Cited by 657Mitochondrial Function and PathologyAutophagy in Disease and TherapyAdipose Tissue and Metabolism

Mitochondrial dynamics in type 2 diabetes: Pathophysiological implications

Open access
Rovira-Llopis, Susana, Bañuls, Celia, Diaz-Morales, Noelia, Hernandez-Mijares, Antonio, Rocha, Milagros, Victor, Victor M.·2017·Redox Biology

Abstract

Mitochondria play a key role in maintaining cellular metabolic homeostasis. These organelles have a high plasticity and are involved in dynamic processes such as mitochondrial fusion and fission, mitophagy and mitochondrial biogenesis. Type 2 diabetes is characterised by mitochondrial dysfunction, high production of reactive oxygen species (ROS) and low levels of ATP. Mitochondrial fusion is modulated by different proteins, including mitofusin-1 (MFN1), mitofusin-2 (MFN2) and optic atrophy (OPA-1), while fission is controlled by mitochondrial fission 1 (FIS1), dynamin-related protein 1 (DRP1) and mitochondrial fission factor (MFF). PARKIN and (PTEN)-induced putative kinase 1 (PINK1) participate in the process of mitophagy, for which mitochondrial fission is necessary. In this review, we discuss the molecular pathways of mitochondrial dynamics, their impairment under type 2 diabetes, and pharmaceutical approaches for targeting mitochondrial dynamics, such as mitochondrial division inhibitor-1 (mdivi-1), dynasore, P110 and 15-oxospiramilactone. Furthermore, we discuss the pathophysiological implications of impaired mitochondrial dynamics, especially in type 2 diabetes.

The claims and statistics of this paper haven’t been checked yet.

Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.

A few free checks a day · papers already verified open instantly · results are public

Integrity signals

Registry

Crossref · 10.1016/j.redox.2017.01.013

Cites

18 of 18 references verified0 citation errors · 0 not checkable

Statistics

Claims the paper makes

The claims and statistics of this paper haven’t been checked yet.

Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.

A few free checks a day · papers already verified open instantly · results are public

Claims other papers make about this one

Each is checked against this paper’s own text: does it say what the citing paper says it does?

  • Mitochondrial dysfunction, characterized by reduced mitochondrial size and activity, is prevalent in individuals with obesity and T2DM.

    “Mitochondrial dysfunction, characterized by reduced mitochondrial size and activity, is prevalent in individuals with obesity and T2DM and is a known contributor to muscle wasting in ageing and some chronic diseases.”

    From The Effects of Glucagon-Like Peptide-1 Receptor Agonists on Mitochondrial Function Within Skeletal Muscle: A Systematic Review (2025) · cites this paper as [31]

    The ‘Type 2 diabetes and mitochondrial dynamics’ section reports smaller mitochondria in people with T2DM and impaired mitochondrial function in insulin-resistant patients. It also reports reduced expression of mitochondrial oxidative pathways in obese patients, but does not establish reduced mitochondrial size in obesity. No page number is available in our copy. (LLM, conf=0.84)

    Experimental — accuracy not yet measured

Self-check

Percentages, sums and reported differences re-computed from the paper’s own numbers.

The self-check needs the paper’s full text.

