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ABSTRACT: Rationale
Activation of NLRP3 (nucleotide-binding domain and leucine-rich repeat pyrin domain containing 3) inflammasome-mediating interleukin (IL)-1β secretion has emerged as an important component of inflammatory processes in atherosclerosis. Mitochondrial DNA (mtDNA) damage is detrimental in atherosclerosis, and mitochondria are central regulators of the nucleotide-binding domain and leucine-rich repeat pyrin domain containing 3 inflammasome. Human atherosclerotic plaques express increased mtDNA damage. The major DNA glycosylase, 8-oxoguanine glycosylase (OGG1), is responsible for removing the most abundant form of oxidative DNA damage.Objective
To test the role of OGG1 in the development of atherosclerosis in mouse.Methods and results
We observed that Ogg1 expre
SUBMITTER: Tumurkhuu G
PROVIDER: S-EPMC5010464 | biostudies-literature | 2016 Sep
REPOSITORIES: biostudies-literature