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Acute nutrient regulation of mitochondrial glutathione redox state in pancreatic β-cells

Bibliographic reference Takahashi, Hilton ; Romagueira Bichara Dos Santos, Laila ; Prates Roma, Leticia ; Duprez, Jessica ; Broca, Christophe ; et. al. Acute nutrient regulation of mitochondrial glutathione redox state in pancreatic β-cells. In: Biochemical Journal, Vol. 460, no. 3, p. 411-423 (2014)
Permanent URL http://hdl.handle.net/2078.1/142143
  1. MacDonald M. J., Perspective: emerging evidence for signaling roles of mitochondrial anaplerotic products in insulin secretion, 10.1152/ajpendo.00218.2004
  2. Jitrapakdee S., Wutthisathapornchai A., Wallace J. C., MacDonald M. J., Regulation of insulin secretion: role of mitochondrial signalling, 10.1007/s00125-010-1685-0
  3. Henquin J. C., Regulation of insulin secretion: a matter of phase control and amplitude modulation, 10.1007/s00125-009-1314-y
  4. Maechler Pierre, Mitochondrial function and insulin secretion, 10.1016/j.mce.2013.06.019
  5. Prentki Marc, Matschinsky Franz M., Madiraju S.R. Murthy, Metabolic Signaling in Fuel-Induced Insulin Secretion, 10.1016/j.cmet.2013.05.018
  6. Bindokas Vytautas P., Kuznetsov Andrey, Sreenan Seamus, Polonsky Kenneth S., Roe Michael W., Philipson Louis H., Visualizing Superoxide Production in Normal and Diabetic Rat Islets of Langerhans, 10.1074/jbc.m206913200
  7. Pi Jingbo, Bai Yushi, Reece Jeffrey M., Williams Jason, Liu Dianxin, Freeman Michael L., Fahl William E., Shugar David, Liu Jie, Qu Wei, Molecular mechanism of human Nrf2 activation and degradation: Role of sequential phosphorylation by protein kinase CK2, 10.1016/j.freeradbiomed.2007.03.001
  8. Leloup C., Tourrel-Cuzin C., Magnan C., Karaca M., Castel J., Carneiro L., Colombani A.-L., Ktorza A., Casteilla L., Penicaud L., Mitochondrial Reactive Oxygen Species Are Obligatory Signals for Glucose-Induced Insulin Secretion, 10.2337/db07-1056
  9. Martens Geert A., Cai Ying, Hinke Simon, Stangé Geert, Van de Casteele Mark, Pipeleers Daniel, Glucose Suppresses Superoxide Generation in Metabolically Responsive Pancreatic β Cells, 10.1074/jbc.m411869200
  10. Rebelato Eduardo, Abdulkader Fernando, Curi Rui, Carpinelli Angelo Rafael, Control of the Intracellular Redox State by Glucose Participates in the Insulin Secretion Mechanism, 10.1371/journal.pone.0024507
  11. Sarre Alexandre, Gabrielli Jessica, Vial Guillaume, Leverve Xavier M., Assimacopoulos-Jeannet Françoise, Reactive oxygen species are produced at low glucose and contribute to the activation of AMPK in insulin-secreting cells, 10.1016/j.freeradbiomed.2011.10.437
  12. Li N., Li B., Brun T., Deffert-Delbouille C., Mahiout Z., Daali Y., Ma X.-J., Krause K.-H., Maechler P., NADPH Oxidase NOX2 Defines a New Antagonistic Role for Reactive Oxygen Species and cAMP/PKA in the Regulation of Insulin Secretion, 10.2337/db12-0009
  13. Lortz S., Gurgul-Convey E., Naujok O., Lenzen S., Overexpression of the antioxidant enzyme catalase does not interfere with the glucose responsiveness of insulin-secreting INS-1E cells and rat islets, 10.1007/s00125-012-2823-7
  14. Grankvist K, Biochem. J., 199, 393 (1981)
  15. Tiedge M., Lortz S., Drinkgern J., Lenzen S., Relation Between Antioxidant Enzyme Gene Expression and Antioxidative Defense Status of Insulin-Producing Cells, 10.2337/diab.46.11.1733
