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Persistent Oxidative Stress Due to Absence of Uncoupling Protein 2 Associated with Impaired Pancreatic β-Cell Function

Divisions of Translational Biology (J.P., Y.B., K.W.D., D.L., S.C.) and Toxicology and Preclinical Studies (O.L.), The Hamner Institutes for Health Sciences, Research Triangle Park, North Carolina 27709; Diabetes Research Center (D.E., M.B.), Albert Einstein College of Medicine, The Bronx, New York 10461; Obesity Research Center (B.E.C.), Boston University School of Medicine, Boston, Massachusetts 02118; and Psychiatry and Behavioral Sciences (S.C.), Duke University Medical Center, Durham North Carolina 27710

Address all correspondence and requests for reprints to: Sheila Collins, Ph.D., or Jingbo Pi, M.D., Ph.D., Division of Translational Biology, The Hamner Institutes for Health Sciences, Research Triangle Park, North Carolina 27709. E-mail: scollins{at}thehamner.org, sheila.collins{at}duke.edu, or jpi{at}thehamner.org.

Uncoupling protein (UCP) 2 is a widely expressed mitochondrial protein whose precise function is still unclear but has been linked to mitochondria-derived reactive oxygen species production. Thus, the chronic absence of UCP2 has the potential to promote persistent reactive oxygen species accumulation and an oxidative stress response. Here, we show that Ucp2–/– mice on three highly congenic (N >10) strain backgrounds (C57BL/6J, A/J, 129/SvImJ), including two independently generated sources of Ucp2-null animals, all exhibit increased oxidative stress. Ucp2-null animals exhibit a decreased ratio of reduced glutathione to its oxidized form in blood and tissues that normally express UCP2, including pancreatic islets. Islets from Ucp2–/– mice exhibit elevated levels of numerous antioxidant enzymes, increased nitrotyrosine and F4/80 staining, but no change in insulin content. Contrary to results in Ucp2–/– mice of mixed 129/B6 strain background, glucose-stimulated insulin secretion in Ucp2–/– islets of each congenic strain was significantly decreased. These data show that the chronic absence of UCP2 causes oxidative stress, including in islets, and is accompanied by impaired glucose-stimulated insulin secretion.

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