4.7 Article

Oxidative Stress and Lipid Dysregulation in Lipid Droplets: A Connection to Chronic Kidney Disease Revealed in Human Kidney Cells

期刊

ANTIOXIDANTS
卷 11, 期 7, 页码 -

出版社

MDPI
DOI: 10.3390/antiox11071387

关键词

lipid droplets (LDs); chronic kidney disease (CKD); oxidative stress; ectopic lipid accumulation; lipid hydroperoxides; triglycerides; phosphatidylcholines; phosphatidylethanolamines; cholesteryl esters; molecular species

资金

  1. Regional Innovation Strategy Support Program, Sapporo Health Innovation Smart-H, of the Ministry of Education, Culture, Sports, Science, and Technology, Japan
  2. Japan Society for the Promotion of Science (JSPS) KAKENHI [19K07861]

向作者/读者索取更多资源

This study investigated the chemical composition of lipid droplets (LDs) in human kidney cells under the influence of free fatty acids and oxidized lipoproteins. The results showed that both the fatty acids and oxidized lipoproteins significantly altered the lipid content and composition of LDs. The accumulation of oxidized lipids and dysregulation of lipid metabolism in LDs may be potential targets for the diagnosis and treatment of chronic kidney disease (CKD).
Chronic kidney disease (CKD), which is defined as a condition causing the gradual loss of kidney function, shows renal lipid droplet (LD) accumulation that is associated with oxidative damage. There is a possibility that an LD abnormality in quality plays a role in CKD development. This study aimed to explore the chemical composition of LDs that are induced in human kidney cells during exposure to free fatty acids as an LD source and oxidized lipoproteins as oxidative stress. The LDs were aspirated directly from cells using nanotips, followed by in-tip microextraction, and the LD lipidomic profiling was conducted using nanoelectrospray mass spectrometry. As a result, the free fatty acids increased the LD lipid content and, at the same time, changed their composition significantly. The oxidized lipoproteins caused distorted proportions of intact lipids, such as triacylglycerols (TG), phosphatidylcholines (PC), phosphatidylethanolamines (PE), and cholesteryl esters (CE). Notably, the oxidized lipids, including the hydroperoxides of TG, PC, and PE, exhibited significant elevations in dose-dependent manners. Furthermore, the dysregulation of intact lipids was paralleled with the accumulation of lipid hydroperoxides. The present study has revealed that the oxidation of lipids and the dysregulation of the lipid metabolism coexisted in LDs in the kidney cells, which has provided a potential new target for diagnosis and new insights into CKD.

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