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蛋氨酸调节下肌萎缩侧索硬化症代谢动力学的光学成像

Optical imaging of metabolic dynamics in ALS under methionine regulation.

作者信息

Hoang Khang, Prayotamornkul Sirasit, Kuo Chan-Yu, Jang Hongje, Shi Lingyan

机构信息

University of California San Diego, Shu Chien-Gene Lay Department of Bioengineering, La Jolla, California, United States.

University of California San Diego, Aiiso Yufeng Li Family Department of Chemical and Nano Engineering, La Jolla, California, United States.

出版信息

J Biomed Opt. 2025 Feb;30(Suppl 2):S23906. doi: 10.1117/1.JBO.30.S2.S23906. Epub 2025 May 24.

Abstract

SIGNIFICANCE

Excessive reactive oxygen species (ROS) in dysfunctional mitochondria, combined with inefficient antioxidant defenses, can drive amyotrophic lateral sclerosis (ALS) progression. L-methionine (Met) can neutralize ROS by modulating metabolism and activating antioxidants; however, its impact on ALS remains unknown.

AIM

We aim to investigate the influence of excess Met on cellular metabolism and ROS accumulation and its role in ALS using multimodal optical imaging techniques.

APPROACH

We applied deuterium oxide-probed stimulated Raman scattering imaging to study metabolic changes of lipids, proteins, and cytochrome and two-photon excitation fluorescence imaging to assess mitochondrial redox state (nicotinamide adenine dinucleotide and flavin adenine dinucleotide ratio) in ALS cellular models under excess Met treatment. With three-dimensional (3D) image reconstruction, we investigated morphological changes of lipid droplets (LDs) and stress granules (SGs) in ALS models.

RESULTS

Excess Met not only promoted syntheses of lipids and unsaturated lipid membranes but also reduced protein synthesis, cytochrome oxidation, and oxidative stress. Moreover, 3D image reconstruction showed that LDs increased in volume and number to promote cellular repair, whereas SGs decreased in volume but increased in number in response to reduced cellular stress.

CONCLUSIONS

Excess Met offers a protective mechanism against oxidative stress and promotes cellular repair in ALS.

摘要

意义

功能失调的线粒体中过量的活性氧(ROS),加上低效的抗氧化防御,可推动肌萎缩侧索硬化症(ALS)的进展。L-蛋氨酸(Met)可通过调节代谢和激活抗氧化剂来中和ROS;然而,其对ALS的影响尚不清楚。

目的

我们旨在使用多模态光学成像技术研究过量Met对细胞代谢和ROS积累的影响及其在ALS中的作用。

方法

我们应用氧化氘探测的受激拉曼散射成像来研究脂质、蛋白质和细胞色素的代谢变化,并应用双光子激发荧光成像来评估过量Met处理下ALS细胞模型中的线粒体氧化还原状态(烟酰胺腺嘌呤二核苷酸和黄素腺嘌呤二核苷酸比率)。通过三维(3D)图像重建,我们研究了ALS模型中脂滴(LDs)和应激颗粒(SGs)的形态变化。

结果

过量Met不仅促进了脂质和不饱和脂质膜的合成,还减少了蛋白质合成、细胞色素氧化和氧化应激。此外,3D图像重建显示,LDs的体积和数量增加以促进细胞修复,而SGs的体积减小但数量增加以应对细胞应激的降低。

结论

过量Met提供了一种针对氧化应激的保护机制,并促进了ALS中的细胞修复。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9324/12102500/2c2997124a50/JBO-030-S23906-g001.jpg

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