Cites

Flagged first, then by citations

Research works printed but not linked: 74

  1. [2]Petersen K.F. Befroy D. Dufour S. Dziura J. Ariyan C. Rothman D.L. DiPietro L. Cline G.W. Shulman G.I. Mitochondrial dysfunction in the elderly: possible role in insulin resistance Science 300 5622 2003 1140 1142 12750520 PMC3004429
  2. [3]Brownlee M. Biochemistry and molecular cell biology of diabetic complications Nature 414 6865 2001 813 820 11742414
  3. [5]van der Bliek A.M. Shen Q. Kawajiri S. Mechanisms of mitochondrial fission and fusion Cold Spring Harb. Perspect. Biol. 5 6 2013 PMC3660830 23732471
  4. [7]Lemasters J.J. Variants of mitochondrial autophagy: Types 1 and 2 mitophagy and micromitophagy (Type 3) Redox Biol. 2 2014 749 754 eCollection 2014 25009776 PMC4085350
  5. [10]Sharma K. Mitochondrial hormesis and diabetic complications Diabetes 64 3 2015 663 672 25713188 PMC4338592
  6. [11]Ni H.M. Williams J.A. Ding W.X. Mitochondrial dynamics and mitochondrial quality control Redox Biol. 4 2015 6 13 25479550 PMC4309858
  7. [14]Galloway C.A. Yoon Y. Mitochondrial morphology in metabolic diseases Antioxid. Redox Signal. 19 4 2013 415 430 22793999 PMC3700066
  8. [15]Detmer S.A. Chan D.C. Complementation between mouse Mfn1 and Mfn2 protects mitochondrial fusion defects caused by CMT2A disease mutations J. Cell Biol. 176 4 2007 405 414 17296794 PMC2063976
  9. [16]de Brito O.M. Scorrano L. Mitofusin 2 tethers endoplasmic reticulum to mitochondria Nature 456 7222 2008 605 610 19052620
  10. [17]Otera H. Mihara K. Molecular mechanisms and physiologic functions of mitochondrial dynamics J. Biochem. 149 3 2011 241 251 21233142
  11. [18]Yoon Y. Galloway C.A. Jhun B.S. Yu T. Mitochondrial dynamics in diabetes Antioxid. Redox Signal. 14 3 2011 439 457 20518704 PMC3025181
  12. [19]Loson O.C. Song Z. Chen H. Chan D.C. Fis1, Mff, MiD49, and MiD51 mediate Drp1 recruitment in mitochondrial fission Mol. Biol. Cell 24 5 2013 659 667 23283981 PMC3583668
  13. [20]Liesa M. Shirihai O.S. Mitochondrial dynamics in the regulation of nutrient utilization and energy expenditure Cell Metab. 17 4 2013 491 506 23562075 PMC5967396
  14. [21]Wai T. Langer T. Mitochondrial Dynamics and Metabolic Regulation Trends Endocrino. Metab. 27 2 2016 105 117 26754340
  15. [23]Sebastián D. Hernández-Alvarez M.I. Segalés J. Sorianello E. Muñoz J.P. Sala D. Waget A. Liesa M. Paz J.C. Gopalacharyulu P. Orešič M. Pich S. Burcelin R. Palacín M. Zorzano A. Mitofusin 2 (Mfn2) links mitochondrial and endoplasmic reticulum function with insulin signaling and is essential for normal glucose homeostasis Proc Natl. Acad. Sci. USA 109 14 2012 5523 5528 22427360 PMC3325712
  16. [24]Kulkarni S.S. Joffraud M. Boutant M. Ratajczak J. Gao A.W. Maclachlan C. Hernandez-Alvarez M.I. Raymond F. Metairon S. Descombes P. Houtkooper R.H. Zorzano A. Cantó C6. Mfn1 Deficiency in the liver protects against diet-induced insulin resistance and enhances the hypoglycemic effect of metformin Diabetes 2016 27613809
  17. [25]Wang L. Ishihara T. Ibayashi Y. Tatsushima K. Setoyama D. Hanada Y. Takeichi Y. Sakamoto S. Yokota S. Mihara K. Kang D. Ishihara N. Takayanagi R. Nomura M. Disruption of mitochondrial fission in the liver protects mice from diet-induced obesity and metabolic deterioration Diabetologia 58 10 2015 2371 2380 26233250
  18. [26]Mizushima N. Komatsu M. Autophagy: renovation of cells and tissues Cell 147 4 2011 728 741 22078875
