Regulatory effects of antioxidants on indoxyl sulfate-enhanced intracellular oxidation and impaired phagocytic activity in differentiated U937 human macrophage cells

Author:

Iwamoto Wakana1,Ikeda Tomohiro1,Nishikawa Hirotaka1,Hirano Masashi12,Kinoshita Hideki12ORCID,Ono Masateru12,Kurogi Katsuhisa3ORCID,Sakakibara Yoichi3,Suiko Masahito4,Yasuda Shin12ORCID

Affiliation:

1. Graduate School of Agriculture, Tokai University , Mashiki-Cho, Kamimashiki-Gun, Kumamoto , Japan

2. Department of Food and Life Sciences, School of Agriculture, Tokai University , Mashiki-Cho, Kamimashiki-Gun, Kumamoto , Japan

3. Department of Biochemistry and Applied Biosciences, Faculty of Agriculture, University of Miyazaki , Miyazaki , Japan

4. Support Office for the Next Generation Researcher, University of Miyazaki , Miyazaki , Japan

Abstract

ABSTRACT Indoxyl sulfate (IS), a uremic toxin, is a physiologically active sulfated metabolite, specifically in kidney failure patients. Our previous studies have shown that IS downregulates phagocytic immune function in a differentiated HL-60 human macrophage cell model. However, it remains unclear whether IS exerts similar effects on macrophage function in other cell types or in lipopolysaccharide (LPS)-sensitive immune cell models. Therefore, this study aimed to investigate the effects of IS on intracellular oxidation levels and phagocytic activity in a differentiated U937 human macrophage cell model, both in the absence and presence of LPS. Our results demonstrated that IS significantly increases intracellular oxidation levels and decreases phagocytic activity, particularly in cells activated by LPS. Furthermore, we found that 2-acetylphenothiazine, an NADH oxidase inhibitor, attenuates the effects of IS in LPS-activated macrophage cells. Representative antioxidants, trolox, α-tocopherol, and ascorbic acid, significantly mitigated the effects of IS on the macrophages responding to LPS.

Funder

JSPS

Tokai University

Publisher

Oxford University Press (OUP)

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