Netosis contributes to the pathogenesis of diabetes and its complications

dc.contributor.authorNjeim, Rachel
dc.contributor.authorAzar, William S.
dc.contributor.authorFares, Angie H.
dc.contributor.authorAzar, Sami T.
dc.contributor.authorK̈foury, Hala Kassouf
dc.contributor.authorEid, Assaad A.
dc.contributor.departmentAnatomy, Cell Biology, and Physiological Sciences
dc.contributor.departmentInternal Medicine
dc.contributor.departmentPathology and Laboratory Medicine
dc.contributor.departmentDiabetes Program
dc.contributor.facultyFaculty of Medicine (FM)
dc.contributor.institutionAmerican University of Beirut
dc.date.accessioned2025-01-24T11:36:58Z
dc.date.available2025-01-24T11:36:58Z
dc.date.issued2020
dc.description.abstractNETosis, a novel form of neutrophil-related cell death, acts as a major regulator of diabetes and diabetes-associated complications. In this review, we show that the extrusion of neutrophil extracellular traps, termed NETs, plays an important role in the pathogenesis of type 1 diabetes mellitus (T1DM), type 2 diabetes mellitus (T2DM), and diabetes-induced complications. In T1DM, β-cell death induces the sequestration of neutrophils in the pancreas and seems to be correlated with increased NETosis. In T2DM patients, products of NETs release are significantly elevated. Increased levels of dsDNA are correlated with the presence of cardiovascular disease and diabetic kidney disease, further supporting the role of NETosis in the pathogenesis of other diabetesinduced complications such as impaired wound healing and diabetic retinopathy. NETosis is induced by high glucose through incompletely understood mechanisms, but it also appears to be elevated in patients with diabetes who have tightly controlled glucose levels. We hypothesize that hyperglycemia worsens the already elevated baseline of NETosis in diabetic patients to further increase its detrimental effects. © 2020 Society for Endocrinology Published by Bioscientifica Ltd.
dc.identifier.doihttps://doi.org/10.1530/JME-20-0128
dc.identifier.eid2-s2.0-85092886473
dc.identifier.pmid33048064
dc.identifier.urihttp://hdl.handle.net/10938/28767
dc.language.isoen
dc.publisherBioScientifica Ltd.
dc.relation.ispartofJournal of Molecular Endocrinology
dc.sourceScopus
dc.subjectDiabetes mellitus
dc.subjectDiabetes-induced complications
dc.subjectNadph oxidases
dc.subjectNetosis
dc.subjectNeutrophil extracellular traps
dc.subjectAnimals
dc.subjectBiomarkers
dc.subjectDiabetes complications
dc.subjectDisease susceptibility
dc.subjectExtracellular traps
dc.subjectHumans
dc.subjectNeutrophils
dc.subjectGlucose
dc.subjectBiological marker
dc.subjectReduced nicotinamide adenine dinucleotide phosphate oxidase
dc.subjectCardiovascular disease
dc.subjectCell death
dc.subjectDiabetic nephropathy
dc.subjectDiabetic retinopathy
dc.subjectExtracellular trap
dc.subjectGlycemic control
dc.subjectHuman
dc.subjectHyperglycemia
dc.subjectInsulin dependent diabetes mellitus
dc.subjectNeutrophil
dc.subjectNon insulin dependent diabetes mellitus
dc.subjectNonhuman
dc.subjectPancreas islet beta cell
dc.subjectPathogenesis
dc.subjectPriority journal
dc.subjectReview
dc.subjectVascular disease
dc.subjectWound healing impairment
dc.subjectAnimal
dc.subjectDiabetic complication
dc.subjectDisease predisposition
dc.subjectGenetics
dc.subjectImmunology
dc.subjectMetabolism
dc.subjectPathology
dc.titleNetosis contributes to the pathogenesis of diabetes and its complications
dc.typeReview

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