N-Glycomic Changes in Serum Proteins in Type 2 Diabetes Mellitus Correlate with Complications and with Metabolic Syndrome Parameters

被引:76
作者
Testa, Roberto [1 ]
Vanhooren, Valerie [2 ,3 ]
Bonfigli, Anna Rita [4 ]
Boemi, Massimo [5 ]
Olivieri, Fabiola [6 ,7 ]
Ceriello, Antonio [8 ,9 ]
Genovese, Stefano [10 ]
Spazzafumo, Liana [11 ]
Borelli, Vincenzo [12 ]
Bacalini, Maria Giulia [12 ]
Salvioli, Stefano [12 ]
Garagnani, Paolo [12 ,13 ,14 ]
Dewaele, Sylviane [2 ,3 ]
Libert, Claude [2 ,3 ]
Franceschi, Claudio [12 ,13 ,14 ,15 ]
机构
[1] INRCA Ancona, Expt Models Clin Pathol, I-60127 Ancona, Italy
[2] VIB Inflammat Res Ctr, B-9052 Ghent, Belgium
[3] Univ Ghent, Dept Mol Biol, B-9052 Ghent, Belgium
[4] INRCA Ancona, Sci Direct, I-60124 Ancona, Italy
[5] INRCA Ancona, Metab Dis & Diabetol Unit, I-60127 Ancona, Italy
[6] Univ Politecn Marche, Dept Clin & Mol Sci, I-60020 Ancona, Italy
[7] INRCA Ancona, Ctr Clin Pathol & Innovat Therapy, I-60127 Ancona, Italy
[8] Inst Invest Biomed August Pi & Sunyer IDIBAPS, Barcelona 08036, Spain
[9] Ctr Invest Biomed Red Diabet & Enfermedades Metab, Barcelona 08017, Spain
[10] IRCCS Grp Multimed Sesto San Giovanni MI, Dept Cardiovasc & Metab Dis, I-20099 Sesto San Giovanni, Italy
[11] INRCA Ancona, Ctr Biostat, I-60124 Ancona, Italy
[12] Univ Bologna, Dept Expt Diagnost & Specialty Med Expt Pathol, I-40126 Bologna, Italy
[13] St Orsola Malpighi Univ Hosp, Ctr Appl Biomed Res, I-40138 Bologna, Italy
[14] Univ Bologna, Interdept Ctr L Galvani CIG, I-40126 Bologna, Italy
[15] Inst Neurol Sci Bologna, IRCCS, I-40124 Bologna, Italy
关键词
O-GLCNAC MODIFICATION; INSULIN-RESISTANCE; GLYCOSYLATION; GLYCAN; GLYCOPROTEIN; OLIGOSACCHARIDES; MECHANISMS; PATHWAY; BLOOD; MICE;
D O I
10.1371/journal.pone.0119983
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Background Glycosylation, i.e the enzymatic addition of oligosaccharides (or glycans) to proteins and lipids, known as glycosylation, is one of the most common co-/posttranslational modifications of proteins. Many important biological roles of glycoproteins are modulated by N-linked oligosaccharides. As glucose levels can affect the pathways leading to glycosylation of proteins, we investigated whether metabolic syndrome (MS) and type 2 diabetes mellitus (T2DM), pathological conditions characterized by altered glucose levels, are associated with specific modifications in serum N-glycome. Methods We enrolled in the study 562 patients with Type 2 Diabetes Mellitus (T2DM) (mean age 65.6 +/- 8.2 years) and 599 healthy control subjects (CTRs) (mean age, 58.5 +/- 12.4 years). N-glycome was evaluated in serum glycoproteins. Results We found significant changes in N-glycan composition in the sera of T2DM patients. In particular, alpha(1,6)-linked arm monogalactosylated, core-fucosylated diantennary N-glycans (NG1(6)A2F) were significantly reduced in T2DM compared with CTR subjects. Importantly, they were equally reduced in diabetic patients with and without complications (P<0.001) compared with CTRs. Macro vascular-complications were found to be related with decreased levels of NG1(6) A2F. In addition, NG1(6) A2F and NG1(3) A2F, identifying, respectively, monogalactosylated N-glycans with alpha(1,6)- and alpha(1,3)-antennary galactosylation, resulted strongly correlated with most MS parameters. The plasmatic levels of these two glycans were lower in T2DM as compared to healthy controls, and even lower in patients with complications and MS, that is the extreme "unhealthy" phenotype (T2DM+ with MS). Conclusions Imbalance of glycosyltransferases, glycosidases and sugar nucleotide donor levels is able to cause the structural changes evidenced by our findings. Serum N-glycan profiles are thus sensitive to the presence of diabetes and MS. Serum N-glycan levels could therefore provide a non-invasive alternative marker for T2DM and MS.
