Glycoblotting method allows for rapid and efficient glycome profiling of human Alzheimer's disease brain, serum and cerebrospinal fluid towards potential biomarker discovery

被引:65
作者
Gizaw, Solomon T. [1 ,2 ]
Ohashi, Tetsu [3 ]
Tanaka, Masakazu [3 ]
Hinou, Hiroshi [1 ,2 ,3 ]
Nishimura, Shin-Ichiro [1 ,2 ,3 ]
机构
[1] Hokkaido Univ, Field Drug Discovery Res, Fac Adv Life Sci, N21 W11, Sapporo, Hokkaido 0010021, Japan
[2] Hokkaido Univ, Grad Sch Life Sci, N21 W11, Sapporo, Hokkaido 0010021, Japan
[3] Med Chem Pharmaceut Co Ltd, N21 W12, Sapporo, Hokkaido 0010021, Japan
来源
BIOCHIMICA ET BIOPHYSICA ACTA-GENERAL SUBJECTS | 2016年 / 1860卷 / 08期
基金
日本科学技术振兴机构;
关键词
Alzheimer's disease; Glycome; Human brain; Serum; Cerebrospinal fluid; Biomarker; AMYLOID PRECURSOR PROTEIN; N-GLYCAN; NEURODEGENERATIVE DISEASE; PRION PROTEIN; BETA-PEPTIDE; GLYCOSYLATION; TRANSFERRIN; DIFFERENTIATION; IDENTIFICATION; GLYCOPROTEIN;
D O I
10.1016/j.bbagen.2016.03.009
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
Background: Understanding of the significance of posttranslational glycosylation in Alzheimer's disease (AD) is of growing importance for the investigation of the pathogenesis of AD as well as discovery research of the disease specific serum biomarkers. Methods: We designed a standard protocol for the glycoblotting combined with MALDI-TOFMS to perform rapid and quantitative profiling of the glycan parts of glycoproteins (N-glycans) and glycosphingolipids (GSLs) using human AD's post-mortem samples such as brain tissues (dissected cerebral cortices such as frontal, parietal, occipital, and temporal domains), serum and cerebrospinal fluid (CSF). Results: The structural profiles of the major N-glycans released from glycoproteins and the total expression levels of the glycans were found to be mostly similar between the brain tissues of the AD patients and those of the normal control group. In contrast, the expression levels of the serum and CSF protein N-glycans such as bisect-type and multiply branched glycoforms were increased significantly in AD patient group. In addition, the levels of some gangliosides such as GM1, GM2 and GM3 appeared to alter in the AD patient brain and serum samples when compared with the normal control groups. Conclusion: Alteration of the expression levels of major N- and GSL-glycans in human brain tissues, serum and CSF of AD patients can be monitored quantitatively by means of the glycoblotting-based standard protocols. General significance: The changes in the expression levels of the glycans derived from the human post-mortem samples uncovered by the standardized glycoblotting method provides potential serum biomarkers in central nervous system disorders and can contribute to the insight into the molecular mechanisms in the pathogenesis of neurodegenerative diseases and future drug discovery. Most importantly, the present preliminary trials using human post-mortem samples of AD patients suggest that large-scale serum glycomics cohort by means of various-types of human AD patients as well as the normal control sera can facilitate the discovery research of highly sensitive and reliable serum biomarkers for an early diagnosis of AD.. This article is part of a Special Issue entitled "Glycans in personalised medicine" Guest Editor: Professor Gordan Lauc. (C) 2016 Elsevier B.V. All rights reserved.
引用
收藏
页码:1716 / 1727
页数:12
相关论文
共 51 条
  • [1] Increased bisecting and core-fucosylated N-glycans on mutant human amyloid precursor proteins
    Akasaka-Manya, Keiko
    Manya, Hiroshi
    Sakurai, Yoko
    Wojczyk, Boguslaw S.
    Spitalnik, Steven L.
    Endo, Tamao
    [J]. GLYCOCONJUGATE JOURNAL, 2008, 25 (08) : 775 - 786
  • [2] Threshold in Stage-specific Embryonic Glycotypes Uncovered by a Full Portrait of Dynamic N-Glycan Expression during Cell Differentiation
    Amano, Maho
    Yamaguchi, Misa
    Takegawa, Yasuhiro
    Yamashita, Tadashi
    Terashima, Michiyo
    Furukawa, Jun-ichi
    Miura, Yoshiaki
    Shinohara, Yasuro
    Iwasaki, Norimasa
    Minami, Akio
    Nishimura, Shin-ichiro
    [J]. MOLECULAR & CELLULAR PROTEOMICS, 2010, 9 (03) : 523 - 537
  • [3] LOSS OF NEURONS IN THE NUCLEUS BASALIS OF MEYNERT IN ALZHEIMERS-DISEASE, PARALYSIS AGITANS AND KORSAKOFFS DISEASE
    ARENDT, T
    BIGL, V
    ARENDT, A
    TENNSTEDT, A
    [J]. ACTA NEUROPATHOLOGICA, 1983, 61 (02) : 101 - 108
  • [4] Ariga T, 2011, INT J ALZHEIMERS DIS
  • [5] Role of ganglioside metabolism in the pathogenesis of Alzheimer's disease - a review
    Ariga, Toshio
    McDonald, Michael P.
    Yu, Robert K.
    [J]. JOURNAL OF LIPID RESEARCH, 2008, 49 (06) : 1157 - 1175
  • [6] CARBOHYDRATE-SPECIFIC RECEPTORS OF THE LIVER
    ASHWELL, G
    HARFORD, J
    [J]. ANNUAL REVIEW OF BIOCHEMISTRY, 1982, 51 : 531 - 554
  • [7] Glycomics of pediatric and adulthood diseases of the central nervous system
    Barone, Rita
    Sturiale, Luisa
    Palmigiano, Angelo
    Zappia, Mario
    Garozzo, Domenico
    [J]. JOURNAL OF PROTEOMICS, 2012, 75 (17) : 5123 - 5139
  • [8] N-glycans in liver-secreted and immunoglogulin-derived protein fractions
    Bekesova, S.
    Kosti, O.
    Chandler, K. B.
    Wu, J.
    Madej, H. L.
    Brown, K. C.
    Simonyan, V.
    Goldman, R.
    [J]. JOURNAL OF PROTEOMICS, 2012, 75 (07) : 2216 - 2224
  • [9] Human IgG Fc-glycosylation profiling reveals associations with age, sex, female sex hormones and thyroid cancer
    Chen, Guoqiang
    Wang, Yanmin
    Qiu, Ling
    Qin, Xuzhen
    Liu, Hui
    Wang, Xiaodong
    Wang, Yanying
    Song, Gaoguang
    Li, Fang
    Guo, Yumei
    Li, Fenjie
    Guo, Shuai
    Li, Zhili
    [J]. JOURNAL OF PROTEOMICS, 2012, 75 (10) : 2824 - 2834
  • [10] MUTATION OF THE BETA-AMYLOID PRECURSOR PROTEIN IN FAMILIAL ALZHEIMERS-DISEASE INCREASES BETA-PROTEIN PRODUCTION
    CITRON, M
    OLTERSDORF, T
    HAASS, C
    MCCONLOGUE, L
    HUNG, AY
    SEUBERT, P
    VIGOPELFREY, C
    LIEBERBURG, I
    SELKOE, DJ
    [J]. NATURE, 1992, 360 (6405) : 672 - 674