  19. [27]Dorn G.W. 2nd Kitsis R.N. The mitochondrial dynamism-mitophagy-cell death interactome: multiple roles performed by members of a mitochondrial molecular ensemble Circ. Res. 116 1 2015 167 182 25323859 PMC4282600
  20. [28]Stotland A. Gottlieb R.A. Mitochondrial quality control: Easy come, easy go Biochim. Biophys. Acta 1853 10 Pt B 2015 2802 2811 25596427 PMC4501896
  21. [30]Shirihai O.S. Song M. Dorn G.W. 2nd How mitochondrial dynamism orchestrates mitophagy Circ. Res. 116 11 2015 1835 1849 25999423 PMC4443843
  22. [31]Lee J.Y. Nagano Y. Taylor J.P. Lim K.L. Yao T.P. Disease-causing mutations in parkin impair mitochondrial ubiquitination, aggregation, and HDAC6-dependent mitophagy J. Cell. Biol. 189 4 2010 671 679 20457763 PMC2872903
  23. [32]Liesa M. Palacín M. Zorzano A. Mitochondrial dynamics in mammalian health and disease Physiol. Rev. 89 3 2009 799 845 19584314
  24. [33]Kytövuori L. Lipponen J. Rusanen H. Komulainen T. Martikainen M.H. Majamaa K. A novel mutation m.8561C>G in MT-ATP6/8 causing a mitochondrial syndrome with ataxia, peripheral neuropathy, diabetes mellitus, and hypergonadotropic hypogonadism J. Neurol. 263 11 2016 2188 2195 27502083
  25. [34]Hoeks J. Hesselink M.K. Russell A.P. Mensink M. Saris W.H. Mensink R.P. Schrauwen P. Peroxisome proliferator-activated receptor-gamma coactivator-1 and insulin resistance: acute effect of fatty acids Diabetologia 49 10 2006 2419 2426 16896940
  26. [35]Maechler P. Wollheim C.B. Mitochondrial function in normal and diabetic beta-cells Nature 414 6865 2001 807 812 11742413
  27. [36]Diaz-Morales N. Rovira-Llopis S. Bañuls C. Escribano-Lopez I. de Marañon A.M. Lopez-Domenech S. Orden S. Roldan-Torres I. Alvarez A. Veses S. Jover A. Rocha M. Hernandez-Mijares A. Victor V.M. Are Mitochondrial Fusion and Fission Impaired in Leukocytes of Type 2 Diabetic Patients? Antioxid. Redox Signal. 25 2 2016 108 115 27043041
  28. [37]Hernandez-Mijares A. Rocha M. Apostolova N. Borras C. Jover A. Bañuls C. Sola E. Victor V.M. Mitochondrial complex I impairment in leukocytes from type 2 diabetic patients Free Radic. Biol. Med. 50 10 2011 1215 1221 21262346
  29. [39]Rovira-Llopis S. Díaz-Morales N. Bañuls C. Blas-García A. Polo M. López-Domenech S. Jover A. Rocha M. Hernández-Mijares A. Víctor V.M. Is Autophagy Altered in the Leukocytes of Type 2 Diabetic Patients? Antioxid. Redox Signal. 23 13 2015 1050 1056 26218267
  30. [40]Kelley D.E. He J. Menshikova E.V. Ritov V.B. Dysfunction of mitochondria in human skeletal muscle in type 2 diabetes Diabetes 51 10 2002 2944 2950 12351431
  31. [41]Mootha V.K. Lindgren C.M. Eriksson K.F. Subramanian A. Sihag S. Lehar J. Puigserver P. Carlsson E. Ridderstråle M. Laurila E. Houstis N. Daly M.J. Patterson N. Mesirov J.P. Golub T.R. Tamayo P. Spiegelman B. Lander E.S. Hirschhorn J.N. Altshuler D. Groop L.C. PGC-1alpha-responsive genes involved in oxidative phosphorylation are coordinately downregulated in human diabetes Nat. Genet. 34 3 2003 267 273 12808457
  32. [43]Apostolova N. Victor V.M. Molecular strategies for targeting antioxidants to mitochondria: therapeutic implications Antioxid. Redox Signal. 22 8 2015 686 729 25546574 PMC4350006
  33. [44]Escribano-Lopez I. Diaz-Morales N. Rovira-Llopis S. de Marañon A.M. Orden S. Alvarez A. Bañuls C. Rocha M. Murphy M.P. Hernandez-Mijares A. Victor V.M. The mitochondria-targeted antioxidant MitoQ modulates oxidative stress, inflammation and leukocyte-endothelium interactions in leukocytes isolated from type 2 diabetic patients Redox Biol. 10 2016 200 205 27810734 PMC5094376