  16. Laclau Muriel, Lu Feng, MacDonald Michael J., 10.1023/a:1012238709063
  17. Godoy José Rodrigo, Funke Maria, Ackermann Waltraud, Haunhorst Petra, Oesteritz Sabrina, Capani Francisco, Elsässer Hans-Peter, Lillig Christopher Horst, Redox atlas of the mouse, 10.1016/j.bbagen.2010.05.006
  18. Bensellam M., Van Lommel L., Overbergh L., Schuit F. C., Jonas J. C., Cluster analysis of rat pancreatic islet gene mRNA levels after culture in low-, intermediate- and high-glucose concentrations, 10.1007/s00125-008-1245-z
  19. Go Young-Mi, Jones Dean P., Redox compartmentalization in eukaryotic cells, 10.1016/j.bbagen.2008.01.011
  20. Spégel Peter, Sharoyko Vladimir V., Goehring Isabel, Danielsson Anders P. H., Malmgren Siri, Nagorny Cecilia L. F., Andersson Lotta E., Koeck Thomas, Sharp Geoffrey W. G., Straub Susanne G., Wollheim Claes B., Mulder Hindrik, Time-resolved metabolomics analysis of β-cells implicates the pentose phosphate pathway in the control of insulin release, 10.1042/bj20121349
  21. Ivarsson R., Quintens R., Dejonghe S., Tsukamoto K., in 't Veld P., Renstrom E., Schuit F. C., Redox Control of Exocytosis: Regulatory Role of NADPH, Thioredoxin, and Glutaredoxin, 10.2337/diabetes.54.7.2132
  22. Reinbothe Thomas M., Ivarsson Rosita, Li Dai-Qing, Niazi Omid, Jing Xingjun, Zhang Enming, Stenson Lena, Bryborn Ulrika, Renström Erik, Glutaredoxin-1 Mediates NADPH-Dependent Stimulation of Calcium-Dependent Insulin Secretion, 10.1210/me.2008-0306
  23. Marí Montserrat, Morales Albert, Colell Anna, García-Ruiz Carmen, Kaplowitz Neil, Fernández-Checa José C., Mitochondrial glutathione: Features, regulation and role in disease, 10.1016/j.bbagen.2012.10.018
  24. Meyer Andreas J., Brach Thorsten, Marty Laurent, Kreye Susanne, Rouhier Nicolas, Jacquot Jean-Pierre, Hell Rüdiger, Redox-sensitive GFP inArabidopsis thalianais a quantitative biosensor for the redox potential of the cellular glutathione redox buffer, 10.1111/j.1365-313x.2007.03280.x
  25. Roma Leticia P., Duprez Jessica, Takahashi Hilton K., Gilon Patrick, Wiederkehr Andreas, Jonas Jean-Christophe, Dynamic measurements of mitochondrial hydrogen peroxide concentration and glutathione redox state in rat pancreatic β-cells using ratiometric fluorescent proteins: confounding effects of pH with HyPer but not roGFP1, 10.1042/bj20111770
  26. Gutscher Marcus, Pauleau Anne-Laure, Marty Laurent, Brach Thorsten, Wabnitz Guido H, Samstag Yvonne, Meyer Andreas J, Dick Tobias P, Real-time imaging of the intracellular glutathione redox potential, 10.1038/nmeth.1212
  27. Meyer Andreas J., Dick Tobias P., Fluorescent Protein-Based Redox Probes, 10.1089/ars.2009.2948
  28. Quoix N., Cheng-Xue R., Mattart L., Zeinoun Z., Guiot Y., Beauvois M. C., Henquin J.-C., Gilon P., Glucose and Pharmacological Modulators of ATP-Sensitive K+ Channels Control [Ca2+]c by Different Mechanisms in Isolated Mouse  -Cells, 10.2337/db07-1298
  29. Khaldi M. Z., Increased glucose sensitivity of both triggering and amplifying pathways of insulin secretion in rat islets cultured for 1 wk in high glucose, 10.1152/ajpendo.00426.2003
  30. Ricordi C., Lacy P. E., Finke E. H., Olack B. J., Scharp D. W., Automated Method for Isolation of Human Pancreatic Islets, 10.2337/diab.37.4.413
  31. Bucher Pascal, Mathe Zoltan, Morel Philippe, Bosco Domenico, Andres Axel, Kurfuest Manfred, Friedrich Olaf, Raemsch-Guenther Nicole, Buhler Leo H., Berney Thierry, Assessment of a Novel Two-Component Enzyme Preparation for Human Islet Isolation and Transplantation : , 10.1097/01.tp.0000147344.73915.c8
