The role of proteomics in dementia and Alzheimer's disease

被引:48
作者
Zellner, Maria [1 ]
Veitinger, Michael [2 ]
Umlauf, Ellen [2 ]
机构
[1] Med Univ Vienna, Inst Physiol, Ctr Physiol Pathophysiol & Immunol, A-1090 Vienna, Austria
[2] Med Univ Vienna, Surg Res Labs, A-1090 Vienna, Austria
关键词
MILD COGNITIVE IMPAIRMENT; DIFFERENCE GEL-ELECTROPHORESIS; CEREBROSPINAL-FLUID BIOMARKERS; OXIDATIVELY MODIFIED PROTEINS; CREUTZFELDT-JAKOB-DISEASE; NEURONAL GENE-EXPRESSION; DOWN-SYNDROME; BRAIN PROTEINS; REDOX PROTEOMICS; MASS-SPECTROMETRY;
D O I
10.1007/s00401-009-0502-7
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Proteomic analysis enables us to identify dementia-related protein profiles of both genetic and environmental origins. In this review, current proteomics technologies are described including many examples of clinical proteomics studies. Many of these studies present only results of the discovery phase. Progression to the validation phase was achieved by developing more advanced proteomics technologies such as fluorescence two-dimensional differential gel electrophoresis or isobaric tagging for relative and absolute protein quantification. These technologies will lead to the design of several new Alzheimer's disease-related protein panels for the analysis of CSF. On these new panels, established markers such as tau and A beta 42 will be used in combination with novel markers, for example beta-2-microglobulin, brain-derived neurotrophic factor 1 and fragments of cystatin C. However, there are still limitations to using proteomic assays. The preparation of homogeneous sample material is difficult due the complexity of brain tissue. Laser capture microdissection and recently developed more sensitive proteomics methods, for example fluorescence saturation labelling, will overcome these limitations. Combining proteomics with approaches at the level of the genome and transcriptome followed by interpretation by systems biology will soon shed further light on dementia-related pathogenesis.
引用
收藏
页码:181 / 195
页数:15
相关论文
共 116 条
[1]  
Abdi F, 2006, J ALZHEIMERS DIS, V9, P293
[2]   INCREASED ACTIVITY OF BRAIN AND PLATELET MONOAMINE-OXIDASE IN DEMENTIA OF ALZHEIMER TYPE [J].
ADOLFSSON, R ;
GOTTFRIES, CG ;
ORELAND, L ;
WIBERG, A ;
WINBLAD, B .
LIFE SCIENCES, 1980, 27 (12) :1029-1034
[3]   A SERUM-PROTEIN INVOLVED IN AGING [J].
AI, KZ ;
VERMUYTEN, K ;
DEDEYN, PP ;
LOWENTHAL, A ;
KARCHER, D .
MOLECULAR AND CHEMICAL NEUROPATHOLOGY, 1989, 11 (03) :131-141
[4]   Changes in thiol content and expression of glutathione redox system genes in the hippocampus and cerebellum in Alzheimer's disease [J].
Aksenov, MY ;
Markesbery, WR .
NEUROSCIENCE LETTERS, 2001, 302 (2-3) :141-145
[5]   ISOELECTRIC-FOCUSING AND TWO-DIMENSIONAL GEL-ELECTROPHORESIS IN PLASMA AND CEREBROSPINAL-FLUID FROM PATIENTS WITH DEMENTIA [J].
ALAFUZOFF, I ;
ADOLFSSON, R ;
BUCHT, G ;
JELLUM, E ;
MEHTA, PD ;
WINBLAD, B .
EUROPEAN NEUROLOGY, 1986, 25 (04) :285-289
[6]   A novel experimental design for comparative two-dimensional gel analysis: Two-dimensional difference gel electrophoresis incorporating a pooled internal standard [J].
Alban, A ;
David, SO ;
Bjorkesten, L ;
Andersson, C ;
Sloge, E ;
Lewis, S ;
Currie, I .
PROTEOMICS, 2003, 3 (01) :36-44
[7]   DISTRIBUTION OF ALZHEIMER-TYPE PATHOLOGICAL-CHANGES IN NONDEMENTED ELDERLY INDIVIDUALS MATCHES THE PATTERN IN ALZHEIMERS-DISEASE [J].
ARRIAGADA, PV ;
MARZLOFF, K ;
HYMAN, BT .
NEUROLOGY, 1992, 42 (09) :1681-1688
[8]   CSF biomarkers for Alzheimer's disease: use in early diagnosis and evaluation of drug treatment [J].
Blennow, K .
EXPERT REVIEW OF MOLECULAR DIAGNOSTICS, 2005, 5 (05) :661-672
[9]   CSF markers for incipient Alzheimer's disease [J].
Blennow, K ;
Hampel, H .
LANCET NEUROLOGY, 2003, 2 (10) :605-613
[10]   Cerebrospinal fluid-optimized two-dimensional difference gel electrophoresis (2-D DIGE) facilitates the differential diagnosis of Creutzfeldt-Jakob disease [J].
Brechlin, Peter ;
Jahn, Olaf ;
Steinacker, Petra ;
Cepek, Lukas ;
Kratzin, Hartmut ;
Lehnert, Stefan ;
Jesse, Sarah ;
Mollenhauer, Brit ;
Kretzschmar, Hans A. ;
Wiltfang, Jens ;
Otto, Markus .
PROTEOMICS, 2008, 8 (20) :4357-4366