  34. [45]Larson-Meyer D.E. Heilbronn L.K. Redman L.M. Newcomer B.R. Frisard M.I. Anton S. Smith S.R. Alfonso A. Ravussin E. Effect of calorie restriction with or without exercise on insulin sensitivity, beta-cell function, fat cell size, and ectopic lipid in overweight subjects Diabetes Care 29 6 2006 1337 1344 16732018 PMC2677812
  35. [46]Rimbert V. Boirie Y. Bedu M. Hocquette J.F. Ritz P. Morio B. Muscle fat oxidative capacity is not impaired by age but by physical inactivity: association with insulin sensitivity FASEB J. 18 6 2004 737 739 14977873
  36. [47]Toledo F.G. Menshikova E.V. Ritov V.B. Azuma K. Radikova Z. DeLany J. Kelley D.E. Effects of physical activity and weight loss on skeletal muscle mitochondria and relationship with glucose control in type 2 diabetes Diabetes 56 8 2007 2142 2147 17536063
  37. [49]Hou Y. Li S. Wu M. Wei J. Ren Y. Du C. Wu H. Han C. Duan H. Shi Y. Mitochondria-targeted peptide SS-31 attenuates renal injury via an antioxidant effect in diabetic nephropathy Am. J. Physiol. Renal Physiol. 310 6 2016 F547 F559 26719366
  38. [50]Byrne H. Caulfield B. De Vito G. Effects of Self-directed Exercise Programmes on Individuals with Type 2 Diabetes Mellitus: A Systematic Review Evaluating Their Effect on HbA1c and Other Metabolic Outcomes, Physical Characteristics, Cardiorespiratory Fitness and Functional Outcomes Sports Med. 2016 27459860
  39. [51]Sathananthan M. Shah M. Edens K.L. Grothe K.B. Piccinini F. Farrugia L.P. Micheletto F. Man C.D. Cobelli C. Rizza R.A. Camilleri M. Vella A. Six and 12 Weeks of Caloric Restriction Increases β Cell Function and Lowers Fasting and Postprandial Glucose Concentrations in People with Type 2 Diabetes J. Nutr. 145 9 2015 2046 2051 26246321 PMC4548160
  40. [52]Lo M.C. Chen M.H. Lee W.S. Lu C.I. Chang C.R. Kao S.H. Lee H.M. Nε-(carboxymethyl) lysine-induced mitochondrial fission and mitophagy cause decreased insulin secretion from β-cells Am. J. Physiol. Endocrinol. Metab. 309 10 2015 E829 E839 26394662
  41. [53]Reinhardt F. Schultz J. Waterstradt R. Baltrusch S. Drp1 guarding of the mitochondrial network is important for glucose-stimulated insulin secretion in pancreatic beta cells Biochem. Biophys. Res. Commun. 474 4 2016 10 646 651 27154223
  42. [54]Cerqueira F.M. Chausse B. Baranovski B.M. Liesa M. Lewis E.C. Shirihai O.S. Kowaltowski A.J. Diluted serum from calorie-restricted animals promotes mitochondrial β-cell adaptations and protect against glucolipotoxicity FEBS J. 283 5 2016 822 833 26732506
  43. [55]Molina A.J. Wikstrom J.D. Stiles L. Las G. Mohamed H. Elorza A. Walzer G. Twig G. Katz S. Corkey B.E. Shirihai O.S. Mitochondrial networking protects beta-cells from nutrient-induced apoptosis Diabetes 58 10 2009 2303 2315 19581419 PMC2750232
  44. [56]Cang X. Wang X. Liu P. Wu X. Yan J. Chen J. Wu G. Jin Y. Xu F. Su J. Wan C. Wang X. PINK1 alleviates palmitate induced insulin resistance in HepG2 cells by suppressing ROS mediated MAPK pathways Biochem. Biophys. Res. Commun. 478 1 2016 431 438 27423393
  45. [57]Zorzano A. Liesa M. Palacín M. Mitochondrial dynamics as a bridge between mitochondrial dysfunction and insulin resistance Arch. Physiol. Biochem. 115 1 2009 1 12 19267277
