Particulate matter induces ferroptosis by accumulating iron and dysregulating the antioxidant system

Cited 14 time in scopus
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dc.contributor.authorMinkyung Park-
dc.contributor.authorYoung Lai Cho-
dc.contributor.authorYumin Choi-
dc.contributor.authorJ K Min-
dc.contributor.authorYoung-Jun Park-
dc.contributor.authorSung Jin Yoon-
dc.contributor.authorDae Soo Kim-
dc.contributor.authorMi-Young Son-
dc.contributor.authorS W Chung-
dc.contributor.authorH Lee-
dc.contributor.authorSeon-Jin Lee-
dc.date.accessioned2023-02-28T16:32:51Z-
dc.date.available2023-02-28T16:32:51Z-
dc.date.issued2023-
dc.identifier.issn1976-6696-
dc.identifier.urihttps://oak.kribb.re.kr/handle/201005/31129-
dc.description.abstractParticulate matter is an air pollutant composed of various components, and has adverse effects on the human body. Particulate matter is known to induce cell death by generating an imbalance in the antioxidant system; however, the underlying mechanism has not been elucidated. In the present study, we demonstrated the cytotoxic effects of the size and composition of particulate matter on small intestine cells. We found that particulate matter 2.5 (PM2.5) with extraction ion (EI) components (PM2.5 EI), is more cytotoxic than PM containing only polycyclic aromatic hydrocarbons (PAHs). Additionally, PM-induced cell death is characteristic of ferroptosis, and includes iron accumulation, lipid peroxidation, and reactive oxygen species (ROS) generation. Furthermore, ferroptosis inhibitor as liproxstatin-1 and iron-chelator as deferiprone attenuated cell mortality, lipid peroxidation, iron accumulation, and ROS production after PM2.5 EI treatment in human small intestinal cells. These results suggest that PM2.5 EI may increase ferroptotic-cell death by iron accumulation and ROS generation, and offer a potential therapeutic clue for inflammatory bowel diseases in human small intestinal cells.-
dc.publisherKorea Soc-Assoc-Inst-
dc.titleParticulate matter induces ferroptosis by accumulating iron and dysregulating the antioxidant system-
dc.title.alternativeParticulate matter induces ferroptosis by accumulating iron and dysregulating the antioxidant system-
dc.typeArticle-
dc.citation.titleBMB Reports-
dc.citation.number2-
dc.citation.endPage101-
dc.citation.startPage96-
dc.citation.volume56-
dc.contributor.affiliatedAuthorMinkyung Park-
dc.contributor.affiliatedAuthorYoung Lai Cho-
dc.contributor.affiliatedAuthorYumin Choi-
dc.contributor.affiliatedAuthorYoung-Jun Park-
dc.contributor.affiliatedAuthorSung Jin Yoon-
dc.contributor.affiliatedAuthorDae Soo Kim-
dc.contributor.affiliatedAuthorMi-Young Son-
dc.contributor.affiliatedAuthorSeon-Jin Lee-
dc.contributor.alternativeName박민경-
dc.contributor.alternativeName조영래-
dc.contributor.alternativeName최유민-
dc.contributor.alternativeName민정기-
dc.contributor.alternativeName박영준-
dc.contributor.alternativeName윤성진-
dc.contributor.alternativeName김대수-
dc.contributor.alternativeName손미영-
dc.contributor.alternativeName정수월-
dc.contributor.alternativeName이희두-
dc.contributor.alternativeName이선진-
dc.identifier.bibliographicCitationBMB Reports, vol. 56, no. 2, pp. 96-101-
dc.identifier.doi10.5483/BMBRep.2022-0139-
dc.subject.keywordCell death-
dc.subject.keywordFerroptosis-
dc.subject.keywordIron accumulation-
dc.subject.keywordParticulate matter-
dc.subject.keywordROS-
dc.subject.localCell death-
dc.subject.localcell death-
dc.subject.localFerroptosis-
dc.subject.localferroptosis-
dc.subject.localParticulate Matter-
dc.subject.localParticulate matter-
dc.subject.localparticulate matter-
dc.subject.localROS-
dc.subject.localReactive Oxygen Species (ROS)-
dc.subject.localReactive oxidative species-
dc.subject.localReactive oxygen species-
dc.subject.localReactive oxygen species (ROS)-
dc.subject.localreactive oxygen species-
dc.subject.localreactive oxygen species (ROS)-
dc.subject.localReactive Oxygen Species-
dc.subject.localReactive oxygen species(ROS)-
dc.description.journalClassY-
Appears in Collections:
Division of Research on National Challenges > Environmental diseases research center > 1. Journal Articles
Division of A.I. & Biomedical Research > Digital Biotech Innovation Center > 1. Journal Articles
Division of Research on National Challenges > 1. Journal Articles
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