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Circulating Cell-Free mtDNA Contributes to AIM2 Inflammasome-Mediated Chronic Inflammation in Patients with Type 2 Diabetes

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dc.contributor.authorBae, Jung Hwan-
dc.contributor.authorJo, Seung, II-
dc.contributor.authorKim, Seong Jin-
dc.contributor.authorLee, Jong Min-
dc.contributor.authorJeong, Ji Hun-
dc.contributor.authorKang, Jeong Suk-
dc.contributor.authorCho, Nam-Jun-
dc.contributor.authorKim, Sang Soo-
dc.contributor.authorLee, Eun Young-
dc.contributor.authorMoon, Jong-Seok-
dc.date.accessioned2021-08-11T09:44:15Z-
dc.date.available2021-08-11T09:44:15Z-
dc.date.issued2019-04-
dc.identifier.issn2073-4409-
dc.identifier.urihttps://scholarworks.bwise.kr/sch/handle/2021.sw.sch/4593-
dc.description.abstractMitochondrial dysfunction has been implicated in the pathogenesis of insulin resistance and type 2 diabetes. Damaged mitochondria DNA (mtDNA) may have a role in regulating hyperglycemia during type 2 diabetes. Circulating cell-free mitochondria DNA (ccf-mtDNA) was found in serum and plasma from patients and has been linked to the prognosis factors in various human diseases. However, the role of ccf-mtDNA in chronic inflammation in type 2 diabetes is unclear. In this study, we hypothesized that the ccf-mtDNA levels are associated with chronic inflammation in patients with type 2 diabetes. The mtDNA levels were elevated in the plasma from patients with type 2 diabetes compared to healthy subjects. The elevated mtDNA levels were associated with interleukin-1 (IL-1) levels in patients with type 2 diabetes. The mtDNA, from patients with type 2 diabetes, induced absent in melanoma 2 (AIM2) inflammasome-dependent caspase-1 activation and IL-1 and IL-18 secretion in macrophages. Our results suggest that the ccf-mtDNA might contribute to AIM2 inflammasome-mediated chronic inflammation in type 2 diabetes.-
dc.language영어-
dc.language.isoENG-
dc.publisherMultidisciplinary Digital Publishing Institute (MDPI)-
dc.titleCirculating Cell-Free mtDNA Contributes to AIM2 Inflammasome-Mediated Chronic Inflammation in Patients with Type 2 Diabetes-
dc.typeArticle-
dc.publisher.location스위스-
dc.identifier.doi10.3390/cells8040328-
dc.identifier.wosid000467304300042-
dc.identifier.bibliographicCitationCells, v.8, no.4-
dc.citation.titleCells-
dc.citation.volume8-
dc.citation.number4-
dc.type.docTypeArticle-
dc.description.isOpenAccessY-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaCell Biology-
dc.relation.journalWebOfScienceCategoryCell Biology-
dc.subject.keywordPlusFREE MITOCHONDRIAL-DNA-
dc.subject.keywordPlusPLASMA NUCLEAR-
dc.subject.keywordPlusRELEASE-
dc.subject.keywordPlusDAMAGE-
dc.subject.keywordPlusACTIVATION-
dc.subject.keywordPlusBIOMARKER-
dc.subject.keywordPlusDISEASE-
dc.subject.keywordPlusNEPHROPATHY-
dc.subject.keywordPlusDYSFUNCTION-
dc.subject.keywordPlusMECHANISM-
dc.subject.keywordAuthorccf-mtDNA-
dc.subject.keywordAuthorchronic inflammation-
dc.subject.keywordAuthorAIM2 inflammasome-
dc.subject.keywordAuthortype 2 diabetes-
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