  46. [59]Veeranki S. Givvimani S. Kundu S. Metreveli N. Pushpakumar S. Tyagi S.C. Moderate intensity exercise prevents diabetic cardiomyopathy associated contractile dysfunction through restoration of mitochondrial function and connexin 43 levels in db/db mice J. Mol. Cell. Cardiol. 92 2016 163 173 26827898 PMC4789087
  47. [60]Arruda A.P. Pers B.M. Parlakgül G. Güney E. Inouye K. Hotamisligil G.S. Chronic enrichment of hepatic endoplasmic reticulum-mitochondria contact leads to mitochondrial dysfunction in obesity Nat. Med. 20 12 2014 1427 1435 25419710 PMC4412031
  48. [61]Rovira-Llopis S. Bañuls C. Apostolova N. Morillas C. Hernandez-Mijares A. Rocha M. Victor V.M. Is glycemic control modulating endoplasmic reticulum stress in leukocytes of type 2 diabetic patients? Antioxid. Redox Signal. 21 12 2014 1759 1765 25000244
  49. [62]Paltauf-Doburzynska J. Malli R. Graier W.F. Hyperglycemic conditions affect shape and Ca2+ homeostasis of mitochondria in endothelial cells J. Cardiovasc. Pharmacol. 44 4 2004 423 436 15454850
  50. [63]Yu T. Robotham J.L. Yoon Y. Increased production of reactive oxygen species in hyperglycemic conditions requires dynamic change of mitochondrial morphology Proc. Natl. Acad. Sci. USA 103 8 2006 2653 2658 16477035 PMC1413838
  51. [64]Vanhorebeek I. De Vos R. Mesotten D. Wouters P.J. De Wolf-Peeters C. Van den Berghe G. Protection of hepatocyte mitochondrial ultrastructure and function by strict blood glucose control with insulin in critically ill patients Lancet 365 9453 2005 53 59 15639679
  52. [66]Montaigne D. Marechal X. Coisne A. Debry N. Modine T. Fayad G. Potelle C. El Arid J.M. Mouton S. Sebti Y. Duez H. Preau S. Remy-Jouet I. Zerimech F. Koussa M. Richard V. Neviere R. Edme J.L. Lefebvre P. Staels B. Myocardial contractile dysfunction is associated with impaired mitochondrial function and dynamics in type 2 diabetic but not in obese patients Circulation 130 7 2014 554 564 24928681
  53. [67]Schultz J. Waterstradt R. Kantowski T. Rickmann A. Reinhardt F. Sharoyko V. Mulder H. Tiedge M. Baltrusch S. Precise expression of Fis1 is important for glucose responsiveness of beta cells J. Endocrinol. 230 1 2016 81 91 27179109
  54. [68]Jheng H.F. Huang S.H. Kuo H.M. Hughes M.W. Tsai Y.S. Molecular insight and pharmacological approaches targeting mitochondrial dynamics in skeletal muscle during obesity Ann. N. Y. Acad. Sci. 1350 2015 82 94 26301786
  55. [70]Ong S.B. Subrayan S. Lim S.Y. Yellon D.M. Davidson S.M. Hausenloy D.J. Inhibiting mitochondrial fission protects the heart against ischemia/reperfusion injury Circulation 121 18 2010 2012 2022 20421521
  56. [71]Jheng H.F. Tsai P.J. Guo S.M. Kuo L.H. Chang C.S. Su I.J. Chang C.R. Tsai Y.S. Mitochondrial fission contributes to mitochondrial dysfunction and insulin resistance in skeletal muscle Mol. Cell Biol. 32 2 2012 309 319 22083962 PMC3255771
  57. [73]Kim B. Kim J.S. Yoon Y. Santiago M.C. Brown M.D. Park J.Y. Inhibition of Drp1-dependent mitochondrial division impairs myogenic differentiation Am. J. Physiol. Regul. Integr. Comp. Physiol. 305 8 2013 R927 R938 23904108
  58. [74]Salabei J.K. Hill B.G. Mitochondrial fission induced by platelet-derived growth factor regulates vascular smooth muscle cell bioenergetics and cell proliferation Redox Biol. 1 2013 542 551 24273737 PMC3836280
  59. [75]Wang J. Hansen K. Edwards R. Van Houten B. Qian W. Mitochondrial division inhibitor 1 (mdivi-1) enhances death receptor-mediated apoptosis in human ovarian cancer cells Biochem. Biophys. Res. Commun. 456 1 2015 7 12 25446129 PMC4297922
