Differential proteomic and oxidative profiles unveil dysfunctional protein import to adipocyte mitochondria in obesity-associated aging and diabetes

被引:39
作者
Gomez-Serrano, Maria [1 ,2 ]
Camafeita, Emilio [3 ]
Lopez, Juan A. [3 ]
Rubio, Miguel A. [4 ]
Breton, Irene [5 ]
Garcia-Consuegra, Ines [6 ,7 ]
Garcia-Santos, Eva [1 ,2 ]
Lago, Jesus [8 ]
Sanchez-Pernaute, Andres [9 ]
Torres, Antonio [9 ]
Vazquez, Jesus [3 ]
Peral, Belen [1 ,2 ]
机构
[1] CSIC, Inst Invest Biomed Alberto Sols IIBM, Arturo Duperier 4, E-28029 Madrid, Spain
[2] Univ Autonoma Madrid, CSIC, Madrid, Spain
[3] Ctr Nacl Invest Cardiovasc, Lab Cardiovasc Prote, Madrid 28029, Spain
[4] Univ Complutense, Hosp Clin San Carlos IDISSC, Fac Med, Dept Endocrinol, E-28040 Madrid, Spain
[5] Hosp Gen Univ Gregorio Maranon HSGM, Dept Endocrinol & Nutr, Madrid 28007, Spain
[6] Hosp Univ 12 Octubre i 12, Inst Invest, Madrid 28041, Spain
[7] Ctr Invest Biomed Red Enfermedades Raras CIBERER, U723, Madrid 28029, Spain
[8] Hosp Gen Univ Gregorio Maranon IISGM, Dept Surg, Madrid 28007, Spain
[9] Univ Complutense, Hosp Clin San Carlos IDISSC, Fac Med, Dept Surg, E-28040 Madrid, Spain
关键词
Adipose tissue; Mitochondria; OXPHOS; Redox proteomics; Thiol oxidation; Type; 2; diabetes; ADIPOSE-TISSUE; QUANTITATIVE PROTEOMICS; TRANSCRIPTION FACTOR; INSULIN-RESISTANCE; REDOX PROTEOMICS; EXPRESSION; DNA; ENCEPHALOMYOPATHY; ELECTROPHORESIS; IDENTIFICATION;
D O I
10.1016/j.redox.2016.12.013
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Human age-related diseases, including obesity and type 2 diabetes (T2DM), have long been associated to mitochondrial dysfunction; however, the role for adipose tissue mitochondria in these conditions remains unknown. We have tackled the impact of aging and T2DM on adipocyte mitochondria from obese patients by quantitating not only the corresponding abundance changes of proteins, but also the redox alterations undergone by Cys residues thereof. For that, we have resorted to a high-throughput proteomic approach based on isobaric labeling, liquid chromatography and mass spectrometry. The alterations undergone by the mitochondrial proteome revealed aging-and T2DM-specific hallmarks. Thus, while a global decrease of oxidative phosphorylation (OXPHOS) subunits was found in aging, the diabetic patients exhibited a reduction of specific OXPHOS complexes as well as an up-regulation of the anti-oxidant response. Under both conditions, evidence is shown for the first time of a link between increased thiol protein oxidation and decreased protein abundance in adipose tissue mitochondria. This association was stronger in T2DM, where OXPHOS mitochondrial-vs. nuclear-encoded protein modules were found altered, suggesting impaired mitochondrial protein translocation and complex assembly. The marked down-regulation of OXPHOS oxidized proteins and the alteration of oxidized Cys residues related to protein import through the redox-active MIA (Mitochondrial Intermembrane space Assembly) pathway support that defects in protein translocation to the mitochondria may be an important underlying mechanism for mitochondrial dysfunction in T2DM and physiological aging. The present draft of redox targets together with the quantification of protein and oxidative changes may help to better understand the role of oxidative stress in both a physiological process like aging and a pathological condition like T2DM.
引用
收藏
页码:415 / 428
页数:14
相关论文
共 74 条
[1]   Mitochondrial complex IV deficiency, caused by mutated COX6B1, is associated with encephalomyopathy, hydrocephalus and cardiomyopathy [J].
Abdulhag, Ulla Najwa ;
Soiferman, Devorah ;
Schueler-Furman, Ora ;
Miller, Chaya ;
Shaag, Avraham ;
Elpeleg, Orly ;
Edvardson, Simon ;
Saada, Ann .
EUROPEAN JOURNAL OF HUMAN GENETICS, 2015, 23 (02) :159-164
[2]   Increased proton leak and SOD2 expression in myotubes from obese non-diabetic subjects with a family history of type 2 diabetes [J].
Aguer, Celine ;
Pasqua, Melissa ;
Thrush, A. Brianne ;
Moffat, Cynthia ;
McBurney, Michael ;
Jardine, Karen ;
Zhang, Rui ;
Beauchamp, Brittany ;
Dent, Robert ;
McPherson, Ruth ;
Harper, Mary-Ellen .
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR BASIS OF DISEASE, 2013, 1832 (10) :1624-1633
[3]   Digging deeper into obesity [J].
Ahima, Rexford S. .
JOURNAL OF CLINICAL INVESTIGATION, 2011, 121 (06) :2076-2079
[4]  
Alberts B., 2002, Molecular Biology of the Cell. (4th edition), V4th ed
[5]   Impaired mitochondrial oxidative phosphorylation and supercomplex assembly in rectus abdominis muscle of diabetic obese individuals [J].
Antoun, Ghadi ;
McMurray, Fiona ;
Thrush, A. Brianne ;
Patten, David A. ;
Peixoto, Alyssa C. ;
Slack, Ruth S. ;
McPherson, Ruth ;
Dent, Robert ;
Harper, Mary-Ellen .
DIABETOLOGIA, 2015, 58 (12) :2861-2866
[6]   Cysteine-mediated redox signalling in the mitochondria [J].
Bak, D. W. ;
Weerapana, E. .
MOLECULAR BIOSYSTEMS, 2015, 11 (03) :678-697
[7]   The Critical Role of Metabolic Pathways in Aging [J].
Barzilai, Nir ;
Huffman, Derek M. ;
Muzumdar, Radhika H. ;
Bartke, Andrzej .
DIABETES, 2012, 61 (06) :1315-1322
[8]   Mitochondrial function/dysfunction in white adipose tissue [J].
Boudina, Sihem ;
Graham, Timothy E. .
EXPERIMENTAL PHYSIOLOGY, 2014, 99 (09) :1168-1178
[9]   MitoCarta2.0: an updated inventory of mammalian mitochondrial proteins [J].
Calvo, Sarah E. ;
Clauser, Karl R. ;
Mootha, Vamsi K. .
NUCLEIC ACIDS RESEARCH, 2016, 44 (D1) :D1251-D1257
[10]   Mitochondrial transcription factor A regulates mitochondrial transcription initiation, DNA packaging, and genome copy number [J].
Campbell, Christopher T. ;
Kolesar, Jill E. ;
Kaufman, Brett A. .
BIOCHIMICA ET BIOPHYSICA ACTA-GENE REGULATORY MECHANISMS, 2012, 1819 (9-10) :921-929