  32. Chuang Y, Cancer Res., 62, 6246 (2002)
  33. Wiederkehr Andreas, Park Kyu-Sang, Dupont Olivier, Demaurex Nicolas, Pozzan Tullio, Cline Gary W, Wollheim Claes B, Matrix alkalinization: a novel mitochondrial signal for sustained pancreatic β-cell activation, 10.1038/emboj.2008.302
  34. Tonooka N, Clin. Transplant., 21, 767 (2007)
  35. Reference deleted
  36. Ortsäter Henrik, Åkerman Karl, Bergsten Peter, Liss Per, Contribution of glycolytic and mitochondrial pathways in glucose-induced changes in islet respiration and insulin secretion, 10.1007/s00424-002-0842-9
  37. Lash Lawrence H., Role of glutathione transport processes in kidney function, 10.1016/j.taap.2004.10.004
  38. Garcia Jerome, Han Derick, Sancheti Harsh, Yap Li-Peng, Kaplowitz Neil, Cadenas Enrique, Regulation of Mitochondrial Glutathione Redox Status and Protein Glutathionylation by Respiratory Substrates, 10.1074/jbc.m110.164160
  39. Hu Jingjing, Dong Lixue, Outten Caryn E., The Redox Environment in the Mitochondrial Intermembrane Space Is Maintained Separately from the Cytosol and Matrix, 10.1074/jbc.m803028200
  40. Østergaard Henrik, Tachibana Christine, Winther Jakob R., Monitoring disulfide bond formation in the eukaryotic cytosol, 10.1083/jcb.200402120
  41. Patterson G. H., Knobel S. M., Arkhammar P., Thastrup O., Piston D. W., Separation of the glucose-stimulated cytoplasmic and mitochondrial NAD(P)H responses in pancreatic islet beta cells, 10.1073/pnas.090098797
  42. Gilon P, J. Biol. Chem., 267, 20713 (1992)
  43. Martens Geert A., Cai Ying, Hinke Simon, Stangé Geert, Van de Casteele Mark, Pipeleers Daniel, Glucose Suppresses Superoxide Generation in Metabolically Responsive Pancreatic β Cells, 10.1074/jbc.m411869200
  44. Nodin Christina, Zhu Changlian, Blomgren Klas, Nilsson Michael, Blomstrand Fredrik, Decreased oxidative stress during glycolytic inhibition enables maintenance of ATP production and astrocytic survival, 10.1016/j.neuint.2012.05.017
  45. Gray J. P., Alavian K. N., Jonas E. A., Heart E. A., NAD kinase regulates the size of the NADPH pool and insulin secretion in pancreatic  -cells, 10.1152/ajpendo.00465.2011
  46. Mailloux Ryan J., Fu Accalia, Robson-Doucette Christine, Allister Emma M., Wheeler Michael B., Screaton Robert, Harper Mary-Ellen, Glutathionylation State of Uncoupling Protein-2 and the Control of Glucose-stimulated Insulin Secretion, 10.1074/jbc.m112.393538
  47. Beer Samantha M., Taylor Ellen R., Brown Stephanie E., Dahm Christina C., Costa Nikola J., Runswick Michael J., Murphy Michael P., Glutaredoxin 2 Catalyzes the Reversible Oxidation and Glutathionylation of Mitochondrial Membrane Thiol Proteins : IMPLICATIONS FOR MITOCHONDRIAL REDOX REGULATION AND ANTIOXIDANT DEFENSE, 10.1074/jbc.m408011200
  48. Mailloux Ryan J., Xuan Jian Ying, Beauchamp Brittany, Jui Linda, Lou Marjorie, Harper Mary-Ellen, Glutaredoxin-2 Is Required to Control Proton Leak through Uncoupling Protein-3, 10.1074/jbc.m112.442905
  49. Roma L. P., Pascal S. M., Duprez J., Jonas J.-C., Mitochondrial oxidative stress contributes differently to rat pancreatic islet cell apoptosis and insulin secretory defects after prolonged culture in a low non-stimulating glucose concentration, 10.1007/s00125-012-2581-6