  60. [76]Macia E. Ehrlich M. Massol R. Boucrot E. Brunner C. Kirchhausen T. Dynasore, a cell-permeable inhibitor of dynamin Dev. Cell. 10 6 2006 839 850 16740485
  61. [77]Gao D. Zhang L. Dhillon R. Hong T.T. Shaw R.M. Zhu J. Dynasore protects mitochondria and improves cardiac lusitropy in Langendorff perfused mouse heart PLoS One 8 4 2013 e60967 23596510 PMC3626591
  62. [78]Qi X. Qvit N. Su Y.C. Mochly-Rosen D. A novel Drp1 inhibitor diminishes aberrant mitochondrial fission and neurotoxicity J. Cell Sci. 126 Pt 3 2013 789 802 23239023 PMC3619809
  63. [79]Guo X. Sesaki H. Qi X. Drp1 stabilizes p53 on the mitochondria to trigger necrosis under oxidative stress conditions in vitro and in vivo Biochem. J. 461 1 2014 137 146 24758576 PMC4381936
  64. [80]Su Y.C. Qi X. Inhibition of excessive mitochondrial fission reduced aberrant autophagy and neuronal damage caused by LRRK2 G2019S mutation Hum. Mol. Genet. 22 22 2013 4545 4561 23813973
  65. [81]Filichia E. Hoffer B. Qi X. Luo Y. Inhibition of Drp1 mitochondrial translocation provides neural protection in dopaminergic system in a Parkinson's disease model induced by MPTP Sci. Rep. 6 2016 32656 27619562 PMC5020318
  66. [82]Zhan L. Cao H. Wang G. Lyu Y. Sun X. An J. Wu Z. Huang Q. Liu B. Xing J. Drp1-mediated mitochondrial fission promotes cell proliferation through crosstalk of p53 and NF-κB pathways in hepatocellular carcinoma Oncotarget 2016 PMC5323133 27542250
  67. [83]Liu J. Mu C. Yue W. Li J. Ma B. Zhao L. Liu L. Chen Q. Yan C. Liu H. Hao X. Zhu Y. A diterpenoid derivate compound targets selenocysteine of thioredoxin reductases and induces Bax/Bak-independent apoptosis Free Radic. Biol. Med. 63 2013 485 494 23732520
  68. [84]Yue W. Chen Z. Liu H. Yan C. Chen M. Feng D. Yan C. Wu H. Du L. Wang Y. Liu J. Huang X. Xia L. Liu L. Wang X. Jin H. Wang J. Song Z. Hao X. Chen Q. A small natural molecule promotes mitochondrial fusion through inhibition of the deubiquitinase USP30 Cell Res. 24 4 2014 482 496 24513856 PMC3975501
  69. [85]Jimenez R.E. Kubli D.A. Gustafsson Å.B. Autophagy and mitophagy in the myocardium: therapeutic potential and concerns Br. J. Pharmacol. 171 8 2014 1907 1916 24148024 PMC3976612
  70. [86]Higgins G.C. Coughlan M.T. Mitochondrial dysfunction and mitophagy: the beginning and end to diabetic nephropathy? Br. J. Pharmacol. 171 8 2014 1917 1942 24720258 PMC3976613
  71. [87]Zhang T. Xue L. Li L. Tang C. Wan Z. Wang R. Tan J. Tan Y. Han H. Tian R. Billiar T.R. Tao W.A. Zhang Z. BNIP Suppresses PINK1 Proteolytic Cleavage to Promote Mitophagy J. Biol. Chem. 2016 PMC5076832 27528605
  72. [89]Mori H. Inoki K. Masutani K. Wakabayashi Y. Komai K. Nakagawa R. Guan K.L. Yoshimura A. The mTOR pathway is highly activated in diabetic nephropathy and rapamycin has a strong therapeutic potential Biochem. Biophys. Res. Commun. 384 4 2009 471 475 19422788
  73. [90]Sakaguchi M. Isono M. Isshiki K. Sugimoto T. Koya D. Kashiwagi A. Inhibition of mTOR signaling with rapamycin attenuates renal hypertrophy in the early diabetic mice Biochem. Biophys. Res. Commun. 340 1 2006 296 301 16364254
  74. [91]Yang Y. Wang J. Qin L. Shou Z. Zhao J. Wang H. Chen Y. Chen J. Rapamycin prevents early steps of the development of diabetic nephropathy in rats Am. J. Nephrol. 27 5 2007 495 502 17671379

