Presentation + Paper
6 March 2023 Subcellular resolution DO-SRS and 2PEF imaging of metabolic dynamics regulated by L-methionine in amyotrophic lateral sclerosis
Author Affiliations +
Abstract
Amyotrophic lateral sclerosis (ALS) is a type of motor neuron disease that results in paralysis and death from a progressive loss of both upper and lower motor neurons. Emerging studies have indicated that excess production of reactive oxygen species (ROS) in dysfunctional mitochondria in addition to an inefficient antioxidant defense may contribute to the progression of the disease. L-methionine (Met) plays important roles in regulating cellular metabolism and activating endogenous antioxidant enzymes. We hypothesized that excess methionine treatment can provide ALS patients with an efficient antioxidant defense mechanism to control their disease. Here, we apply an optical imaging approach that combines deuterium oxide (D2O)-probed stimulated Raman scattering (DO-SRS) and two photon excitation fluorescence (2PEF) microscopies to directly image the effects of methionine-enriched diet on oxidative imbalance and cellular metabolism in neurodegenerative cells. Our preliminary data revealed that excess methionine increases syntheses of lipid and unsaturated lipid membranes. Meanwhile, the same diet decreases protein synthesis and oxidative imbalance. Our study suggests that excess methionine can provide a protective mechanism against oxidative imbalance and promote cellular repair in neurodegenerative diseases.
Conference Presentation
© (2023) COPYRIGHT Society of Photo-Optical Instrumentation Engineers (SPIE). Downloading of the abstract is permitted for personal use only.
Khang Hoang, Chan-yu Kuo, Sirasit Prayotamornkul, Hongje Jang, Hetvi Trivedi, Pegah Bagheri, and Lingyan Shi "Subcellular resolution DO-SRS and 2PEF imaging of metabolic dynamics regulated by L-methionine in amyotrophic lateral sclerosis", Proc. SPIE 12373, Optical Biopsy XXI: Toward Real-Time Spectroscopic Imaging and Diagnosis, 1237303 (6 March 2023); https://doi.org/10.1117/12.2649560
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KEYWORDS
Biological imaging

Raman spectroscopy

Raman scattering

Two photon excitation microscopy

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