引用
收藏
页数:16
相关论文
共 46 条
[11]  
Durand G, 2000, CLIN CHEM, V46, P795
[12]   The metabolic syndrome [J].
Eckel, RH ;
Grundy, SM ;
Zimmet, PZ .
LANCET, 2005, 365 (9468) :1415-1428
[13]   Comparison of the Fc glycosylation of fetal and maternal immunoglobulin G [J].
Einarsdottir, Helga K. ;
Selman, Maurice H. J. ;
Kapur, Rick ;
Scherjon, Sicco ;
Koeleman, Carolien A. M. ;
Deelder, Andre M. ;
van der Schoot, C. Ellen ;
Vidarsson, Gestur ;
Wuhrer, Manfred .
GLYCOCONJUGATE JOURNAL, 2013, 30 (02) :147-157
[14]   Diabetic Retinopathy and Atherosclerosis: is there a Link? [J].
Ellis, Thomas Phillip ;
Choudhury, Ruhul Hassan ;
Kaul, Kirti ;
Chopra, Mohit ;
Kohner, Eva Maria ;
Tarr, Joanna Mary ;
Chibber, Rakesh .
CURRENT DIABETES REVIEWS, 2013, 9 (02) :146-160
[15]   Stability of N-glycan profiles in human plasma [J].
Gornik, Olga ;
Wagner, Jasenka ;
Pucic, Maja ;
Knezevic, Ana ;
Redzic, Irma ;
Lauc, Gordan .
GLYCOBIOLOGY, 2009, 19 (12) :1547-1553
[16]   O-glycosylation of nuclear and cytoplasmic proteins: Regulation analogous to phosphorylation? [J].
Haltiwanger, RS ;
Busby, S ;
Grove, K ;
Li, S ;
Mason, D ;
Medina, L ;
Moloney, D ;
Philipsberg, G ;
Scartozzi, R .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1997, 231 (02) :237-242
[17]   Altered glycosylation of α1-acid glycoprotein in patients with inflammation and diabetes mellitus [J].
Higai, K ;
Azuma, Y ;
Aoki, Y ;
Matsumoto, K .
CLINICA CHIMICA ACTA, 2003, 329 (1-2) :117-125
[18]   Prevalence of the metabolic syndrome and its relation to all-cause and cardiovascular mortality in nondiabetic European men and women [J].
Hu, G ;
Qiao, Q ;
Tuomilehto, J ;
Balkau, B ;
Borch-Johnsen, K ;
Pyorala, K .
ARCHIVES OF INTERNAL MEDICINE, 2004, 164 (10) :1066-1076
[19]   O-GlcNAc modification, insulin signaling and diabetic complications [J].
Issad, T. ;
Masson, E. ;
Pagesy, P. .
DIABETES & METABOLISM, 2010, 36 (06) :423-435
[20]   Analysis of N-glycan in serum glycoproteins from db/db mice and humans with type 2 diabetes [J].
Itoh, Naofumi ;
Sakaue, Shinji ;
Nakagawa, Hiroaki ;
Kurogochi, Masaki ;
Ohira, Hiroshi ;
Deguchi, Kisaburo ;
Nishimura, Shin-Ichiro ;
Nishimura, Masaharu .
AMERICAN JOURNAL OF PHYSIOLOGY-ENDOCRINOLOGY AND METABOLISM, 2007, 293 (04) :E1069-E1077