Fiche publication
Date publication
mars 2017
Journal
Annals of transplantation
Auteurs
Membres identifiés du Cancéropôle Est :
Pr SCHINI-KERTH Valérie
,
Dr AUGER Cyril
Tous les auteurs :
Kassem M, Niazi ZR, Abbas M, El Habhab A, Kreutter G, Khemais-Benkhiat S, Auger C, Antal MC, Schini-Kerth VB, Toti F, Kessler L
Lien Pubmed
Résumé
BACKGROUND In organ transplantation, particularly pancreas transplantation, donor age is a determinant factor for graft survival. Physiological aging is crucial in the progressive deterioration of organs in adulthood. We compared the senescence and function features of pancreas and vascular tissues in young rats and middle-aged rats. MATERIAL AND METHODS Islet morphology and the area of cells secreting insulin or glucagon was investigated using immunohistology in young rats (12 weeks) and middle-aged rats (52 weeks) (n=8). Senescence markers, oxidative stress (ROS), and tissue factor (TF) were measured in the rat pancreases. Circulating microparticles (MPs) were measured as surrogates of vascular cell injury. Vascular function was studied in mesenteric arterial rings. RESULTS Larger islets were twice as frequent in young rats versus middle-aged rats. In middle-aged rats there was a significant decrease of the β-cells/islet area ratio. Western blot analysis showed an increased expression of p53, p21, and p16 senescence markers (2-, 7- and 3-fold respectively) with no modification in caspase-3 activation. A 30% decrease of endothelial nitric oxide synthase (eNOS) was observed together with a 4-fold increase in TF expression. ROS formation increased significantly (2-fold) in middle-aged rats and their main source, determined by pharmacological inhibition, was NADPH oxidase and uncoupled nitric-oxide (NO) synthase. No sign of vascular injury (microparticles) or dysfunction was evidenced. CONCLUSIONS Modification in islet morphology and function were detected in middle-aged rats before any measurement of macro-vascular dysfunction. The data indicate a pancreatic senescence in the process of aging associated with uncontrolled accumulation of oxidative species that suggests a determining role of donor age in transplantation.
Mots clés
Aging, physiology, Animals, Caspase 3, metabolism, Endothelium, Vascular, physiology, Glucagon, metabolism, Insulin, metabolism, Insulin-Secreting Cells, metabolism, Male, NADPH Oxidases, metabolism, Nitric Oxide Synthase, metabolism, Oxidative Stress, physiology, Pancreas, metabolism, Rats, Rats, Wistar, Reactive Oxygen Species, metabolism
Référence
Ann. Transplant.. 2017 Mar 31;22:177-186
