕榈酰化。此外,在小鼠体内注射铁下垂抑制剂fer1和CD36 shRNA后,评估了眼表和泪腺的损伤。结果:在本研究中,我们发现与限热相比,IF能更有效地减少糖尿病db/db小鼠泪腺脂质积累,降低脂质过氧化和铁下垂,改善功能。IF下调CD36表达及其棕榈酰化,可能由ZDHHC20介导。CD36 shRNA和铁下垂抑制(fer1)可明显恢复泪液分泌功能,但只有敲低CD36才能同时解决脂质停滞和铁下垂。结论:该分析确定CD36是糖尿病泪腺功能障碍中脂毒性应激和铁致下降的关键调节因子。重要的是,我们的研究结果表明,铁下垂可能是将代谢超载转化为腺体功能障碍的关键效应机制,这表明在脂质平衡和细胞死亡途径的双重靶向方面具有潜在的治疗价值。意义:间歇性禁食似乎比热量限制更有效,可能与泪腺细胞膜上CD36表达及其棕榈酰化减少导致的脂质吸收减少有关。这些发现揭示了一种潜在的治疗糖尿病性干眼症的新策略。
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
Cellular & Molecular Biology Letters
Cellular & Molecular Biology Letters 生物-生化与分子生物学
CiteScore
11.60
自引率
13.30%
发文量
101
审稿时长
3 months
期刊介绍: Cellular & Molecular Biology Letters is an international journal dedicated to the dissemination of fundamental knowledge in all areas of cellular and molecular biology, cancer cell biology, and certain aspects of biochemistry, biophysics and biotechnology.
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