Cited by

Sorted by citations

Authors
Rovira-Llopis, S., Bañuls, C., Diaz-Morales, N., Hernandez-Mijares, A., Rocha, M., & Victor, V. M.
Affiliations
  • Fundación para el Fomento de la Investigación Sanitaria y Biomédica de la Comunitat Valenciana (ES)
  • Universitat de València (ES)
Venue
Redox Biology
Publisher
Elsevier BV
Published
2017-04
Volume
11
Pages
637-645
ISSN
2213-2317 (ISSN-L)
OpenAlex
W2572344066
Cited by
657
References
18
Citations by year
2026: 60 · 2025: 95 · 2024: 102 · 2023: 91 · 2022: 92 · 2021: 82 · 2020: 54 · 2019: 35 · 2018: 33 · 2017: 13
FWCI
3.46
Type
journal article
Language
en
Open access
Locations
  • Redox Biology (publishedVersion, cc-by-nc-nd)
  • PubMed Central (publishedVersion, cc-by-nc-nd)
  • PubMed (publishedVersion)
  • DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion, cc-by-sa)
Funders
  • European Regional Development Fund (UGP15-193, UGP15-220)
  • Fundación para el Fomento de la Investigación Sanitaria y Biomédica de la Comunitat Valenciana (GV/2016/169)
  • Instituto de Salud Carlos III
  • Ministerio de Economía y Competitividad (FJCI-2015–25040)
Topics
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Mitochondrial Function and Pathology
  • Health Sciences › Medicine › Epidemiology › Autophagy in Disease and Therapy
  • Health Sciences › Medicine › Physiology › Adipose Tissue and Metabolism
Keywords
mitochondrial dynamics, type 2 diabetes, mitochondrial fusion, mitochondrial fission, mitophagy, mitochondrial biogenesis, reactive oxygen species, mitochondrial dysfunction, mitofusin 1, mitofusin 2, OPA1, Drp1, PINK1, Parkin, Mdivi-1, dynasore, p110, metabolic homeostasis
MeSH terms
Adenosine Triphosphate, Diabetes Mellitus, Type 2, Humans, Mitochondria, Reactive Oxygen Species, Mitochondrial Proteins, Mitochondrial Dynamics, Mitophagy

About these checks

Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.

Statistics and arithmetic are recomputed, not judged.

Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.

What counts as a claim ›How we measure confidence ›How we check this ›

Are you an author, or do you see a problem with this page? Request a review